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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_evidenceWBPaper00005655
WBPaper00013529
WBPaper00026715
WBPaper00028482
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_model (3)
Models_disease_assertedWBDOannot00000569
Molecular_infoCorresponding_CDSE04F6.3
Corresponding_transcriptE04F6.3.1
Other_sequenceEX006989.1
Acan_isotig10756
FG619760.1
EX008982.1
FK809128.1
EX566264.1
HG11687
EX014924.1
PPC04898_1
EG025491.1
PPC05274_1
EX912399.1
ES744495.1
Hbac_isotig02356
ES743508.1
EX008313.1
HC09716
ES412591.1
EX011407.1
Tcir_isotig03219
EX912964.1
ES742298.1
EX911139.1
FD514985.1
EX557803.1
Name_isotig02945
EG025490.1
EX010418.1
EG025545.1
HCC12479_1
EX009626.1
PPC02385_1
AYC03850_1
EX010876.1
EX910330.1
EX012884.1
HBC16435_1
EG025801.1
ES743599.1
Tcir_isotig03220
EX913511.1
PP00778
CSC01660_1
ES409188.1
ES410840.1
FG619779.1
Tcol_isotig14942
EX015001.1
ES741458.1
EX013930.1
EX010278.1
ES740980.1
MIC08102_1
ES411837.1
HBC00225_1
ACC02301_1
EX913713.1
ES742423.1
CR05028
EX014155.1
EX909970.1
AE04662
EX007773.1
EX013959.1
ACC15576_1
EX015284.1
BXC01731_1
EX914775.1
Oden_isotig20736
JO469556.1
EX012762.1
CRC10657_1
JI174652.1
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
Reference (19)
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