CA14 (carbonic anhydrase 14) - Rat Genome Database

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Gene: CA14 (carbonic anhydrase 14) Homo sapiens
Analyze
Symbol: CA14
Name: carbonic anhydrase 14
RGD ID: 1317436
HGNC Page HGNC
Description: Predicted to have carbonate dehydratase activity. Predicted to be involved in one-carbon metabolic process. Predicted to localize to plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CA-XIV; carbonate dehydratase XIV; carbonic anhydrase XIV; carbonic dehydratase; CAXiV
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: AL451074.1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1150,257,251 - 150,265,078 (+)EnsemblGRCh38hg38GRCh38
GRCh381150,257,258 - 150,265,862 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371150,230,169 - 150,237,478 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361148,488,047 - 148,504,102 (+)NCBINCBI36hg18NCBI36
Build 341147,043,290 - 147,050,549NCBI
Celera1123,345,949 - 123,353,209 (+)NCBI
Cytogenetic Map1q21.2NCBI
HuRef1121,608,885 - 121,616,145 (+)NCBIHuRef
CHM1_11151,625,869 - 151,633,204 (+)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
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
1. GOA_HUMAN data from the GO Consortium
2. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10512682   PMID:11172051   PMID:12028451   PMID:12477932   PMID:12611920   PMID:12975309   PMID:14578124   PMID:14702039   PMID:15342556   PMID:15489334   PMID:16710414   PMID:17881426  
PMID:20170095   PMID:20379614   PMID:21873635   PMID:21988832   PMID:24374484   PMID:25056061   PMID:26186194   PMID:28514442  


Genomics

Comparative Map Data
CA14
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1150,257,251 - 150,265,078 (+)EnsemblGRCh38hg38GRCh38
GRCh381150,257,258 - 150,265,862 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371150,230,169 - 150,237,478 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361148,488,047 - 148,504,102 (+)NCBINCBI36hg18NCBI36
Build 341147,043,290 - 147,050,549NCBI
Celera1123,345,949 - 123,353,209 (+)NCBI
Cytogenetic Map1q21.2NCBI
HuRef1121,608,885 - 121,616,145 (+)NCBIHuRef
CHM1_11151,625,869 - 151,633,204 (+)NCBICHM1_1
Car14
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39395,805,080 - 95,812,443 (-)NCBIGRCm39mm39
GRCm39 Ensembl395,805,080 - 95,812,003 (-)Ensembl
GRCm38395,897,768 - 95,905,117 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl395,897,768 - 95,904,691 (-)EnsemblGRCm38mm10GRCm38
MGSCv37395,701,723 - 95,708,562 (-)NCBIGRCm37mm9NCBIm37
MGSCv36395,983,205 - 95,990,044 (-)NCBImm8
Celera397,331,353 - 97,338,218 (-)NCBICelera
Cytogenetic Map3F2.1NCBI
Ca14
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.22183,442,263 - 183,449,207 (-)NCBI
Rnor_6.0 Ensembl2198,010,349 - 198,016,898 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.02198,010,142 - 198,017,635 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02217,500,302 - 217,507,935 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42190,683,916 - 190,690,229 (-)NCBIRGSC3.4rn4RGSC3.4
Celera2175,971,924 - 175,978,237 (-)NCBICelera
Cytogenetic Map2q34NCBI
Ca14
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955413510,089 - 516,892 (-)EnsemblChiLan1.0
ChiLan1.0NW_004955413510,089 - 516,892 (-)NCBIChiLan1.0ChiLan1.0
CA14
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11129,253,787 - 129,261,676 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1129,253,787 - 129,261,676 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01125,602,521 - 125,610,323 (+)NCBIMhudiblu_PPA_v0panPan3
CA14
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11759,504,181 - 59,510,497 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1759,504,483 - 59,510,127 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1758,950,038 - 58,956,854 (+)NCBI
ROS_Cfam_1.01760,519,100 - 60,525,928 (+)NCBI
UMICH_Zoey_3.11759,349,547 - 59,356,380 (+)NCBI
UNSW_CanFamBas_1.01759,433,284 - 59,440,110 (+)NCBI
UU_Cfam_GSD_1.01760,161,286 - 60,168,105 (+)NCBI
Ca14
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505821,514,788 - 21,521,689 (+)NCBI
SpeTri2.0NW_004936580545,221 - 552,071 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CA14
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl498,821,578 - 98,828,736 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1498,821,577 - 98,828,934 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
CA14
(Chlorocebus sabaeus - African green monkey)
No map positions available.
Ca14
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462477218,011,094 - 18,018,585 (+)NCBI

