Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6102
Gene name Gene Name - the full gene name approved by the HGNC.
RP2 activator of ARL3 GTPase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RP2
Synonyms (NCBI Gene) Gene synonyms aliases
DELXp11.3, NM23-H10, NME10, TBCCD2, XRP2
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xp11.3
Summary Summary of gene provided in NCBI Entrez Gene.
The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefo
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs28933687 G>A,T Pathogenic Coding sequence variant, missense variant
rs104894925 C>T Pathogenic Coding sequence variant, stop gained
rs104894926 C>G Pathogenic Coding sequence variant, stop gained
rs104894927 C>T Pathogenic Coding sequence variant, stop gained
rs137852284 TCC>- Pathogenic Coding sequence variant, inframe deletion
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020630 hsa-miR-155-5p Proteomics 18668040
MIRT002407 hsa-miR-21-5p Microarray 18591254
MIRT726709 hsa-miR-181a-5p HITS-CLIP 22473208
MIRT726707 hsa-miR-181b-5p HITS-CLIP 22473208
MIRT726708 hsa-miR-181c-5p HITS-CLIP 22473208
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000287 Function Magnesium ion binding IDA 26455799
GO:0005096 Function GTPase activator activity IBA
GO:0005096 Function GTPase activator activity IDA 11847227, 18376416, 26455799
GO:0005096 Function GTPase activator activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300757 10274 ENSG00000102218
Protein
UniProt ID O75695
Protein name Protein XRP2
Protein function Acts as a GTPase-activating protein (GAP) involved in trafficking between the Golgi and the ciliary membrane. Involved in localization of proteins, such as NPHP3, to the cilium membrane by inducing hydrolysis of GTP ARL3, leading to the release
PDB 2BX6 , 3BH6 , 3BH7
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07986 TBCC 59 177 Tubulin binding cofactor C Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Expressed in the rod and cone photoreceptors, extending from the tips of the outer segment (OS) through the inner segment (IS) and outer nuclear layer (ONL) and into the synaptic terminals of the outer plexiform layer (ONL)
Sequence
MGCFFSKRRKADKESRPENEEERPKQYSWDQREKVDPKDYMFSGLKDETVGRLPGTVAGQ
QFLIQDCENCNIYIFDHSATVTIDDCTNCIIFLGPVKGSVFFRNCRDCKCTLACQQFRVR
DCRKLEVFLCCATQPIIESSSNIKFGCFQWYYPELAFQFKDAGLSIFNNTWSNIHDF
TPV
SGELNWSLLPEDAVVQDYVPIPTTEELKAVRVSTEANRSIVPISRGQRQKSSDESCLVVL
FAGDYTIANARKLIDEMVGKGFFLVQTKEVSMKAEDAQRVFREKAPDFLPLLNKGPVIAL
EFNGDGAVEVCQLIVNEIFNGTKMFVSESKETASGDVDSFYNFADIQMGI
Sequence length 350
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Trafficking of myristoylated proteins to the cilium
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
retinal dystrophy Retinal dystrophy rs1925389524, rs1924904597, rs1556318633, rs1924521211, rs1924895234, rs104894927, rs1924896735, rs1924897230, rs1924901288, rs878853381, rs1924521431, rs1924904407, rs1064797368, rs1925035229, rs28933687
View all (1 more)
N/A
Retinitis Pigmentosa retinitis pigmentosa 3, Retinitis pigmentosa 2, retinitis pigmentosa rs1602347637, rs1924904597, rs2147081376, rs1924900389, rs1556318627, rs1602355025, rs28933687, rs1602342597, rs104894927, rs1556318633, rs1602347786, rs1602347851, rs1556318642, rs1602342663, rs137852284
View all (11 more)
N/A
Leber Congenital Amaurosis leber congenital amaurosis rs1556313557, rs1569531639, rs1556313552 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
cone-rod dystrophy Cone-rod dystrophy N/A N/A ClinVar
Macular dystrophy macular dystrophy N/A N/A ClinVar
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adrenal Hyperplasia Congenital Associate 10207042
Atrophy Associate 20625056, 37643038
Carcinoma Renal Cell Associate 36035369
Choroideremia Associate 20625056, 28112135
Chromosome Deletion Associate 7977353
Cone Rod Dystrophies Associate 39596324
Emphysema Associate 16504044
Glioma Associate 37602882
Hypertensive Retinopathy Associate 26448634, 37977507
Immunoglobulin G4 Related Disease Associate 22126752