CA7 (carbonic anhydrase 7) - Rat Genome Database

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Gene: CA7 (carbonic anhydrase 7) Homo sapiens
Analyze
Symbol: CA7
Name: carbonic anhydrase 7
RGD ID: 1315686
HGNC Page HGNC
Description: Predicted to have hydro-lyase activity. Predicted to be involved in one-carbon metabolic process and regulation of intracellular pH. Predicted to localize to cytosol.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CA-VII; carbonate dehydratase VII; carbonic anhydrase VII; carbonic dehydratase VII; CAVII
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 Ensembl1666,844,414 - 66,854,153 (+)EnsemblGRCh38hg38GRCh38
GRCh381666,844,414 - 66,854,149 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371666,878,317 - 66,888,050 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361665,435,783 - 65,445,551 (+)NCBINCBI36hg18NCBI36
Build 341665,435,891 - 65,445,541NCBI
Celera1651,386,593 - 51,396,359 (+)NCBI
Cytogenetic Map16q22.1NCBI
HuRef1652,752,480 - 52,762,235 (+)NCBIHuRef
CHM1_11668,285,378 - 68,295,146 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytosol  (TAS)

Molecular Function

References

Additional References at PubMed
PMID:1783392   PMID:7574487   PMID:10493829   PMID:11875253   PMID:12417987   PMID:12477932   PMID:15489334   PMID:15528236   PMID:15686895   PMID:20493921   PMID:21873635   PMID:22020285  
PMID:23851572   PMID:25885898   PMID:27688658  


Genomics

Comparative Map Data
CA7
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1666,844,414 - 66,854,153 (+)EnsemblGRCh38hg38GRCh38
GRCh381666,844,414 - 66,854,149 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371666,878,317 - 66,888,050 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361665,435,783 - 65,445,551 (+)NCBINCBI36hg18NCBI36
Build 341665,435,891 - 65,445,541NCBI
Celera1651,386,593 - 51,396,359 (+)NCBI
Cytogenetic Map16q22.1NCBI
HuRef1652,752,480 - 52,762,235 (+)NCBIHuRef
CHM1_11668,285,378 - 68,295,146 (+)NCBICHM1_1
Car7
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398105,261,326 - 105,276,979 (+)NCBIGRCm39mm39
GRCm39 Ensembl8105,261,321 - 105,276,975 (+)Ensembl
GRCm388104,534,694 - 104,550,347 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8104,534,689 - 104,550,343 (+)EnsemblGRCm38mm10GRCm38
MGSCv378107,064,707 - 107,074,243 (+)NCBIGRCm37mm9NCBIm37
MGSCv368107,429,936 - 107,439,472 (+)NCBImm8
Celera8108,773,242 - 108,782,734 (+)NCBICelera
Cytogenetic Map8D3NCBI
Car7
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.219429,063 - 438,478 (-)NCBI
Rnor_6.0 Ensembl19636,545 - 645,937 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.019636,545 - 645,935 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.019630,356 - 639,746 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.419365,680 - 375,074 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.119365,695 - 375,513 (-)NCBI
Celera19424,600 - 433,992 (-)NCBICelera
Cytogenetic Map19p14NCBI
Ca7
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543323,365,718 - 23,374,548 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495543323,365,832 - 23,374,517 (+)NCBIChiLan1.0ChiLan1.0
CA7
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11666,262,259 - 66,272,316 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1666,262,362 - 66,271,665 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01647,161,021 - 47,170,800 (+)NCBIMhudiblu_PPA_v0panPan3
CA7
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1582,446,239 - 82,455,445 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl582,446,246 - 82,455,590 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha582,434,936 - 82,444,145 (-)NCBI
ROS_Cfam_1.0582,882,872 - 82,892,083 (-)NCBI
UMICH_Zoey_3.1582,706,026 - 82,715,234 (-)NCBI
UNSW_CanFamBas_1.0582,392,889 - 82,402,094 (-)NCBI
UU_Cfam_GSD_1.0583,031,862 - 83,041,073 (-)NCBI
Ca7
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934942,469,000 - 42,477,123 (-)NCBI
SpeTri2.0NW_00493647517,112,004 - 17,120,105 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CA7
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl627,548,706 - 27,563,861 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1627,548,647 - 27,563,966 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
CA7
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1552,541,008 - 52,551,307 (+)NCBI
ChlSab1.1 Ensembl552,541,527 - 52,551,389 (+)Ensembl
Ca7
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474619,640,436 - 19,648,708 (-)NCBI

