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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)
InteractionWBInteraction000050841
WBInteraction000050842
WBInteraction000052700
WBInteraction000052701
WBInteraction000114275
WBInteraction000162600
WBInteraction000164450
WBInteraction000167720
WBInteraction000169865
WBInteraction000174125
WBInteraction000233128
WBInteraction000233163
WBInteraction000272831
WBInteraction000280493
WBInteraction000344046
WBInteraction000349645
WBInteraction000354521
WBInteraction000361956
WBInteraction000382122
WBInteraction000392059
WBInteraction000403023
WBInteraction000406220
WBInteraction000406467
WBInteraction000411016
WBInteraction000420238
WBInteraction000427604
WBInteraction000438704
WBInteraction000456265
WBInteraction000459125
WBInteraction000459539
WBInteraction000461115
WBInteraction000503896
WBInteraction000503897
WBInteraction000503898
WBInteraction000503899
WBInteraction000534831
WBInteraction000536172
WBInteraction000583590
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