CA1 (carbonic anhydrase 1) - Rat Genome Database

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Gene: CA1 (carbonic anhydrase 1) Homo sapiens
Analyze
Symbol: CA1
Name: carbonic anhydrase 1
RGD ID: 1320302
HGNC Page HGNC
Description: Exhibits arylesterase activity and carbonate dehydratase activity. Predicted to be involved in one-carbon metabolic process. Localizes to extracellular exosome.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CA-I; CAB; Car1; carbonate dehydratase I; carbonic anhydrase B; carbonic anhydrase I; carbonic dehydratase; epididymis secretory protein Li 11; HEL-S-11
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl885,327,608 - 85,379,014 (-)EnsemblGRCh38hg38GRCh38
GRCh38885,327,608 - 85,378,113 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37886,239,837 - 86,290,342 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36886,427,709 - 86,477,594 (-)NCBINCBI36hg18NCBI36
Build 34886,427,708 - 86,477,594NCBI
Celera882,245,509 - 82,295,378 (-)NCBI
Cytogenetic Map8q21.2NCBI
HuRef881,734,656 - 81,784,498 (-)NCBIHuRef
CHM1_1886,292,190 - 86,342,064 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
1H-1,2,4-triazole  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dinitrotoluene  (ISO)
2,6-di-tert-butylphenol  (EXP)
2,6-dinitrotoluene  (ISO)
2-hydroxypropanoic acid  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acetazolamide  (EXP)
aflatoxin B1  (EXP)
anthocyanin  (EXP)
benzo[a]pyrene  (EXP)
bleomycin A2  (ISO)
bromobenzene  (ISO)
butylated hydroxyanisole  (EXP)
C60 fullerene  (ISO)
cadmium dichloride  (ISO)
candesartan  (EXP)
carbon nanotube  (ISO)
carbonates  (EXP)
chalcone  (EXP)
chloric acid  (EXP)
cobalt atom  (EXP)
cobalt dichloride  (EXP)
coumarin  (EXP)
dibutyl phthalate  (ISO)
diclofenac  (ISO)
erythromycin estolate  (ISO)
ethanol  (ISO)
ethoxzolamide  (EXP)
ferroheme b  (ISO)
flavonoids  (EXP)
guaiacol  (EXP)
heme b  (ISO)
hydrazinecarbothioamide  (EXP)
hydrogencarbonate  (EXP)
indometacin  (EXP)
irbesartan  (EXP)
lead(0)  (EXP)
lead(2+)  (EXP)
malvidin 3-O-beta-D-glucoside  (EXP)
malvin  (EXP)
mercury atom  (EXP)
mercury(0)  (EXP)
methamphetamine  (ISO)
Methazolamide  (EXP)
methylamines  (EXP)
N-(3-methyl-5-sulfamoyl-1,3,4-thiadiazol-2-ylidene)acetamide  (EXP)
N-nitrosodiethylamine  (ISO)
N-phenylthiourea  (EXP)
nitric acid  (EXP)
orphenadrine  (ISO)
oryzalin  (EXP)
oxaliplatin  (ISO)
paracetamol  (EXP,ISO)
pelargonidin 3-O-beta-D-glucoside  (EXP)
pelargonidin 3-O-beta-D-glucoside chloride  (EXP)
perchlorate  (EXP)
phenobarbital  (ISO)
phenylephrine  (EXP)
pirinixic acid  (ISO)
potassium dichromate  (ISO)
propofol  (EXP)
pyrimidines  (EXP)
rac-lactic acid  (EXP)
rifampicin  (EXP)
rotenone  (ISO)
silychristin  (EXP)
sodium dichromate  (ISO)
sodium fluoride  (ISO)
sulfamic acid  (EXP)
sulfates  (EXP)
synephrine  (EXP)
tetrachloromethane  (ISO)
thiazolidines  (EXP)
thioacetamide  (ISO)
thiophenes  (EXP)
thiourea  (EXP)
topiramate  (EXP)
topotecan  (ISO)
trans-chalcone  (EXP)
triazoles  (EXP)
triphenyl phosphate  (ISO)
Triptolide  (ISO)
tungstate  (EXP)
valproic acid  (ISO)
vanillin  (EXP)
voriconazole  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)
zonisamide  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IBA,IEA)
cytosol  (TAS)
extracellular exosome  (HDA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:406674   PMID:804171   PMID:827930   PMID:1602151   PMID:1908227   PMID:1916821   PMID:2114290   PMID:2121614   PMID:2511043   PMID:3088232   PMID:3104879   PMID:3124707  
PMID:4207120   PMID:4217196   PMID:4625868   PMID:4632246   PMID:6781336   PMID:7574487   PMID:7758465   PMID:7866410   PMID:9879596   PMID:11392054   PMID:11680594   PMID:12009884  
