Trpm1 (transient receptor potential cation channel, subfamily M, member 1) - Rat Genome Database

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Gene: Trpm1 (transient receptor potential cation channel, subfamily M, member 1) Rattus norvegicus
Analyze
Symbol: Trpm1
Name: transient receptor potential cation channel, subfamily M, member 1
RGD ID: 1597140
Description: Predicted to enable calcium channel activity. Predicted to be involved in G protein-coupled glutamate receptor signaling pathway; calcium ion import across plasma membrane; and visual perception. Predicted to act upstream of or within several processes, including cellular response to light stimulus; protein localization; and retinal rod cell development. Predicted to be located in endoplasmic reticulum and new growing cell tip. Predicted to be active in cell tip; dendrite; and plasma membrane. Human ortholog(s) of this gene implicated in congenital stationary night blindness and congenital stationary night blindness 1C. Orthologous to human TRPM1 (transient receptor potential cation channel subfamily M member 1); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; amphetamine; bisphenol A.
Type: protein-coding
RefSeq Status: PROVISIONAL
Previously known as: melastatin; melastatin-1; transient receptor potential cation channel subfamily M member 1
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81127,130,686 - 127,247,219 (+)NCBIGRCr8
mRatBN7.21117,718,896 - 117,835,434 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1117,718,896 - 117,834,605 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1125,693,996 - 125,809,613 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01132,876,553 - 132,992,162 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01125,707,003 - 125,822,518 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01124,983,391 - 125,101,759 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1124,983,452 - 125,099,573 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01126,092,991 - 126,210,809 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41118,583,516 - 118,700,653 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1109,974,992 - 110,090,741 (+)NCBICelera
Cytogenetic Map1q22NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
Object Symbol
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Original Reference(s)
Trpm1Ratcongenital stationary night blindness  ISORGD:13126077175555DNA:mutations:exon, intron:multiple (human)RGD 
Trpm1Ratcongenital stationary night blindness  ISORGD:13126077183084DNA:deletion, missense mutations:cds:multiple (human)RGD 
Trpm1Ratcongenital stationary night blindness  ISORGD:13126077183085DNA:mutations:multiple (human)RGD 
Trpm1RatHypertriglyceridemia  ISORGD:13126077175561DNA:SNP:intron:g.59080C>T (rs11070811) (human)RGD 
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Trpm1Ratautism spectrum disorder  ISORGD:13126078554872ClinVar Annotator: match by term: Autism spectrum disorderClinVarPMID:19050728|PMID:19289393|PMID:21844811|PMID:23044707|PMID:25255310|PMID:25741868|PMID:27569545
Trpm1Ratautistic disorder  ISORGD:13126078554872ClinVar Annotator: match by term: AutismClinVarPMID:21681106|PMID:30208311
Trpm1Ratchromosome 15q13.3 microdeletion syndrome  ISORGD:13126078554872ClinVar Annotator: match by term: Chromosome 15q13.3 microdeletion syndromeClinVarPMID:31690835
Trpm1Ratcolorectal cancer  ISORGD:13126078554872ClinVar Annotator: match by term: Familial colorectal cancerClinVarPMID:22561515|PMID:25992589|PMID:26493165|PMID:28492532
