| C50H2.1 | SMap | S_parent | Sequence | C50H2
|
|---|
| Chromosome | V |
|
Identity (5)
|
|
Gene_info
| Gene_class | fshr
|
| |
Allele
| ok778
| Inferred_automatically | From strain object: RB911 |
| | | pkP714
|
| | | pkP741
|
| | | pkP5197
|
| | Strain | RB911
|
| |
GO_term (8)
|
| |
Structured_description
| Provisional_description | C50H2.1 is orthologous to the human gene FORKHEAD BOX O1A (RHABDOMYOSARCOMA) (FSHR; OMIM:136533), which when mutated leads to disease. | Person_evidence | WBPerson567
|
| | | | | Curator_confirmed | WBPerson567
|
| | | Concise_description | C50H2.1 is orthologous to the human gene FORKHEAD BOX O1A (RHABDOMYOSARCOMA) (FSHR; OMIM:136533), which when mutated leads to disease. |
|
Molecular_info (7)
|
|
Experimental_info
|
RNAi_result (7)
|
| |
WB_RNAi_result (7)
|
| 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
|
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