1. Gene
  2. CA6 - carbonic anhydrase 6 Gene

CA6 - carbonic anhydrase 6 Gene

Homo sapiens

Also known as CA-VI; GUSTIN

Gene ID: 765 | Gene type: protein coding

About CA6

Cytogenetic location: 1p36.23 Genomic coordinates (GRCh38): 1:8,945,868-8,975,092 (from NCBI)

This gene has 6 transcripts (splice variants), 228 orthologues and 14 paralogues. Restricted expression toward salivary gland (RPKM 1381.7).

Summary

The protein encoded by this gene is one of several isozymes of Carbonic Anhydrase. This protein is found only in salivary glands and saliva and protein may play a role in the reversible hydratation of carbon dioxide though its function in saliva is unknown. [provided by RefSeq, Jul 2008]

CA6 Products(4)

mRNA Protein Name
NM_001215.4 NP_001206.2 carbonic anhydrase 6 isoform 1 precursor
NM_001270500.2 NP_001257429.1 carbonic anhydrase 6 isoform 2 precursor
NM_001270501.2 NP_001257430.1 carbonic anhydrase 6 isoform 3 precursor
NM_001270502.2 NP_001257431.1 carbonic anhydrase 6 isoform 4

CA6 Protein Structure

Carb_anhydrase

Carb_anhydrase: Eukaryotic-type carbonic anhydrase (23 - 278)

  • 0
  • 100
  • 200
  • 308 a.a.
Protein Preferred Names Protein Names

carbonic anhydrase 6

carbonate dehydratase VI

Related Diseases

Diseases Alias
Mammary Analogue Secretory Carcinoma
Dental Caries

Dental Caries Extending Into Pulp

Dental Caries Of Smooth Surface

Dental Caries Pit And Fissure

Smooth Surface Dental Caries

Dental Decay

Carious Teeth

Dental Cavity

Saprodontia

Teeth Decayed

Tooth Caries

Tooth Decay

Enamel Erosion
Tooth Erosion

Generalized Erosion

Localized Erosion

Generalized Erosions

Erosion, Localized

Multilocular Clear Cell Renal Cell Carcinoma

Cystadenocarcinoma Of Kidney

Renal Cystadenocarcinoma

Aseptic Meningitis

Acute Aseptic Meningitis

Meningitis Aseptic

Meningitis, Aseptic

Parotid Disease

Parotid Diseases

Xerophthalmia

Conjunctival Xerosis

Potocki-Shaffer Syndrome

Proximal 11p Deletion Syndrome

Chromosome 11p11.2 Deletion Syndrome

Pss

11p11.2 Deletion

P11pds

Defect11 Syndrome

Deletion Of Chromosome 11p11.2

POSHS

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus CA6 VGNC VGNC:26656
Mus musculus CA6 MGD MGI:1333786
Macaca mulatta CA6 VGNC VGNC:70493
Felis catus CA6 VGNC VGNC:60277
Canis familiaris CA6 VGNC VGNC:38614
Rattus norvegicus CA6 RGD RGD:70516
Others CA6 NCBI