Trpm1Ratcongenital stationary night blindness  ISORGD:13126078554872ClinVar Annotator: match by term: Congenital Stationary Night Blindness, Recessive | ClinVar Annotator: match by more ...ClinVarPMID:17576681|PMID:19878917|PMID:19896113|PMID:19966281|PMID:20300565|PMID:25741868|PMID:27803854|PMID:28041643|PMID:28492532|PMID:29074561|PMID:33691579|PMID:35633130|PMID:9536098
Trpm1Ratcongenital stationary night blindness 1C  ISORGD:13126078554872ClinVar Annotator: match by term: Congenital stationary night blindness 1C | ClinVar Annotator: match by more ...ClinVarPMID:16199547|PMID:17576681|PMID:19436059|PMID:19878917|PMID:19896109|PMID:19896113|PMID:19966281|PMID:20300565|PMID:22277662|PMID:25307992|PMID:25741868|PMID:25999674|PMID:26493165|PMID:26872967|PMID:27803854|PMID:28492532|PMID:28559085|PMID:28838317|PMID:29522070|PMID:30487145|PMID:30718709|PMID:31589614|PMID:31908403|PMID:33691579|PMID:35456422|PMID:35457050|PMID:35633130|PMID:9536098
Trpm1RatEpendymomas  ISORGD:13126078554872ClinVar Annotator: match by term: EpendymomaClinVar 
Trpm1Ratfundus dystrophy  ISORGD:13126078554872ClinVar Annotator: match by term: Retinal dystrophyClinVarPMID:16199547|PMID:17576681|PMID:19896109|PMID:19896113|PMID:19966281|PMID:20300565|PMID:23714322|PMID:24715752|PMID:25307992|PMID:25741868|PMID:26633542|PMID:28341476|PMID:28492532|PMID:28559085|PMID:28726569|PMID:29522070|PMID:30487145|PMID:31427709|PMID:31589614|PMID:31645983|PMID:31725702|PMID:32141364|PMID:3378126|PMID:33781268|PMID:34426522|PMID:35119454|PMID:35456422|PMID:35457050|PMID:35567543|PMID:35633130|PMID:9536098
Trpm1Ratgenetic disease  ISORGD:13126078554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:25741868|PMID:28492532
Trpm1Ratintellectual disability  ISORGD:13126078554872ClinVar Annotator: match by term: Intellectual disabilityClinVarPMID:25741868
Trpm1RatNeurodevelopmental Disorders  ISORGD:13126078554872ClinVar Annotator: match by term: Neurodevelopmental disorderClinVarPMID:25741868
Trpm1Ratnight blindness  ISORGD:13126078554872ClinVar Annotator: match by term: Night blindnessClinVarPMID:19896113|PMID:25741868|PMID:33691579
Trpm1Ratoptic atrophy  ISORGD:13126078554872ClinVar Annotator: match by term: Optic atrophyClinVarPMID:25741868|PMID:28492532
Trpm1Ratretinitis pigmentosa  ISORGD:13126078554872ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Tapetoretinal degenerationClinVarPMID:25741868|PMID:28492532|PMID:30718709
Trpm1Ratschizophrenia  ISORGD:13126078554872ClinVar Annotator: match by term: SchizophreniaClinVarPMID:21681106|PMID:30208311
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Original Reference(s)
Trpm1Ratcongenital stationary night blindness  ISORGD:131260711554173CTD Direct Evidence: marker/mechanismCTD 
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Original Reference(s)
Trpm1Ratcongenital stationary night blindness 1C  ISSRGD:131260813592920OMIM:613216MouseDO 
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Original Reference(s)
Trpm1Ratcongenital stationary night blindness 1C  ISORGD:13126077240710 OMIM 

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Original Reference(s)
Trpm1Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionISORGD:13126086480464Tetrachlorodibenzodioxin affects the expression of TRPM1 mRNACTDPMID:21570461
Trpm1Rat2,3,7,8-tetrachlorodibenzodioxine increases expressionEXP 6480464Tetrachlorodibenzodioxin results in increased expression of TRPM1 mRNACTDPMID:33387578
