SHMARQL

CA5A

<http://www.wikidata.org/entity/Q17854478>

protein-coding gene in the species Homo sapiens
rdfs:label
"CA5A"@en
skos:altLabel "CA5"@en
"CA5AD"@en
"CAV"@en
"CAVA"@en
"GS1-21A4.1"@en
"carbonic anhydrase 5A"@en
schema:description
"protein-coding gene in the species Homo sapiens"@en
schema:dateModified "2026-05-20T05:11:22+00:00"^^xsd:dateTime
schema:version 2494674693
wikibase:identifiers 20
wikibase:sitelinks 4
wikibase:statements 47
p:P1057 wd:statement/Q17854478-F78C5E50-DAC7-426A-91A1-44AC94DFFB34
p:P2293 wd:statement/Q17854478-1F78F960-DA9A-4383-956E-405E9366E8CB
p:P2548 wd:statement/Q17854478-76D1B078-F5D1-4BB3-8738-BC6B7EDC9952
p:P2671 wd:statement/Q17854478-115B7385-DE81-4259-931E-C4E793B614D3
p:P279 wd:statement/Q17854478-8BDC171F-881B-4907-AEDE-972174660228
p:P2888 wd:statement/Q17854478-ED5495DC-9EEA-44B7-8F86-A60298C2E01E
p:P2892 wd:statement/Q17854478-8FFEAC39-55F9-47CB-B949-065C2A0E5210
p:P31 wd:statement/Q17854478-D8D3966D-D0C9-49D5-88CF-D0620A7D2B7C
p:P351 wd:statement/Q17854478-4E76B0FE-B395-4BF0-B7D9-48090B4DB6E1
p:P353 wd:statement/Q17854478-080E7B40-EF67-46EF-82E3-488B674BB3D2
p:P354 wd:statement/Q17854478-C78F1CE6-76BD-46FE-8C7C-374D38F95D29
p:P4196 wd:statement/Q17854478-39CE9D07-4FCE-4361-A780-31C81CA69F96
p:P492 wd:statement/Q17854478-88CA2BB1-962D-4793-9A29-DAB00A1D37DD
p:P5572 wd:statement/Q17854478-0D2AB7B0-587F-420F-B384-E389EB381249
wd:statement/Q17854478-2851CF88-C7E4-4D6E-B2B0-7F7E8AFC525E
wd:statement/Q17854478-4315DE56-C3C1-4F6A-B695-42CEDFBBE94C
wd:statement/Q17854478-5FBAA267-E3F1-4904-ABC7-245F4774ACD9
wd:statement/Q17854478-6DE7B4C3-860E-4769-9F03-27C0394A98CF
wd:statement/Q17854478-8CE4552B-A4F1-4098-99AE-826F4D7C9D81
wd:statement/Q17854478-BABEA6C8-4C0B-4254-9AF8-FDB5508A7807
wd:statement/Q17854478-ED5F45B8-C088-4DEE-B30D-4D5FD277FF69
wd:statement/Q17854478-F08DB1A6-C82F-4728-807C-82A6837F2222
wd:statement/Q17854478-FA4EFFBB-CB42-460F-99AD-5D0162806461
p:P593 wd:statement/Q17854478-74B2F96A-BDAB-48E0-AEE1-6533BA9D5A1E
p:P594 wd:statement/Q17854478-57F06A0D-92E4-4247-87E2-AB168E45728C
p:P639 wd:statement/Q17854478-0A240B80-AD37-4A4C-8359-AE029A454CE4
wd:statement/Q17854478-1000859A-4859-496E-A7BA-68CAECD10CA4
wd:statement/Q17854478-4C7F76B1-CA98-47C1-9BCE-A176514B3969
wd:statement/Q17854478-677A8D02-F7F5-4D40-ADB1-F9352592D0F4
wd:statement/Q17854478-81A918B9-D1E1-4425-886D-3069EA965F9A
wd:statement/Q17854478-85029117-E7B1-4D9E-A02B-D3F2BF77F2D4
wd:statement/Q17854478-AF75E0AB-31CD-4058-84DB-5E2D71BF2E7B
