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Pigmentary skin disorders v1.43 USP9X Arina Puzriakova Tag Q4_21_rating was removed from gene: USP9X.
Tag Q4_21_NHS_review was removed from gene: USP9X.
Pigmentary skin disorders v1.42 USP9X Arina Puzriakova commented on gene: USP9X
Pigmentary skin disorders v1.41 USP9X Arina Puzriakova Source Expert Review Green was added to USP9X.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Pigmentary skin disorders v1.37 USP9X Ivone Leong Tag Q4_21_rating tag was added to gene: USP9X.
Tag Q4_21_NHS_review tag was added to gene: USP9X.
Pigmentary skin disorders v1.37 USP9X Ivone Leong Classified gene: USP9X as Amber List (moderate evidence)
Pigmentary skin disorders v1.37 USP9X Ivone Leong Added comment: Comment on list classification: New gene added by Tom Cullup (Great Ormond Street Hospital). This gene is associated with a phenotype in OMIM and Gene2Phenotype (probable). There is enough evidence to support a gene-disease association, this gene should be rated Green at the next review.
Pigmentary skin disorders v1.37 USP9X Ivone Leong Gene: usp9x has been classified as Amber List (Moderate Evidence).
Pigmentary skin disorders v1.36 USP9X Ivone Leong Phenotypes for gene: USP9X were changed from Intellectual developmental disorder, X-linked 99, syndromic, female-restricted, OMIM:300968; Intellectual developmental disorder, X-linked 99, OMIM:300072 to Intellectual developmental disorder, X-linked 99, syndromic, female-restricted, OMIM:300968
Pigmentary skin disorders v1.35 USP9X Ivone Leong Phenotypes for gene: USP9X were changed from INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED to Intellectual developmental disorder, X-linked 99, syndromic, female-restricted, OMIM:300968; Intellectual developmental disorder, X-linked 99, OMIM:300072
Pigmentary skin disorders v1.16 USP9X Tom Cullup gene: USP9X was added
gene: USP9X was added to Pigmentary skin disorders. Sources: Expert list
Mode of inheritance for gene: USP9X was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: USP9X were set to 26833328
Phenotypes for gene: USP9X were set to INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED
Penetrance for gene: USP9X were set to unknown
Review for gene: USP9X was set to GREEN
Added comment: Sources: Expert list