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WormBase Tree Display for Gene: WBGene00000972

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Name Class

WBGene00000972SMapS_parentSequenceK10H10
IdentityVersion1
NameCGC_namedhs-8Person_evidenceWBPerson651
Sequence_nameK10H10.3
Molecular_nameK10H10.3a
K10H10.3a.1
CE16253
K10H10.3c
CE49107
K10H10.3d
CE48898
K10H10.3b
K10H10.3c.1
K10H10.3d.1
Other_nameCELE_K10H10.3Accession_evidenceNDBBX284602
Public_namedhs-8
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdhs
AlleleWBVar00789360
WBVar00789361
WBVar00789362
WBVar01499702
WBVar00789363
WBVar00789364
WBVar01944224
WBVar00001206
WBVar01498435
WBVar00232328
WBVar00385262
WBVar00385263
WBVar00385264
WBVar00385265
WBVar00385266
WBVar00385267
WBVar02041028
WBVar01767528
WBVar00016088
WBVar00016093
WBVar00016098
WBVar00016103
WBVar01253265
WBVar01540260
WBVar01817802
WBVar01498941
WBVar01442355
WBVar01896056
WBVar01442357
WBVar01442359
WBVar01442362
WBVar01442364
WBVar01320358
WBVar00789356
WBVar00789357
WBVar01320362
WBVar00789358
WBVar00789359
RNASeq_FPKM (74)
GO_annotation00034972
Ortholog (21)
Paralog (11)
Structured_descriptionAutomated_descriptionPredicted to enable oxidoreductase activity. Human ortholog(s) of this gene implicated in autosomal recessive spinocerebellar ataxia 12; developmental and epileptic encephalopathy 28; and esophagus squamous cell carcinoma. Is an ortholog of human WWOX (WW domain containing oxidoreductase).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:3748Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12799)
DOID:5041Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12799)
DOID:0080452Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12799)
DOID:0080060Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12799)
DOID:1749Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12799)
Molecular_infoCorresponding_CDSK10H10.3a
K10H10.3c
K10H10.3d
Corresponding_transcriptK10H10.3b
K10H10.3a.1
K10H10.3c.1
K10H10.3d.1
Associated_featureWBsf644859
WBsf657184
WBsf222470
WBsf222471
Experimental_infoRNAi_resultWBRNAi00022401Inferred_automaticallyRNAi_primary
WBRNAi00034272Inferred_automaticallyRNAi_primary
WBRNAi00050567Inferred_automaticallyRNAi_primary
Expr_patternExpr1024651
Expr1030606
Expr1154276
Expr2010922
Expr2029161
Drives_constructWBCnstr00037167
Construct_productWBCnstr00037167
Microarray_results (24)
Expression_cluster (189)
InteractionWBInteraction000047019
WBInteraction000047023
WBInteraction000047024
WBInteraction000305809
WBInteraction000309034
WBInteraction000425512
WBInteraction000444353
WBInteraction000505030
Map_infoMapIIPosition23.0371Error0.002143
PositivePositive_cloneK10H10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00042257
WBPaper00055090
PictureWBPicture0000013093
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