Gene
ahsg1
- ID
- ZDB-GENE-041114-50
- Name
- alpha-2-HS-glycoprotein 1
- Symbol
- ahsg1 Nomenclature History
- Previous Names
-
- ahsg
- wu:fb63g02
- zgc:103687
- Type
- protein_coding_gene
- Location
- Chr: 22 Mapping Details/Browsers
- Description
- Predicted to have endopeptidase inhibitor activity. Predicted to be involved in negative regulation of endopeptidase activity. Predicted to localize to extracellular region. Human ortholog(s) of this gene implicated in alopecia-mental retardation syndrome 1; coronary artery disease; and type 2 diabetes mellitus. Is expressed in liver. Orthologous to human AHSG (alpha 2-HS glycoprotein).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 5 figures from 5 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| alopecia-mental retardation syndrome 1 | Alliance | ?Alopecia-intellectual disability syndrome 1 | 203650 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Cystatin domain | Cystatin superfamily | Fetuin-A-type cystatin domain | Kininogen/Fetuin/Histidine-rich Glycoprotein |
|---|---|---|---|---|---|
|
UniProtKB:Q800S8
|
455 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available