CA7
Carbonic anhydrase 7
Also known as: CAH7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P43166
- Gene
- CA7
- Ensembl
- ENSG00000168748
- Chromosome
- 16
- Canonical length
- 264 aa
- Protein class
- Enzymes, FDA approved drug targets, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Cytosol
OverviewNCBI Gene
Carbonic anhydrases are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. The cytosolic protein encoded by this gene is predominantly expressed in the brain and contributes to bicarbonate driven GABAergic neuron excitation. Alternative splicing in the coding region results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2018]
Canonical amino-acid sequenceUniProt
264 residues, UniProt reviewed canonical sequence.
>P43166|CA7
1 MTGHHGWGYG QDDGPSHWHK LYPIAQGDRQ SPINIISSQA VYSPSLQPLE LSYEACMSLS
61 ITNNGHSVQV DFNDSDDRTV VTGGPLEGPY RLKQFHFHWG KKHDVGSEHT VDGKSFPSEL
121 HLVHWNAKKY STFGEAASAP DGLAVVGVFL ETGDEHPSMN RLTDALYMVR FKGTKAQFSC
181 FNPKCLLPAS RHYWTYPGSL TTPPLSESVT WIVLREPICI SERQMGKFRS LLFTSEDDER
241 IHMVNNFRPP QPLKGRVVKA SFRALocalizationUniProt · AlphaFold · HPA
Whether an antibody against CA7 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 53 nTPM
Expression across tissuesHPA
Tissue
- colon: 53 nTPM
- rectum: 46 nTPM
- cerebral cortex: 10 nTPM
- small intestine: 9.4 nTPM
- basal ganglia: 9.1 nTPM
- hippocampal formation: 8.9 nTPM
Single-cell type
- colonocytes: 504 nCPM
- tuft cells: 311 nCPM
- enterocytes: 104 nCPM
- enteric transient amplifying cells: 40 nCPM
- goblet cells: 9.9 nCPM
- enteric stem cells: 7.5 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 15 nTPM
- hippocampal formation: 14 nTPM
- basal ganglia: 11 nTPM
- white matter: 8.5 nTPM
- cerebellum: 6.8 nTPM
- thalamus: 6.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.68
- gnomAD pLI
- 0.11
- gnomAD missense Z
- 2.27
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- neuron cellular homeostasis
- positive regulation of cellular pH reduction
- positive regulation of synaptic transmission, GABAergic
- regulation of chloride transport
- regulation of intracellular pH
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CA7 as an antibody target. Whether an autoantibody or antibody against CA7 could matter depends on whether native CA7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CA7 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CA7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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