PMID:12477932   PMID:14675565   PMID:15342556   PMID:15489334   PMID:15836783   PMID:15837325   PMID:16870440   PMID:17192395   PMID:17314045   PMID:17464559   PMID:18029348   PMID:19536309  
PMID:20624682   PMID:21143847   PMID:21873635   PMID:21900206   PMID:21988832   PMID:22360420   PMID:22416960   PMID:22619369   PMID:22838845   PMID:22996014   PMID:23213568   PMID:23218470  
PMID:23327700   PMID:23339426   PMID:23356845   PMID:23376485   PMID:23389367   PMID:23533145   PMID:23557951   PMID:23720494   PMID:23774970   PMID:23798711   PMID:23859774   PMID:23867389  
PMID:23892086   PMID:23993330   PMID:24289818   PMID:24670789   PMID:24878360   PMID:25165709   PMID:25416956   PMID:25910212   PMID:26232327   PMID:26459317   PMID:26475450   PMID:27413740  
PMID:27475498   PMID:27809276   PMID:28270370   PMID:28445001   PMID:28514442   PMID:28544359   PMID:28613396   PMID:28782909   PMID:30463901   PMID:30916466   PMID:31963697   PMID:32031891  
PMID:32992797  


Genomics

Comparative Map Data
CA1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl885,327,608 - 85,379,014 (-)EnsemblGRCh38hg38GRCh38
GRCh38885,327,608 - 85,378,113 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37886,239,837 - 86,290,342 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36886,427,709 - 86,477,594 (-)NCBINCBI36hg18NCBI36
Build 34886,427,708 - 86,477,594NCBI
Celera882,245,509 - 82,295,378 (-)NCBI
Cytogenetic Map8q21.2NCBI
HuRef881,734,656 - 81,784,498 (-)NCBIHuRef
CHM1_1886,292,190 - 86,342,064 (-)NCBICHM1_1
Car1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39314,831,274 - 14,873,425 (-)NCBIGRCm39mm39
GRCm39 Ensembl314,831,276 - 14,873,428 (-)Ensembl
GRCm38314,766,214 - 14,808,365 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl314,766,216 - 14,808,368 (-)EnsemblGRCm38mm10GRCm38
MGSCv37314,766,214 - 14,808,365 (-)NCBIGRCm37mm9NCBIm37
MGSCv36314,742,975 - 14,767,557 (-)NCBImm8
Celera314,771,712 - 14,813,913 (-)NCBICelera
Cytogenetic Map3A1NCBI
cM Map33.18NCBI
Car1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2286,829,436 - 86,872,209 (+)NCBI
Rnor_6.0 Ensembl288,217,188 - 88,227,479 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0288,185,204 - 88,227,486 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02107,958,483 - 108,000,765 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4288,166,412 - 88,210,693 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1288,143,727 - 88,155,654 (+)NCBI
Celera282,427,032 - 82,469,698 (+)NCBICelera
Cytogenetic Map2q23NCBI
Ca1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554173,270,619 - 3,305,756 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554173,270,619 - 3,313,261 (-)NCBIChiLan1.0ChiLan1.0
CA1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1883,464,680 - 83,515,359 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl883,463,434 - 83,526,899 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0881,854,390 - 81,905,728 (-)NCBIMhudiblu_PPA_v0panPan3
CA1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12931,858,644 - 31,868,135 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2931,858,636 - 31,868,158 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2932,144,441 - 32,154,240 (-)NCBI
ROS_Cfam_1.02932,007,771 - 32,017,260 (-)NCBI
UMICH_Zoey_3.12932,058,957 - 32,068,728 (-)NCBI
UNSW_CanFamBas_1.02932,080,387 - 32,089,882 (-)NCBI
UU_Cfam_GSD_1.02932,466,958 - 32,476,446 (-)NCBI
Ca1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440530347,504,905 - 47,545,941 (+)NCBI
SpeTri2.0NW_004936544246,797 - 257,798 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CA1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl451,302,406 - 51,353,127 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1451,343,548 - 51,353,127 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2456,358,354 - 56,367,895 (+)NCBISscrofa10.2Sscrofa10.2susScr3
