TRPC2 (transient receptor potential cation channel subfamily C member 2 (pseudogene)) - Rat Genome Database

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Gene: TRPC2 (transient receptor potential cation channel subfamily C member 2 (pseudogene)) Homo sapiens
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Symbol: TRPC2
Name: transient receptor potential cation channel subfamily C member 2 (pseudogene)
RGD ID: 1350987
HGNC Page HGNC:12334
Description: Predicted to enable diacylglycerol binding activity; inositol 1,4,5 trisphosphate binding activity; and store-operated calcium channel activity. Predicted to act upstream of or within several processes, including female courtship behavior; inter-male aggressive behavior; and mating behavior, sex discrimination. Predicted to be located in dendrite membrane and endomembrane system.
Type: pseudo (Ensembl: transcribed_unprocessed_pseudogene)
RefSeq Status: VALIDATED
Previously known as: transient receptor potential cation channel subfamily C member 2, pseudogene
RGD Orthologs
Mouse
Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38113,626,460 - 3,637,559 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl113,616,679 - 3,637,549 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p14 Ensembl113,626,438 - 3,637,677 (+)EnsemblGRCh38hg38GRCh38
GRCh37113,647,690 - 3,658,789 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36113,604,290 - 3,615,365 (+)NCBINCBI36Build 36hg18NCBI36
Build 34113,604,289 - 3,615,365NCBI
Celera113,659,826 - 3,663,093 (+)NCBICelera
Cytogenetic Map11p15.4NCBI
HuRef113,384,984 - 3,396,073 (+)NCBIHuRef
CHM1_1113,646,765 - 3,657,866 (+)NCBICHM1_1
T2T-CHM13v2.0113,671,928 - 3,682,997 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7568191   PMID:11290752   PMID:12032305   PMID:12601176   PMID:12631698   PMID:14505576   PMID:14699131   PMID:16382100   PMID:17217050   PMID:20210993   PMID:24756702  


Genomics

Comparative Map Data
TRPC2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38113,626,460 - 3,637,559 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl113,616,679 - 3,637,549 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p14 Ensembl113,626,438 - 3,637,677 (+)EnsemblGRCh38hg38GRCh38
GRCh37113,647,690 - 3,658,789 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36113,604,290 - 3,615,365 (+)NCBINCBI36Build 36hg18NCBI36
Build 34113,604,289 - 3,615,365NCBI
Celera113,659,826 - 3,663,093 (+)NCBICelera
Cytogenetic Map11p15.4NCBI
HuRef113,384,984 - 3,396,073 (+)NCBIHuRef
CHM1_1113,646,765 - 3,657,866 (+)NCBICHM1_1
T2T-CHM13v2.0113,671,928 - 3,682,997 (+)NCBIT2T-CHM13v2.0
Trpc2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397101,732,323 - 101,746,071 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7101,732,323 - 101,745,603 (+)EnsemblGRCm39 Ensembl
GRCm387102,083,116 - 102,096,864 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7102,083,116 - 102,096,396 (+)EnsemblGRCm38mm10GRCm38
MGSCv377109,214,227 - 109,244,930 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367101,949,701 - 101,970,155 (+)NCBIMGSCv36mm8
Celera7102,440,894 - 102,463,475 (+)NCBICelera
Cytogenetic Map7E2NCBI
cM Map754.71NCBI
Trpc2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81165,871,991 - 165,885,339 (+)NCBIGRCr8
mRatBN7.21156,460,009 - 156,473,039 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1156,440,305 - 156,473,073 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1164,437,596 - 164,450,988 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01171,617,684 - 171,631,076 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01164,494,996 - 164,508,394 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01167,180,103 - 167,192,456 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1167,169,442 - 167,192,801 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01173,368,155 - 173,381,696 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41159,542,801 - 159,576,294 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11159,642,649 - 159,655,999 (+)NCBI
Celera1154,528,993 - 154,541,346 (+)NCBICelera
Cytogenetic Map1q32NCBI

