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WormBase Tree Display for Gene: WBGene00001796

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Name Class

WBGene00001796SMapS_parentSequenceF54D1
IdentityVersion1
NameCGC_namegtl-2Person_evidenceWBPerson51
Sequence_nameF54D1.5
Molecular_nameF54D1.5
F54D1.5.1
CE40563
Other_nameCELE_F54D1.5Accession_evidenceNDBBX284604
Public_namegtl-2
DB_infoDatabaseAceViewgene4M45
WormQTLgeneWBGene00001796
WormFluxgeneWBGene00001796
NDBlocus_tagCELE_F54D1.5
PanthergeneCAEEL|WormBase=WBGene00001796|UniProtKB=Q20766
familyPTHR13800
NCBIgene178036
RefSeqproteinNM_069717.7
TrEMBLUniProtAccQ20766
UniProt_GCRPUniProtAccQ20766
OMIMgene603576
605692
608961
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgtl
AlleleWBVar01490501
WBVar01500079
WBVar02058954
WBVar02058955
WBVar02058956
WBVar01731092
WBVar00275570
WBVar00275571
WBVar00250456
WBVar00275572
WBVar00601259
WBVar02079211
WBVar01498996
WBVar01499925
WBVar02134676
WBVar01499585
WBVar01499586
WBVar00942256
WBVar00942257
WBVar00942258
WBVar00942259
WBVar00942260
WBVar00942261
WBVar01966975
WBVar01966976
WBVar00942262
WBVar01857939
WBVar00942263
WBVar01857940
WBVar00942264
WBVar01857941
WBVar00942265
WBVar01857942
WBVar00942266
WBVar00942267
WBVar00942268
WBVar00942269
WBVar00942270
WBVar00942271
WBVar00942272
WBVar00942273
WBVar00942274
WBVar00942275
WBVar00942276
WBVar00942277
WBVar00942278
WBVar00942279
WBVar00942280
WBVar00942281
WBVar00942282
WBVar00942283
WBVar00942284
WBVar00942285
WBVar00942286
WBVar00942287
WBVar00942288
WBVar00942289
WBVar00942290
WBVar00942291
WBVar00942292
WBVar00942293
WBVar00942294
WBVar00942295
WBVar00942296
WBVar00942297
WBVar00942298
WBVar00191986
WBVar00191987
WBVar00191988
WBVar00264929
WBVar01894155
WBVar00435609
WBVar00435610
WBVar00435611
WBVar00435612
WBVar00435613
WBVar00435614
WBVar00435615
WBVar00435616
WBVar00435617
WBVar00435618
WBVar00435619
WBVar00435620
WBVar00435621
WBVar00435622
WBVar01795542
WBVar00435623
WBVar00435624
WBVar00435625
WBVar01500245
WBVar00601218
WBVar01454192
WBVar01454193
WBVar01846963
StrainWBStrain00024196
WBStrain00005419
WBStrain00049842
WBStrain00049843
RNASeq_FPKM (74)
GO_annotation00069079
00069080
00069081
00069082
00069083
00109391
00109392
00109393
00109394
Ortholog (48)
ParalogWBGene00001651Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00001795Caenorhabditis 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-2 encodes a predicted receptor-activated calcium channel and represents a family of calcium channels, the other two family members being gtl-1 and gon-2.Paper_evidenceWBPaper00011683
WBPaper00023556
Curator_confirmedWBPerson324
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable monoatomic cation channel activity. Predicted to be involved in monoatomic cation transmembrane transport. Located in basal plasma membrane. Expressed in excretory canal; excretory cell; hypodermis; pharyngeal muscle cell; and pharynx. Used to study MASA syndrome. 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_infoExperimental_modelDOID:0060246
Potential_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)
Models_disease_assertedWBDOannot00000053
Molecular_infoCorresponding_CDSF54D1.5
Corresponding_CDS_historyF54D1.5:wp57
F54D1.5:wp167
Corresponding_transcriptF54D1.5.1
Other_sequence (12)
Associated_featureWBsf718194
WBsf997800
WBsf997801
WBsf1018191
WBsf021262
WBsf229125
Experimental_infoRNAi_resultWBRNAi00109632Inferred_automaticallyRNAi_primary
WBRNAi00015597Inferred_automaticallyRNAi_primary
WBRNAi00109535Inferred_automaticallyRNAi_primary
WBRNAi00109341Inferred_automaticallyRNAi_primary
WBRNAi00048282Inferred_automaticallyRNAi_primary
WBRNAi00109244Inferred_automaticallyRNAi_primary
WBRNAi00109438Inferred_automaticallyRNAi_primary
WBRNAi00001304Inferred_automaticallyRNAi_primary
Expr_pattern (8)
Drives_constructWBCnstr00007205
WBCnstr00011623
WBCnstr00013198
WBCnstr00013672
WBCnstr00013883
WBCnstr00036677
WBCnstr00042689
Construct_productWBCnstr00011623
WBCnstr00013198
WBCnstr00013672
WBCnstr00013883
WBCnstr00036677
WBCnstr00042689
WBCnstr00042690
Microarray_results (19)
Expression_cluster (120)
Interaction (21)
Map_infoMapIVPosition4.94064Error0.001769
PositivePositive_cloneF54D1Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4386
Pseudo_map_position
Reference (24)
RemarkSequence connection from Kwan CSM, Ragnauth CD and Baylis HA [021008 ck1]
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