{"count":220504,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2028","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2026","results":[{"created":"2019-12-24T11:04:54.678483+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LRP2 was added\ngene: LRP2 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: LRP2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LRP2 were set to Donnai-Barrow syndrome, MIM#222448\nReview for gene: LRP2 was set to GREEN\nAdded comment: Iris coloboma is part of the phenotype. \nSources: Expert list","entity_name":"LRP2","entity_type":"gene"},{"created":"2019-12-24T11:03:00.951453+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HMX1 as ready","entity_name":"HMX1","entity_type":"gene"},{"created":"2019-12-24T11:03:00.940413+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hmx1 has been classified as Green List (High Evidence).","entity_name":"HMX1","entity_type":"gene"},{"created":"2019-12-24T11:02:56.312908+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HMX1 as Green List (high evidence)","entity_name":"HMX1","entity_type":"gene"},{"created":"2019-12-24T11:02:56.302196+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hmx1 has been classified as Green List (High Evidence).","entity_name":"HMX1","entity_type":"gene"},{"created":"2019-12-24T11:02:29.368975+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HMX1 was added\ngene: HMX1 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: HMX1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HMX1 were set to Oculoauricular syndrome, MIM#612109\nReview for gene: HMX1 was set to GREEN\nAdded comment: Microphthalmia and ocular coloboma are part of the phenotype. \nSources: Expert list","entity_name":"HMX1","entity_type":"gene"},{"created":"2019-12-24T11:00:28.841017+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLDN19 as ready","entity_name":"CLDN19","entity_type":"gene"},{"created":"2019-12-24T11:00:28.827566+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn19 has been classified as Green List (High Evidence).","entity_name":"CLDN19","entity_type":"gene"},{"created":"2019-12-24T11:00:25.235672+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLDN19 as Green List (high evidence)","entity_name":"CLDN19","entity_type":"gene"},{"created":"2019-12-24T11:00:25.224787+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn19 has been classified as Green List (High Evidence).","entity_name":"CLDN19","entity_type":"gene"},{"created":"2019-12-24T10:59:57.689141+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CLDN19 was added\ngene: CLDN19 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: CLDN19 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CLDN19 were set to Hypomagnesemia 5, renal, with ocular involvement, MIM#248190\nReview for gene: CLDN19 was set to GREEN\nAdded comment: Macular coloboma is part of the phenotype. \nSources: Expert list","entity_name":"CLDN19","entity_type":"gene"},{"created":"2019-12-24T10:58:13.317113+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CC2D2A as ready","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2019-12-24T10:58:13.306220+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cc2d2a has been classified as Green List (High Evidence).","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2019-12-24T10:58:07.953614+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CC2D2A as Green List (high evidence)","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2019-12-24T10:58:07.942993+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cc2d2a has been classified as Green List (High Evidence).","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2019-12-24T10:57:40.184069+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CC2D2A was added\ngene: CC2D2A was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: CC2D2A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CC2D2A were set to COACH syndrome, MIM#216360\nReview for gene: CC2D2A was set to GREEN\nAdded comment: Ocular coloboma is part of the phenotype. \nSources: Expert list","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2019-12-24T10:55:30.142965+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C12orf57 as ready","entity_name":"C12orf57","entity_type":"gene"},{"created":"2019-12-24T10:55:30.131686+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c12orf57 has been classified as Green List (High Evidence).","entity_name":"C12orf57","entity_type":"gene"},{"created":"2019-12-24T10:55:25.352207+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C12orf57 as Green List (high evidence)","entity_name":"C12orf57","entity_type":"gene"},{"created":"2019-12-24T10:55:25.340690+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c12orf57 has been classified as Green List (High Evidence).","entity_name":"C12orf57","entity_type":"gene"},{"created":"2019-12-24T10:54:56.886988+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"gene: C12orf57 was added\ngene: C12orf57 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: C12orf57 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: C12orf57 were set to Temtamy syndrome, MIM#218340\nReview for gene: C12orf57 was set to GREEN\nAdded comment: Ocular coloboma is part of the phenotype. \nSources: Expert list","entity_name":"C12orf57","entity_type":"gene"},{"created":"2019-12-24T10:52:49.983367+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B3GLCT