Gene
apoc2
- ID
- ZDB-GENE-030131-2168
- Name
- apolipoprotein C-II
- Symbol
- apoc2 Nomenclature History
- Previous Names
-
- fb71a04
- fb98g08
- wu:fb52e03
- wu:fb71a04
- wu:fb98g08
- Type
- protein_coding_gene
- Location
- Chr: 16 Mapping Details/Browsers
- Description
- Predicted to have enzyme activator activity. Involved in definitive hemopoiesis and lipoprotein catabolic process. Predicted to localize to chylomicron. Used to study familial hyperlipidemia; familial lipoprotein lipase deficiency; and hyperlipoproteinemia type IV. Human ortholog(s) of this gene implicated in familial apolipoprotein C-II deficiency; familial hyperlipidemia; and multiple sclerosis. Is expressed in intestine; liver; pancreas; and yolk. Orthologous to human APOC2 (apolipoprotein C2).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 5 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 19 figures from 6 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
familial apolipoprotein C-II deficiency | Alliance | Hyperlipoproteinemia, type Ib | 207750 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | ApoC-II domain superfamily | Apolipoprotein C-II |
---|---|---|---|
UniProtKB:E9QEQ1
|
100 |
Interactions and Pathways
No data available
Plasmids
No data available