WormBase Tree Display for Gene: WBGene00015332
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WBGene00015332 | SMap | S_parent | Sequence | C02C2 | ||
---|---|---|---|---|---|---|
Identity (6) | ||||||
Gene_info | Biotype | SO:0001217 | ||||
Gene_class | tyr | |||||
Allele (34) | ||||||
Strain | WBStrain00032008 | |||||
RNASeq_FPKM (74) | ||||||
GO_annotation | 00041196 | |||||
00041197 | ||||||
00041198 | ||||||
00041199 | ||||||
00121250 | ||||||
Ortholog (44) | ||||||
Paralog | WBGene00009001 | Caenorhabditis elegans | From_analysis | TreeFam | ||
Panther | ||||||
WormBase-Compara | ||||||
WBGene00010060 | Caenorhabditis elegans | From_analysis | Panther | |||
WormBase-Compara | ||||||
WBGene00010661 | Caenorhabditis elegans | From_analysis | TreeFam | |||
Panther | ||||||
WormBase-Compara | ||||||
WBGene00021553 | Caenorhabditis elegans | From_analysis | TreeFam | |||
Panther | ||||||
WormBase-Compara | ||||||
WBGene00016419 | Caenorhabditis elegans | From_analysis | TreeFam | |||
Panther | ||||||
WormBase-Compara | ||||||
WBGene00022231 | Caenorhabditis elegans | From_analysis | TreeFam | |||
Panther | ||||||
WormBase-Compara | ||||||
WBGene00017483 | Caenorhabditis elegans | From_analysis | Panther | |||
Structured_description | Concise_description | C02C2.1 encodes a tyrosinase homolog with a glutamine/asparagine-rich domain. | Paper_evidence | WBPaper00005068 | ||
WBPaper00012788 | ||||||
WBPaper00012830 | ||||||
WBPaper00012882 | ||||||
WBPaper00012897 | ||||||
WBPaper00013003 | ||||||
Curator_confirmed | WBPerson567 | |||||
Date_last_updated | 17 Jun 2004 00:00:00 | |||||
Automated_description | Predicted 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_evidence | WBPaper00065943 | |||
Curator_confirmed (2) | ||||||
Inferred_automatically | This description was generated automatically by a script based on data from the WS291 version of WormBase | |||||
Date_last_updated | 29 Nov 2023 00:00:00 | |||||
Disease_info | Potential_model | DOID:0050633 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442) | |
DOID:8465 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442) | |||
DOID:0070097 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12450) | |||
DOID:8923 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442) | |||
DOID:0050632 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442,HGNC:12450,HGNC:2709) | |||
DOID:12306 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442) | |||
DOID:0070095 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442) | |||
DOID:0070094 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442) | |||
DOID:1909 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442) | |||
DOID:10123 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12442,HGNC:12450) | |||
Molecular_info | Corresponding_CDS | C02C2.1 | ||||
Corresponding_transcript | C02C2.1.1 | |||||
Other_sequence (31) | ||||||
Associated_feature | WBsf993180 | |||||
WBsf993181 | ||||||
WBsf993182 | ||||||
WBsf993183 | ||||||
WBsf1015330 | ||||||
WBsf225291 | ||||||
WBsf225292 | ||||||
WBsf225293 | ||||||
WBsf225294 | ||||||
Experimental_info | RNAi_result | WBRNAi00098213 | Inferred_automatically | RNAi_primary | ||
WBRNAi00039406 | Inferred_automatically | RNAi_primary | ||||
WBRNAi00028334 | Inferred_automatically | RNAi_primary | ||||
WBRNAi00098217 | Inferred_automatically | RNAi_primary | ||||
WBRNAi00005452 | Inferred_automatically | RNAi_primary | ||||
WBRNAi00007421 | Inferred_automatically | RNAi_primary | ||||
WBRNAi00009978 | Inferred_automatically | RNAi_primary | ||||
WBRNAi00039403 | Inferred_automatically | RNAi_primary | ||||
WBRNAi00005197 | Inferred_automatically | RNAi_primary | ||||
Expr_pattern | Expr1020752 | |||||
Expr1143519 | ||||||
Expr2017685 | ||||||
Expr2035823 | ||||||
Drives_construct | WBCnstr00028927 | |||||
Construct_product | WBCnstr00028927 | |||||
Microarray_results (19) | ||||||
Expression_cluster (186) | ||||||
Interaction (17) | ||||||
Map_info (4) | ||||||
Reference | WBPaper00011697 | |||||
WBPaper00022302 | ||||||
WBPaper00038491 | ||||||
WBPaper00044177 | ||||||
WBPaper00055090 | ||||||
WBPaper00061115 | ||||||
WBPaper00065140 | ||||||
Picture | WBPicture0000013093 | |||||
Remark | Map 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 | ||||
Method | Gene |