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WormBase Tree Display for Gene: WBGene00016588

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Name Class

WBGene00016588SMapS_parentSequenceC42C1
IdentityVersion4
NameCGC_namehpo-12Paper_evidenceWBPaper00038231
Person_evidenceWBPerson26
Sequence_nameC42C1.10
Molecular_nameC42C1.10
C42C1.10.1
CE29222
C42C1.10.2
Other_nameCELE_C42C1.10Accession_evidenceNDBBX284604
Public_namehpo-12
DB_infoDatabaseAceViewgene4N47
WormQTLgeneWBGene00016588
WormFluxgeneWBGene00016588
NDBlocus_tagCELE_C42C1.10
NCBIgene36804989
RefSeqproteinNM_001392411.1
TrEMBLUniProtAccA3QMB9
UniProt_GCRPUniProtAccA3QMB9
OMIMgene606521
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
226 Apr 2011 13:31:47WBPerson2970Name_changeCGC_namehpo-12
310 Jun 2014 12:12:12WBPerson1983EventAcquires_mergeWBGene00016593
406 Mar 2018 14:45:19WBPerson4025EventSplit_intoWBGene00302978
Acquires_mergeWBGene00016593
Split_intoWBGene00302978
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhpo
Allele (32)
StrainWBStrain00032586
RNASeq_FPKM (74)
GO_annotation00004367
00004368
00004369
00004370
00004371
00004372
00122163
Contained_in_operonCEOP4508
CEOP5599
Ortholog (37)
Paralog (36)
Structured_descriptionAutomated_descriptionPredicted to enable thiamine transmembrane transporter activity. Predicted to be involved in thiamine pyrophosphate transmembrane transport. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in inherited metabolic disorder and microcephaly. Is an ortholog of human SLC25A19 (solute carrier family 25 member 19).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_infoPotential_modelDOID:10907Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14409)
DOID:655Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14409)
Molecular_infoCorresponding_CDSC42C1.10
Corresponding_CDS_historyC42C1.10a:wp264
C42C1.10b:wp219
C42C1.10b:wp264
C42C1.10c:wp264
C42C1.10d:wp264
Corresponding_transcriptC42C1.10.1
C42C1.10.2
Other_sequence (27)
Associated_featureWBsf660799
WBsf998069
WBsf229269
Experimental_infoRNAi_resultWBRNAi00088614Inferred_automaticallyRNAi_primary
WBRNAi00042329Inferred_automaticallyRNAi_primary
WBRNAi00011858Inferred_automaticallyRNAi_primary
WBRNAi00088721Inferred_automaticallyRNAi_primary
WBRNAi00024798Inferred_automaticallyRNAi_primary
WBRNAi00042330Inferred_automaticallyRNAi_primary
WBRNAi00027220Inferred_automaticallyRNAi_primary
Expr_patternExpr1027070
Expr1037118
Expr1146323
Expr2012557
Expr2030794
Drives_constructWBCnstr00027954
WBCnstr00027959
Construct_productWBCnstr00027954
WBCnstr00027959
Microarray_results (19)
Expression_cluster (63)
Interaction (59)
Map_infoMapIVPosition5.83418Error0.000997
PositivePositive_cloneC42C1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
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
[140610 pad] Gene was missing Acquires_merge Event history data so inferred from Acquires_merge tag.
MethodGene