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WormBase Tree Display for Gene: WBGene00000583

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Name Class

WBGene00000583EvidencePerson_evidenceWBPerson651
WBPerson260
WBPerson385
SMapS_parentSequenceC48E7
IdentityVersion1
NameCGC_namecof-2Person_evidenceWBPerson260
Sequence_nameC48E7.5
Molecular_nameC48E7.5
C48E7.5.1
CE36279
Other_namecol-57
ofm-2Person_evidenceWBPerson260
CELE_C48E7.5Accession_evidenceNDBBX284601
Public_namecof-2
DB_infoDatabaseAceViewgene1G827
WormQTLgeneWBGene00000583
WormFluxgeneWBGene00000583
NDBlocus_tagCELE_C48E7.5
PanthergeneCAEEL|WormBase=WBGene00000583|UniProtKB=G5EBT7
familyPTHR23192
NCBIgene183582
RefSeqproteinNM_059403.5
TrEMBLUniProtAccG5EBT7
UniProt_GCRPUniProtAccG5EBT7
OMIMgene608603
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcof
Allele (28)
RNASeq_FPKM (74)
GO_annotation00010186
00010187
00010188
00010189
Ortholog (50)
ParalogWBGene00006845Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00008543Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptioncof-2 encodes a type II transmembrane protein containing extracellular collage-like repeats and a highly conserved olfactomedin (OLF) domain, and is homologous to human GLC1A, which when mutated leads to glaucome primary open angle (OMIM:137750); a cof-2::gfp promoter fusion is expressed in muscle cells.Paper_evidenceWBPaper00004103
WBPaper00006427
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated13 Jul 2015 00:00:00
Automated_descriptionPredicted to be involved in signal transduction. Predicted to be located in extracellular space. Human ortholog(s) of this gene implicated in lethal congenital contracture syndrome. Is an ortholog of human GLDN (gliomedin).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:0060558Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29514)
Molecular_infoCorresponding_CDSC48E7.5
Corresponding_CDS_historyC48E7.5:wp116
Corresponding_transcriptC48E7.5.1
Other_sequenceJI166496.1
JI167173.1
Dviv_isotig26478
Oden_isotig21470
Associated_featureWBsf643344
WBsf217778
WBsf217779
Experimental_infoRNAi_resultWBRNAi00029947Inferred_automaticallyRNAi_primary
WBRNAi00042743Inferred_automaticallyRNAi_primary
WBRNAi00042737Inferred_automaticallyRNAi_primary
WBRNAi00003197Inferred_automaticallyRNAi_primary
WBRNAi00003196Inferred_automaticallyRNAi_primary
WBRNAi00042744Inferred_automaticallyRNAi_primary
Expr_patternExpr3194
Expr1014871
Expr1146734
Expr2010288
Expr2028530
Drives_constructWBCnstr00037446
Construct_productWBCnstr00037446
AntibodyWBAntibody00000826
Microarray_results (25)
Expression_cluster (88)
InteractionWBInteraction000354025
WBInteraction000501569
Map_infoMapIPosition0.885296Error0.001203
PositivePositive_cloneC48E7Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4841
4805
4217
Pseudo_map_position
ReferenceWBPaper00006427
WBPaper00024680
WBPaper00038491
WBPaper00055090
RemarkC48E7.4 has been merged into C48E7.5Person_evidenceWBPerson260
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