Renal and urinary tract disorders
Gene: COL4A4EnsemblGeneIds (GRCh38): ENSG00000081052
EnsemblGeneIds (GRCh37): ENSG00000081052
OMIM: 120131, Gene2Phenotype
COL4A4 is in 9 panels
1 review
Sarah Leigh (Genomics England Curator)
Comment when marking as ready: Associated with phenotype in OMIM and G2P. Numerous variants reportedCreated: 4 Aug 2016, 11:43 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Phenotypes
-
- Alport syndrome, autosomal recessive, 203780
- Hematuria,familial benign
- OMIM
- 120131
- Clinvar variants
- Variants in COL4A4
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Eleanor Williams (Genomics England Curator)Sarah Leigh: Comment when marking as ready:
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: COL4A4 was added gene: COL4A4 was added to Renal and urinary tract disorders. Sources: Expert Review Green Mode of inheritance for gene: COL4A4 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: COL4A4 were set to 25381091 Phenotypes for gene: COL4A4 were set to Alport syndrome, autosomal recessive, 203780; Hematuria,familial benign