Position Markers
SHGC-60620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371666,887,465 - 66,887,684UniSTSGRCh37
Build 361665,444,966 - 65,445,185RGDNCBI36
Celera1651,395,774 - 51,395,993RGD
Cytogenetic Map16q22.1UniSTS
HuRef1652,761,650 - 52,761,869UniSTS
Whitehead-RH Map16299.8UniSTS
NCBI RH Map16508.6UniSTS
CA7_4490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371666,887,331 - 66,888,131UniSTSGRCh37
Build 361665,444,832 - 65,445,632RGDNCBI36
Celera1651,395,640 - 51,396,440RGD
HuRef1652,761,516 - 52,762,316UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1199
Count of miRNA genes:457
Interacting mature miRNAs:499
Transcripts:ENST00000338437, ENST00000394069, ENST00000548332
Prediction methods:Miranda, Rnahybrid, Targetscan
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 adipose tissue appendage pharyngeal arch
High
Medium 342 1 56 3 546 4
Low 398 5 70 16 137 7 196 28 1804 23 440 114 9 4 16 1
Below cutoff 1033 1795 1207 250 766 123 2367 1207 1164 211 755 1139 127 765 1673 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000338437   ⟹   ENSP00000345659
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1666,844,414 - 66,854,147 (+)Ensembl
RefSeq Acc Id: ENST00000394069   ⟹   ENSP00000377632
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1666,844,932 - 66,854,153 (+)Ensembl
RefSeq Acc Id: ENST00000548332   ⟹   ENSP00000447178
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1666,844,932 - 66,853,720 (+)Ensembl
RefSeq Acc Id: NM_001014435   ⟹   NP_001014435
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,844,929 - 66,854,147 (+)NCBI
GRCh371666,878,282 - 66,888,052 (+)NCBI
Build 361665,436,338 - 65,445,551 (+)NCBI Archive
Celera1651,386,593 - 51,396,359 (+)RGD
HuRef1652,752,480 - 52,762,235 (+)RGD
CHM1_11668,285,937 - 68,295,146 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001365337   ⟹   NP_001352266
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,844,929 - 66,854,147 (+)NCBI
RefSeq Acc Id: NM_005182   ⟹   NP_005173
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,844,414 - 66,854,147 (+)NCBI
GRCh371666,878,282 - 66,888,052 (+)NCBI
Build 361665,435,783 - 65,445,551 (+)NCBI Archive
Celera1651,386,593 - 51,396,359 (+)RGD
HuRef1652,752,480 - 52,762,235 (+)RGD
CHM1_11668,285,378 - 68,295,146 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011523312   ⟹   XP_011521614
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,844,440 - 66,854,149 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_005173   ⟸   NM_005182
- Peptide Label: isoform 1
- UniProtKB: P43166 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001014435   ⟸   NM_001014435
- Peptide Label: isoform 2
- UniProtKB: P43166 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011521614   ⟸   XM_011523312
- Peptide Label: isoform X1
- UniProtKB: P43166 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001352266   ⟸   NM_001365337
- Peptide Label: isoform 2
RefSeq Acc Id: ENSP00000447178   ⟸   ENST00000548332
RefSeq Acc Id: ENSP00000345659   ⟸   ENST00000338437
RefSeq Acc Id: ENSP00000377632   ⟸   ENST00000394069
Protein Domains
Alpha-carbonic anhydrase

