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WormBase Tree Display for Gene: WBGene00000991

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Name Class

WBGene00000991SMapS_parentSequenceM03A8
IdentityVersion1
NameCGC_namedhs-28Person_evidenceWBPerson651
Sequence_nameM03A8.1
Molecular_nameM03A8.1
M03A8.1.1
CE04770
Other_nameCELE_M03A8.1Accession_evidenceNDBBX284606
Public_namedhs-28
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdhs
AlleleWBVar02146417
WBVar02159306
WBVar01498964
WBVar02124851
WBVar02122483
WBVar02146407
WBVar02146408
WBVar02146409
WBVar02146410
WBVar02146411
WBVar02146412
WBVar02146413
WBVar02146414
WBVar02146415
WBVar02146416
WBVar02146418
WBVar02146419
WBVar02146420
WBVar02146421
WBVar01156822
WBVar00251445
WBVar01156823
WBVar01156824
WBVar01156825
WBVar01156826
WBVar01156827
WBVar01820160
WBVar01156828
WBVar01156829
WBVar00087888
WBVar01156830
WBVar00034941
WBVar00087889
WBVar00087890
WBVar00087891
WBVar02120886
WBVar02122728
WBVar00091741
WBVar00506998
WBVar00506999
WBVar00507000
WBVar02064447
WBVar01815814
WBVar01500067
StrainWBStrain00035626
WBStrain00040189
WBStrain00050737
WBStrain00050738
WBStrain00050736
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (37)
Paralog (38)
Structured_descriptionConcise_descriptiondhs-28 encodes an ortholog of human 17-BETA-HYDROXYSTEROID DEHYDROGENASE 4 (HSD17B4; OMIM:601860, mutated in D-bifunctional protein deficiency), which contains a C-terminal SCP-2 sterol transfer domain; the deletion allele dhs-28(ok450) is superficially wild-type.Paper_evidenceWBPaper00004424
Curator_confirmedWBPerson48
WBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable oxidoreductase activity. Involved in several processes, including carbohydrate derivative metabolic process; dauer entry; and positive regulation of developmental process. Located in peroxisome. Expressed in hypodermis. Used to study obesity. Human ortholog(s) of this gene implicated in D-bifunctional protein deficiency; Perrault syndrome; and Stiff-Person syndrome. Is an ortholog of human HSD17B4 (hydroxysteroid 17-beta dehydrogenase 4).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_infoExperimental_modelDOID:9970Homo sapiensPaper_evidenceWBPaper00035972
Curator_confirmedWBPerson38202
Date_last_updated29 Jun 2018 00:00:00
Potential_modelDOID:13366Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5213)
DOID:0090031Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5213)
DOID:0050857Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5213)
Models_disease_assertedWBDOannot00000570
WBDOannot00000571
Molecular_infoCorresponding_CDSM03A8.1
Corresponding_transcriptM03A8.1.1
Other_sequence (107)
Associated_featureWBsf648263
WBsf648264
WBsf662918
WBsf235872
WBsf235873
Experimental_infoRNAi_resultWBRNAi00108444Inferred_automaticallyRNAi_primary
WBRNAi00008998Inferred_automaticallyRNAi_primary
WBRNAi00050847Inferred_automaticallyRNAi_primary
WBRNAi00034393Inferred_automaticallyRNAi_primary
WBRNAi00025981Inferred_automaticallyRNAi_primary
WBRNAi00092604Inferred_automaticallyRNAi_primary
Expr_patternExpr8991
Expr1020554
Expr1030616
Expr1154542
Expr2010912
Expr2029151
Drives_constructWBCnstr00013659
WBCnstr00037154
Construct_product (3)
AntibodyWBAntibody00001955
WBAntibody00002918
Microarray_results (27)
Expression_cluster (216)
Interaction (99)
Map_infoMapXPosition-2.40245Error0.010942
PositivePositive_cloneM03A8Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4258
4343
5031
Pseudo_map_position
Reference (31)
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