as ready","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2019-12-24T10:52:49.972461+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3glct has been classified as Green List (High Evidence).","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2019-12-24T10:52:45.951928+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B3GLCT as Green List (high evidence)","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2019-12-24T10:52:45.940993+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3glct has been classified as Green List (High Evidence).","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2019-12-24T10:52:17.614120+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"gene: B3GLCT was added\ngene: B3GLCT was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: B3GLCT was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: B3GLCT were set to Peters-plus syndrome, MIM#261540\nReview for gene: B3GLCT was set to GREEN\nAdded comment: Retinal coloboma is part of the phenotype. \nSources: Expert list","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2019-12-24T10:50:28.112249+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACTG1 as ready","entity_name":"ACTG1","entity_type":"gene"},{"created":"2019-12-24T10:50:28.101013+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actg1 has been classified as Green List (High Evidence).","entity_name":"ACTG1","entity_type":"gene"},{"created":"2019-12-24T10:50:23.147336+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACTG1 as Green List (high evidence)","entity_name":"ACTG1","entity_type":"gene"},{"created":"2019-12-24T10:50:23.135028+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actg1 has been classified as Green List (High Evidence).","entity_name":"ACTG1","entity_type":"gene"},{"created":"2019-12-24T10:49:55.703611+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ACTG1 was added\ngene: ACTG1 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: ACTG1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: ACTG1 were set to Baraitser-Winter syndrome 2, MIM#614583\nReview for gene: ACTG1 was set to GREEN\nAdded comment: Microphthalmia and coloboma are part of the phenotype. \nSources: Expert list","entity_name":"ACTG1","entity_type":"gene"},{"created":"2019-12-24T10:48:10.169673+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACTB as ready","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-24T10:48:10.156969+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actb has been classified as Green List (High Evidence).","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-24T10:48:04.886169+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACTB as Green List (high evidence)","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-24T10:48:04.874825+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actb has been classified as Green List (High Evidence).","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-24T10:47:37.751997+11:00","panel_name":"Anophthalmia, microphthalmia, coloboma_VCGS","panel_id":42,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ACTB was added\ngene: ACTB was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: ACTB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: ACTB were set to Baraitser-Winter syndrome 1, MIM#243310\nReview for gene: ACTB was set to GREEN\nAdded comment: Iris coloboma is part of the phenotype. \nSources: Expert list","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-24T10:34:12.585689+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ZNF513 was added\ngene: ZNF513 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ZNF513 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ZNF513 were set to Retinitis pigmentosa 58, 613617","entity_name":"ZNF513","entity_type":"gene"},{"created":"2019-12-24T10:34:12.511296+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ZNF408 was added\ngene: ZNF408 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ZNF408 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: ZNF408 were set to Retinitis pigmentosa 72; Familial exudative vitreoretinopathy (FEVR)","entity_name":"ZNF408","entity_type":"gene"},{"created":"2019-12-24T10:34:12.432040+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ZFYVE26 was added\ngene: ZFYVE26 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: ZFYVE26 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ZFYVE26 were set to 18394578\nPhenotypes for gene: ZFYVE26 were set to Spastic paraplegia 15","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2019-12-24T10:34:12.353141+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: USH2A was added\ngene: USH2A was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: USH2A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: USH2A were set to Retinitis pigmentosa 39, 613809; Usher syndrome, type 2A, 276901","entity_name":"USH2A","entity_type":"gene"},{"created":"2019-12-24T10:34:12.278375+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: USH1C was added\ngene: USH1C was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: USH1C was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: USH1C were set to Usher syndrome, type 1C","entity_name":"USH1C","entity_type":"gene"},{"created":"2019-12-24T10:34:12.205788+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TULP1 was added\ngene: TULP1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TULP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TULP1 were set to Leber congenital amaurosis 15, 613843; Retinitis pigmentosa 14, 600132","entity_name":"TULP1","entity_type":"gene"},{"created":"2019-12-24T10:34:12.129808+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TTC8 was added\ngene: TTC8 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TTC8 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TTC8 were set to Retinitis pigmentosa 51, 613464; Bardet-Biedl syndrome 8, 209900","entity_name":"TTC8","entity_type":"gene"},{"created":"2019-12-24T10:34:11.983263+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TRNT1 was added\ngene: TRNT1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TRNT1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TRNT1 were set to Retinitis pigmentosa and erythrocytic microcytosis","entity_name":"TRNT1","entity_type":"gene"},{"created":"2019-12-24T10:34:11.908335+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SPATA7 was added\ngene: SPATA7 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SPATA7 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SPATA7 were set to Leber Congenital Amaurosis; Retinitis pigmentosa, juvenile, autosomal recessive, 604232; Leber congenital amaurosis 3","entity_name":"SPATA7","entity_type":"gene"},{"created":"2019-12-24T10:34:11.827247+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SLC7A14 was added\ngene: SLC7A14 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: SLC7A14 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC7A14 were set to 27028480; 24670872\nPhenotypes for gene: SLC7A14 were set to Retinitis pigmentosa 68, 615725 (3)","entity_name":"SLC7A14","entity_type":"gene"},{"created":"2019-12-24T10:34:11.750052+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SEMA4A was added\ngene: SEMA4A was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SEMA4A was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: SEMA4A were set to Cone-rod dystrophy 10, 610283; Retinitis pigmentosa 35, 610282","entity_name":"SEMA4A","entity_type":"gene"},{"created":"2019-12-24T10:34:11.676969+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SAMD11 was added\ngene: SAMD11 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: SAMD11 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SAMD11 were set to 27734943\nPhenotypes for gene: SAMD11 were set to Autosomal recessive retinitis pigmentosa","entity_name":"SAMD11","entity_type":"gene"},{"created":"2019-12-24T10:34:11.604307+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SAG was added\ngene: SAG was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SAG was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SAG were set to Oguchi disease-1, 258100; Retinitis  pigmentosa 47","entity_name":"SAG","entity_type":"gene"},{"created":"2019-12-24T10:34:11.529718+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RPGRIP1 was added\ngene: RPGRIP1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RPGRIP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RPGRIP1 were set to Leber congenital amaurosis 6, 613826; Cone-rod dystrophy 13, 608194","entity_name":"RPGRIP1","entity_type":"gene"},{"created":"2019-12-24T10:34:11.451910+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RPGR was added\ngene: RPGR was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RPGR was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPhenotypes for gene: RPGR were set to Cone-rod dystrophy, X-linked, 1, 304020; Macular degeneration, X-linked atrophic, 300834; Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness, 300455; Retinitis pigmentosa 3, 300029","entity_name":"RPGR","entity_type":"gene"},{"created":"2019-12-24T10:34:11.380307+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RPE65 was added\ngene: RPE65 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RPE65 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RPE65 were set to Retinitis  pigmentosa 20; Leber congenital amaurosis 2, 204100","entity_name":"RPE65","entity_type":"gene"},{"created":"2019-12-24T10:34:11.308058+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RP2 was added\ngene: RP2 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RP2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: RP2 were set to Retinitis Pigmentosa, X-linked; Retinitis pigmentosa 2, 312600","entity_name":"RP2","entity_type":"gene"},{"created":"2019-12-24T10:34:11.235392+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RP1L1 was added\ngene: RP1L1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RP1L1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: RP1L1 were set to 31833436; 31236346; 30025130\nPhenotypes for gene: RP1L1 were set to retinitis pigmentosa; Occult macular dystrophy, 613587","entity_name":"RP1L1","entity_type":"gene"},{"created":"2019-12-24T10:34:11.163774+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RP1 was added\ngene: RP1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RP1 were set to Retinitis pigmentosa 1, 180100","entity_name":"RP1","entity_type":"gene"},{"created":"2019-12-24T10:34:11.086293+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RLBP1 was added\ngene: RLBP1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RLBP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RLBP1 were set to Retinitis punctata  albescens; Newfoundland