Promoters
RGD ID:7232449
Promoter ID:EPDNEW_H21969
Type:initiation region
Name:CA7_1
Description:carbonic anhydrase 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H21970  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,844,417 - 66,844,477EPDNEW
RGD ID:7232447
Promoter ID:EPDNEW_H21970
Type:initiation region
Name:CA7_2
Description:carbonic anhydrase 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H21969  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,844,929 - 66,844,989EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16q13-22.2(chr16:56883592-71279975)x3 copy number gain See cases [RCV000052405] Chr16:56883592..71279975 [GRCh38]
Chr16:56917504..71313878 [GRCh37]
Chr16:55475005..69871379 [NCBI36]
Chr16:16q13-22.2
pathogenic
GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3 copy number gain See cases [RCV000052408] Chr16:58456122..74708723 [GRCh38]
Chr16:58490026..74742621 [GRCh37]
Chr16:57047527..73300122 [NCBI36]
Chr16:16q21-23.1
pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3 copy number gain See cases [RCV000052421] Chr16:65313395..90081985 [GRCh38]
Chr16:65347298..90148393 [GRCh37]
Chr16:63904799..88675894 [NCBI36]
Chr16:16q21-24.3
pathogenic
GRCh38/hg38 16q21-22.1(chr16:62179331-67770414)x1 copy number loss See cases [RCV000053333] Chr16:62179331..67770414 [GRCh38]
Chr16:62213235..67804317 [GRCh37]
Chr16:60770736..66361818 [NCBI36]
Chr16:16q21-22.1
pathogenic
GRCh38/hg38 16q21-22.1(chr16:63318997-70555249)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]|See cases [RCV000053334] Chr16:63318997..70555249 [GRCh38]
Chr16:63352901..70589152 [GRCh37]
Chr16:61910402..69146653 [NCBI36]
Chr16:16q21-22.1
pathogenic
GRCh38/hg38 16q21-22.1(chr16:64311275-68062011)x1 copy number loss See cases [RCV000053335] Chr16:64311275..68062011 [GRCh38]
Chr16:64345179..68095914 [GRCh37]
Chr16:62902680..66653415 [NCBI36]
Chr16:16q21-22.1
pathogenic
GRCh38/hg38 16q22.1(chr16:66694180-67865445)x1 copy number loss See cases [RCV000053336] Chr16:66694180..67865445 [GRCh38]
Chr16:66728083..67899348 [GRCh37]
Chr16:65285584..66456849 [NCBI36]
Chr16:16q22.1
pathogenic
NM_001014435.1(CA7):c.65G>A (p.Arg22Gln) single nucleotide variant Malignant melanoma [RCV000071177] Chr16:66847222 [GRCh38]
Chr16:66881125 [GRCh37]
Chr16:65438626 [NCBI36]
Chr16:16q22.1
not provided
GRCh38/hg38 16q21-22.1(chr16:66245888-67473023)x1 copy number loss See cases [RCV000134709] Chr16:66245888..67473023 [GRCh38]
Chr16:66279791..67506926 [GRCh37]
Chr16:64837292..66064427 [NCBI36]
Chr16:16q21-22.1
pathogenic
GRCh38/hg38 16q21-24.1(chr16:62925929-84585795)x3 copy number gain See cases [RCV000135863] Chr16:62925929..84585795 [GRCh38]
Chr16:62959833..84619401 [GRCh37]
Chr16:61517334..83176902 [NCBI36]
Chr16:16q21-24.1
pathogenic
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3 copy number gain See cases [RCV000139426] Chr16:65511483..90096995 [GRCh38]
Chr16:65545386..90163403 [GRCh37]
Chr16:64102887..88690904 [NCBI36]
Chr16:16q21-24.3
pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3 copy number gain See cases [RCV000142578] Chr16:64389378..90081985 [GRCh38]
Chr16:64423281..90148393 [GRCh37]
Chr16:62980782..88675894 [NCBI36]
Chr16:16q21-24.3
pathogenic|likely pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3 copy number gain See cases [RCV000143425] Chr16:52899183..90088654 [GRCh38]
Chr16:52933095..90155062 [GRCh37]
Chr16:51490596..88682563 [NCBI36]
Chr16:16q12.2-24.3
pathogenic
GRCh38/hg38 16q12.1-22.1(chr16:49685521-68401712)x3 copy number gain See cases [RCV000143752] Chr16:49685521..68401712 [GRCh38]
Chr16:49719432..68435615 [GRCh37]
Chr16:48276933..66993116 [NCBI36]
Chr16:16q12.1-22.1
pathogenic
GRCh38/hg38 16q21-23.3(chr16:65957829-83611443)x3 copy number gain See cases [RCV000143742] Chr16:65957829..83611443 [GRCh38]
Chr16:65991732..83645048 [GRCh37]
Chr16:64549233..82202549 [NCBI36]
Chr16:16q21-23.3
pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1 copy number loss Ductal breast carcinoma [RCV000207138] Chr16:46615804..90142285 [GRCh37]
Chr16:16q11.2-24.3
uncertain significance
GRCh37/hg19 16q12.2-22.2(chr16:55359026-70884455)x1 copy number loss Ductal breast carcinoma [RCV000207067] Chr16:55359026..70884455 [GRCh37]
Chr16:16q12.2-22.2
likely pathogenic|uncertain significance
Single allele complex Ductal breast carcinoma [RCV000207314] Chr16:56368689..90141355 [GRCh37]
Chr16:16q12.2-24.3
uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3 copy number gain See cases [RCV000446110] Chr16:46464488..90155062 [GRCh37]
Chr16:16q11.2-24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16q21-22.1(chr16:66537021-67369281)x3 copy number gain See cases [RCV000510388] Chr16:66537021..67369281 [GRCh37]
Chr16:16q21-22.1
uncertain significance
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3
uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1 copy number loss PARP Inhibitor response [RCV000626435] Chr16:46455960..90354753 [GRCh37]
Chr16:16q11.2-24.3
drug response
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3 copy number gain See cases [RCV000512511] Chr16:57051473..89797669 [GRCh37]
Chr16:16q13-24.3
pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1 copy number loss PARP Inhibitor response [RCV000626429] Chr16:46497599..90354753 [GRCh37]
Chr16:16q11.2-24.3
drug response
GRCh37/hg19 16q12.2-22.2(chr16:54416050-72453266)x3 copy number gain not provided [RCV000683820] Chr16:54416050..72453266 [GRCh37]
Chr16:16q12.2-22.2
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16q21-22.1(chr16:65669673-70180183)x1 copy number loss not provided [RCV001006797] Chr16:65669673..70180183 [GRCh37]
Chr16:16q21-22.1
pathogenic
NM_005182.3(CA7):c.444T>C (p.Val148=) single nucleotide variant not provided [RCV000897775] Chr16:66851549 [GRCh38]
Chr16:66885452 [GRCh37]
Chr16:16q22.1
likely benign
GRCh37/hg19 16q22.1(chr16:66797153-67109495)x3 copy number gain not provided [RCV000848721] Chr16:66797153..67109495 [GRCh37]
Chr16:16q22.1
uncertain significance
NM_005182.3(CA7):c.65A>T (p.Tyr22Phe) single nucleotide variant not provided [RCV000963147] Chr16:66847054 [GRCh38]
Chr16:66880957 [GRCh37]
Chr16:16q22.1
likely benign
GRCh37/hg19 16q22.1(chr16:66876199-67150370)x3 copy number gain not provided [RCV000846681] Chr16:66876199..67150370 [GRCh37]
Chr16:16q22.1
uncertain significance
NM_005182.3(CA7):c.198C>T (p.His66=) single nucleotide variant not provided [RCV000885799] Chr16:66847187 [GRCh38]
Chr16:66881090 [GRCh37]
Chr16:16q22.1
benign
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3 copy number gain not provided [RCV001249359] Chr16:61524229..90155062 [GRCh37]
Chr16:16q21-24.3
not provided