CA1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1880,699,114 - 80,729,932 (-)NCBI
ChlSab1.1 Ensembl880,699,651 - 80,712,858 (-)Ensembl
Ca1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247446,244,872 - 6,324,722 (+)NCBI

Position Markers
RH118415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37886,248,048 - 86,248,347UniSTSGRCh37
Build 36886,435,300 - 86,435,599RGDNCBI36
Celera882,253,099 - 82,253,398RGD
Cytogenetic Map8q21.2UniSTS
HuRef881,742,246 - 81,742,545UniSTS
TNG Radiation Hybrid Map842602.0UniSTS
SHGC-31642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37886,240,666 - 86,240,790UniSTSGRCh37
Build 36886,427,918 - 86,428,042RGDNCBI36
Celera882,245,717 - 82,245,841RGD
Cytogenetic Map8q21.2UniSTS
HuRef881,734,864 - 81,734,988UniSTS
GeneMap99-GB4 RH Map8419.67UniSTS
Whitehead-RH Map8521.6UniSTS
GeneMap99-G3 RH Map83337.0UniSTS
CA1_3942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37886,240,282 - 86,240,883UniSTSGRCh37
Build 36886,427,534 - 86,428,135RGDNCBI36
Celera882,245,333 - 82,245,934RGD
HuRef881,734,480 - 81,735,081UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3261
Count of miRNA genes:935
Interacting mature miRNAs:1081
Transcripts:ENST00000256119, ENST00000431316, ENST00000432364, ENST00000517429, ENST00000517590, ENST00000517618, ENST00000518233, ENST00000518341, ENST00000519129, ENST00000519991, ENST00000520093, ENST00000520663, ENST00000520692, ENST00000520990, ENST00000521679, ENST00000521846, ENST00000522389, ENST00000522579, ENST00000522662, ENST00000522814, ENST00000523022, ENST00000523712, ENST00000523858, ENST00000523953, ENST00000524324, ENST00000542576
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 12 3 8
Medium 339 610 22 12 698 12 4 6 8 3 2 56 13 3 1
Low 392 380 354 103 382 98 243 144 323 44 84 518 6 1 199 145 1 1
Below cutoff 1404 1657 1155 357 389 210 3428 1705 3077 210 1086 805 153 871 2266 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_016221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001128829 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001128830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001128831 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001291967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001291968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC025800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI802646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC027890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP261967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU655910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU656154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU658617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU659301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU659695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU661390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU663330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU664306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU665210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU794595 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ891527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JC427562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M33987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S81738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X05014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000431316   ⟹   ENSP00000392338
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,229 - 85,349,901 (-)Ensembl
RefSeq Acc Id: ENST00000517429   ⟹   ENSP00000430710
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,332,494 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000517590   ⟹   ENSP00000429843