Trpm1Rat4,4'-sulfonyldiphenol decreases methylationISORGD:13126076480464bisphenol S results in decreased methylation of TRPM1 geneCTDPMID:31601247
Trpm1Rat4,4'-sulfonyldiphenol affects methylationISORGD:13126086480464bisphenol S affects the methylation of TRPM1 geneCTDPMID:31683443
Trpm1Rataflatoxin B1 increases methylationISORGD:13126076480464Aflatoxin B1 results in increased methylation of TRPM1 gene; Aflatoxin B1 results in increased methylation more ...CTDPMID:27153756|PMID:30157460
Trpm1RatAflatoxin B2 alpha increases methylationISORGD:13126076480464aflatoxin B2 results in increased methylation of TRPM1 intronCTDPMID:30157460
Trpm1Ratamphetamine increases expressionEXP 6480464Amphetamine results in increased expression of TRPM1 mRNACTDPMID:30779732
Trpm1RatAzoxymethane multiple interactionsISORGD:13126086480464[titanium dioxide co-treated with Azoxymethane co-treated with Dextran Sulfate] affects the expression of TRPM1 mRNACTDPMID:29950665
Trpm1Ratbenzo[a]pyrene affects methylationISORGD:13126076480464Benzo(a)pyrene affects the methylation of TRPM1 5' UTRCTDPMID:27901495
Trpm1Ratbenzo[a]pyrene increases methylationISORGD:13126076480464Benzo(a)pyrene results in increased methylation of TRPM1 promoterCTDPMID:27901495
Trpm1Ratbenzo[e]pyrene increases methylationISORGD:13126076480464benzo(e)pyrene results in increased methylation of TRPM1 intronCTDPMID:30157460
Trpm1Ratbisphenol A decreases expressionEXP 6480464bisphenol A results in decreased expression of TRPM1 mRNACTDPMID:25181051
Trpm1Ratbisphenol A multiple interactionsISORGD:13126076480464[bisphenol A co-treated with Fulvestrant] results in decreased methylation of TRPM1 geneCTDPMID:31601247
Trpm1Ratbisphenol A decreases methylationISORGD:13126076480464bisphenol A results in decreased methylation of TRPM1 geneCTDPMID:31601247
Trpm1Ratcadmium atom multiple interactionsISORGD:13126076480464[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of TRPM1 more ...CTDPMID:35301059
Trpm1Ratcadmium dichloride multiple interactionsISORGD:13126076480464[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of TRPM1 more ...CTDPMID:35301059
Trpm1Ratcarbon nanotube decreases expressionISORGD:13126086480464Nanotubes, Carbon analog results in decreased expression of TRPM1 mRNA; Nanotubes, Carbon results in decreased more ...CTDPMID:25554681
Trpm1RatCGP 52608 multiple interactionsISORGD:13126076480464CGP 52608 promotes the reaction [RORA protein binds to TRPM1 gene]CTDPMID:28238834
Trpm1Ratchlorpyrifos increases expressionISORGD:13126086480464Chlorpyrifos results in increased expression of TRPM1 mRNACTDPMID:37019170
Trpm1Ratcopper atom increases expressionEXP 6480464Copper deficiency results in increased expression of TRPM1 mRNACTDPMID:26033743

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Biological Process
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Original Reference(s)
Trpm1Ratcalcium ion import across plasma membrane involved_inISSUniProtKB:Q7Z4N21600115GO_REF:0000024UniProtGO_REF:0000024
Trpm1Ratcalcium ion import across plasma membrane involved_inIEAUniProtKB:Q7Z4N2|ensembl:ENSP000002565521600115GO_REF:0000107EnsemblGO_REF:0000107
Trpm1Ratcalcium ion import across plasma membrane involved_inISORGD:13126071624291 PMID:23452348RGDPMID:23452348
Trpm1Ratcellular response to light stimulus involved_inISORGD:13126081624291 PMID:19861548RGDPMID:19861548
