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WormBase Tree Display for Gene: WBGene00008239

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Name Class

WBGene00008239SMapS_parentSequenceC50H2
IdentityVersion2
NameCGC_namefshr-1Paper_evidenceWBPaper00026667
Person_evidenceWBPerson1139
Sequence_nameC50H2.1
Molecular_nameC50H2.1a
C50H2.1a.1
CE28214
C50H2.1b
CE48138
C50H2.1b.1
Other_namelgrAccession_evidenceEMBLAF224743
CELE_C50H2.1Accession_evidenceNDBBX284605
Public_namefshr-1
DB_infoDatabaseAceViewgene5K373
WormQTLgeneWBGene00008239
WormFluxgeneWBGene00008239
NDBlocus_tagCELE_C50H2.1
PanthergeneCAEEL|WormBase=WBGene00008239|UniProtKB=L8EC40
familyPTHR24372
NCBIgene179381
RefSeqproteinNM_073147.7
NM_001276924.3
TrEMBLUniProtAccL8EC40
G5EG04
UniProt_GCRPUniProtAccL8EC40
OMIMgene136435
152790
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
212 Sep 2005 16:03:13WBPerson2970Name_changeCGC_namefshr-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfshr
Allele (65)
StrainWBStrain00031623
WBStrain00007212
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (51)
ParalogWBGene00011454Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionfshr-1 encodes a putative neuropeptide receptor required for normalacetylcholine secretion by synapses; FSHR-1 is orthologous to humanfollicle-stimulating hormone receptor (OMIM:136435; mutated in ovariandysgenesis), thyrotropin receptor (OMIM:603372; mutated inhyperthyroidism), and luteinizing hormone receptor (OMIM:152790, mutatedin precocious puberty); fshr-1 mutants have abnormally many GFP::SNB-1puncta at synapses, suggesting exocytotic defects; the requirement forFSHR-1 and ten other predicted neuropeptide signalling proteins incholinergic neurotransmission indicates that such signalling isimportant for regulating acetylcholine release at neuromuscularjunctions; possible ligands of FSHR-1 are FLP-1 and NLP-12.Paper_evidenceWBPaper00026667
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated09 Nov 2006 00:00:00
Automated_descriptionPredicted to enable G protein-coupled peptide receptor activity. Involved in defense response to other organism; response to oxidative stress; and stress response to cadmium ion. Predicted to be located in plasma membrane. Expressed in intestine; neurons; pharynx; spermatheca; and vulva. Human ortholog(s) of this gene implicated in several diseases, including cystadenocarcinoma (multiple); disorder of sexual development (multiple); and sex cord-gonadal stromal tumor (multiple). Is an ortholog of human FSHR (follicle stimulating hormone receptor) and LHCGR (luteinizing hormone/choriogonadotropin receptor).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_model (16)
Molecular_infoCorresponding_CDSC50H2.1a
C50H2.1b
Corresponding_CDS_historyC50H2.1:wp52
Corresponding_transcriptC50H2.1a.1
C50H2.1b.1
Other_sequenceJI171853.1
Tcol_isotig10998
JI473293.1
CJC04547_1
Tcol_isotig10997
JI468453.1
Associated_featureWBsf647114
WBsf647115
WBsf661588
WBsf232300
WBsf232301
Experimental_infoRNAi_result (12)
Expr_patternExpr3541
Expr4567
Expr7940
Expr16472
Expr1012556
Expr1033582
Expr1146942
Expr2011911
Expr2030148
Drives_constructWBCnstr00006333
WBCnstr00007211
WBCnstr00007212
WBCnstr00007213
WBCnstr00011465
WBCnstr00013014
WBCnstr00033124
WBCnstr00043063
Construct_productWBCnstr00006333
WBCnstr00007211
WBCnstr00007212
WBCnstr00007213
WBCnstr00020873
WBCnstr00033124
WBCnstr00041283
WBCnstr00041284
WBCnstr00041285
WBCnstr00043063
Regulate_expr_clusterWBPaper00048530:fshr-1(ok778)_PA14_upregulated
WBPaper00048530:fshr-1(ok778)_upregulated
Microarray_results (22)
Expression_cluster (125)
Interaction (38)
WBProcessWBbiopr:00000039
Map_infoMapVPosition2.20466Error0.001111
PositivePositive_cloneC50H2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5520
5436
Pseudo_map_position
Reference (45)
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