WormBase Tree Display for Gene: WBGene00020842
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WBGene00020842 | SMap | S_parent | Sequence | T27A3 | |||
---|---|---|---|---|---|---|---|
Identity | Version | 4 | |||||
Name | CGC_name | nmrk-1 | Person_evidence | WBPerson1983 | |||
Sequence_name | T27A3.6 | ||||||
Molecular_name | T27A3.6 | ||||||
T27A3.6.1 | |||||||
CE14227 | |||||||
Other_name | moc-4 | Paper_evidence | WBPaper00056452 | ||||
CELE_T27A3.6 | Accession_evidence | NDB | BX284601 | ||||
Public_name | nmrk-1 | ||||||
DB_info | Database (13) | ||||||
Species | Caenorhabditis elegans | ||||||
History | Version_change (4) | ||||||
Status | Live | ||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | nmrk | ||||||
Allele (17) | |||||||
Strain | WBStrain00032639 | ||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (13) | |||||||
Contained_in_operon | CEOP1300 | ||||||
Ortholog (34) | |||||||
Structured_description (2) | |||||||
Disease_info | Potential_model | DOID:0111163 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:7193) | ||
Disease_relevance | Mutations in the human gene Molybdenum cofactor synthesis gene 2 (MOCS2; orthologous to elegans T27A3.6), are associated with Molybdenum cofactor deficiency, type B, which is an autosomal recessive disease where there is a loss of all molybdoenzyme activities, characterized by neurological damage, seizures and early childhood death. | Homo sapiens | Accession_evidence | OMIM | 252150 | ||
603708 | |||||||
Curator_confirmed | WBPerson324 | ||||||
Date_last_updated | 26 Jun 2012 00:00:00 | ||||||
Molecular_info | Corresponding_CDS | T27A3.6 | |||||
Corresponding_transcript | T27A3.6.1 | ||||||
Other_sequence | CBC15288_1 | ||||||
CR05650 | |||||||
CRC00288_1 | |||||||
Associated_feature | WBsf649219 | ||||||
WBsf219542 | |||||||
Experimental_info | RNAi_result | WBRNAi00054263 | Inferred_automatically | RNAi_primary | |||
WBRNAi00054264 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00036016 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00004319 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00076715 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00103547 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00116636 | Inferred_automatically | RNAi_primary | |||||
Expr_pattern | Expr1012188 | ||||||
Expr1039085 | |||||||
Expr1157811 | |||||||
Expr2014334 | |||||||
Expr2032575 | |||||||
Drives_construct | WBCnstr00024844 | ||||||
Construct_product | WBCnstr00024844 | ||||||
Microarray_results (21) | |||||||
Expression_cluster (89) | |||||||
Interaction (55) | |||||||
Map_info | Map | I | Position | 0.784315 | |||
Positive | Positive_clone | T27A3 | Inferred_automatically | From sequence, transcript, pseudogene data | |||
Pseudo_map_position | |||||||
Reference | WBPaper00038491 | ||||||
WBPaper00051761 | |||||||
WBPaper00055090 | |||||||
WBPaper00056452 | |||||||
WBPaper00064339 | |||||||
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 |