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WormBase Tree Display for Gene: WBGene00015332

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Name Class

WBGene00015332SMapS_parentSequenceC02C2
IdentityVersion2
NameCGC_nametyr-1Person_evidenceWBPerson69
Sequence_nameC02C2.1
Molecular_nameC02C2.1
C02C2.1.1
CE06754
Other_nameCELE_C02C2.1Accession_evidenceNDBBX284603
Public_nametyr-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:55WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
211 Feb 2005 11:34:52WBPerson2970Name_changeCGC_nametyr-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtyr
Allele (34)
StrainWBStrain00032008
RNASeq_FPKM (74)
GO_annotation00041006
00041007
00041008
00041009
00121040
Ortholog (45)
ParalogWBGene00009001Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010060Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010661Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00021553Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016419Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00022231Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00017483Caenorhabditis elegansFrom_analysisPanther
Structured_descriptionConcise_descriptionC02C2.1 encodes a tyrosinase homolog with a glutamine/asparagine-rich domain.Paper_evidenceWBPaper00005068
WBPaper00012788
WBPaper00012830
WBPaper00012882
WBPaper00012897
WBPaper00013003
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable metal ion binding activity and monooxygenase activity. Human ortholog(s) of this gene implicated in several diseases, including ocular albinism 1; oculocutaneous albinism (multiple); and vitiligo. Is an ortholog of human DCT (dopachrome tautomerase) and TYR (tyrosinase).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS290 version of WormBase
Date_last_updated11 Sep 2023 00:00:00
Disease_infoPotential_modelDOID:0050633Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442)
DOID:8465Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442)
DOID:0070097Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12450)
DOID:8923Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442)
DOID:0050632Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442,HGNC:12450,HGNC:2709)
DOID:12306Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442)
DOID:0070095Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442)
DOID:0070094Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442)
DOID:1909Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442)
DOID:10123Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12442,HGNC:12450)
Molecular_infoCorresponding_CDSC02C2.1
Corresponding_transcriptC02C2.1.1
Other_sequence (31)
Associated_featureWBsf993180
WBsf993181
WBsf993182
WBsf993183
WBsf1015330
WBsf225291
WBsf225292
WBsf225293
WBsf225294
Experimental_infoRNAi_resultWBRNAi00098213Inferred_automaticallyRNAi_primary
WBRNAi00039406Inferred_automaticallyRNAi_primary
WBRNAi00028334Inferred_automaticallyRNAi_primary
WBRNAi00098217Inferred_automaticallyRNAi_primary
WBRNAi00005452Inferred_automaticallyRNAi_primary
WBRNAi00007421Inferred_automaticallyRNAi_primary
WBRNAi00009978Inferred_automaticallyRNAi_primary
WBRNAi00039403Inferred_automaticallyRNAi_primary
WBRNAi00005197Inferred_automaticallyRNAi_primary
Expr_patternExpr1020752
Expr1143519
Expr2017685
Expr2035823
Drives_constructWBCnstr00028927
Construct_productWBCnstr00028927
Microarray_results (19)
Expression_cluster (176)
Interaction (17)
Map_infoMapIIIPosition-0.517852Error0.006315
PositivePositive_cloneC02C2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5055
Pseudo_map_position
ReferenceWBPaper00011697
WBPaper00022302
WBPaper00038491
WBPaper00044177
WBPaper00055090
WBPaper00061115
WBPaper00065140
PictureWBPicture0000013093
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