Gene: F19C6.1
F19C6.1 | Evidence | Person_evidence | WBPerson242 | ||
---|---|---|---|---|---|
SMap | S_parent | Sequence | F19C6 | ||
Chromosome | X | ||||
Identity (5) | |||||
Gene_info | Gene_class | grk | |||
Allele (5) | |||||
Strain | RB1194 | ||||
GO_term | GO:0004703 | IEA | Inferred_automatically | ||
GO:0005524 | IEA | Inferred_automatically | |||
GO:0006468 | IEA | Inferred_automatically | |||
GO:0007165 | IEA | Inferred_automatically | |||
GO:0004674 | IEA | Inferred_automatically | |||
GO:0004672 | IEA | Inferred_automatically | |||
GO:0004871 | IEA | Inferred_automatically | |||
Molecular_info (5) | |||||
Experimental_info | RNAi_result | Cenix:66-h4 | |||
JA:F19C6.1 | |||||
WB_RNAi_result | JA:F19C6.1 | ||||
MV_SV:mv_F19C6.1 | |||||
Cenix:66-h4 | |||||
Expr_pattern | Expr5574 | ||||
Remark | no mutant available yet for this gene [Hart A][030331 ck1] | ||||
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 |