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WormBase Tree Display for Gene: WBGene00019503

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Name Class

WBGene00019503SMapS_parentSequenceK07H8
IdentityVersion2
NameCGC_nametbce-1Person_evidenceWBPerson1836
Sequence_nameK07H8.1
Molecular_nameK07H8.1
K07H8.1.1
CE18021
Other_nameCELE_K07H8.1Accession_evidenceNDBBX284604
Public_nametbce-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:01WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
221 Jul 2014 15:41:21WBPerson2970Name_changeCGC_nametbce-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtbce
Allele (30)
RNASeq_FPKM (74)
GO_annotation00067037
00067038
00067039
00067040
00067041
00067042
00067043
00124345
00124346
Contained_in_operonCEOP4280
Ortholog (32)
ParalogWBGene00016866Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionK07H8.1 encodes a putative tubulin chaperone cofactor orthologous to human TBCE (OMIM:604934, mutated in HRD), and paralogous to COEL-1 and human TBCEL (LRRC35; OMIM:610451); K07H8.1 is required for normally short lifespan and for embryonic viability.Paper_evidenceWBPaper00005599
WBPaper00025054
WBPaper00026643
WBPaper00031580
WBPaper00031581
Curator_confirmedWBPerson567
Date_last_updated12 Mar 2008 00:00:00
Automated_descriptionPredicted to enable alpha-tubulin binding activity. Predicted to be involved in microtubule cytoskeleton organization; post-chaperonin tubulin folding pathway; and tubulin complex assembly. Located in cytoplasm. Human ortholog(s) of this gene implicated in Kenny-Caffey syndrome type 1; hypoparathyroidism; and hypoparathyroidism-retardation-dysmorphism syndrome. Is an ortholog of human TBCE (tubulin folding cofactor E).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:11199Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11582)
DOID:0080722Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11582)
DOID:0060348Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11582)
Molecular_infoCorresponding_CDSK07H8.1
Corresponding_transcriptK07H8.1.1
Other_sequence (21)
Associated_featureWBsf646155
WBsf660394
WBsf228655
Experimental_infoRNAi_resultWBRNAi00065250Inferred_automaticallyRNAi_primary
WBRNAi00050202Inferred_automaticallyRNAi_primary
WBRNAi00016756Inferred_automaticallyRNAi_primary
WBRNAi00103445Inferred_automaticallyRNAi_primary
WBRNAi00008228Inferred_automaticallyRNAi_primary
WBRNAi00081158Inferred_automaticallyRNAi_primary
WBRNAi00034092Inferred_automaticallyRNAi_primary
Expr_patternExpr9571
Expr1020653
Expr1038427
Expr1153898
Expr2017341
Expr2035477
Drives_constructWBCnstr00025793
Construct_productWBCnstr00014136
WBCnstr00025793
Microarray_results (20)
Expression_cluster (114)
SAGE_tag (13)
Interaction (98)
Map_infoMapIVPosition3.7055
PositivePositive_cloneK07H8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00031320
WBPaper00034662
WBPaper00038444
WBPaper00038491
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