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,329,831 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000517618   ⟹   ENSP00000430861
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,593 - 85,341,714 (-)Ensembl
RefSeq Acc Id: ENST00000518233
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,332,371 - 85,342,825 (-)Ensembl
RefSeq Acc Id: ENST00000518341
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,333,528 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000519129   ⟹   ENSP00000429688
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,338,420 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000519991   ⟹   ENSP00000430543
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,594 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000520093
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,337,985 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000520663   ⟹   ENSP00000430571
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,329,756 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000520692
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,341,415 - 85,342,800 (-)Ensembl
RefSeq Acc Id: ENST00000520990
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,338,019 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000521679   ⟹   ENSP00000429300
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,489 - 85,338,295 (-)Ensembl
RefSeq Acc Id: ENST00000521846   ⟹   ENSP00000430471
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,333,527 - 85,378,108 (-)Ensembl
RefSeq Acc Id: ENST00000522389   ⟹   ENSP00000427773
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,439 - 85,341,659 (-)Ensembl
RefSeq Acc Id: ENST00000522579   ⟹   ENSP00000427852
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,333,528 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000522662   ⟹   ENSP00000430372
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,336,945 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000522814   ⟹   ENSP00000430737
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,333,530 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000523022   ⟹   ENSP00000429798
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,230 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000523712
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,329,698 - 85,337,212 (-)Ensembl
RefSeq Acc Id: ENST00000523858   ⟹   ENSP00000430975
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,337,002 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000523953   ⟹   ENSP00000430656
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,327,608 - 85,379,014 (-)Ensembl
RefSeq Acc Id: ENST00000524324   ⟹   ENSP00000428923
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,565 - 85,378,113 (-)Ensembl
RefSeq Acc Id: ENST00000542576   ⟹   ENSP00000443517
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,328,229 - 85,342,843 (-)Ensembl
RefSeq Acc Id: ENST00000626824   ⟹   ENSP00000486171
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl885,327,608 - 85,379,014 (-)Ensembl
RefSeq Acc Id: NM_001128829   ⟹   NP_001122301
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,327,608 - 85,378,113 (-)NCBI
GRCh37886,240,458 - 86,290,342 (-)ENTREZGENE
HuRef881,734,656 - 81,784,498 (-)ENTREZGENE
CHM1_1886,292,190 - 86,342,064 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001128830   ⟹   NP_001122302
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,327,608 - 85,378,113 (-)NCBI
GRCh37886,240,458 - 86,290,342 (-)ENTREZGENE
HuRef881,734,656 - 81,784,498 (-)ENTREZGENE
CHM1_1886,292,190 - 86,342,064 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001128831   ⟹   NP_001122303
