Ocular and Oculocutaneous Albinism
Gene: DCTEnsemblGeneIds (GRCh38): ENSG00000080166
EnsemblGeneIds (GRCh37): ENSG00000080166
OMIM: 191275, Gene2Phenotype
DCT is in 3 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Two unrelated families reported. Functional data including mouse model.
Sources: LiteratureCreated: 31 Jan 2021, 6:26 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Oculocutaneous albinism, type VIII, MIM# 619165
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Oculocutaneous albinism, type VIII, MIM# 619165
- OMIM
- 191275
- Clinvar variants
- Variants in DCT
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: dct has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: dct has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: DCT was added gene: DCT was added to Ocular and Oculocutaneous Albinism. Sources: Literature Mode of inheritance for gene: DCT was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DCT were set to 33100333 Phenotypes for gene: DCT were set to Oculocutaneous albinism, type VIII, MIM# 619165 Review for gene: DCT was set to GREEN