| Common name: | POB25,RPG1,RPGRIP1 |
| Defline: | Retinitis pigmentosa GTPase regulator-interacting protein 1; (1 of 1) PF11618 - First C2 domain of RPGR-interacting protein 1 (C2-C2_1) |
| Description: | Found in basal body proteome as POB25; Similar to X-linked retinitis pigmentosa GTPase regulator-interacting protein 1 (RPGRIP1) in humans |
| Synonyms: | RPGRIP1,POB25,Cre14.g632050.t1.1,g15231.t1 |
| Chromosome: | chromosome 14 |
We did not create a plasmid for this gene.
We did not determine any protein-protein interactions for this gene.
| PFAM: | PF00168, PF11618, PF13499 |
| PANTHER: | PTHR14240 |
| KEGG_ec: | |
| KEGG_orthology: | |
| KOG: | KOG0027 |
| Gene ontology terms:: | GO:0005509, GO:0005515 |
| Best arabidopsis TAIR name: | AT2G41100.1 |
| Best arabidopsis TAIR symbol: | ATCAL4,TCH3 |
| Best arabidopsis TAIR defline: | Calcium-binding EF hand family protein |
| Phytozome Locus Page |
Mutants in this gene exhibit a phenotype under the following conditions:
| High pH, screen 2 of 2 ( 74% confidence (FDR = 0.26)) |
Note: FDR indicates the likelihood that a particular genotype-phenotype relationship is incorrect. Not all mutants in a particular gene show the same phenotype. Please see the mutant pages for each mutant's phenotypes. Complementation is needed to definitively prove a genotype-phenotype link. These data are from a pooled phenotyping experiment.
If you reference the phenotypic data above in a manuscript, please cite: Fauser et al. 2022 Nature Genetics.