Gene Symbol | RPGR |
Entrez Gene ID | 403726 |
Full Name | retinitis pigmentosa GTPase regulator |
Gene Type | protein-coding |
Organism | Canis lupus familiaris(dog) |
ORF » Species Summary » Canis lupus familiaris » RPGR cDNA ORF clone
Gene Symbol | RPGR |
Entrez Gene ID | 403726 |
Full Name | retinitis pigmentosa GTPase regulator |
Gene Type | protein-coding |
Organism | Canis lupus familiaris(dog) |
mRNA | Protein | Name |
---|---|---|
NM_001003126.1 | NP_001003126.1 | X-linked retinitis pigmentosa GTPase regulator |
Pan troglodytes (chimpanzee) | RPGR | XP_003954016.1 |
Mus musculus (house mouse) | Rpgr | NP_001171421.1 |
Rattus norvegicus (Norway rat) | Rpgr | XP_006256751.1 |
Xenopus tropicalis (tropical clawed frog) | rpgr | NP_001037872.1 |
Danio rerio (zebrafish) | rpgrb | XP_005169406.1 |
Canis lupus familiaris (dog) | RPGR | NP_001003126.1 |
Homo sapiens (human) | RPGR | NP_000319.1 |
Molecular studies of phenotype variation in canine RPGR-XLPRA1.
Appelbaum T, Becker D, Santana E, Aguirre GD
Molecular vision22319-31(2016)
Muscular dystrophy in the Japanese Spitz: an inversion disrupts the DMD and RPGR genes.
Atencia-Fernandez S, Shiel RE, Mooney CT, Nolan CM
Animal genetics46(2)175-84(2015 Apr)
Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration.
Zhang Q, Acland GM, Wu WX, Johnson JL, Pearce-Kelling S, Tulloch B, Vervoort R, Wright AF, Aguirre GD
Human molecular genetics11(9)993-1003(2002 May)
Mapping of X-linked progressive retinal atrophy (XLPRA), the canine homolog of retinitis pigmentosa 3 (RP3).
Zeiss CJ, Ray K, Acland GM, Aguirre GD
Human molecular genetics9(4)531-7(2000 Mar)
GeneRIFs: Gene References Into Functions What's a GeneRIF?
Lack of association between haplotypes and the disease phenotype suggests that these genes are not genetic modifiers of XLPRA1
Title: Molecular studies of phenotype variation in canine RPGR-XLPRA1.
a chromosome inversion disrupting the DMD and RPGR genes is the causative mutation for X-linked muscular dystrophy in the Japanese Spitz breed
Title: Muscular dystrophy in the Japanese Spitz: an inversion disrupts the DMD and RPGR genes.
The following RPGR gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the RPGR 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 | OCe00104 | |
Clone ID Related Accession (Same CDS sequence) | NM_001003126.1 | |
Accession Version | NM_001003126.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 3012bp) 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 | 2019-12-24 | |
Organism | Canis lupus familiaris(dog) | |
Product | X-linked retinitis pigmentosa GTPase regulator | |
Comment | Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from AF148801.1. ##Evidence-Data-START## Transcript exon combination :: AF148801.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA103936001, SAMEA103936002 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. |
1 | ATGGGGGAAC CCGAGGAGGT GATGCCCGGT TCAGGTGCTG TGTTTACATT TGGGAAAACT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001003126.1 |
CDS | 81..3092 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001003126.1 |
1 | ATGGGGGAAC CCGAGGAGGT GATGCCCGGT TCAGGTGCTG TGTTTACATT TGGGAAAACT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
Molecular studies of phenotype variation in canine RPGR-XLPRA1. |
Muscular dystrophy in the Japanese Spitz: an inversion disrupts the DMD and RPGR genes. |
Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration. |
Mapping of X-linked progressive retinal atrophy (XLPRA), the canine homolog of retinitis pigmentosa 3 (RP3). |