Gene: F40G9.11
F40G9.11 | Evidence | Person_evidence | WBPerson2322 | ||
---|---|---|---|---|---|
SMap | S_parent | Sequence | F40G9 | ||
Chromosome | III | ||||
Identity (5) | |||||
Gene_info | Gene_class | mxl | |||
Allele | tm1440 | ||||
tm1516 | |||||
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:327-g10 | |||
JA:F40G9.11 | |||||
TH:327G10 | |||||
WB_RNAi_result | TH:327G10 | ||||
JA:F40G9.11 | |||||
MV_SV:mv_G_YK4505 | |||||
Cenix:327-g10 | |||||
Reference | WBPaper00025527 | ||||
Remark | mxl-2 naming is based on high level of sequence identity between F40G9.11 and its human orthologues Max and Mlx [Pickett CL][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 |