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Intellectual disability syndromic and non-syndromic v0.5779 ACBD6 Zornitza Stark Phenotypes for gene: ACBD6 were changed from Neurodevelopmental disorder (MONDO#0700092), ACBD6-related to Neurodevelopmental disorder with progressive movement abnormalities, MIM# 620785
Intellectual disability syndromic and non-syndromic v0.5778 ACBD6 Zornitza Stark reviewed gene: ACBD6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with progressive movement abnormalities, MIM# 620785; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.5239 ACBD6 Elena Savva Classified gene: ACBD6 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.5239 ACBD6 Elena Savva Gene: acbd6 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5237 ACBD6 Elena Savva Classified gene: ACBD6 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.5237 ACBD6 Elena Savva Gene: acbd6 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5238 ACBD6 Elena Savva Marked gene: ACBD6 as ready
Intellectual disability syndromic and non-syndromic v0.5238 ACBD6 Elena Savva Gene: acbd6 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5238 ACBD6 Elena Savva Classified gene: ACBD6 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.5238 ACBD6 Elena Savva Gene: acbd6 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5234 ACBD6 Lucy Spencer gene: ACBD6 was added
gene: ACBD6 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: ACBD6 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ACBD6 were set to 36457943; 21937992; 35446914
Phenotypes for gene: ACBD6 were set to Neurodevelopmental disorder (MONDO#0700092), ACBD6-related
Review for gene: ACBD6 was set to GREEN
Added comment: PMID: 36457943
2 siblings with a neurodevelopmental disorder: severely delayed development, obesity, pancytopenia, diabetes, liver cirrhosis, intravertebral disc herniation, mild brain atrophy. Consanguineous family both siblings found to have a homozygous frameshift.

This paper also mentioned 3 other reported variants in 6 individuals (only 3 unrelated) all homozygous, 2 frameshift, 1 canonical splice. All reported to have a neurodevelopmental disorder, some with limited information but one family also has obesity, spasticity, and dysmorphism. PMIDs: 21937992, 35446914
Sources: Literature