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,327,608 - 85,378,113 (-)NCBI
GRCh37886,240,458 - 86,290,342 (-)ENTREZGENE
HuRef881,734,656 - 81,784,498 (-)ENTREZGENE
CHM1_1886,292,190 - 86,342,064 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001164830   ⟹   NP_001158302
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,327,608 - 85,341,714 (-)NCBI
GRCh37886,240,458 - 86,290,342 (-)ENTREZGENE
HuRef881,734,656 - 81,784,498 (-)ENTREZGENE
CHM1_1886,292,190 - 86,305,681 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001291967   ⟹   NP_001278896
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,327,608 - 85,378,113 (-)NCBI
CHM1_1886,292,190 - 86,342,064 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001291968   ⟹   NP_001278897
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,327,608 - 85,378,113 (-)NCBI
CHM1_1886,292,190 - 86,342,064 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001738   ⟹   NP_001729
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,327,608 - 85,378,113 (-)NCBI
GRCh37886,240,458 - 86,290,342 (-)ENTREZGENE
Build 36886,427,709 - 86,477,594 (-)NCBI Archive
HuRef881,734,656 - 81,784,498 (-)ENTREZGENE
CHM1_1886,292,190 - 86,342,064 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001122301   ⟸   NM_001128829
- Peptide Label: isoform a
- UniProtKB: P00915 (UniProtKB/Swiss-Prot),   V9HWE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001729   ⟸   NM_001738
- Peptide Label: isoform a
- UniProtKB: P00915 (UniProtKB/Swiss-Prot),   V9HWE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001122302   ⟸   NM_001128830
- Peptide Label: isoform a
- UniProtKB: P00915 (UniProtKB/Swiss-Prot),   V9HWE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158302   ⟸   NM_001164830
- Peptide Label: isoform a
- UniProtKB: P00915 (UniProtKB/Swiss-Prot),   V9HWE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001122303   ⟸   NM_001128831
- Peptide Label: isoform a
- UniProtKB: P00915 (UniProtKB/Swiss-Prot),   V9HWE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001278897   ⟸   NM_001291968
- Peptide Label: isoform c
- Sequence:
RefSeq Acc Id: NP_001278896   ⟸   NM_001291967
- Peptide Label: isoform b
- Sequence:
RefSeq Acc Id: ENSP00000443517   ⟸   ENST00000542576
RefSeq Acc Id: ENSP00000429843   ⟸   ENST00000517590
RefSeq Acc Id: ENSP00000430861   ⟸   ENST00000517618
RefSeq Acc Id: ENSP00000430710   ⟸   ENST00000517429
RefSeq Acc Id: ENSP00000429688   ⟸   ENST00000519129
RefSeq Acc Id: ENSP00000430543   ⟸   ENST00000519991
RefSeq Acc Id: ENSP00000486171   ⟸   ENST00000626824
RefSeq Acc Id: ENSP00000430571   ⟸   ENST00000520663
RefSeq Acc Id: ENSP00000429300   ⟸   ENST00000521679
RefSeq Acc Id: ENSP00000430471   ⟸   ENST00000521846
RefSeq Acc Id: ENSP00000430372   ⟸   ENST00000522662
RefSeq Acc Id: ENSP00000427852   ⟸   ENST00000522579
RefSeq Acc Id: ENSP00000427773   ⟸   ENST00000522389
RefSeq Acc Id: ENSP00000430737   ⟸   ENST00000522814
RefSeq Acc Id: ENSP00000430656   ⟸   ENST00000523953
RefSeq Acc Id: ENSP00000430975   ⟸   ENST00000523858
RefSeq Acc Id: ENSP00000429798   ⟸   ENST00000523022
RefSeq Acc Id: ENSP00000392338   ⟸   ENST00000431316
RefSeq Acc Id: ENSP00000428923   ⟸   ENST00000524324
Protein Domains
Alpha-carbonic anhydrase

Promoters
RGD ID:7213679
Promoter ID:EPDNEW_H12585
Type:initiation region
Name:CA1_2
Description:carbonic anhydrase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12586  EPDNEW_H12591  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,341,714 - 85,341,774EPDNEW
RGD ID:7213683
Promoter ID:EPDNEW_H12586
Type:multiple initiation site
Name:CA1_1
Description:carbonic anhydrase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12585  EPDNEW_H12591  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38885,378,113 - 85,378,173EPDNEW
