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WormBase Tree Display for Gene: WBGene00004402

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Name Class

WBGene00004402EvidencePaper_evidenceWBPaper00018136
SMapS_parentSequenceY116A8C
IdentityVersion1
NameCGC_namerom-3Person_evidenceWBPerson232
Sequence_nameY116A8C.14
Molecular_nameY116A8C.14a
Y116A8C.14a.1
CE39642
Y116A8C.14b
CE50609
Y116A8C.14b.1
Other_nameCELE_Y116A8C.14Accession_evidenceNDBBX284604
Public_namerom-3
DB_infoDatabaseAceViewgene4R906
WormQTLgeneWBGene00004402
WormFluxgeneWBGene00004402
NDBlocus_tagCELE_Y116A8C.14
PanthergeneCAEEL|EnsemblGenome=WBGene00004402|UniProtKB=Q9U2S3
familyPTHR45965
NCBIgene191000
RefSeqproteinNM_070612.2
NM_001313037.1
TrEMBLUniProtAccA0A0K3AV34
Q9U2S3
UniProt_GCRPUniProtAccQ9U2S3
OMIMgene614404
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:35WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrom
Allele (163)
RNASeq_FPKM (74)
GO_annotation00001380
00001381
00001382
00001383
00099565
00099566
00099567
00099568
00112780
00112781
Ortholog (36)
ParalogWBGene00020683Caenorhabditis elegansFrom_analysisTreeFam
WBGene00004403Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00004400Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004401Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004404Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable serine-type endopeptidase activity. Predicted to be involved in regulation of epidermal growth factor receptor signaling pathway and regulation of protein secretion. Predicted to be located in endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in palmoplantar keratoderma-esophageal carcinoma syndrome. Is an ortholog of human RHBDF1 (rhomboid 5 homolog 1) and RHBDF2 (rhomboid 5 homolog 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:0111506Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20788)
Molecular_infoCorresponding_CDSY116A8C.14a
Y116A8C.14b
Corresponding_CDS_historyY116A8C.14:wp153
Corresponding_transcriptY116A8C.14a.1
Y116A8C.14b.1
Other_sequence (12)
Associated_featureWBsf1018935
Experimental_infoRNAi_resultWBRNAi00055430Inferred_automaticallyRNAi_primary
WBRNAi00019916Inferred_automaticallyRNAi_primary
WBRNAi00062579Inferred_automaticallyRNAi_primary
Expr_patternExpr1027458
Expr1158944
Expr2015408
Expr2033643
Microarray_results (18)
Expression_cluster (90)
Interaction (32)
Map_infoMapIVPosition15.8195Error0.008429
PositivePositive_cloneY116A8CInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00011463
WBPaper00018136
WBPaper00024876
WBPaper00038491
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