WormBase Tree Display for Gene: WBGene00017123
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WBGene00017123 | SMap | S_parent | Sequence | E04F6 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | maoc-1 | Person_evidence | WBPerson1157 | |||||
Sequence_name | E04F6.3 | ||||||||
Molecular_name | E04F6.3 | ||||||||
E04F6.3.1 | |||||||||
CE01215 | |||||||||
Other_name | CELE_E04F6.3 | Accession_evidence | NDB | BX284602 | |||||
Public_name | maoc-1 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 28 May 2004 13:30:58 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
2 | 31 Aug 2005 14:07:05 | WBPerson2970 | Name_change | CGC_name | maoc-1 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | maoc | ||||||||
Allele (21) | |||||||||
Strain | WBStrain00032684 | ||||||||
WBStrain00040194 | |||||||||
WBStrain00040195 | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (11) | |||||||||
Ortholog (40) | |||||||||
Structured_description | Concise_description | maoc-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 | WBPaper00005655 | |||||
WBPaper00013529 | |||||||||
WBPaper00026715 | |||||||||
WBPaper00028482 | |||||||||
Curator_confirmed | WBPerson567 | ||||||||
WBPerson1843 | |||||||||
Date_last_updated | 16 Dec 2007 00:00:00 | ||||||||
Automated_description | Enables 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_evidence | WBPaper00065943 | ||||||
Curator_confirmed | WBPerson324 | ||||||||
WBPerson37462 | |||||||||
Inferred_automatically | This description was generated automatically by a script based on data from the WS292 version of WormBase | ||||||||
Date_last_updated | 24 Apr 2024 00:00:00 | ||||||||
Disease_info | Experimental_model | DOID:9970 | Homo sapiens | Paper_evidence | WBPaper00035972 | ||||
Curator_confirmed | WBPerson38202 | ||||||||
Date_last_updated | 29 Jun 2018 00:00:00 | ||||||||
Potential_model | DOID:13366 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:5213) | |||||
DOID:0090031 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:5213) | ||||||
DOID:0050857 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:5213) | ||||||
Models_disease_asserted | WBDOannot00000569 | ||||||||
Molecular_info | Corresponding_CDS | E04F6.3 | |||||||
Corresponding_transcript | E04F6.3.1 | ||||||||
Other_sequence (73) | |||||||||
Associated_feature | WBsf644358 | ||||||||
WBsf221572 | |||||||||
Experimental_info | RNAi_result | WBRNAi00065091 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00063963 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00012692 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00108443 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00080807 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00023398 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00030502 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00043682 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00063964 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr12049 | ||||||||
Expr13909 | |||||||||
Expr1016601 | |||||||||
Expr1037356 | |||||||||
Expr1147666 | |||||||||
Expr2013373 | |||||||||
Expr2031605 | |||||||||
Drives_construct | WBCnstr00020137 | ||||||||
WBCnstr00027554 | |||||||||
WBCnstr00040240 | |||||||||
Construct_product | WBCnstr00020137 | ||||||||
WBCnstr00023003 | |||||||||
WBCnstr00027554 | |||||||||
Microarray_results (20) | |||||||||
Expression_cluster (200) | |||||||||
Interaction (23) | |||||||||
Map_info | Map | II | Position | 0.498761 | Error | 7.7e-05 | |||
Positive | Positive_clone | E04F6 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
Pseudo_map_position | |||||||||
Reference (19) | |||||||||
Remark | Map 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 | |||||||
Method | Gene |