RGD ID:6806550
Promoter ID:HG_KWN:61626
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:NM_001128830,   UC003YDH.2,   UC003YDI.2,   UC010MAE.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36886,477,606 - 86,478,106 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001738.5(CA1):c.760G>C (p.Gly254Arg) single nucleotide variant Carbonic anhydrase I, Guam [RCV000019171] Chr8:85328586 [GRCh38]
Chr8:86240815 [GRCh37]
Chr8:8q21.2
pathogenic
NM_001738.5(CA1):c.740G>A (p.Arg247His) single nucleotide variant Carbonic anhydrase I deficiency [RCV000019172] Chr8:85328606 [GRCh38]
Chr8:86240835 [GRCh37]
Chr8:8q21.2
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.11-21.2(chr8:73879385-85611466)x1 copy number loss See cases [RCV000054259] Chr8:73879385..85611466 [GRCh38]
Chr8:74791620..86523695 [GRCh37]
Chr8:74954174..86710947 [NCBI36]
Chr8:8q21.11-21.2
pathogenic
GRCh38/hg38 8q21.13-21.3(chr8:77765431-91839285)x1 copy number loss See cases [RCV000054261] Chr8:77765431..91839285 [GRCh38]
Chr8:78677666..92851513 [GRCh37]
Chr8:78840221..92920689 [NCBI36]
Chr8:8q21.13-21.3
pathogenic
GRCh38/hg38 8q21.13-22.1(chr8:78672463-95366868)x1 copy number loss See cases [RCV000054262] Chr8:78672463..95366868 [GRCh38]
Chr8:79584698..96379096 [GRCh37]
Chr8:79747253..96448272 [NCBI36]
Chr8:8q21.13-22.1
pathogenic
NM_001164830.1(CA1):c.198C>T (p.Ser66=) single nucleotide variant Malignant melanoma [RCV000068422] Chr8:85338289 [GRCh38]
Chr8:86250518 [GRCh37]
Chr8:86437770 [NCBI36]
Chr8:8q21.2
not provided
NM_001738.4(CA1):c.-79+12860C>T single nucleotide variant Lung cancer [RCV000107812] Chr8:85365186 [GRCh38]
Chr8:86277415 [GRCh37]
Chr8:8q21.2
uncertain significance
GRCh38/hg38 8q13.1-22.1(chr8:66171669-93505509)x3 copy number gain See cases [RCV000137050] Chr8:66171669..93505509 [GRCh38]
Chr8:67083904..94517737 [GRCh37]
Chr8:67246458..94586913 [NCBI36]
Chr8:8q13.1-22.1
pathogenic
GRCh38/hg38 8q21.2(chr8:84246857-85606287)x1 copy number loss See cases [RCV000136883] Chr8:84246857..85606287 [GRCh38]
Chr8:85159092..86518516 [GRCh37]
Chr8:85321647..86705768 [NCBI36]
Chr8:8q21.2
uncertain significance
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q21.2-21.3(chr8:83721453-87866414)x3 copy number gain See cases [RCV000143246] Chr8:83721453..87866414 [GRCh38]
Chr8:84633688..88878642 [GRCh37]
Chr8:84796243..88947758 [NCBI36]
Chr8:8q21.2-21.3
uncertain significance
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.2(chr8:86163125-86262003)x1 copy number loss See cases [RCV000449254] Chr8:86163125..86262003 [GRCh37]
Chr8:8q21.2
likely benign
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
NM_001128831.4(CA1):c.368_369del (p.His123fs) deletion Metabolic acidosis [RCV000856819] Chr8:85333606..85333607 [GRCh38]
Chr8:86245835..86245836 [GRCh37]
Chr8:8q21.2
uncertain significance
NM_001128831.4(CA1):c.587C>T (p.Pro196Leu) single nucleotide variant not provided [RCV000965777] Chr8:85329771 [GRCh38]
Chr8:86242000 [GRCh37]
Chr8:8q21.2
benign
NM_001128831.4(CA1):c.500C>T (p.Ala167Val) single nucleotide variant not provided [RCV000968466] Chr8:85332503 [GRCh38]
Chr8:86244732 [GRCh37]
Chr8:8q21.2
benign
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3
pathogenic
GRCh37/hg19 8q21.2(chr8:85635587-86553130)x3 copy number gain not provided [RCV001006118] Chr8:85635587..86553130 [GRCh37]
Chr8:8q21.2
uncertain significance
GRCh37/hg19 8q21.13-21.3(chr8:84358585-89159915)x1 copy number loss not provided [RCV000845762] Chr8:84358585..89159915 [GRCh37]
Chr8:8q21.13-21.3
uncertain significance
NM_001128831.4(CA1):c.360C>T (p.His120=) single nucleotide variant not provided [RCV000975188] Chr8:85333615 [GRCh38]
Chr8:86245844 [GRCh37]
Chr8:8q21.2
benign
