Infantile nystagmus
Gene: GNAI3Comment on list classification: Should remain red as this is a candidate gene.Created: 21 Dec 2016, 12:41 p.m.
Candidate gene for ocular albinism reported in PMID: 27607449. The study involved comparison of GNAI3 gene sequences from 26 patients with ocular albinism who were negative for OA1 variants, and 6 healthy controls. Many variants were identified accross the gene, and though some were not found in the control group, comparison with allele frequencies in available databases such as ExAC was not reported in order to determine whether the variants uniquely found in the patients were rare. No comparisons with family members was reported, therefore segregation with the disease was not confirmed. 6 variants were reported as have likely functional effects due to computation prediction. No in vitro functional work was done to confirm the functional effect of the variants, only computational modelling.Created: 21 Dec 2016, 12:40 p.m.
Mode of inheritance
Unknown
Phenotypes
Ocular Albinism
Publications
21/Dec/2016: panel revised according to expert review, addition of green genes from the Ocular and oculo-cutaneous albinism (Version 1.1) gene panel and further curation.
This gene has been classified as Red List (Low Evidence).
This gene has been classified as Red List (Low Evidence).
Mode of inheritance for GNAI3 was changed to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
GNAI3 was created by ellenmcdonagh
GNAI3 was added to Infantile nystagmuspanel. Sources: Literature