Position Markers
SGC31751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371150,237,829 - 150,237,958UniSTSGRCh37
Build 361148,504,453 - 148,504,582RGDNCBI36
Celera1123,353,560 - 123,353,689RGD
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.13-q31.3UniSTS
HuRef1121,616,496 - 121,616,625UniSTS
GeneMap99-GB4 RH Map1542.76UniSTS
GeneMap99-GB4 RH Map1540.36UniSTS
Whitehead-RH Map1634.9UniSTS
SHGC-32182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371150,237,331 - 150,237,433UniSTSGRCh37
Build 361148,503,955 - 148,504,057RGDNCBI36
Celera1123,353,062 - 123,353,164RGD
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.13-q31.3UniSTS
HuRef1121,615,998 - 121,616,100UniSTS
GeneMap99-GB4 RH Map1537.26UniSTS
GeneMap99-GB4 RH Map1553.37UniSTS
Whitehead-RH Map1627.7UniSTS
NCBI RH Map11003.6UniSTS
CA14_9388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371150,237,054 - 150,237,484UniSTSGRCh37
Build 361148,503,678 - 148,504,108RGDNCBI36
Celera1123,352,785 - 123,353,215RGD
HuRef1121,615,721 - 121,616,151UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1079
Count of miRNA genes:638
Interacting mature miRNAs:741
Transcripts:ENST00000369111, ENST00000483993, ENST00000607082, ENST00000607652, ENST00000607751
Prediction methods: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
High
Medium 101 112 21 21 44 20 291 107 448 9 32 4 2 63
Low 1541 711 998 349 396 340 2395 1484 3100 192 933 837 20 1 22 1739 2
Below cutoff 783 2027 700 250 1423 102 1612 595 173 214 484 762 150 1146 945 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_012113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006711259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006711261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB025904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC242988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074765 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308964 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL138795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC034412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP361793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT020054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000369111   ⟹   ENSP00000358107
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1150,257,774 - 150,265,078 (+)Ensembl
RefSeq Acc Id: ENST00000483993   ⟹   ENSP00000475869
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1150,258,094 - 150,263,376 (+)Ensembl
RefSeq Acc Id: ENST00000582010
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1150,257,851 - 150,261,331 (+)Ensembl
RefSeq Acc Id: ENST00000607082   ⟹   ENSP00000475238
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1150,263,044 - 150,264,891 (+)Ensembl
RefSeq Acc Id: ENST00000607652
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1150,257,875 - 150,263,831 (+)Ensembl
RefSeq Acc Id: ENST00000647854   ⟹   ENSP00000498013
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1150,257,251 - 150,265,049 (+)Ensembl
RefSeq Acc Id: NM_012113   ⟹   NP_036245
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,774 - 150,265,078 (+)NCBI
GRCh371150,229,554 - 150,237,478 (+)NCBI
Build 361148,488,047 - 148,504,102 (+)NCBI Archive
Celera1123,345,949 - 123,353,209 (+)RGD
HuRef1121,608,885 - 121,616,145 (+)RGD
CHM1_11151,625,869 - 151,633,204 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245059   ⟹   XP_005245116
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
GRCh371150,229,554 - 150,237,478 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245060   ⟹   XP_005245117
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
GRCh371150,229,554 - 150,237,478 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006711259   ⟹   XP_006711322
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006711261   ⟹   XP_006711324
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509379   ⟹   XP_011507681
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000893   ⟹   XP_016856382
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000894   ⟹   XP_016856383
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000895   ⟹   XP_016856384
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000896   ⟹   XP_016856385
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,265,862 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_036245   ⟸   NM_012113
- Peptide Label: precursor
- UniProtKB: Q9ULX7 (UniProtKB/Swiss-Prot),   A8K3J4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245117   ⟸   XM_005245060
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_005245116   ⟸   XM_005245059
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_006711322   ⟸   XM_006711259
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_006711324   ⟸   XM_006711261
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011507681   ⟸   XM_011509379
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016856382   ⟸   XM_017000893
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016856385   ⟸   XM_017000896
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_016856383   ⟸   XM_017000894
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016856384   ⟸   XM_017000895
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: ENSP00000475869   ⟸   ENST00000483993
RefSeq Acc Id: ENSP00000358107   ⟸   ENST00000369111
RefSeq Acc Id: ENSP00000475238   ⟸   ENST00000607082
RefSeq Acc Id: ENSP00000498013   ⟸   ENST00000647854
Protein Domains
Alpha-carbonic anhydrase

