Gene: F38C2.2
F38C2.2 | Evidence | CGC_data_submission | |||
---|---|---|---|---|---|
SMap | S_parent | Sequence | F38C2 | ||
Chromosome | IV | ||||
Identity (5) | |||||
Gene_info | Gene_class | hlh | |||
Allele | ok487 | Inferred_automatically | From strain object: VC486 | ||
tm277 | |||||
tm279 | |||||
Strain | VC486 | ||||
GO_term | GO:0030528 | IEA | Inferred_automatically | ||
GO:0045449 | IEA | Inferred_automatically | |||
GO:0005634 | IEA | Inferred_automatically | |||
Molecular_info (5) | |||||
Experimental_info | RNAi_result | Cenix:134-f2 | |||
WB_RNAi_result | JA:F38C2.2 | ||||
Cenix:134-f2 | |||||
Expr_pattern | Expr3311 | ||||
Expr3312 | |||||
Reference | WBPaper00025524 | ||||
WBPaper00026651 | |||||
Remark | Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC. | CGC_data_submission | |||
Method | Gene |