Gene: F52B11.2
F52B11.2 | SMap | S_parent | Sequence | F52B11 | ||
---|---|---|---|---|---|---|
Chromosome | IV | |||||
Identity (5) | ||||||
Gene_info | GO_term (3) | |||||
Contained_in_operon | CEOP4576 | |||||
Structured_description | Provisional_description | F52B11.2 is orthologous to the human gene PHOSPHOMANNOMUTASE 2 (PMS2; OMIM:601785), which when mutated leads to congenital disorder of glycosylation, type Ia. | Person_evidence | WBPerson567 | ||
Curator_confirmed | WBPerson567 | |||||
Concise_description | F52B11.2 is orthologous to the human gene PHOSPHOMANNOMUTASE 2 (PMS2; OMIM:601785), which when mutated leads to congenital disorder of glycosylation, type Ia. | |||||
Molecular_info (6) | ||||||
Experimental_info | RNAi_result (6) | |||||
WB_RNAi_result (7) | ||||||
Method | Gene |