Gene: C54G6.2
C54G6.2 | SMap | S_parent | Sequence | C54G6 | ||
---|---|---|---|---|---|---|
Chromosome | I | |||||
Identity (5) | ||||||
Gene_info | Allele | snp_C54G6[7] | ||||
snp_C54G6[8] | ||||||
GO_term | GO:0016020 | IEA | Inferred_automatically | |||
Structured_description | Provisional_description | The C54G6.2 gene encodes a homolog of human RP2, which when mutated leads to X-linked retinitis pigmentosa 2 (OMIM:312600). | Paper_evidence | WBPaper00004103 | ||
Person_evidence | WBPerson567 | |||||
Curator_confirmed | WBPerson567 | |||||
Date_last_updated | 17 Jun 2004 00:00:00 | |||||
Concise_description | The C54G6.2 gene encodes a homolog of human RP2, which when mutated leads to X-linked retinitis pigmentosa 2 (OMIM:312600). | |||||
Molecular_info (6) | ||||||
Experimental_info | RNAi_result | Cenix:119-d7 | ||||
JA:C54G6.2 | ||||||
WB_RNAi_result | JA:C54G6.2 | |||||
Cenix:119-d7 | ||||||
Method | Gene |