Trpm1Ratcellular response to light stimulus involved_inIEAUniProtKB:Q7Z4N2|ensembl:ENSP000002565521600115GO_REF:0000107EnsemblGO_REF:0000107
Trpm1Ratcellular response to light stimulus acts_upstream_of_or_withinISORGD:13126081624291MGI:4421441 PMID:19966281, PMID:21052544RGDPMID:19966281|PMID:21052544
Trpm1Ratcellular response to light stimulus involved_inISORGD:13126071624291 PMID:19896109RGDPMID:19896109
Trpm1RatG protein-coupled glutamate receptor signaling pathway involved_inISORGD:13126071624291 PMID:23452348RGDPMID:23452348
Trpm1RatG protein-coupled glutamate receptor signaling pathway involved_inIEAUniProtKB:Q7Z4N2|ensembl:ENSP000002565521600115GO_REF:0000107EnsemblGO_REF:0000107
Trpm1RatG protein-coupled glutamate receptor signaling pathway involved_inISSUniProtKB:Q7Z4N21600115GO_REF:0000024UniProtGO_REF:0000024
Trpm1Ratmetal ion transport involved_inIBAFB:FBgn0265194|MGI:1351901|MGI:1915917|MGI:1929996|MGI:2181435|MGI:2675603|PANTHER:PTN001013045|RGD:1311889|RGD:620053|RGD:620762|UniProtKB:A7T1N0|UniProtKB:O94759|UniProtKB:Q7Z4N2|UniProtKB:Q8TD43|UniProtKB:Q96QT4|UniProtKB:Q9BX84|UniProtKB:Q9HCF6|ZFIN:ZDB-GENE-021115-2|ZFIN:ZDB-GENE-061214-41600115GO_REF:0000033GO_CentralGO_REF:0000033
Trpm1Ratmonoatomic cation transmembrane transport involved_inISORGD:13126071624291 PMID:21278253RGDPMID:21278253
Trpm1Ratmonoatomic cation transmembrane transport involved_inIEAUniProtKB:Q7Z4N2|ensembl:ENSP000002565521600115GO_REF:0000107EnsemblGO_REF:0000107
Trpm1Ratmonoatomic cation transmembrane transport involved_inIBAFB:FBgn0265194|MGI:1351901|MGI:1929996|PANTHER:PTN001013045|RGD:1311889|RGD:620762|UniProtKB:A7T1N0|UniProtKB:O94759|UniProtKB:Q7Z4N2|UniProtKB:Q8TD43|UniProtKB:Q96QT4|UniProtKB:Q9BX84|UniProtKB:Q9HCF6|ZFIN:ZDB-GENE-061214-41600115GO_REF:0000033GO_CentralGO_REF:0000033
Trpm1Ratmonoatomic cation transmembrane transport involved_inIEAGO:00052611600115GO_REF:0000108GOCGO_REF:0000108
Trpm1Ratmonoatomic cation transmembrane transport involved_inIEAARBA:ARBA000266331600115GO_REF:0000117UniProtGO_REF:0000117
Trpm1Ratmonoatomic cation transmembrane transport involved_inISSUniProtKB:Q7Z4N21600115GO_REF:0000024UniProtGO_REF:0000024
Trpm1Ratmonoatomic ion transmembrane transport involved_inIEAUniProtKB-KW:KW-04071600115GO_REF:0000043UniProtGO_REF:0000043
Trpm1Ratmonoatomic ion transport involved_inIEAUniProtKB-KW:KW-04061600115GO_REF:0000043UniProtGO_REF:0000043
Trpm1Ratmonoatomic ion transport involved_inIEAInterPro:IPR0058211600115GO_REF:0000002InterProGO_REF:0000002
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Cellular Component
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Original Reference(s)
Trpm1Rataxon located_inIEAUniProtKB-SubCell:SL-02791600115GO_REF:0000044UniProtGO_REF:0000044
Trpm1Ratcell projection located_inIEAUniProtKB-KW:KW-09661600115GO_REF:0000043UniProtGO_REF:0000043
Trpm1Ratcell tip is_active_inISORGD:13126081624291 PMID:25997951RGDPMID:25997951
Trpm1Ratdendrite is_active_inISORGD:13126081624291 PMID:25997951RGDPMID:25997951
Trpm1Ratendoplasmic reticulum located_inISSUniProtKB:Q7Z4N21600115GO_REF:0000024UniProtGO_REF:0000024
Trpm1Ratendoplasmic reticulum located_inIEAUniProtKB-KW:KW-02561600115GO_REF:0000043UniProtGO_REF:0000043
Trpm1Ratendoplasmic reticulum located_inIEAUniProtKB:Q7Z4N2|ensembl:ENSP000002565521600115GO_REF:0000107EnsemblGO_REF:0000107
Trpm1Ratendoplasmic reticulum located_inISORGD:13126071624291 PMID:30027108RGDPMID:30027108
