The following RPGRIP1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the RPGRIP1 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.
| CloneID | OCe17484 | |
| Clone ID Related Accession (Same CDS sequence) | NM_001313773.1 | |
| Accession Version | NM_001313773.1 Latest version! | Documents for ORF clone product in default vector |
| Sequence Information | ORF Nucleotide Sequence (Length: 3630bp) Protein sequence SNP |
|
| Vector | pcDNA3.1-C-(k)DYK or customized vector |  User Manual |
| Clone information | Clone Map | MSDS |
| Tag on pcDNA3.1+/C-(K)DYK | C terminal DYKDDDDK tags | |
| ORF Insert Method | CloneEZ™ Seamless cloning technology | |
| Insert Structure | linear | |
| Update Date | 2019-07-01 | |
| Organism | Canis lupus familiaris(dog) | |
| Product | X-linked retinitis pigmentosa GTPase regulator-interacting protein 1 | |
| Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AAEX03009852.1. On Sep 1, 2015 this sequence version replaced XM_846504.3. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. ##Evidence-Data-START## Transcript exon combination :: HM021768.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA103936001, SAMEA103936002 [ECO:0000350] ##Evidence-Data-END## | |
1 | ATGGTACCAG TGTCGAAAGG TAAGAATATG AAAGCTCAAC CACCCTTGAG CAGAATGAGC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
| RefSeq | NP_001300702.1 |
| CDS | 197..3826 |
| Translation |
Target ORF information:
Target ORF information:
|
 NM_001313773.1 |
1 | ATGGTACCAG TGTCGAAAGG TAAGAATATG AAAGCTCAAC CACCCTTGAG CAGAATGAGC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
| CloneID | OCe293353 | |
| Clone ID Related Accession (Same CDS sequence) | XM_022427662.1 | |
| Accession Version | XM_022427662.1 Latest version! | Documents for ORF clone product in default vector |
| Sequence Information | ORF Nucleotide Sequence (Length: 3135bp) Protein sequence SNP |
|
| Vector | pcDNA3.1-C-(k)DYK or customized vector | User Manual |
| Clone information | Clone Map | MSDS |
| Tag on pcDNA3.1+/C-(K)DYK | C terminal DYKDDDDK tags | |
| ORF Insert Method | CloneEZ™ Seamless cloning technology | |
| Insert Structure | linear | |
| Update Date | 2017-09-04 | |
| Organism | Canis lupus familiaris(dog) | |
| Product | X-linked retinitis pigmentosa GTPase regulator-interacting protein 1 isoform X1 | |
| Comment | Comment: MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_006597.3) annotated using gene prediction method: Gnomon, supported by mRNA and EST evidence. Also see: Documentation of NCBI's Annotation Process ##Genome-Annotation-Data-START## Annotation Provider :: NCBI Annotation Status :: Full annotation Annotation Version :: Canis lupus familiaris Annotation Release 105 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 7.4 Annotation Method :: Best-placed RefSeq; Gnomon Features Annotated :: Gene; mRNA; CDS; ncRNA ##Genome-Annotation-Data-END## | |
1 | ATGGTACCAG TGTCGAAAGG TAAGAATATG AAAGCTCAAC CACCCTTGAG CAGAATGAGC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
| RefSeq | XP_022283370.1 |
| CDS | 197..3331 |
| Translation |
Target ORF information:
Target ORF information:
|
XM_022427662.1 |
1 | ATGGTACCAG TGTCGAAAGG TAAGAATATG AAAGCTCAAC CACCCTTGAG CAGAATGAGC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
Variabilities in retinal function and structure in a canine model of cone-rod dystrophy associated with RPGRIP1 support multigenic etiology. |
Canine genome assembly correction facilitates identification of a MAP9 deletion as a potential age of onset modifier for RPGRIP1-associated canine retinal degeneration. |
Leber congenital amaurosis caused by mutations in RPGRIP1. |
Genome-wide association study in RPGRIP1(-/-) dogs identifies a modifier locus that determines the onset of retinal degeneration. |
Multiple mechanisms contribute to leakiness of a frameshift mutation in canine cone-rod dystrophy. |