Promoters
RGD ID:6856950
Promoter ID:EPDNEW_H1640
Type:initiation region
Name:CA14_3
Description:carbonic anhydrase 14
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1641  EPDNEW_H1642  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,258 - 150,257,318EPDNEW
RGD ID:6856952
Promoter ID:EPDNEW_H1641
Type:initiation region
Name:CA14_1
Description:carbonic anhydrase 14
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1640  EPDNEW_H1642  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,257,867 - 150,257,927EPDNEW
RGD ID:6856954
Promoter ID:EPDNEW_H1642
Type:initiation region
Name:CA14_2
Description:carbonic anhydrase 14
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1640  EPDNEW_H1641  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381150,258,101 - 150,258,161EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q21.2(chr1:150034379-150414215)x1 copy number loss See cases [RCV000051175] Chr1:150034379..150414215 [GRCh38]
Chr1:150006344..150311095 [GRCh37]
Chr1:148272968..148653315 [NCBI36]
Chr1:1q21.2
uncertain significance
GRCh38/hg38 1q21.2(chr1:150214843-150565007)x3 copy number gain See cases [RCV000138735] Chr1:150214843..150565007 [GRCh38]
Chr1:150187139..150537483 [GRCh37]
Chr1:148453763..148804107 [NCBI36]
Chr1:1q21.2
likely benign
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2
pathogenic
GRCh37/hg19 1q21.1-21.3(chr1:144927578-153223600)x3 copy number gain Chromosome 1q21.1 duplication syndrome [RCV000223957] Chr1:144927578..153223600 [GRCh37]
Chr1:1q21.1-21.3
pathogenic
GRCh37/hg19 1q21.1-21.3(chr1:143753740-151399970)x3 copy number gain See cases [RCV000447109] Chr1:143753740..151399970 [GRCh37]
Chr1:1q21.1-21.3
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_012113.3(CA14):c.863-4C>T single nucleotide variant not provided [RCV000902693] Chr1:150263790 [GRCh38]
Chr1:150236189 [GRCh37]
Chr1:1q21.2
likely benign
NM_012113.3(CA14):c.934G>A (p.Ala312Thr) single nucleotide variant not provided [RCV000906282] Chr1:150263865 [GRCh38]
Chr1:150236264 [GRCh37]
Chr1:1q21.2
benign
NM_012113.3(CA14):c.447G>A (p.Glu149=) single nucleotide variant not provided [RCV000955775] Chr1:150262572 [GRCh38]
Chr1:150234971 [GRCh37]
Chr1:1q21.2
benign
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1372 AgrOrtholog
COSMIC CA14 COSMIC
Ensembl Genes ENSG00000118298 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000358107 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000475238 UniProtKB/TrEMBL
  ENSP00000475869 UniProtKB/TrEMBL
  ENSP00000498013 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000369111 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000483993 UniProtKB/TrEMBL
  ENST00000607082 UniProtKB/TrEMBL
  ENST00000647854 UniProtKB/Swiss-Prot
Gene3D-CATH 3.10.200.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000118298 GTEx
HGNC ID HGNC:1372 ENTREZGENE
Human Proteome Map CA14 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_CA14 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23632 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 23632 ENTREZGENE
OMIM 604832 OMIM
PANTHER PTHR18952 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR18952:SF84 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Carb_anhydrase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25988 PharmGKB
PROSITE 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 A8K3J4 ENTREZGENE, UniProtKB/TrEMBL
  CAH14_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  U3KPU6_HUMAN UniProtKB/TrEMBL
  U3KQH0_HUMAN UniProtKB/TrEMBL
UniProt Secondary Q5TB24 UniProtKB/Swiss-Prot
  Q8NCF4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-28 CA14  carbonic anhydrase 14    carbonic anhydrase XIV  Symbol and/or name change 5135510 APPROVED