Trpm1Ratendoplasmic reticulum membrane located_inIEAUniProtKB-SubCell:SL-00971600115GO_REF:0000044UniProtGO_REF:0000044
Trpm1Ratmembrane located_inIEAUniProtKB-SubCell:SL-01621600115GO_REF:0000044UniProtGO_REF:0000044
Trpm1Ratmembrane located_inIEAUniProtKB-KW:KW-04721600115GO_REF:0000043UniProtGO_REF:0000043
Trpm1Ratmembrane located_inIEAInterPro:IPR0058211600115GO_REF:0000002InterProGO_REF:0000002
Trpm1Ratnew growing cell tip located_inISORGD:13126081624291 PMID:19966281RGDPMID:19966281
Trpm1Ratplasma membrane located_inIEAUniProtKB-KW:KW-10031600115GO_REF:0000043UniProtGO_REF:0000043
Trpm1Ratplasma membrane located_inIEAUniProtKB-SubCell:SL-00391600115GO_REF:0000044UniProtGO_REF:0000044
Trpm1Ratplasma membrane is_active_inIBAMGI:1351901|MGI:1915917|MGI:1929996|MGI:2181435|MGI:2675603|PANTHER:PTN001013045|RGD:620244|RGD:620762|UniProtKB:A7T1N0|UniProtKB:O94759|UniProtKB:Q7Z2W7|UniProtKB:Q8TD43|UniProtKB:Q96QT4|UniProtKB:Q9BX84|UniProtKB:Q9HCF6|WB:WBGene00001796|ZFIN:ZDB-GENE-021115-2|ZFIN:ZDB-GENE-061214-41600115GO_REF:0000033GO_CentralGO_REF:0000033
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Molecular Function
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Original Reference(s)
Trpm1Ratcalcium channel activity enablesISSUniProtKB:Q7Z4N21600115GO_REF:0000024UniProtGO_REF:0000024
Trpm1Ratcalcium channel activity enablesIBAPANTHER:PTN002674408|UniProtKB:Q7Z4N21600115GO_REF:0000033GO_CentralGO_REF:0000033
Trpm1Ratcalcium channel activity enablesIEAUniProtKB:Q7Z4N2|ensembl:ENSP000002565521600115GO_REF:0000107EnsemblGO_REF:0000107
Trpm1Ratcalcium channel activity enablesISORGD:13126071624291 PMID:23452348RGDPMID:23452348
Trpm1Ratmonoatomic cation channel activity enablesIEAARBA:ARBA000266081600115GO_REF:0000117UniProtGO_REF:0000117
Trpm1Ratmonoatomic cation channel activity enablesISORGD:13126081624291 PMID:19966281RGDPMID:19966281
Trpm1Ratmonoatomic cation transmembrane transporter activity enablesISSUniProtKB:Q7Z4N21600115GO_REF:0000024UniProtGO_REF:0000024
Trpm1Ratmonoatomic cation transmembrane transporter activity enablesIEAUniProtKB:Q7Z4N2|ensembl:ENSP000002565521600115GO_REF:0000107EnsemblGO_REF:0000107
Trpm1Ratmonoatomic cation transmembrane transporter activity enablesISORGD:13126071624291 PMID:21278253RGDPMID:21278253
Trpm1Ratmonoatomic ion channel activity enablesISORGD:13126081624291 PMID:36179691RGDPMID:36179691
Trpm1Ratmonoatomic ion channel activity enablesIEAInterPro:IPR0058211600115GO_REF:0000002InterProGO_REF:0000002
Trpm1Ratprotein binding enablesISORGD:1312607,UniProtKB:Q7Z4N2-71624291UniProtKB:P51114-2 PMID:32296183RGDPMID:32296183
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Reference Title
Reference Citation
1. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Audo I, etal., Am J Hum Genet. 2009 Nov;85(5):720-9. doi: 10.1016/j.ajhg.2009.10.013. Epub 2009 Nov 5.
2. Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Gaudet P, etal., Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
3. Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. Li Z, etal., Am J Hum Genet. 2009 Nov;85(5):711-9. doi: 10.1016/j.ajhg.2009.10.003. Epub 2009 Oct 29.
4. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
5. GOA pipeline RGD automated data pipeline
6. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
8. Genetic variants in transient receptor potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans. Thameem F, etal., Clin Chim Acta. 2011 Nov 20;412(23-24):2058-62. doi: 10.1016/j.cca.2011.03.024. Epub 2011 Apr 1.
9. Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. van Genderen MM, etal., Am J Hum Genet. 2009 Nov;85(5):730-6. doi: 10.1016/j.ajhg.2009.10.012. Epub 2009 Nov 5.
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PMID:17712480   PMID:19861548   PMID:19966281   PMID:21052544   PMID:23452348   PMID:27435061  



Trpm1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81127,130,686 - 127,247,219 (+)NCBIGRCr8
mRatBN7.21117,718,896 - 117,835,434 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1117,718,896 - 117,834,605 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1125,693,996 - 125,809,613 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01132,876,553 - 132,992,162 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01125,707,003 - 125,822,518 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01124,983,391 - 125,101,759 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1124,983,452 - 125,099,573 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01126,092,991 - 126,210,809 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41118,583,516 - 118,700,653 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1109,974,992 - 110,090,741 (+)NCBICelera
Cytogenetic Map1q22NCBI
TRPM1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381531,001,065 - 31,161,160 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1531,001,065 - 31,161,160 (-)EnsemblGRCh38hg38GRCh38
GRCh371531,293,268 - 31,453,363 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361529,080,829 - 29,181,216 (-)NCBINCBI36Build 36hg18NCBI36
Build 341529,080,844 - 29,181,216NCBI
Celera159,019,006 - 9,119,394 (-)NCBICelera
Cytogenetic Map15q13.3NCBI
HuRef158,470,226 - 8,630,487 (-)NCBIHuRef
CHM1_11531,284,115 - 31,444,331 (-)NCBICHM1_1
T2T-CHM13v2.01528,795,157 - 28,955,270 (-)NCBIT2T-CHM13v2.0
Trpm1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39763,803,583 - 63,923,630 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl763,803,583 - 63,919,523 (+)EnsemblGRCm39 Ensembl
GRCm38764,153,835 - 64,269,772 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl764,153,835 - 64,269,775 (+)EnsemblGRCm38mm10GRCm38
MGSCv37771,298,721 - 71,414,658 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36764,032,878 - 64,148,722 (+)NCBIMGSCv36mm8
Celera761,596,535 - 61,712,952 (+)NCBICelera
Cytogenetic Map7CNCBI
cM Map734.61NCBI
Trpm1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541629,814,077 - 29,939,344 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541629,846,374 - 29,880,922 (-)NCBIChiLan1.0ChiLan1.0
TRPM1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21619,808,237 - 19,886,134 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11524,532,668 - 24,693,365 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0159,492,500 - 9,653,644 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11528,530,878 - 28,690,947 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1528,530,878 - 28,690,947 (-)Ensemblpanpan1.1panPan2
TRPM1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1337,860,730 - 37,949,108 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl337,817,339 - 37,949,108 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha340,503,547 - 40,626,849 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0338,199,294 - 38,329,018 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl338,191,370 - 38,329,018 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1337,731,034 - 37,854,661 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0337,984,595 - 38,114,581 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0338,194,873 - 38,318,556 (+)NCBIUU_Cfam_GSD_1.0
Trpm1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640145,477,644 - 145,610,678 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936483724,018 - 858,855 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936483723,784 - 856,839 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TRPM1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1143,709,864 - 143,855,984 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11143,718,295 - 143,856,968 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21159,663,385 - 159,801,269 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TRPM1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12651,560,992 - 51,660,857 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2651,586,041 - 51,660,171 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604889,165,059 - 89,239,923 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Trpm1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247681,757,293 - 1,873,627 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247681,802,601 - 1,873,627 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in Trpm1
955 total Variants

Predicted Target Of
Summary Value
Count of predictions:38
Count of miRNA genes:16
Interacting mature miRNAs:19
Transcripts:ENSRNOT00000021262, ENSRNOT00000065343
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.


