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WormBase Tree Display for Gene: WBGene00008832

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Name Class

WBGene00008832SMapS_parentSequenceF14H8
IdentityVersion2
NameCGC_nameobr-2Person_evidenceWBPerson1105
Sequence_nameF14H8.1
Molecular_nameF14H8.1a
F14H8.1a.1
CE35859
F14H8.1b
CE42504
F14H8.1c
CE46315
F14H8.1b.1
F14H8.1c.1
Other_nameCELE_F14H8.1Accession_evidenceNDBBX284605
Public_nameobr-2
DB_infoDatabaseAceViewgene5P492
WormQTLgeneWBGene00008832
WormFluxgeneWBGene00008832
NDBlocus_tagCELE_F14H8.1
PanthergeneCAEEL|WormBase=WBGene00008832|UniProtKB=Q93485
familyPTHR10972
NCBIgene180003
RefSeqproteinNM_001269713.3
NM_074294.5
NM_001129445.5
TrEMBLUniProtAccB2D6P3
G1K0Y0
Q93485
UniProt_GCRPUniProtAccQ93485
OMIMgene606731
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
202 Jul 2004 16:55:44WBPerson1971Name_changeCGC_nameobr-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classobr
Allele (52)
RNASeq_FPKM (74)
GO_annotation00005827
00005828
00005829
00005830
00005831
00005832
00005833
00005834
00116678
Contained_in_operonCEOP5436
Ortholog (40)
ParalogWBGene00016331Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00014215Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00012930Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable sterol binding activity and sterol transporter activity. Predicted to be involved in sterol transport. Predicted to be located in cytosol; perinuclear endoplasmic reticulum; and plasma membrane. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 67. Is an ortholog of human OSBPL2 (oxysterol binding protein like 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:0110588Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15761)
Molecular_infoCorresponding_CDSF14H8.1a
F14H8.1b
F14H8.1c
Corresponding_CDS_historyF14H8.1:wp111
Corresponding_transcriptF14H8.1a.1
F14H8.1b.1
F14H8.1c.1
Other_sequenceJI166695.1
BUC02044_1
JO473702.1
JI178404.1
CJC17892_1
Associated_featureWBsf717282
WBsf718455
WBsf718456
WBsf1020962
WBsf235016
Experimental_infoRNAi_resultWBRNAi00091954Inferred_automaticallyRNAi_primary
WBRNAi00023422Inferred_automaticallyRNAi_primary
WBRNAi00002181Inferred_automaticallyRNAi_primary
WBRNAi00023711Inferred_automaticallyRNAi_primary
WBRNAi00023199Inferred_automaticallyRNAi_primary
WBRNAi00023999Inferred_automaticallyRNAi_primary
WBRNAi00030972Inferred_automaticallyRNAi_primary
WBRNAi00044661Inferred_automaticallyRNAi_primary
WBRNAi00013328Inferred_automaticallyRNAi_primary
Expr_patternExpr1026580
Expr1033851
Expr1148634
Expr2014592
Expr2032825
Drives_constructWBCnstr00032649
Construct_productWBCnstr00032649
Microarray_results (21)
Expression_cluster (148)
InteractionWBInteraction000036699
WBInteraction000043519
WBInteraction000360775
WBInteraction000376388
WBInteraction000399470
WBInteraction000406894
WBInteraction000425665
WBInteraction000447238
Map_infoMapVPosition7.16225Error0.005018
PositivePositive_cloneF14H8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00010008
WBPaper00010145
WBPaper00025402
WBPaper00030935
WBPaper00038491
WBPaper00055090
WBPaper00062625
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