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WormBase Tree Display for Gene: WBGene00017123

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Name Class

WBGene00017123SMapS_parentSequenceE04F6
IdentityVersion2
NameCGC_namemaoc-1Person_evidenceWBPerson1157
Sequence_nameE04F6.3
Molecular_nameE04F6.3
E04F6.3.1
CE01215
Other_nameCELE_E04F6.3Accession_evidenceNDBBX284602
Public_namemaoc-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
231 Aug 2005 14:07:05WBPerson2970Name_changeCGC_namemaoc-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmaoc
Allele (21)
StrainWBStrain00032684
WBStrain00040194
WBStrain00040195
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (40)
Structured_descriptionConcise_descriptionmaoc-1 encodes an ortholog of human HSD17B4 (OMIM:601860, mutated in D-bifunctional protein deficiency); MAOC-1 contains a MaoC-like domain found in diverse enzymes (HSD17B4, peroxisomal hydratase-dehydrogenase-epimerase, and the fatty acid synthase beta subunit) and by homology, is predicted to function in peroxisomal fatty acid beta-oxidation; loss of maoc-1 activity via RNAi results in lifespan extension, increased fat content, and an increased susceptibility to pathogens.Paper_evidence (4)
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated16 Dec 2007 00:00:00
Automated_descriptionEnables identical protein binding activity. Involved in defense response to Gram-negative bacterium and innate immune response. Predicted to be located in peroxisomal membrane. 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_assertedWBDOannot00000569
Molecular_infoCorresponding_CDSE04F6.3
Corresponding_transcriptE04F6.3.1
Other_sequence (73)
Associated_featureWBsf644358
WBsf221572
Experimental_infoRNAi_resultWBRNAi00065091Inferred_automaticallyRNAi_primary
WBRNAi00063963Inferred_automaticallyRNAi_primary
WBRNAi00012692Inferred_automaticallyRNAi_primary
WBRNAi00108443Inferred_automaticallyRNAi_primary
WBRNAi00080807Inferred_automaticallyRNAi_primary
WBRNAi00023398Inferred_automaticallyRNAi_primary
WBRNAi00030502Inferred_automaticallyRNAi_primary
WBRNAi00043682Inferred_automaticallyRNAi_primary
WBRNAi00063964Inferred_automaticallyRNAi_primary
Expr_patternExpr12049
Expr13909
Expr1016601
Expr1037356
Expr1147666
Expr2013373
Expr2031605
Drives_constructWBCnstr00020137
WBCnstr00027554
WBCnstr00040240
Construct_productWBCnstr00020137
WBCnstr00023003
WBCnstr00027554
Microarray_results (20)
Expression_cluster (200)
Interaction (23)
Map_infoMapIIPosition0.498761Error7.7e-05
PositivePositive_cloneE04F6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00026715
WBPaper00028482
WBPaper00033162
WBPaper00035972
WBPaper00038491
WBPaper00040624
WBPaper00041771
WBPaper00042257
WBPaper00044266
WBPaper00049625
WBPaper00054648
WBPaper00055090
WBPaper00057654
WBPaper00058717
WBPaper00059191
WBPaper00062224
WBPaper00064105
WBPaper00064202
WBPaper00065140
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