rod - cone dystrophy; Fundus albipunctatus, 136880; Fundus  albipunctatus; Bothnia retinal  dystrophy","entity_name":"RLBP1","entity_type":"gene"},{"created":"2019-12-24T10:34:11.011057+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RHO was added\ngene: RHO was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RHO was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RHO were set to Retinitis pigmentosa 4, autosomal dominant or recessive, 613731; Retinitis punctata albescens; Congenital Stationary Night Blindness","entity_name":"RHO","entity_type":"gene"},{"created":"2019-12-24T10:34:10.937030+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RGR was added\ngene: RGR was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RGR was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RGR were set to Retinitis pigmentosa 44, 613769","entity_name":"RGR","entity_type":"gene"},{"created":"2019-12-24T10:34:10.856536+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: REEP6 was added\ngene: REEP6 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: REEP6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: REEP6 were set to Retinitis pigmentosa 77","entity_name":"REEP6","entity_type":"gene"},{"created":"2019-12-24T10:34:10.785861+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RDH12 was added\ngene: RDH12 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RDH12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RDH12 were set to Leber congenital amaurosis 13, 612712; Retinitis Pigmentosa, Recessive","entity_name":"RDH12","entity_type":"gene"},{"created":"2019-12-24T10:34:10.713850+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RD3 was added\ngene: RD3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RD3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RD3 were set to Leber congenital amaurosis 12, 610612","entity_name":"RD3","entity_type":"gene"},{"created":"2019-12-24T10:34:10.642966+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RBP3 was added\ngene: RBP3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RBP3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RBP3 were set to 19074801; 25766589; 19357286; 9614228\nPhenotypes for gene: RBP3 were set to Retinitis pigmentosa 66, 615233","entity_name":"RBP3","entity_type":"gene"},{"created":"2019-12-24T10:34:10.568383+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PROM1 was added\ngene: PROM1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PROM1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: PROM1 were set to Stargardt disease 4, 603786; Macular dystrophy, retinal, 2, 608051; Retinitis pigmentosa 41, 612095; Cone-rod dystrophy 12, 612657","entity_name":"PROM1","entity_type":"gene"},{"created":"2019-12-24T10:34:10.497955+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PRCD was added\ngene: PRCD was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PRCD was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PRCD were set to Retinitis pigmentosa 36, 610599","entity_name":"PRCD","entity_type":"gene"},{"created":"2019-12-24T10:34:10.428072+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: POMGNT1 was added\ngene: POMGNT1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: POMGNT1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: POMGNT1 were set to Retinitis pigmentosa 76","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2019-12-24T10:34:10.358734+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PMPCA was added\ngene: PMPCA was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Red\nMode of inheritance for gene: PMPCA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PMPCA were set to Spinocerebellar ataxia, autosomal recessive 2","entity_name":"PMPCA","entity_type":"gene"},{"created":"2019-12-24T10:34:10.288340+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PLA2G5 was added\ngene: PLA2G5 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Red\nMode of inheritance for gene: PLA2G5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PLA2G5 were set to Fleck retina, familial benign","entity_name":"PLA2G5","entity_type":"gene"},{"created":"2019-12-24T10:34:10.218276+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PHYH was added\ngene: PHYH was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PHYH was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PHYH were set to Refsum disease","entity_name":"PHYH","entity_type":"gene"},{"created":"2019-12-24T10:34:10.145320+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PEX7 was added\ngene: PEX7 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PEX7 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PEX7 were set to Refsum disease","entity_name":"PEX7","entity_type":"gene"},{"created":"2019-12-24T10:34:10.000255+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PDE6G was added\ngene: PDE6G was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PDE6G was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PDE6G were set to Retinitis pigmentosa 57, 613582","entity_name":"PDE6G","entity_type":"gene"},{"created":"2019-12-24T10:34:09.930687+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PDE6B was added\ngene: PDE6B was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PDE6B was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: PDE6B were set to Retinitis  pigmentosa 40; Night blindness,  congenital  