1 to 10 of 54 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1582234Gluco18Glucose level QTL 183.40.0003blood glucose amount (VT:0000188)blood glucose level (CMO:0000046)178479925123479925Rat
1358359Sradr1Stress Responsive Adrenal Weight QTL 14.74adrenal gland mass (VT:0010420)both adrenal glands wet weight (CMO:0000164)130882023123479925Rat
1578780Cm52Cardiac mass QTL 523.30.0001heart mass (VT:0007028)heart wet weight (CMO:0000069)181591954219808434Rat
1578654Bss10Bone structure and strength QTL 104femur morphology trait (VT:0000559)femoral neck cortical cross-sectional area (CMO:0001702)149393172159356837Rat
9590300Scort16Serum corticosterone level QTL 164.390.001blood corticosterone amount (VT:0005345)plasma corticosterone level (CMO:0001173)1103111621148111621Rat
2298545Neuinf8Neuroinflammation QTL 84.6nervous system integrity trait (VT:0010566)spinal cord beta-2 microglobulin mRNA level (CMO:0002125)157336763151090257Rat
7794788Mcs32Mammary carcinoma susceptibility QTL 322.61mammary gland integrity trait (VT:0010552)mammary tumor incidence/prevalence measurement (CMO:0000946)1115540693238914717Rat
631199Cm23Cardiac mass QTL 234.60.0004heart left ventricle mass (VT:0007031)heart left ventricle wet weight (CMO:0000071)1115585465172949803Rat
1302788Scl19Serum cholesterol QTL 194.60.001blood cholesterol amount (VT:0000180)plasma total cholesterol level (CMO:0000585)190532338123479925Rat
631569Bp93Blood pressure QTL 930.0001arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)1106047847121834139Rat

1 to 10 of 54 rows
BF410273  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21117,806,492 - 117,806,661 (+)MAPPERmRatBN7.2
Rnor_6.01125,071,071 - 125,071,239NCBIRnor6.0
Rnor_5.01126,180,121 - 126,180,289UniSTSRnor5.0
RGSC_v3.41118,671,352 - 118,671,520UniSTSRGSC3.4
Celera1110,062,683 - 110,062,851UniSTS
RH 3.4 Map11563.11UniSTS
Cytogenetic Map1q22UniSTS
BI279791  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21117,782,705 - 117,782,862 (+)MAPPERmRatBN7.2
Rnor_6.01125,047,286 - 125,047,442NCBIRnor6.0
Rnor_5.01126,156,336 - 126,156,492UniSTSRnor5.0
RGSC_v3.41118,647,566 - 118,647,722UniSTSRGSC3.4
Celera1110,038,888 - 110,039,044UniSTS
RH 3.4 Map21657.71UniSTS
Cytogenetic Map1q22UniSTS
Mlsn1  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21117,792,495 - 117,792,625 (+)MAPPERmRatBN7.2
Rnor_6.01125,057,074 - 125,057,203NCBIRnor6.0
Rnor_5.01126,166,124 - 126,166,253UniSTSRnor5.0
RGSC_v3.41118,657,355 - 118,657,484UniSTSRGSC3.4
Celera1110,048,677 - 110,048,806UniSTS
Cytogenetic Map1q22UniSTS




alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
8 11 9 76 41 47 17 24 17 6 123 49 63 41 50 30



Ensembl Acc Id: ENSRNOT00000021262   ⟹   ENSRNOP00000021262
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1117,718,896 - 117,834,605 (+)Ensembl
Rnor_6.0 Ensembl1124,983,452 - 125,099,573 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000107676   ⟹   ENSRNOP00000091126
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1117,718,896 - 117,834,605 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000117805   ⟹   ENSRNOP00000089212
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1117,718,896 - 117,792,697 (+)Ensembl
RefSeq Acc Id: NM_001037733   ⟹   NP_001032822
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81127,130,686 - 127,246,390 (+)NCBI
mRatBN7.21117,718,896 - 117,834,605 (+)NCBI
Rnor_6.01124,983,452 - 125,099,573 (+)NCBI
