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Gene: T14G10.1 
| T14G10.1 | Evidence | Author_evidence | Bergeron KF | |||
|---|---|---|---|---|---|---|
| SMap | S_parent | Sequence | T14G10 | |||
| Chromosome | IV | |||||
| Identity (5) | ||||||
| Gene_info | Gene_class | pps | ||||
| Allele | tm1109 | |||||
| GO_term (5) | ||||||
| Structured_description | Provisional_description | pps-1 is orthologous to human PAPSS1 (OMIM:603262) and human PAPSS2 (OMIM:603005, mutated in spondyloepimetaphyseal dysplasia). | Person_evidence | WBPerson567 | ||
| Curator_confirmed | WBPerson567 | |||||
| Concise_description | pps-1 is orthologous to human PAPSS1 (OMIM:603262) and human PAPSS2 (OMIM:603005, mutated in spondyloepimetaphyseal dysplasia). | |||||
| Molecular_info (5) | ||||||
| Experimental_info | RNAi_result | Cenix:38-e2 | ||||
| WB_RNAi_result | MV_SV:mv_T14G10.1 | |||||
| Cenix:38-e2 | ||||||
| Expr_pattern | Expr5496 | |||||
| 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 |
