WormBase Tree Display for Gene: WBGene00004337
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WBGene00004337 | Evidence | CGC_data_submission | |||||
---|---|---|---|---|---|---|---|
SMap | S_parent | Sequence | C54G10 | ||||
Identity (6) | |||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | rfc | ||||||
Allele (143) | |||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (17) | |||||||
Ortholog (37) | |||||||
Paralog | WBGene00010676 | Caenorhabditis elegans | From_analysis | Panther | |||
Structured_description | Automated_description | Predicted to enable DNA binding activity. Predicted to be involved in DNA repair and DNA replication. Predicted to be located in nucleus. Predicted to be part of DNA replication factor C complex. Human ortholog(s) of this gene implicated in West Nile fever. Is an ortholog of human RFC1 (replication factor C subunit 1). | Paper_evidence | WBPaper00065943 | |||
Curator_confirmed | WBPerson324 | ||||||
WBPerson37462 | |||||||
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:2366 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9969) | ||
DOID:1682 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9969) | ||||
Molecular_info | Corresponding_CDS | C54G10.2a | |||||
Corresponding_transcript | C54G10.2b | ||||||
C54G10.2a.1 | |||||||
C54G10.2a.2 | |||||||
Other_sequence (28) | |||||||
Associated_feature | WBsf653399 | ||||||
WBsf1002090 | |||||||
WBsf1020892 | |||||||
WBsf234972 | |||||||
Experimental_info | RNAi_result (13) | ||||||
Expr_pattern | Expr1022325 | ||||||
Expr1032155 | |||||||
Expr1147151 | |||||||
Expr2015303 | |||||||
Expr2033537 | |||||||
Drives_construct | WBCnstr00035558 | ||||||
Construct_product | WBCnstr00035558 | ||||||
Microarray_results (25) | |||||||
Expression_cluster (139) | |||||||
Interaction (135) | |||||||
Map_info | Map | V | Position | 6.56404 | Error | 0.004106 | |
Positive | Positive_clone | C54G10 | Inferred_automatically | From sequence, transcript, pseudogene data | |||
Pseudo_map_position | |||||||
Reference | WBPaper00005486 | ||||||
WBPaper00005736 | |||||||
WBPaper00027740 | |||||||
WBPaper00028457 | |||||||
WBPaper00038491 | |||||||
WBPaper00055090 | |||||||
Remark | Sequence connection from [Boulton S, Vidal M] | ||||||
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 |