Rnor_5.01126,092,991 - 126,210,809 (+)NCBI
RGSC_v3.41118,583,516 - 118,700,653 (+)RGD
Celera1109,974,992 - 110,090,741 (+)RGD
Sequence:
RefSeq Acc Id: NM_001037734   ⟹   NP_001032823
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81127,130,686 - 127,246,390 (+)NCBI
mRatBN7.21117,718,896 - 117,834,605 (+)NCBI
Rnor_6.01124,983,452 - 125,099,573 (+)NCBI
Rnor_5.01126,092,991 - 126,210,809 (+)NCBI
RGSC_v3.41118,583,516 - 118,700,653 (+)RGD
Celera1109,974,992 - 110,090,741 (+)RGD
Sequence:
RefSeq Acc Id: XM_039082296   ⟹   XP_038938224
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81127,207,891 - 127,247,219 (+)NCBI
mRatBN7.21117,796,103 - 117,835,434 (+)NCBI
RefSeq Acc Id: XM_063266876   ⟹   XP_063122946
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81127,172,044 - 127,247,219 (+)NCBI
1 to 9 of 9 rows
Protein RefSeqs NP_001032822 (Get FASTA)   NCBI Sequence Viewer  
  NP_001032823 (Get FASTA)   NCBI Sequence Viewer  
  XP_038938224 (Get FASTA)   NCBI Sequence Viewer  
  XP_063122946 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein CAI30141 (Get FASTA)   NCBI Sequence Viewer  
  CAI30142 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000021262
  ENSRNOP00000021262.7
GenBank Protein Q2WEA5 (Get FASTA)   NCBI Sequence Viewer  
1 to 9 of 9 rows
RefSeq Acc Id: NP_001032822   ⟸   NM_001037733
- Peptide Label: isoform 2
- UniProtKB: Q2WEA5 (UniProtKB/Swiss-Prot),   Q2WEA4 (UniProtKB/Swiss-Prot),   F1M9X0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001032823   ⟸   NM_001037734
- Peptide Label: isoform 1
- UniProtKB: Q2WEA4 (UniProtKB/Swiss-Prot),   Q2WEA5 (UniProtKB/Swiss-Prot),   F1M9X0 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000021262   ⟸   ENSRNOT00000021262
RefSeq Acc Id: XP_038938224   ⟸   XM_039082296
- Peptide Label: isoform X2
Ensembl Acc Id: ENSRNOP00000091126   ⟸   ENSRNOT00000107676
TRPM SLOG   TRPM tetramerisation

Name Modeler Protein Id AA Range Protein Structure
AF-Q2WEA5-F1-model_v2 AlphaFold Q2WEA5 1-1628 view protein structure


eQTL   View at Phenogen
WGCNA   View at Phenogen
Tissue/Strain Expression   View at Phenogen



1 to 26 of 26 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-59079 BioCyc
Ensembl Genes ENSRNOG00000015829 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENSRNOT00000021262 ENTREZGENE
  ENSRNOT00000021262.7 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.5.1010 UniProtKB/Swiss-Prot
InterPro Ion_trans_dom UniProtKB/Swiss-Prot
  TRPM UniProtKB/Swiss-Prot
  TRPM_SLOG UniProtKB/Swiss-Prot
  TRPM_tetra UniProtKB/Swiss-Prot
  TRPM_tetra_sf UniProtKB/Swiss-Prot
KEGG Report rno:361586 UniProtKB/Swiss-Prot
NCBI Gene 361586 ENTREZGENE
PANTHER PTHR13800:SF13 UniProtKB/Swiss-Prot
  TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY M, MEMBER 6 UniProtKB/Swiss-Prot
Pfam Ion_trans UniProtKB/Swiss-Prot
  LSDAT_euk UniProtKB/Swiss-Prot
  TRPM_tetra UniProtKB/Swiss-Prot
PhenoGen Trpm1 PhenoGen
RatGTEx ENSRNOG00000015829 RatGTEx
UniProt A0A8I6A7P2_RAT UniProtKB/TrEMBL
  A0A8I6AEQ8_RAT UniProtKB/TrEMBL
  F1M9X0 ENTREZGENE
  Q2WEA4 ENTREZGENE
  Q2WEA5 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary F1M9X0 UniProtKB/Swiss-Prot
  Q2WEA4 UniProtKB/Swiss-Prot
1 to 26 of 26 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2006-11-20 Trpm1  transient receptor potential cation channel, subfamily M, member 1      Symbol and Name status set to provisional 70820 PROVISIONAL