stationary,  autosomal  dominant 2","entity_name":"PDE6B","entity_type":"gene"},{"created":"2019-12-24T10:34:09.857494+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PDE6A was added\ngene: PDE6A was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PDE6A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PDE6A were set to Retinitis pigmentosa 43, 613810","entity_name":"PDE6A","entity_type":"gene"},{"created":"2019-12-24T10:34:09.769762+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: C2orf71 was added\ngene: C2orf71 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: C2orf71 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: C2orf71 were set to Retinitis pigmentosa 54","entity_name":"C2orf71","entity_type":"gene"},{"created":"2019-12-24T10:34:09.696959+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: OFD1 was added\ngene: OFD1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: OFD1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: OFD1 were set to 28191358; 22619378; 29843741\nPhenotypes for gene: OFD1 were set to Retinitis pigmentosa 23, 300424; Joubert syndrome 10, 300804; Orofaciodigital syndrome I, 311200Simpson-Golabi-Behmel syndrome, type 2, 300209","entity_name":"OFD1","entity_type":"gene"},{"created":"2019-12-24T10:34:09.626387+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: OAT was added\ngene: OAT was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: OAT was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: OAT were set to Gyrate atrophy of choroid and retina","entity_name":"OAT","entity_type":"gene"},{"created":"2019-12-24T10:34:09.551682+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: NRL was added\ngene: NRL was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: NRL was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: NRL were set to Retinitis  pigmentosa 27 (AD); Retinal  degeneration,  autosomal  recessive, clumped pigment type (AR)","entity_name":"NRL","entity_type":"gene"},{"created":"2019-12-24T10:34:09.472705+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: NR2E3 was added\ngene: NR2E3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: NR2E3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: NR2E3 were set to Enhanced S - cone syndrome (AR); Retinitis  pigmentosa 37 (AD and AR)","entity_name":"NR2E3","entity_type":"gene"},{"created":"2019-12-24T10:34:09.402527+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: NEUROD1 was added\ngene: NEUROD1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: NEUROD1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NEUROD1 were set to 25477324; 29521454; 25684977\nPhenotypes for gene: NEUROD1 were set to ?retinitis pigmentosa; neonatal diabetes, systematic neurological abnormalities, and early-onset retinal dystrophy","entity_name":"NEUROD1","entity_type":"gene"},{"created":"2019-12-24T10:34:09.330674+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: NEK2 was added\ngene: NEK2 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: NEK2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NEK2 were set to 24043777\nPhenotypes for gene: NEK2 were set to ?Retinitis pigmentosa 67, 615565","entity_name":"NEK2","entity_type":"gene"},{"created":"2019-12-24T10:34:09.254183+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: MVK was added\ngene: MVK was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: MVK was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: MVK were set to Mevalonic aciduria; Hyper-IgD syndrome","entity_name":"MVK","entity_type":"gene"},{"created":"2019-12-24T10:34:09.184563+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: MFRP was added\ngene: MFRP was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: MFRP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: MFRP were set to Posterior Microphthalmia with Retinitis Pigmentosa, Foveoschisis, and Optic Disc Drusen","entity_name":"MFRP","entity_type":"gene"},{"created":"2019-12-24T10:34:09.107984+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: MERTK was added\ngene: MERTK was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: MERTK was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: MERTK were set to childhood onset rod-cone dystrophy with early macular atrophy; Leber congenital amaurosisRetinitis pigmentosa 38, 613862","entity_name":"MERTK","entity_type":"gene"},{"created":"2019-12-24T10:34:08.964264+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: MAK was added\ngene: MAK was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: MAK was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: MAK were set to Retinitis pigmentosa 62, 614181","entity_name":"MAK","entity_type":"gene"},{"created":"2019-12-24T10:34:08.890567+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: LRAT was added\ngene: LRAT was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: LRAT was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LRAT were set to Leber Congenital Amaurosis; Leber congenital  amaurosis 14; Retinitis  pigmentosa,  juvenile; Retinal dystrophy, early-onset severe, 613341","entity_name":"LRAT","entity_type":"gene"},{"created":"2019-12-24T10:34:08.816736+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: LCA5 was added\ngene: LCA5 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: LCA5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LCA5 were set to Leber congenital