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WormBase Tree Display for Gene: WBGene00000983

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Name Class

WBGene00000983SMapS_parentSequenceF35B12
IdentityVersion1
NameCGC_namedhs-20Person_evidenceWBPerson651
Sequence_nameF35B12.2
Molecular_nameF35B12.2
F35B12.2.1
CE39496
Other_nameCELE_F35B12.2Accession_evidenceNDBBX284605
Public_namedhs-20
DB_infoDatabaseAceViewgene5M84
WormQTLgeneWBGene00000983
WormFluxgeneWBGene00000983
NDBlocus_tagCELE_F35B12.2
PanthergeneCAEEL|WormBase=WBGene00000983|UniProtKB=Q20012
familyPTHR43313
NCBIgene179590
RefSeqproteinNM_073540.6
TrEMBLUniProtAccQ20012
UniProt_GCRPUniProtAccQ20012
OMIMgene601617
609769
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdhs
Allele (29)
RNASeq_FPKM (74)
GO_annotation00066820
00066821
00066822
00066823
Ortholog (61)
Paralog (38)
Structured_descriptionConcise_descriptiondhs-20 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 DHRS9 (dehydrogenase/reductase 9); HSD17B6 (hydroxysteroid 17-beta dehydrogenase 6); 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_CDSF35B12.2
Corresponding_CDS_historyF35B12.2:wp87
F35B12.2:wp152
Corresponding_transcriptF35B12.2.1
Other_sequenceBUC00455_1
EX552147.1
EX011702.1
Dviv_isotig25160
MI04755
Acan_isotig19791
JI168263.1
ASC18420_1
OOC03846_1
EX911177.1
FE914564.1
EX007595.1
JO472247.1
MIC03584_1
EX913201.1
HBC11358_1
ACC20641_1
ES739621.1
EX007868.1
EG025495.1
JI176856.1
BXC00012_1
JI180277.1
Oden_isotig15965
HGC11427_1
JI474127.1
JI175479.1
JI175319.1
BXC01909_1
HBC11251_1
ASC29930_1
Oden_isotig27721
BF599168.1
AI124431.1
EX914028.1
EX916778.1
ES740185.1
PPC07993_1
ASC15616_1
JI175797.1
FE918974.1
AS16268
HBC00338_1
CBC01352_1
Hbac_isotig00437
JI225118.1
HG04506
Acan_isotig14282
EX914877.1
JI480695.1
JI212600.1
OVC00959_1
JI174137.1
CRC05036_1
ES744368.1
GRC02377_1
Oden_isotig15964
CR10640
FE914522.1
ES412243.1
Oden_isotig26888
EX014058.1
ES739569.1
AS00780
AS07273
EX010975.1
ACC25662_1
EX537589.1
AS08209
JI172943.1
EX009064.1
XIC05283_1
XI04690
JI172552.1
Hbac_isotig00436
Associated_featureWBsf653131
WBsf669390
WBsf234552
Experimental_infoRNAi_resultWBRNAi00014283Inferred_automaticallyRNAi_primary
WBRNAi00046270Inferred_automaticallyRNAi_primary
WBRNAi00046271Inferred_automaticallyRNAi_primary
WBRNAi00031741Inferred_automaticallyRNAi_primary
Expr_patternExpr1025422
Expr1150162
Expr2010904
Expr2029143
Drives_constructWBCnstr00037159
Construct_productWBCnstr00037159
Microarray_results (19)
Expression_cluster (225)
Interaction (35)
Map_infoMapVPosition3.21084Error0.00022
PositivePositive_cloneF35B12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (4)
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