Entity Details

Primary name CAH12_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO43570
EntryNameCAH12_HUMAN
FullNameCarbonic anhydrase 12
TaxID9606
Evidenceevidence at protein level
Length354
SequenceStatuscomplete
DateCreated1999-07-15
DateModified2021-06-02

Ontological Relatives

GenesCA12

GO terms

Show/Hide Table
GOName
GO:0004089 carbonate dehydratase activity
GO:0005886 plasma membrane
GO:0006730 one-carbon metabolic process
GO:0008270 zinc ion binding
GO:0015701 bicarbonate transport
GO:0016021 integral component of membrane
GO:0016836 hydro-lyase activity
GO:0055064 chloride ion homeostasis

Subcellular Location

Show/Hide Table
Subcellular Location
Cell membrane
Membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR001148 Alpha carbonic anhydrase domainDomainDomain
IPR018338 Carbonic anhydrase, alpha-class, conserved siteSiteConserved site
IPR018430 Carbonic anhydrase, CA-XIIFamilyFamily
IPR023561 Carbonic anhydrase, alpha-classFamilyFamily
IPR036398 Alpha carbonic anhydrase domain superfamilyFamilyHomologous superfamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
143860 OMIMHyperchlorhidrosis, isolated (HYCHL)An autosomal recessive disorder characterized by excessive sweating and increased sweat chloride levels. Affected individuals suffer from episodes of hyponatremic dehydration and report increased amounts of visible salt precipitates in sweat. The disease is caused by variants affecting the gene represented in this entry.

Drugs

Show/Hide Table
DrugNameSourceType
DB00562 BenzthiazideDrugbanksmall molecule
DB00774 HydroflumethiazideDrugbanksmall molecule
DB00819 AcetazolamideDrugbanksmall molecule
DB00909 ZonisamideDrugbanksmall molecule
DB08846 Ellagic acidDrugbanksmall molecule