amaurosis 5, 604537","entity_name":"LCA5","entity_type":"gene"},{"created":"2019-12-24T10:34:08.746294+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: KIZ was added\ngene: KIZ was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: KIZ was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: KIZ were set to Retinitis pigmentosa 69","entity_name":"KIZ","entity_type":"gene"},{"created":"2019-12-24T10:34:08.678016+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: KIAA1549 was added\ngene: KIAA1549 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: KIAA1549 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: KIAA1549 were set to Retinitis pigmentosa 86","entity_name":"KIAA1549","entity_type":"gene"},{"created":"2019-12-24T10:34:08.607683+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: IMPG2 was added\ngene: IMPG2 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: IMPG2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: IMPG2 were set to Retinitis pigmentosa 56, 613581; Maculopathy,  IMPG2 - related; Retinitis pigmentosa","entity_name":"IMPG2","entity_type":"gene"},{"created":"2019-12-24T10:34:08.538823+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: IFT172 was added\ngene: IFT172 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: IFT172 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: IFT172 were set to Retinitis pigmentosa 71","entity_name":"IFT172","entity_type":"gene"},{"created":"2019-12-24T10:34:08.471461+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: IFT140 was added\ngene: IFT140 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: IFT140 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: IFT140 were set to Retinitis pigmentosa 80","entity_name":"IFT140","entity_type":"gene"},{"created":"2019-12-24T10:34:08.403715+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: IDH3B was added\ngene: IDH3B was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: IDH3B was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: IDH3B were set to Retinitis pigmentosa 46, 612572","entity_name":"IDH3B","entity_type":"gene"},{"created":"2019-12-24T10:34:08.336915+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: HGSNAT was added\ngene: HGSNAT was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: HGSNAT was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HGSNAT were set to Retinitis pigmentosa 73","entity_name":"HGSNAT","entity_type":"gene"},{"created":"2019-12-24T10:34:08.268299+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: GUCY2D was added\ngene: GUCY2D was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GUCY2D was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: GUCY2D were set to Achromatopsia, Cone, and Cone-rod Dystrophy; Cone-rod dystrophy 6 (AD); Leber congenital amaurosis 1, 204000; Retinitis pigmentosa","entity_name":"GUCY2D","entity_type":"gene"},{"created":"2019-12-24T10:34:08.199591+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: FLVCR1 was added\ngene: FLVCR1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: FLVCR1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: FLVCR1 were set to Ataxia, posterior column, with retinitis pigmentosa, 609033","entity_name":"FLVCR1","entity_type":"gene"},{"created":"2019-12-24T10:34:08.130550+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: FAM161A was added\ngene: FAM161A was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: FAM161A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: FAM161A were set to Retinitis pigmentosa 28, 606068","entity_name":"FAM161A","entity_type":"gene"},{"created":"2019-12-24T10:34:08.063792+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: EYS was added\ngene: EYS was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: EYS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: EYS were set to Retinitis pigmentosa 25, 602772","entity_name":"EYS","entity_type":"gene"},{"created":"2019-12-24T10:34:07.982337+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: EMC1 was added\ngene: EMC1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: EMC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EMC1 were set to 29271071; 23105016\nPhenotypes for gene: EMC1 were set to ?Retinitis pigmentosa; Cerebellar atrophy, visual impairment, and psychomotor retardation","entity_name":"EMC1","entity_type":"gene"},{"created":"2019-12-24T10:34:07.914804+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: DHX38 was added\ngene: DHX38 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: DHX38 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DHX38 were set to Retinitis pigmentosa 84, 618220","entity_name":"DHX38","entity_type":"gene"},{"created":"2019-12-24T10:34:07.846640+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: DHDDS was added\ngene: DHDDS was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: DHDDS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DHDDS were set to Retinitis pigmentosa 59, 613861","entity_name":"DHDDS","entity_type":"gene"},{"created":"2019-12-24T10:34:07.778277+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CYP4V2 was added\ngene: CYP4V2 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CYP4V2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CYP4V2 were set to Retinitis pigmentosa; Bietti crystalline corneoretinal dystrophy, 210370","entity_name":"CYP4V2","entity_type":"gene"}]}