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Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Marked gene: SEPT9 as ready
Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Added comment: Comment when marking as ready: New HGNC approved name is SEPTIN9.
Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Gene: sept9 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Tag new gene name tag was added to gene: SEPT9.
Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Tag SV/CNV tag was added to gene: SEPT9.
Tag 5'UTR tag was added to gene: SEPT9.
Tag founder tag was added to gene: SEPT9.
Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Marked gene: SEPT9 as ready
Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Gene: sept9 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.170 SEPT9 Zornitza Stark Phenotypes for gene: SEPT9 were changed from Amyotrophy, hereditary neuralgic; HMSN to Amyotrophy, hereditary neuralgic, MIM# 162100; HMSN
Hereditary Neuropathy_CMT - isolated v0.169 SEPT9 Zornitza Stark Publications for gene: SEPT9 were set to
Hereditary Neuropathy_CMT - isolated v0.168 SEPT9 Zornitza Stark Mode of inheritance for gene: SEPT9 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy_CMT - isolated v0.167 SEPT9 Zornitza Stark reviewed gene: SEPT9: Rating: GREEN; Mode of pathogenicity: None; Publications: 16186812, 19451530, 19939853, 19139049; Phenotypes: Amyotrophy, hereditary neuralgic, MIM# 162100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy_CMT - isolated v0.0 SEPT9 Bryony Thompson gene: SEPT9 was added
gene: SEPT9 was added to Hereditary Neuropathy - isolated_RMH. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: SEPT9 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: SEPT9 were set to Amyotrophy, hereditary neuralgic; HMSN