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WormBase Tree Display for Gene: WBGene00021437

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Name Class

WBGene00021437SMapS_parentSequenceY39A3B
IdentityVersion2
NameCGC_namelgc-42Person_evidenceWBPerson2536
WBPerson1430
Sequence_nameY39A3B.2
Molecular_nameY39A3B.2a
Y39A3B.2a.1
CE46491
Y39A3B.2b
CE54407
Y39A3B.2b.1
Other_nameCELE_Y39A3B.2Accession_evidenceNDBBX284603
Public_namelgc-42
DB_infoDatabaseAceViewgene3D91
WormQTLgeneWBGene00021437
WormFluxgeneWBGene00021437
NDBlocus_tagCELE_Y39A3B.2
PanthergeneCAEEL|WormBase=WBGene00021437|UniProtKB=Q9N517
familyPTHR18945
NCBIgene189722
RefSeqproteinNM_001404273.1
NM_065088.6
TrEMBLUniProtAccA0A8S4QD70
Q9N517
UniProt_GCRPUniProtAccA0A8S4QD70
OMIMgene138491
138492
305990
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:04WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
218 Jan 2008 14:49:34WBPerson2970Name_changeCGC_namelgc-42
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlgc
Allele (153)
StrainWBStrain00050982
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (38)
Paralog (100)
Structured_descriptionAutomated_descriptionPredicted to enable transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential. Predicted to contribute to chloride channel activity. Predicted to be involved in chloride transmembrane transport. Predicted to be located in neuron projection and synapse. Human ortholog(s) of this gene implicated in hyperekplexia 1; hyperekplexia 2; and syndromic X-linked intellectual disability Pilorge type. Is an ortholog of several human genes including GLRA1 (glycine receptor alpha 1); GLRA2 (glycine receptor alpha 2); and GLRB (glycine receptor beta).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:0070422Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4327)
DOID:0060696Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4326)
DOID:0060697Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4329)
Molecular_infoCorresponding_CDSY39A3B.2a
Y39A3B.2b
Corresponding_CDS_historyY39A3B.2:wp104
Y39A3B.2:wp227
Corresponding_transcriptY39A3B.2a.1
Y39A3B.2b.1
Other_sequence (24)
Associated_featureWBsf991436
WBsf991437
WBsf991438
WBsf991439
WBsf991440
WBsf1014340
WBsf1014341
WBsf1014342
WBsf1014343
WBsf1014344
Experimental_infoRNAi_resultWBRNAi00056136Inferred_automaticallyRNAi_primary
WBRNAi00006992Inferred_automaticallyRNAi_primary
WBRNAi00036899Inferred_automaticallyRNAi_primary
Expr_patternExpr1012912
Expr1159649
Expr2013121
Expr2031353
Drives_constructWBCnstr00024553
Construct_productWBCnstr00024553
Microarray_results (19)
Expression_cluster (72)
InteractionWBInteraction000031336
WBInteraction000295740
WBInteraction000354963
WBInteraction000507941
Map_infoMapIIIPosition-15.6805Error0.005588
PositivePositive_cloneY39A3BInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
RemarkMap 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