Gene: Y17G9B.3
Y17G9B.3 | SMap | S_parent | Sequence | Y17G9B | ||
---|---|---|---|---|---|---|
Chromosome | IV | |||||
Identity (5) | ||||||
Gene_info | Gene_class | cyp | ||||
GO_term | GO:0004497 | IEA | Inferred_automatically | |||
GO:0005506 | IEA | Inferred_automatically | ||||
GO:0020037 | IEA | Inferred_automatically | ||||
GO:0006118 | IEA | Inferred_automatically | ||||
Structured_description | Provisional_description | The Y17G9B.3 gene encodes a homolog of the human gene CYP7B1, which when mutated leads to pseudovitamin D deficiency rickets (OMIM:264700). | Paper_evidence | WBPaper00004637 | ||
Person_evidence | WBPerson567 | |||||
Curator_confirmed | WBPerson567 | |||||
Date_last_updated | 17 Jun 2004 00:00:00 | |||||
Concise_description | The Y17G9B.3 gene encodes a homolog of the human gene CYP7B1, which when mutated leads to pseudovitamin D deficiency rickets (OMIM:264700). | |||||
Molecular_info (5) | ||||||
Experimental_info | RNAi_result | Cenix:213-h9 | ||||
Simmer:Y17G9B.h | ||||||
WB_RNAi_result (10) | ||||||
Y2H_bait | Y2H009746 | |||||
Method | Gene |