Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56934
Gene name Gene Name - the full gene name approved by the HGNC.
Carbonic anhydrase 10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CA10
Synonyms (NCBI Gene) Gene synonyms aliases
CA-RPX, CARPX, HUCEP-15
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q21.33-q22
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that belongs to the carbonic anhydrase family of zinc metalloenzymes, which catalyze the reversible hydration of carbon dioxide in various biological processes. The protein encoded by this gene is an acatalytic member of the al
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019406 hsa-miR-148b-3p Microarray 17612493
MIRT856289 hsa-miR-4733-5p CLIP-seq
MIRT856290 hsa-miR-3166 CLIP-seq
MIRT856291 hsa-miR-3185 CLIP-seq
MIRT856292 hsa-miR-3678-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0004089 Function Carbonate dehydratase activity IEA
GO:0005575 Component Cellular_component ND
GO:0006730 Process One-carbon metabolic process IBA 21873635
GO:0007420 Process Brain development NAS 11311946
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604642 1369 ENSG00000154975
Protein
UniProt ID Q9NS85
Protein name Carbonic anhydrase-related protein 10 (Carbonic anhydrase-related protein X) (CA-RP X) (CARP X) (Cerebral protein 15)
Protein function Does not have a catalytic activity.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00194 Carb_anhydrase 32 300 Eukaryotic-type carbonic anhydrase Domain
Tissue specificity TISSUE SPECIFICITY: Strong expression in brain and central nervous system. {ECO:0000269|PubMed:11311946}.
Sequence
Sequence length 328
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cholelithiasis Cholelithiasis rs121918440, rs72552778, rs387906528, rs759202962, rs377160065, rs1051861187, rs757693457, rs752563752 17632509
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Gastroesophageal Reflux Disease Gastroesophageal Reflux Disease GWAS
Myocardial Infarction Myocardial Infarction GWAS
Gastritis Gastritis GWAS
Dementia Dementia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 32736539
Colorectal Neoplasms Associate 29291617
Hashimoto Disease Associate 30926877
Hepatitis B Associate 32736539
Hodgkin Disease Associate 6370286
Metabolic Syndrome Associate 26507551
Osteoarthritis Associate 25880085
Osteoporosis Associate 25880085
Ovarian Neoplasms Associate 39972314
Pulmonary Disease Chronic Obstructive Associate 39223457