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Gene: F11D5.3 
| F11D5.3 | SMap | S_parent | Sequence | F11D5 | ||
|---|---|---|---|---|---|---|
| Chromosome | X | |||||
| Identity (5) | ||||||
| Gene_info | Allele | ok574 | Inferred_automatically | From strain object: RB788 | ||
| tm797 | ||||||
| snp_F11D5[2] | ||||||
| snp_F11D5[3] | ||||||
| Strain | RB788 | |||||
| GO_term (5) | ||||||
| Structured_description | Provisional_description | F11D5.3 encodes a putative tyrosine kinase homologous to human RS1 (OMIM:312700, mutated in juvenile X-linked retinoschisis). | Paper_evidence | WBPaper00004103 | ||
| Person_evidence | WBPerson567 | |||||
| Curator_confirmed | WBPerson567 | |||||
| Date_last_updated | 17 Jun 2004 00:00:00 | |||||
| Concise_description | F11D5.3 encodes a putative tyrosine kinase homologous to human RS1 (OMIM:312700, mutated in juvenile X-linked retinoschisis). | |||||
| Molecular_info (5) | ||||||
| Experimental_info (4) | ||||||
| Method | Gene |
