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Gene: F52B11.2   

F52B11.2SMapS_parentSequenceF52B11
ChromosomeIV
Identity (5)
Gene_info GO_term GO:0004615 IEA Inferred_automatically
GO:0019307 IEA Inferred_automatically
GO:0005737 IEA Inferred_automatically
Contained_in_operonCEOP4576
Structured_description Provisional_descriptionF52B11.2 is orthologous to the human gene PHOSPHOMANNOMUTASE 2 (PMS2; OMIM:601785), which when mutated leads to congenital disorder of glycosylation, type Ia.Person_evidenceWBPerson567
Curator_confirmedWBPerson567
Concise_descriptionF52B11.2 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)
MethodGene