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WormBase Tree Display for Gene: WBGene00010661

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Name Class

WBGene00010661SMapS_parentSequenceK08E3
IdentityVersion2
NameCGC_nametyr-2Person_evidenceWBPerson69
Sequence_nameK08E3.1
Molecular_nameK08E3.1
K08E3.1.1
CE18864
Other_nameCELE_K08E3.1Accession_evidenceNDBBX284603
Public_nametyr-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
211 Feb 2005 11:34:52WBPerson2970Name_changeCGC_nametyr-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtyr
Allele (47)
StrainWBStrain00031972
RNASeq_FPKM (74)
GO_annotation00102039
00102040
00102041
00118004
Ortholog (33)
ParalogWBGene00009001Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010060Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00015332Caenorhabditis 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_descriptionAutomated_descriptionEnables dopachrome isomerase activity. Involved in negative regulation of apoptotic process. Expressed in hypodermis and uterine muscle. Human ortholog(s) of this gene implicated in several diseases, including ocular albinism 1; oculocutaneous albinism (multiple); and vitiligo. Is an ortholog of human TYR (tyrosinase).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: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_CDSK08E3.1
Corresponding_transcriptK08E3.1.1
Other_sequence (32)
Associated_feature (15)
Experimental_infoRNAi_resultWBRNAi00000756Inferred_automaticallyRNAi_primary
WBRNAi00005997Inferred_automaticallyRNAi_primary
WBRNAi00050281Inferred_automaticallyRNAi_primary
WBRNAi00098200Inferred_automaticallyRNAi_primary
WBRNAi00034132Inferred_automaticallyRNAi_primary
WBRNAi00016804Inferred_automaticallyRNAi_primary
WBRNAi00107781Inferred_automaticallyRNAi_primary
WBRNAi00107782Inferred_automaticallyRNAi_primary
Expr_patternExpr9119
Expr1026237
Expr1034659
Expr1153982
Expr2017686
Expr2035824
Drives_constructWBCnstr00006917
WBCnstr00006918
WBCnstr00006921
WBCnstr00006926
WBCnstr00006975
WBCnstr00006976
WBCnstr00006977
WBCnstr00031245
Construct_productWBCnstr00006919
WBCnstr00006920
WBCnstr00006921
WBCnstr00006922
WBCnstr00006923
WBCnstr00006925
WBCnstr00006926
WBCnstr00031245
Microarray_results (19)
Expression_cluster (267)
Interaction (13)
Map_infoMapIIIPosition21.4473Error0.01737
PositivePositive_cloneK08E3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5064
Pseudo_map_position
Reference (8)
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