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Hereditary Neuropathy_CMT - isolated v1.66 DNMT1 Chirag Patel Source Royal Melbourne Hospital was removed from DNMT1.
Source ClinGen was added to DNMT1.
Source Literature was added to DNMT1.
Phenotypes for gene: DNMT1 were changed from Neuropathy, hereditary sensory, type IE, 614116; Dementia, Deafness, and Sensory Neuropathy; HSAN/SFN to Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Publications for gene DNMT1 were changed from 22328086, 23904686, 24727570, 25678562, 23521649, 23365052, 21532572, 27602171, 25033457, 31984424 to 22328086, 23904686, 24727570, 25678562, 23521649, 23365052, 21532572, 27602171, 25033457, 31984424
Hereditary Neuropathy_CMT - isolated v0.82 DNMT1 Zornitza Stark Marked gene: DNMT1 as ready
Hereditary Neuropathy_CMT - isolated v0.82 DNMT1 Zornitza Stark Gene: dnmt1 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.82 DNMT1 Zornitza Stark Publications for gene: DNMT1 were set to
Hereditary Neuropathy_CMT - isolated v0.0 DNMT1 Bryony Thompson gene: DNMT1 was added
gene: DNMT1 was added to Hereditary Neuropathy - isolated_RMH. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: DNMT1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: DNMT1 were set to Neuropathy, hereditary sensory, type IE, 614116; Dementia, Deafness, and Sensory Neuropathy; HSAN/SFN