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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
carbonic anhydrase 4
Summary
- Gene Symbol
-
- CA4
- Aliases
-
- CAIV
- Car4
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Direct protein sequencing
- Disease variant
- Disulfide bond
- GPI-anchor
- Lyase
- Metal-binding
- Reference proteome
- Retinitis pigmentosa
- Signal
- Zinc
- Proteins
| UniProt | Protein Name |
|---|---|
| P22748 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| one-carbon metabolic process | ||
| bicarbonate transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum-Golgi intermediate compartment | ||
| trans-Golgi network | ||
| external side of plasma membrane | ||
| cell surface | ||
| transport vesicle membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbonate dehydratase activity | ||
| zinc ion binding | ||
| protein binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:8499 | night blindness | |
| DOID:0050387 | nonpapillary renal cell carcinoma | |
| DOID:0050534 | congenital stationary night blindness | |
| DOID:0050572 | cone-rod dystrophy | |
| DOID:0050782 | Zollinger-Ellison syndrome | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0110404 | retinitis pigmentosa 17 | |
| DOID:0110870 | congenital stationary night blindness 1A | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:10124 | corneal disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000035 | Abnormal testis morphology |
| HP:0000135 | Hypogonadism |
| HP:0000405 | Conductive hearing impairment |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000501 | Glaucoma |
| HP:0000505 | Visual impairment |
| HP:0000512 | Abnormal electroretinogram |
| HP:0000543 | Optic disc pallor |
| HP:0000546 | Retinal degeneration |
| HP:0000563 | Keratoconus |
| Disease ID | Disease Name |
|---|---|
| ORPHA:791 |
|
PubChem Disease
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 180972 | WB:WBGene00000283 | ||
| 181713 | WB:WBGene00000281 | ||
| 39390 | FB:FBgn0027843 | ||
| 43264 | FB:FBgn0039486 | ||
| 102360700 | LATCH19790 | ||
| 553246 | ZFIN:ZDB-GENE-080815-5 | DANRE08777 | |
| 407683 | ZFIN:ZDB-GENE-080815-6 | ||
| 555196 | ZFIN:ZDB-GENE-080204-85 | ||
| 103038820 | ASTMX09621 | ||
| 108259756 | ICTPU23143 |
