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Ophthalmological ciliopathies v1.30 C8orf37 Arina Puzriakova commented on gene: C8orf37
Ophthalmological ciliopathies v1.30 C8orf37 Arina Puzriakova Tag new-gene-name tag was added to gene: C8orf37.
Ophthalmological ciliopathies v1.27 C8orf37 Ivone Leong Tag for-review was removed from gene: C8orf37.
Ophthalmological ciliopathies v1.27 C8orf37 Ivone Leong commented on gene: C8orf37: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Ophthalmological ciliopathies v1.27 C8orf37 Ivone Leong Source Expert Review Green was added to C8orf37.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ophthalmological ciliopathies v1.13 C8orf37 Ivone Leong Classified gene: C8orf37 as Amber List (moderate evidence)
Ophthalmological ciliopathies v1.13 C8orf37 Ivone Leong Added comment: Comment on list classification: This gene is associated with a relevant phenotype in OMIM and Gene2Phenotype. There is enough evidence to support a gene-disease association. This gene should be promoted to Green at the next review.
Ophthalmological ciliopathies v1.13 C8orf37 Ivone Leong Gene: c8orf37 has been classified as Amber List (Moderate Evidence).
Ophthalmological ciliopathies v1.12 C8orf37 Ivone Leong Tag for-review tag was added to gene: C8orf37.
Ophthalmological ciliopathies v1.12 C8orf37 Ivone Leong Publications for gene: C8orf37 were set to 26854863; 27008867
Ophthalmological ciliopathies v1.11 C8orf37 Ivone Leong Phenotypes for gene: C8orf37 were changed from Bardet-Biedl syndrome 21, 617406 to Bardet-Biedl syndrome 21, OMIM:617406, MONDO:0044308; Cone-rod dystrophy 16, OMIM:614500, MONDO:0013786; Retinitis pigmentosa 64, OMIM:614500, MONDO:0019200
Ophthalmological ciliopathies v1.4 C8orf37 Zornitza Stark reviewed gene: C8orf37: Rating: GREEN; Mode of pathogenicity: None; Publications: 27008867, 26854863, 22177090, 25113443, 2686542625802487; Phenotypes: Bardet-Biedl syndrome 21 617406, Cone-rod dystrophy 16 614500, Retinitis pigmentosa 64 614500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Ophthalmological ciliopathies v0.1 C8orf37 Ivone Leong gene: C8orf37 was added
gene: C8orf37 was added to Ophthalmological ciliopathies. Sources: Other,Expert Review Red
Mode of inheritance for gene: C8orf37 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: C8orf37 were set to 26854863; 27008867
Phenotypes for gene: C8orf37 were set to Bardet-Biedl syndrome 21, 617406