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Cancer Genome Characterization Initiative

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Gene Info

Gene Information For:Hs. RPGRIP1, retinitis pigmentosa GTPase regulator interacting protein 1
Sequence ID:NM_020366
RefSeqGene ID:NG_008933
Entrez Gene ID:57096
Ensembl ID:ENSG00000092200

Database Links

UniGeneEntrez GeneOMIMEnsembl GeneHPRDVegaSNPSNP: GeneViewSNP: VarViewAssembliesCancer AberrationsRNAi

Gene Expression Data


Associated Diseases (from OMIM)

DiseaseOther Genes
CONE-ROD DYSTROPHY 13 
LEBER CONGENITAL AMAUROSIS 6 

Cytogenetic Location (from UniGene)

Cytogenetic Location:14q11Mitelman Breakpoint Data

Chromosomal Position (from UCSC)

Chromosomal Position:14: 21789522 - 21819460

 Exon Info From UCSC:
NM_020366

Full-Length MGC Clones for This Gene

IMAGE IdStatusAccession GenBank Def Line
100015329BC148360retinitis pigmentosa GTPase regulator interacting protein 1

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_020366 NP_065099 Q96KN7  

Related Sequences

 
mRNAGenPeptSwissProt
AF260257 AAF91371 Q96KN7
AF265666 AAG10000 Q96KN7
AF265667 AAG10001 Q96KN7
AF227257 AAG10246 Q96KN7
BC039089 AAH39089 Q96KN7
BC148360 AAI48361  
AY914561 AAX11416 Q5D221
AK301780 BAG63237 B4DX25
AJ417067 CAD01135 Q96KN7
BX571740 CAE11866 Q96KN7

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
H.sapiens RPGRIP1 NP_065099 M.musculus Rpgrip1 77945 Gene Info NP_001161987 67

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)