Entrez Gene ID | 1288 |
---|---|
Official Gene Symbol | COL4A6 (GeneCards) |
Full name | collagen type IV alpha 6 chain |
Location | Xq22.3 |
Other ids | Vega : OTTHUMG00000022179 MIM : 303631 HGNC : HGNC:2208 Ensembl : ENSG00000197565 |
Other names | DFNX6, DELXq22.3, CXDELq22.3 |
Summary | This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013] |
Found 3 variants in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
1232 | 1288 | COL4A6 | X | 107414663 | 107414663 | Autism Spectrum Disorders | NextSeq500 v2 |
24143 | 1288 | COL4A6 | X | 107571866 | 107571866 | Asymptomatic | NextSeq500 v2 Single cell Sequencing Cell cloning |
29036 | 1288 | COL4A6 | X | 107594757 | 107594757 | Asymptomatic | NextSeq500 v2 Single cell Sequencing Cell cloning |