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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
calcium voltage-gated channel auxiliary subunit alpha2delta 4
Summary
- Gene Symbol
-
- CACNA2D4
- Aliases
-
- alpha2delta-4
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Calcium channel
- Disulfide bond
- Glycoprotein
- Metal-binding
- Reference proteome
- Signal
- Transmembrane helix
- Voltage-gated channel
- Proteins
| UniProt | Protein Name |
|---|---|
| Q7Z3S7 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| detection of light stimulus involved in visual perception | ||
| calcium ion transmembrane transport |
| GO Term | Evidence Code | PMID |
|---|---|---|
| voltage-gated calcium channel complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| voltage-gated calcium channel activity | ||
| metal ion binding |
GO Hierarchy
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050534 | congenital stationary night blindness | |
| DOID:0050572 | cone-rod dystrophy | |
| DOID:0050795 | cone dystrophy | |
| DOID:0060224 | atrial fibrillation | |
| DOID:0081023 | retinal cone dystrophy 4 | |
| DOID:0110870 | congenital stationary night blindness 1A | |
| DOID:0111005 | cone-rod dystrophy 2 | |
| DOID:10141 | obsolete asthenopia | |
| DOID:10930 | borderline personality disorder | |
| DOID:11661 | blue color blindness |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001133 | Constriction of peripheral visual field |
| HP:0007663 | Reduced visual acuity |
| HP:0007703 | Abnormality of retinal pigmentation |
| HP:0007814 | Retinal pigment epithelial mottling |
| HP:0007984 | Electronegative electroretinogram |
| Disease ID | Disease Name |
|---|---|
| ORPHA:215 |
|
| OMIM:610478 |
|
| ORPHA:1872 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 176155 | WB:WBGene00006772 | ||
| 34951 | FB:FBgn0261999 | ||
| 100150428 | ZFIN:ZDB-GENE-100422-18 | DANRE27759 | |
| 103042404 | ASTMX08330 | ||
| 108268693 | ICTPU34297 | ||
| 105023094 | ESOLU54634 | ||
| 105031141 | ESOLU58183 | ||
| 106561009 | SALSA11774 | ||
| 106584529 | SALSA85800 | ||
| 115192701 | SALTR30183 |