p:P644 wd:statement/Q17854478-84BDC2B3-AF5E-466F-9567-CBB0E38757F9
wd:statement/Q17854478-A1F4F5AE-39B6-40CB-92CC-BC5066095C76
p:P645 wd:statement/Q17854478-B2E215FE-CCE5-432D-AD38-F2245F64484C
wd:statement/Q17854478-F0D7C30C-8E0B-4585-8463-835FAC300913
p:P684 wd:statement/Q17854478-24133BCC-3C2A-4DC3-A583-70DF9C6D5F2B
wd:statement/Q17854478-6924FD74-07F3-4B6D-ADA3-EB539F344177
wd:statement/Q17854478-EE18087E-FF19-491D-882B-2BA46F73A58D
p:P688 wd:statement/Q17854478-F326C333-5CE1-46C6-B8E3-51FC82935EA5
p:P703 wd:statement/Q17854478-48D2547E-92DF-4260-9588-F8C4876FE671
p:P704 wd:statement/Q17854478-06CCB109-F5D6-4E50-AC76-3090AB5C2CE4
wd:statement/Q17854478-121AF409-5346-4DF3-AD54-8F4E97013AA4
wd:statement/Q17854478-79127B33-2EC2-43FD-B25C-98646BD86DC0
wd:statement/Q17854478-7C24D613-D3EC-48C7-8C75-2F8885E140B4
wd:statement/Q17854478-86542FD5-59F4-489C-A164-DB2AF37F0CD2
wd:statement/Q17854478-9118CEED-C6E7-4500-ADF7-F6CEAEA38DCB
p:direct-normalized/P2671 <http://g.co/kg/g/11gbldswvh>
p:direct-normalized/P351 <http://purl.uniprot.org/geneid/763>
p:direct-normalized/P594 <http://rdf.ebi.ac.uk/resource/ensembl/ENSG00000174990>
p:direct-normalized/P704 <http://rdf.ebi.ac.uk/resource/ensembl/ENST00000566402>
<http://rdf.ebi.ac.uk/resource/ensembl/ENST00000568801>
<http://rdf.ebi.ac.uk/resource/ensembl/ENST00000648022>
<http://rdf.ebi.ac.uk/resource/ensembl/ENST00000648177>
<http://rdf.ebi.ac.uk/resource/ensembl/ENST00000649158>
<http://rdf.ebi.ac.uk/resource/ensembl/ENST00000649794>
wdt:P1057 human chromosome 16
wdt:P2293 Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
wdt:P2548 reverse strand
wdt:P2671 "/g/11gbldswvh"
wdt:P279 protein-coding gene
wdt:P2888 <http://identifiers.org/ncbigene/763>
wdt:P2892 "C1413046"
wdt:P31 gene
wdt:P351 "763"
wdt:P353 "CA5A"
wdt:P354 "1377"
wdt:P4196 "16q24.2"
wdt:P492 "114761"
wdt:P5572 hypothalamus
prefrontal cortex
putamen
right lobe of liver
apex of heart
C1 segment
islet of Langerhans
hippocampus proper
substantia nigra
testicle
wdt:P593 "68200"
wdt:P594 "ENSG00000174990"
wdt:P639 "NM_001367225"
"NM_001739"
"NR_159798"
"NR_159799"
"XM_005256134"
"XM_047434594"
"XM_047434595"
wdt:P644 "87881546"
"87921625"
wdt:P645 "87936580"
"87970135"
wdt:P684 Car5a
Ca5a
cah-4
wdt:P688 Carbonic anhydrase 5A
wdt:P703 man
wdt:P704 "ENST00000566402"
"ENST00000568801"
"ENST00000648022"
"ENST00000648177"
"ENST00000649158"
"ENST00000649794"
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data from SPARQL profile: Wikidata