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WormBase Tree Display for Gene: WBGene00000966

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Name Class

WBGene00000966SMapS_parentSequenceF55A12
IdentityVersion1
NameCGC_namedhs-2Person_evidenceWBPerson651
Sequence_nameF55A12.4
Molecular_nameF55A12.4a
F55A12.4a.1
CE26924
F55A12.4b
CE51265
F55A12.4c
CE11123
F55A12.4b.1
F55A12.4c.1
Other_nameCELE_F55A12.4Accession_evidenceNDBBX284601
Public_namedhs-2
DB_infoDatabaseAceViewgene1F923
WormQTLgeneWBGene00000966
WormFluxgeneWBGene00000966
NDBlocus_tagCELE_F55A12.4
PanthergeneCAEEL|WormBase=WBGene00000966|UniProtKB=O01758
familyPTHR43313
NCBIgene172183
RefSeqproteinNM_001392303.1
NM_059174.9
NM_001322672.3
TrEMBLUniProtAccH2KYZ9
O01758
Q86NJ7
UniProt_GCRPUniProtAccO01758
OMIMgene601617
609769
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdhs
Allele (41)
RNASeq_FPKM (74)
GO_annotation00022005
00022006
00022007
00022008
00025475
Ortholog (46)
Paralog (38)
Structured_descriptionConcise_descriptiondhs-2 encodes a short-chain dehydrogenase predicted to be mitochondrial.Paper_evidenceWBPaper00004424
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable oxidoreductase activity. Predicted to be involved in steroid metabolic process. Predicted to be located in intracellular membrane-bounded organelle. Human ortholog(s) of this gene implicated in autosomal recessive congenital ichthyosis 13; fundus albipunctatus; and night blindness. Is an ortholog of several human genes including HSD17B6 (hydroxysteroid 17-beta dehydrogenase 6); RDH16 (retinol dehydrogenase 16); and RDH5 (retinol dehydrogenase 5).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:0080257Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29958)
DOID:11105Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9940)
DOID:8499Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9940)
Molecular_infoCorresponding_CDSF55A12.4a
F55A12.4b
F55A12.4c
Corresponding_CDS_historyF55A12.4b:wp252
Corresponding_transcriptF55A12.4a.1
F55A12.4b.1
F55A12.4c.1
Other_sequenceCRC07315_1
CJC05535_1
Associated_featureWBsf643287
WBsf643288
WBsf643289
WBsf656310
WBsf983664
WBsf983665
WBsf1009808
Experimental_infoRNAi_resultWBRNAi00032838Inferred_automaticallyRNAi_primary
WBRNAi00002223Inferred_automaticallyRNAi_primary
WBRNAi00003774Inferred_automaticallyRNAi_primary
WBRNAi00114793Inferred_automaticallyRNAi_primary
WBRNAi00048419Inferred_automaticallyRNAi_primary
Expr_patternExpr1011247
Expr1030601
Expr1152208
Expr2010914
Expr2029153
Drives_constructWBCnstr00037173
Construct_productWBCnstr00037173
Microarray_results (27)
Expression_cluster (258)
Interaction (59)
Map_infoMapIPosition-0.057235Error0.008171
PositivePositive_cloneF55A12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00029387
WBPaper00038491
WBPaper00042257
WBPaper00045631
WBPaper00055090
WBPaper00059839
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