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WormBase Tree Display for Gene: WBGene00001795

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Name Class

WBGene00001795EvidenceCGC_data_submission
SMapS_parentSequenceC05C12
IdentityVersion1
NameCGC_namegtl-1Person_evidenceWBPerson51
Sequence_nameC05C12.3
Molecular_nameC05C12.3
C05C12.3.1
CE33754
Other_nametag-33CGC_data_submission
CELE_C05C12.3Accession_evidenceNDBBX284604
Public_namegtl-1
DB_infoDatabaseAceViewgene4M14
WormQTLgeneWBGene00001795
WormFluxgeneWBGene00001795
NDBlocus_tagCELE_C05C12.3
PanthergeneCAEEL|WormBase=WBGene00001795|UniProtKB=G5ECM4
familyPTHR13800
NCBIgene178031
RefSeqproteinNM_069710.6
TrEMBLUniProtAccG5ECM4
UniProt_GCRPUniProtAccG5ECM4
OMIMgene603576
605692
608961
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgtl
Allele (118)
StrainWBStrain00003262
WBStrain00035612
RNASeq_FPKM (74)
GO_annotation00012064
00012065
00012066
00012067
00012068
00012069
Ortholog (46)
ParalogWBGene00001651Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00001796Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000425Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004149Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008731Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020972Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021404Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021408Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptiongtl-1 encodes a TRPM subfamily member of the TRP channel family that affects the periodicity of the defecation cycle in combination with gon-2; expression includes the intestine.Paper_evidenceWBPaper00005092
WBPaper00011328
Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable monoatomic cation channel activity. Involved in defecation. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in amyotrophic lateral sclerosis-parkinsonism/dementia complex 1; cataract; and congenital stationary night blindness 1C. Is an ortholog of human TRPM1 (transient receptor potential cation channel subfamily M member 1); TRPM3 (transient receptor potential cation channel subfamily M member 3); and TRPM7 (transient receptor potential cation channel subfamily M member 7).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:0110867Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7146)
DOID:0050534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7146)
DOID:0111246Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17994)
DOID:83Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17992)
Molecular_infoCorresponding_CDSC05C12.3
Corresponding_CDS_historyC05C12.3:wp99
Corresponding_transcriptC05C12.3.1
Other_sequenceFK807706.1
MHC01321_1
MH01590
Dviv_isotig25122
FM207828.1
Associated_featureWBsf668304
WBsf1018190
WBsf230849
Experimental_infoRNAi_resultWBRNAi00010181Inferred_automaticallyRNAi_primary
WBRNAi00039701Inferred_automaticallyRNAi_primary
WBRNAi00001394Inferred_automaticallyRNAi_primary
WBRNAi00001519Inferred_automaticallyRNAi_primary
Expr_patternChronogram1622
Expr3713
Expr5160
Expr8230
Expr8232
Expr1017897
Expr1031057
Expr1143801
Expr2012342
Expr2030579
Drives_constructWBCnstr00003737
WBCnstr00007204
WBCnstr00007207
WBCnstr00007208
WBCnstr00007209
WBCnstr00011622
WBCnstr00013197
WBCnstr00021190
WBCnstr00036678
Construct_productWBCnstr00011622
WBCnstr00013197
WBCnstr00036678
Microarray_results (18)
Expression_cluster (177)
Interaction (18)
Map_infoMapIVPosition4.92955Error0.001473
PositivePositive_cloneC05C12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4386
4526
Pseudo_map_position
ReferenceWBPaper00010099
WBPaper00011328
WBPaper00011683
WBPaper00023556
WBPaper00024755
WBPaper00024894
WBPaper00025331
WBPaper00026597
WBPaper00027280
WBPaper00028115
WBPaper00029042
WBPaper00031549
WBPaper00031896
WBPaper00035380
WBPaper00035487
WBPaper00036046
WBPaper00036498
WBPaper00038142
WBPaper00038410
WBPaper00038491
WBPaper00040955
WBPaper00041112
WBPaper00045423
WBPaper00048884
WBPaper00055090
WBPaper00059257
WBPaper00059396
WBPaper00059520
WBPaper00064809
RemarkSequence connection from Kwan CSM, Ragnauth CD and Baylis HA [021008 ck1]
Gene name created from parsing 'genotype' field from CGC strain informationCGC_data_submission
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene