ITGA8 Chromosome 10
Integrin subunit alpha 8
Upload your DNA to see your personal genotypes for variants in ITGA8.
What This Gene Does
Integrins are heterodimeric transmembrane receptor proteins that mediate numerous cellular processes including cell adhesion, cytoskeletal rearrangement, and activation of cell signaling pathways. Integrins are composed of alpha and beta subunits. This gene encodes the alpha 8 subunit of the heterodimeric integrin alpha8beta1 protein. The encoded protein is a single-pass type 1 membrane protein that contains multiple FG-GAP repeats. This repeat is predicted to fold into a beta propeller structure. This gene regulates the recruitment of mesenchymal cells into epithelial structures, mediates cell-cell interactions, and regulates neurite outgrowth of sensory and motor neurons. The integrin alpha8beta1 protein thus plays an important role in wound-healing and organogenesis. Mutations in this gene have been associated with renal hypodysplasia/aplasia-1 (RHDA1) and with several animal models of chronic kidney disease. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2014]
Gene Info
Gene Group
Integrin alpha subunits
Locus Type
gene with protein product
Location
10p13
Ensembl
ENSG00000077943
Associated Conditions (3)
Inborn genetic diseases
Renal hypodysplasia/aplasia 1
ITGA8-related disorder
Key Variants
RS147784534
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS150922478
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS151036773
Conflicting classifications of pathogenicity
Renal hypodysplasia/aplasia 1, Inborn genetic diseases, Renal hypodysplasia/aplasia 1
Health Risk
RS1241945430
Likely pathogenic
Health Risk
RS1358182981
Likely pathogenic
Health Risk
RS2491052121
Likely pathogenic
Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1
Health Risk
RS749220565
Likely pathogenic
Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1
Health Risk
RS765166981
Likely pathogenic
Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1
Health Risk
RS1554775668
Pathogenic
Health Risk
RS2491851327
Pathogenic
Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1
Health Risk
RS374664941
Pathogenic
Renal hypodysplasia/aplasia 1, ITGA8-related disorder, Renal hypodysplasia/aplasia 1
Health Risk
RS587777280
Pathogenic
Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1
Health Risk
All Variants (13)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS147784534 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS150922478 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS151036773 | Health Risk | Conflicting classifications of pathogenicity | Renal hypodysplasia/aplasia 1, Inborn genetic diseases, Renal hypodysplasia/aplasia 1 |
| RS1241945430 | Health Risk | Likely pathogenic | — |
| RS1358182981 | Health Risk | Likely pathogenic | — |
| RS2491052121 | Health Risk | Likely pathogenic | Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1 |
| RS749220565 | Health Risk | Likely pathogenic | Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1 |
| RS765166981 | Health Risk | Likely pathogenic | Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1 |
| RS1554775668 | Health Risk | Pathogenic | — |
| RS2491851327 | Health Risk | Pathogenic | Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1 |
| RS374664941 | Health Risk | Pathogenic | Renal hypodysplasia/aplasia 1, ITGA8-related disorder, Renal hypodysplasia/aplasia 1 |
| RS587777280 | Health Risk | Pathogenic | Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1 |
| RS587777279 | Health Risk | Pathogenic/Likely pathogenic | Renal hypodysplasia/aplasia 1, Renal hypodysplasia/aplasia 1 |