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WormBase Tree Display for Gene: WBGene00020184

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Name Class

WBGene00020184SMapS_parentSequenceT03F1
IdentityVersion2
NameCGC_nameuba-5Paper_evidenceWBPaper00042074
Sequence_nameT03F1.1
Molecular_nameT03F1.1
T03F1.1.1
CE13096
T03F1.1.2
T03F1.1.3
Other_nameCELE_T03F1.1Accession_evidenceNDBBX284601
Public_nameuba-5
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:02WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
204 Jun 2013 14:47:04WBPerson2970Name_changeCGC_nameuba-5
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classuba
Allele (41)
StrainWBStrain00033116
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (35)
ParalogWBGene00000142Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00004341Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006699Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006700Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006735Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010882Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00018357Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionEnables UFM1 activating enzyme activity and ubiquitin conjugating enzyme binding activity. Involved in determination of adult lifespan; reproduction; and stress response to metal ion. Predicted to be located in cytosol. Used to study early infantile epileptic encephalopathy. Human ortholog(s) of this gene implicated in autosomal recessive spinocerebellar ataxia 24 and developmental and epileptic encephalopathy 44. Is an ortholog of human UBA5 (ubiquitin like modifier activating enzyme 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_infoExperimental_modelDOID:0050709Homo sapiensPaper_evidenceWBPaper00050013
Curator_confirmedWBPerson324
Date_last_updated27 Sep 2020 00:00:00
Potential_modelDOID:0080424Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:23230)
DOID:0111615Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:23230)
Models_disease_assertedWBDOannot00000813
Molecular_infoCorresponding_CDST03F1.1
Corresponding_transcriptT03F1.1.1
T03F1.1.2
T03F1.1.3
Other_sequence (72)
Associated_featureWBsf643164
WBsf217452
WBsf217453
Experimental_infoRNAi_resultWBRNAi00116513Inferred_automaticallyRNAi_primary
WBRNAi00107652Inferred_automaticallyRNAi_primary
WBRNAi00052280Inferred_automaticallyRNAi_primary
WBRNAi00076636Inferred_automaticallyRNAi_primary
WBRNAi00004114Inferred_automaticallyRNAi_primary
WBRNAi00052277Inferred_automaticallyRNAi_primary
WBRNAi00035091Inferred_automaticallyRNAi_primary
Expr_patternExpr1010853
Expr1038778
Expr1155909
Expr2017697
Expr2035835
Drives_constructWBCnstr00017406
WBCnstr00025317
Construct_productWBCnstr00025317
Microarray_results (23)
Expression_cluster (116)
Interaction (123)
Map_infoMapIPosition-1.95366
PositivePositive_cloneT03F1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00044965
WBPaper00045692
WBPaper00050013
WBPaper00055090
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