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:991
Count of miRNA genes:518
Interacting mature miRNAs:575
Transcripts:ENST00000399582, ENST00000451043, ENST00000526541
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597453421GWAS1549495_Hsmall vessel stroke QTL GWAS1549495 (human)0.000001small vessel stroke1136306483630649Human
1558691SCL8_HSerum cholesterol level QTL 8 (human)1.2Lipid levelHDL cholesterol1115227071Human
1559107SCL32_HSerum cholesterol level QTL 32 (human)3.27Lipid levelLDL cholesterol11289243028892430Human
1559113SCL31_HSerum cholesterol level QTL 31 (human)3.72Lipid levelLDL cholesterol11289243028892430Human

Markers in Region
PMC152292P2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37113,642,574 - 3,642,717UniSTSGRCh37
Build 36113,599,150 - 3,599,293RGDNCBI36
Cytogenetic Map11p15.4-p15.3UniSTS
HuRef113,379,868 - 3,380,011UniSTS
PMC152292P3  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37113,658,422 - 3,658,680UniSTSGRCh37
Build 36113,614,998 - 3,615,256RGDNCBI36
Celera113,662,726 - 3,662,984RGD
Cytogenetic Map11p15.4-p15.3UniSTS
HuRef113,395,706 - 3,395,964UniSTS
PMC21939P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37113,647,723 - 3,647,954UniSTSGRCh37
Build 36113,604,299 - 3,604,530RGDNCBI36
Cytogenetic Map11p15.4-p15.3UniSTS
HuRef113,385,017 - 3,385,248UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1200 2207 2725 2106 4082 1603 2004 3 544 1402 390 2057 6262 5724 10 3043 705 1536 1368 156

Sequence


Ensembl Acc Id: ENST00000451043
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,616,679 - 3,637,549 (+)Ensembl
Ensembl Acc Id: ENST00000526541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,626,448 - 3,637,676 (+)Ensembl
Ensembl Acc Id: ENST00000688797
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,626,454 - 3,637,672 (+)Ensembl
Ensembl Acc Id: ENST00000689523
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,626,439 - 3,637,672 (+)Ensembl
Ensembl Acc Id: ENST00000696867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,626,439 - 3,637,672 (+)Ensembl
Ensembl Acc Id: ENST00000696868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,626,454 - 3,637,672 (+)Ensembl
Ensembl Acc Id: ENST00000744238
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,626,438 - 3,637,677 (+)Ensembl
Ensembl Acc Id: ENST00000744239
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,626,447 - 3,637,677 (+)Ensembl
Ensembl Acc Id: ENST00000744240
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,634,316 - 3,637,677 (+)Ensembl
Ensembl Acc Id: ENST00000744241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl113,634,934 - 3,637,677 (+)Ensembl
RefSeq Acc Id: NR_002720
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38113,626,460 - 3,637,559 (+)NCBI
GRCh37113,647,690 - 3,658,789 (+)NCBI
Build 36113,604,290 - 3,615,365 (+)NCBI Archive
Celera113,659,826 - 3,663,093 (+)RGD
HuRef113,384,984 - 3,396,073 (+)NCBI
CHM1_1113,646,765 - 3,657,866 (+)NCBI
T2T-CHM13v2.0113,671,928 - 3,682,997 (+)NCBI
Sequence:
Protein Sequences
GenBank Protein BAE46900 (Get FASTA)   NCBI Sequence Viewer  


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12334 AgrOrtholog
COSMIC TRPC2 COSMIC
Ensembl Genes ENSG00000182048 Ensembl
  ENSG00000290962 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000526541 ENTREZGENE
GTEx ENSG00000182048 GTEx
  ENSG00000290962 GTEx
HGNC ID HGNC:12334 ENTREZGENE
Human Proteome Map TRPC2 Human Proteome Map
NCBI Gene 7221 ENTREZGENE
PharmGKB PA37007 PharmGKB


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-01-16 TRPC2  transient receptor potential cation channel subfamily C member 2 (pseudogene)    transient receptor potential cation channel subfamily C member 2, pseudogene  Symbol and/or name change 5135510 APPROVED
2016-02-02 TRPC2  transient receptor potential cation channel subfamily C member 2, pseudogene    transient receptor potential cation channel, subfamily C, member 2, pseudogene  Symbol and/or name change 5135510 APPROVED
2011-07-27 TRPC2  transient receptor potential cation channel, subfamily C, member 2, pseudogene  TRPC2  transient receptor potential cation channel, subfamily C, member 2 (pseudogene)  Symbol and/or name change 5135510 APPROVED