Gene: H13N06.4
H13N06.4 | SMap | S_parent | Sequence | H13N06 | ||
---|---|---|---|---|---|---|
Chromosome | X | |||||
Identity (5) | ||||||
Gene_info | Allele | uCE6-1552 | ||||
uCE6-1553 | ||||||
GO_term | GO:0006118 | IEA | Inferred_automatically | |||
GO:0016491 | IEA | Inferred_automatically | ||||
Contained_in_operon | CEOPX136 | |||||
Structured_description | Provisional_description | H13N06.4 is orthologous to the human gene UNKNOWN (PROTEIN FOR MGC:12715) (SUOX; OMIM:602216), which when mutated leads to disease. | Person_evidence | WBPerson567 | ||
Curator_confirmed | WBPerson567 | |||||
Concise_description | H13N06.4 is orthologous to the human gene UNKNOWN (PROTEIN FOR MGC:12715) (SUOX; OMIM:602216), which when mutated leads to disease. | |||||
Molecular_info (5) | ||||||
Experimental_info | RNAi_result (5) | |||||
WB_RNAi_result (7) | ||||||
Method | Gene |