Gene: Y51H1A.4
Y51H1A.4 | SMap | S_parent | Sequence | Y51H1A | ||
---|---|---|---|---|---|---|
Chromosome | II | |||||
Identity (5) | ||||||
Gene_info | GO_term | GO:0005515 | IEA | Inferred_automatically | ||
GO:0008270 | IEA | Inferred_automatically | ||||
GO:0006355 | IEA | Inferred_automatically | ||||
Contained_in_operon | CEOP2620 | |||||
Structured_description | Provisional_description | Y51H1A.4 is orthologous to the human gene P33ING1B (ING1; OMIM:601566), which when mutated leads to disease. | Person_evidence | WBPerson567 | ||
Curator_confirmed | WBPerson567 | |||||
Concise_description | Y51H1A.4 is orthologous to the human gene P33ING1B (ING1; OMIM:601566), which when mutated leads to disease. | |||||
Molecular_info (5) | ||||||
Experimental_info | RNAi_result | Cenix:55-c3 | ||||
WB_RNAi_result | MV_SV:mv_Y51H1A.4 | |||||
Cenix:55-c3 | ||||||
Y2H_target | Y2H009257 | |||||
Method | Gene |