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WormBase Tree Display for Gene: WBGene00001490

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Name Class

WBGene00001490SMapS_parentSequenceCHROMOSOME_X
IdentityVersion2
NameCGC_namefrm-3Person_evidenceWBPerson204
Sequence_nameH05G16.1
Molecular_nameH05G16.1a
H05G16.1a.1
CE43269
H05G16.1b
CE52019
H05G16.1c
CE40652
H05G16.1a.2
H05G16.1b.1
H05G16.1c.1
Other_nameCELE_H05G16.1Accession_evidenceNDBBX284606
Public_namefrm-3
DB_infoDatabaseAceViewgeneXM199
WormQTLgeneWBGene00001490
WormFluxgeneWBGene00001490
NDBlocus_tagCELE_H05G16.1
PanthergeneCAEEL|WormBase=WBGene00001490|UniProtKB=O17905
familyPTHR45858
NCBIgene186110
RefSeqproteinNM_077534.3
NM_001375142.3
NM_001351892.5
TrEMBLUniProtAccA0A1X7RBN3
G5EDC0
O17905
UniProt_GCRPUniProtAccO17905
OMIMgene300628
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
228 Apr 2017 01:35:57WBPerson1983EventAcquires_mergeWBGene00009932
Acquires_mergeWBGene00009932
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfrm
Allele (173)
StrainWBStrain00036481
WBStrain00023645
RNASeq_FPKM (74)
GO_annotation00002734
00002735
00002736
00030973
00030974
00030975
00030976
00030977
00108786
00108787
Ortholog (39)
ParalogWBGene00001366Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006431Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006450Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013682Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionEnables GABA receptor binding activity. Involved in gamma-aminobutyric acid receptor clustering. Predicted to be located in adherens junction and plasma membrane. Expressed in dorsal nerve cord. Human ortholog(s) of this gene implicated in congenital nystagmus 1. Is an ortholog of human FARP2 (FERM, ARH/RhoGEF and pleckstrin domain protein 2).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:0111790Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8079)
Molecular_infoCorresponding_CDSH05G16.1a
H05G16.1b
H05G16.1c
Corresponding_CDS_historyH05G16.1:wp196
Corresponding_transcriptH05G16.1a.1
H05G16.1a.2
H05G16.1b.1
H05G16.1c.1
Other_sequence (11)
Associated_featureWBsf663372
WBsf663373
WBsf1007045
WBsf1007046
WBsf1007047
WBsf1007048
WBsf1023897
WBsf1023898
WBsf1023899
Experimental_infoRNAi_resultWBRNAi00016198Inferred_automaticallyRNAi_primary
WBRNAi00047966Inferred_automaticallyRNAi_primary
WBRNAi00077329Inferred_automaticallyRNAi_primary
WBRNAi00015399Inferred_automaticallyRNAi_primary
WBRNAi00049303Inferred_automaticallyRNAi_primary
WBRNAi00032609Inferred_automaticallyRNAi_primary
WBRNAi00114828Inferred_automaticallyRNAi_primary
WBRNAi00033665Inferred_automaticallyRNAi_primary
Expr_pattern (12)
Drives_constructWBCnstr00013168
WBCnstr00022289
WBCnstr00031805
WBCnstr00036913
Construct_productWBCnstr00013168
WBCnstr00021429
WBCnstr00021430
WBCnstr00031805
WBCnstr00036913
WBCnstr00041671
Microarray_results (44)
Expression_cluster (183)
Interaction (15)
Map_infoMapXPosition4.71117Error0.036864
PositivePositive_cloneH05G16Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point5432
5040
Pseudo_map_position
Reference (11)
Remarkdata submitted by [Gobel V]
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