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WormBase Tree Display for Gene: WBGene00004779

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Name Class

WBGene00004779EvidencePaper_evidenceWBPaper00002710
SMapS_parentSequenceY22D7AR
IdentityVersion3
NameCGC_nameser-4Person_evidenceWBPerson32
Sequence_nameY22D7AR.13
Molecular_nameY22D7AR.13
Y22D7AR.13.1
CE29370
Other_namecer-1Paper_evidenceWBPaper00002710
WBPaper00006180
5HT-CePaper_evidenceWBPaper00002710
WBPaper00006180
CELE_Y22D7AR.13Accession_evidenceNDBBX284603
Public_nameser-4
DB_infoDatabaseAceViewgene3C814
WormQTLgeneWBGene00004779
WormFluxgeneWBGene00004779
NDBlocus_tagCELE_Y22D7AR.13
PanthergeneCAEEL|WormBase=WBGene00004779|UniProtKB=G5EGH0
familyPTHR24247
NCBIgene175322
RefSeqproteinNM_065051.8
TrEMBLUniProtAccG5EGH0
UniProt_GCRPUniProtAccG5EGH0
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
215 Dec 2005 15:56:16WBPerson2970Name_changeOther_namecer-1
315 Dec 2005 15:56:16WBPerson2970Name_changeOther_name5HT-Ce
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classser
Allele (265)
StrainWBStrain00031461
WBStrain00000209
WBStrain00055583
WBStrain00055584
WBStrain00055062
WBStrain00055576
WBStrain00055575
WBStrain00055580
WBStrain00055579
WBStrain00055574
RNASeq_FPKM (74)
GO_annotation (27)
Ortholog (44)
Paralog (20)
Structured_descriptionConcise_descriptionser-4 encodes an ortholog of mammalian 5-HT1 metabotropic serotoninreceptors; SER-4 is required for normal inhibition of movement by 5-HT,with ser-4 mutants being hyperactive; SER-4 is partly required for maletail curling, with ser-4 mutants showing reduced curling in exogenous5-HT; SER-4 is dispensable for the stimulation of egg-laying by 5-HT andby the uptake inhibitor fluoxetine; SER-4 may actually inhibitegg-laying, since egg-laying ser-4 mutants are moderately hypersensitiveto 5-HT, and mutant ser-4 hermaphrodites are partly depleted of eggs,suggesting that their egg-laying is weakly constitutive; however, SER-4is required for stimulation of egg-laying by the tricyclicantidepressant imipramine, suggesting that imipramine drives HSNs tosecrete some non-5-HT neurotransmitter which then activates SER-4; SER-4is expressed in neurons (RIB and RIS, other head, pharyngeal,sublateral, retrovesicular ganglion, PVT, and either DVA or DVC); SER-4has a low affinity for serotonin (5-HT), and overall pharmacologicalsimilarities to mammalian 5-HT1 receptors; SER-4 is probably antagonizedby mianserin; heterologously expressed SER-4, when challenged with 5-HT,diminishes intracellular adenylate cyclase activity; LIM-6 is requiredfor normal expression of SER-4 in RIS interneurons.Paper_evidenceWBPaper00002710
WBPaper00006180
WBPaper00024420
WBPaper00024527
WBPaper00025141
WBPaper00025145
WBPaper00026843
WBPaper00028762
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated20 Dec 2006 00:00:00
Automated_descriptionEnables G protein-coupled serotonin receptor activity. Involved in regulation of locomotion and serotonin receptor signaling pathway. Predicted to be located in dendrite. Expressed in neurons; vm2; and vulval cell. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; attention deficit hyperactivity disorder; conduct disorder; and panic disorder. Is an ortholog of human HTR1A (5-hydroxytryptamine receptor 1A).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:12995Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5287)
DOID:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5286)
DOID:594Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5286)
DOID:0060001Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5286)
DOID:2030Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5286)
DOID:1596Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5286)
DOID:1094Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5287)
DOID:0050741Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5286)
Molecular_infoCorresponding_CDSY22D7AR.13
Corresponding_transcriptY22D7AR.13.1
Other_sequence (32)
Associated_feature (14)
Experimental_infoRNAi_resultWBRNAi00069695Inferred_automaticallyRNAi_primary
WBRNAi00069703Inferred_automaticallyRNAi_primary
WBRNAi00069737Inferred_automaticallyRNAi_primary
WBRNAi00027718Inferred_automaticallyRNAi_primary
WBRNAi00055679Inferred_automaticallyRNAi_primary
WBRNAi00069727Inferred_automaticallyRNAi_primary
WBRNAi00069719Inferred_automaticallyRNAi_primary
WBRNAi00069711Inferred_automaticallyRNAi_primary
Expr_patternExpr2710
Expr4333
Expr10554
Expr13790
Expr13883
Expr16105
Expr1013909
Expr1159204
Expr2015749
Expr2033982
Drives_constructWBCnstr00000004
WBCnstr00006800
WBCnstr00011926
WBCnstr00015416
WBCnstr00042764
Construct_productWBCnstr00040229
Microarray_results (18)
Expression_cluster (171)
InteractionWBInteraction000133998
WBInteraction000136821
WBInteraction000136913
WBInteraction000138057
WBInteraction000139088
WBInteraction000140940
WBInteraction000172909
WBInteraction000175561
WBInteraction000361546
WBProcessWBbiopr:00000001
Map_infoMapIIIPosition-18.935Error0.267694
PositivePositive_cloneY22D7ARInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4656
Pseudo_map_position
ReferenceWBPaper00002710
WBPaper00006180
WBPaper00010752
WBPaper00015026
WBPaper00017010
WBPaper00023946
WBPaper00023951
WBPaper00023953
WBPaper00024420
WBPaper00024527
WBPaper00025141
WBPaper00025145
WBPaper00025350
WBPaper00026263
WBPaper00026843
WBPaper00028134
WBPaper00028135
WBPaper00028157
WBPaper00028260
WBPaper00028762
WBPaper00028865
WBPaper00029150
WBPaper00030761
WBPaper00031241
WBPaper00031915
WBPaper00032196
WBPaper00032335
WBPaper00032677
WBPaper00032852
WBPaper00032881
WBPaper00033168
WBPaper00033181
WBPaper00033950
WBPaper00034151
WBPaper00034152
WBPaper00034156
WBPaper00034162
WBPaper00034655
WBPaper00034731
WBPaper00036766
WBPaper00037320
WBPaper00038382
WBPaper00038491
WBPaper00039260
WBPaper00039294
WBPaper00039349
WBPaper00040158
WBPaper00041535
WBPaper00042584
WBPaper00043522
WBPaper00043908
WBPaper00044457
WBPaper00045105
WBPaper00045634
WBPaper00046292
WBPaper00048542
WBPaper00048791
WBPaper00049202
WBPaper00050753
WBPaper00052771
WBPaper00055090
WBPaper00056790
WBPaper00060134
WBPaper00060405
WBPaper00060976
WBPaper00061107
WBPaper00061589
WBPaper00062289
WBPaper00062298
WBPaper00062563
WBPaper00062573
WBPaper00063695
WBPaper00064144
WBPaper00064652
WBPaper00065366
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