NM_001128831.4(CA1):c.428C>T (p.Ala143Val) single nucleotide variant not provided [RCV000956647] Chr8:85333547 [GRCh38]
Chr8:86245776 [GRCh37]
Chr8:8q21.2
benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1368 AgrOrtholog
COSMIC CA1 COSMIC
Ensembl Genes ENSG00000133742 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000392338 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000427773 UniProtKB/TrEMBL
  ENSP00000427852 UniProtKB/TrEMBL
  ENSP00000428923 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000429300 UniProtKB/TrEMBL
  ENSP00000429688 UniProtKB/TrEMBL
  ENSP00000429798 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000429843 UniProtKB/TrEMBL
  ENSP00000430372 UniProtKB/TrEMBL
  ENSP00000430471 UniProtKB/TrEMBL
  ENSP00000430543 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000430571 UniProtKB/TrEMBL
  ENSP00000430656 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000430710 UniProtKB/TrEMBL
  ENSP00000430737 UniProtKB/TrEMBL
  ENSP00000430861 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000430975 UniProtKB/TrEMBL
  ENSP00000443517 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000486171 UniProtKB/TrEMBL
Ensembl Transcript ENST00000431316 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000517429 UniProtKB/TrEMBL
  ENST00000517590 UniProtKB/TrEMBL
  ENST00000517618 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000519129 UniProtKB/TrEMBL
  ENST00000519991 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000520663 UniProtKB/TrEMBL
  ENST00000521679 UniProtKB/TrEMBL
  ENST00000521846 UniProtKB/TrEMBL
  ENST00000522389 UniProtKB/TrEMBL
  ENST00000522579 UniProtKB/TrEMBL
  ENST00000522662 UniProtKB/TrEMBL
  ENST00000522814 UniProtKB/TrEMBL
  ENST00000523022 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000523858 UniProtKB/TrEMBL
  ENST00000523953 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000524324 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000542576 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000626824 UniProtKB/TrEMBL
Gene3D-CATH 3.10.200.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000133742 GTEx
HGNC ID HGNC:1368 ENTREZGENE
Human Proteome Map CA1 Human Proteome Map
InterPro CA_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CA_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Carbonic_anhydrase_a-class UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Carbonic_anhydrase_a-class_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Carbonic_anhydrase_CA1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:759 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 759 ENTREZGENE
OMIM 114800 OMIM
PANTHER PTHR18952 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR18952:SF82 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Carb_anhydrase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25984 PharmGKB
PROSITE ALPHA_CA_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ALPHA_CA_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Carb_anhydrase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF51069 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt CAH1_HUMAN UniProtKB/Swiss-Prot
  E5RFE7_HUMAN UniProtKB/TrEMBL
  E5RFL2_HUMAN UniProtKB/TrEMBL
  E5RG43_HUMAN UniProtKB/TrEMBL
  E5RG81_HUMAN UniProtKB/TrEMBL
  E5RGU8_HUMAN UniProtKB/TrEMBL
  E5RH81_HUMAN UniProtKB/TrEMBL
  E5RHP7_HUMAN UniProtKB/TrEMBL
  E5RHS7_HUMAN UniProtKB/TrEMBL
  E5RIF9_HUMAN UniProtKB/TrEMBL
  E5RII2_HUMAN UniProtKB/TrEMBL
  E5RJF6_HUMAN UniProtKB/TrEMBL
  E5RJI8_HUMAN UniProtKB/TrEMBL
  H0YBE2_HUMAN UniProtKB/TrEMBL
  P00915 ENTREZGENE
  V9HWE3 ENTREZGENE, UniProtKB/TrEMBL


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-28 CA1  carbonic anhydrase 1    carbonic anhydrase I  Symbol and/or name change 5135510 APPROVED