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1381 AgrOrtholog
COSMIC CA7 COSMIC
Ensembl Genes ENSG00000168748 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000345659 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000377632 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000447178 UniProtKB/TrEMBL
Ensembl Transcript ENST00000338437 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000394069 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000548332 UniProtKB/TrEMBL
Gene3D-CATH 3.10.200.10 UniProtKB/Swiss-Prot
GTEx ENSG00000168748 GTEx
HGNC ID HGNC:1381 ENTREZGENE
Human Proteome Map CA7 Human Proteome Map
InterPro alpha_CA_VII UniProtKB/Swiss-Prot
  CA_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CA_dom_sf UniProtKB/Swiss-Prot
  Carbonic_anhydrase_a-class UniProtKB/Swiss-Prot
  Carbonic_anhydrase_a-class_CS UniProtKB/Swiss-Prot
KEGG Report hsa:766 UniProtKB/Swiss-Prot
NCBI Gene 766 ENTREZGENE
OMIM 114770 OMIM
PANTHER PTHR18952 UniProtKB/Swiss-Prot
Pfam Carb_anhydrase UniProtKB/Swiss-Prot
PharmGKB PA25996 PharmGKB
PROSITE ALPHA_CA_1 UniProtKB/Swiss-Prot
  ALPHA_CA_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Carb_anhydrase UniProtKB/Swiss-Prot
Superfamily-SCOP SSF51069 UniProtKB/Swiss-Prot
UniProt CAH7_HUMAN UniProtKB/Swiss-Prot
  F8W0L0_HUMAN UniProtKB/TrEMBL
  P43166 ENTREZGENE
UniProt Secondary Q541F0 UniProtKB/Swiss-Prot
  Q86YU0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-28 CA7  carbonic anhydrase 7    carbonic anhydrase VII  Symbol and/or name change 5135510 APPROVED
2011-09-01 CA7  carbonic anhydrase VII  CA7  carbonic anhydrase VII  Symbol and/or name change 5135510 APPROVED