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WormBase Tree Display for Gene: WBGene00022231

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Name Class

WBGene00022231SMapS_parentSequenceY73B6BL
IdentityVersion2
NameCGC_nametyr-6Person_evidenceWBPerson260
Sequence_nameY73B6BL.1
Molecular_nameY73B6BL.1
Y73B6BL.1.1
CE37586
Other_nameCELE_Y73B6BL.1Accession_evidenceNDBBX284604
Public_nametyr-6
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:05WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
228 Jan 2010 16:20:10WBPerson2970Name_changeCGC_nametyr-6
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtyr
Allele (65)
StrainWBStrain00036861
RNASeq_FPKM (74)
GO_annotation00088884
00126383
Ortholog (40)
ParalogWBGene00009001Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010060Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010661Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00015332Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016419Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00017483Caenorhabditis elegansFrom_analysisPanther
WBGene00021553Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptiontyr-6 is orthologous to the human gene tyrosinase (TYR), which is involved in the conversion of tyrosine to melanin.Curator_confirmedWBPerson324
WBPerson1823
WBPerson567
Date_last_updated21 May 2013 00:00:00
Automated_descriptionPredicted to enable oxidoreductase activity. Human ortholog(s) of this gene implicated in oculocutaneous albinism type III and pigmentation disease. Is an ortholog of human DCT (dopachrome tautomerase).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:0070097Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12450)
DOID:10123Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12450)
DOID:0050632Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12450,HGNC:2709)
Disease_relevanceMutations in human tyrosinase (TYR), which is involved in the conversion of tyrosine to melanine, are implicated in skin pigmentation disorders, melanoma and albinism.Homo sapiensAccession_evidenceOMIM203100
606952
103470
601800
606933
Curator_confirmedWBPerson324
Date_last_updated28 May 2013 00:00:00
Molecular_infoCorresponding_CDSY73B6BL.1
Corresponding_CDS_historyY73B6BL.1:wp98
Y73B6BL.1:wp131
Corresponding_transcriptY73B6BL.1.1
Other_sequence (19)
Associated_featureWBsf718107
WBsf996754
WBsf996755
WBsf996756
WBsf1017528
WBsf1017529
WBsf1017530
WBsf228416
Experimental_infoRNAi_resultWBRNAi00058309Inferred_automaticallyRNAi_primary
WBRNAi00000744Inferred_automaticallyRNAi_primary
Expr_patternExpr1011954
Expr1161718
Expr2017690
Expr2035828
Drives_constructWBCnstr00024328
Construct_productWBCnstr00024328
Microarray_results (16)
Expression_cluster (113)
Map_infoMapIVPosition3.20057Error0.000208
PositivePositive_cloneY73B6BLInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00065140
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