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WormBase Tree Display for Gene: WBGene00007363

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Name Class

WBGene00007363SMapS_parentSequenceC06B3
IdentityVersion2
NameCGC_namestdh-1
Sequence_nameC06B3.4
Molecular_nameC06B3.4
C06B3.4.1
CE07961
Other_namedod-8
CELE_C06B3.4Accession_evidenceNDBBX284605
Public_namestdh-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:47WBPerson1971EventImportedInitial conversion from CDS class of WS125
225 Aug 2004 14:23:52WBPerson1971Name_changeCGC_namestdh-1
Other_namedod-8
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classstdh
Allele (39)
StrainWBStrain00001275
WBStrain00031499
RNASeq_FPKM (74)
GO_annotation00058973
00058974
00058975
00058976
00058977
Contained_in_operonCEOP5519
Ortholog (67)
Paralog (38)
Structured_descriptionConcise_descriptionstdh-1 encodes a putative steroid dehydrogenase required for normally short lifespan; STDH-1 is orthologous to human HSD17B3 (OMIM:605573, mutated in pseudohermaphroditism), HSD17B12 (OMIM:609574), and HSDL1, and paralogous to LET-767 and STDH-2/-4; STDH-1 is expressed in larval intestine, and in both larval and adult body wall muscle and neurons.Paper_evidenceWBPaper00005976
WBPaper00006204
WBPaper00006525
WBPaper00031006
Curator_confirmedWBPerson567
Date_last_updated26 Nov 2007 00:00:00
Automated_descriptionPredicted to enable oxidoreductase activity. Predicted to be involved in fatty acid elongation. Predicted to be located in endoplasmic reticulum. Expressed in head and tail. Human ortholog(s) of this gene implicated in 17-beta hydroxysteroid dehydrogenase 3 deficiency and Alzheimer's disease. Is an ortholog of human HSD17B12 (hydroxysteroid 17-beta dehydrogenase 12).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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5212)
DOID:1923Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5212)
DOID:0112248Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5212)
Molecular_infoCorresponding_CDSC06B3.4
Corresponding_transcriptC06B3.4.1
Other_sequence (26)
Associated_featureWBsf647494
WBsf647495
WBsf647496
WBsf662060
WBsf232849
Experimental_infoRNAi_resultWBRNAi00063175Inferred_automaticallyRNAi_primary
WBRNAi00010276Inferred_automaticallyRNAi_primary
WBRNAi00028552Inferred_automaticallyRNAi_primary
WBRNAi00039850Inferred_automaticallyRNAi_primary
Expr_patternChronogram834
Expr5184
Expr5185
Expr10720
Expr1026758
Expr1033171
Expr1143932
Expr2016956
Expr2035104
Drives_constructWBCnstr00002170
WBCnstr00004244
WBCnstr00017496
WBCnstr00033799
Construct_productWBCnstr00033799
Microarray_results (16)
Expression_cluster (173)
Interaction (73)
Map_infoMapVPosition5.76716Error0.006468
PositivePositive_cloneC06B3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4895
Pseudo_map_position
Reference (13)
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