RBP3 (retinol binding protein 3)

symbol
RBP3
locus group
protein-coding gene
location
10q11.22
gene_family
-
alias symbol
D10S64|D10S65|D10S66|RP66
alias name
interstitial retinol-binding prote…
entrez id
5949
ensembl gene id
ENSG00000265203
ucsc gene id
uc001jez.3
refseq accession
NM_002900
hgnc_id
HGNC:9921
approved reserved
1986-01-01
10q11.22
ChineseEnglish

Interphotoreceptor retinol-binding protein is a large glycoprotein known to bind retinoids and found primarily in the interphotoreceptor matrix of the retina between the retinal pigment epithelium and the photoreceptor cells. It is thought to transport retinoids between the retinal pigment epithelium and the photoreceptors, a critical role in the visual process.The human IRBP gene is approximately 9.5 kbp in length and consists of four exons separated by three introns. The introns are 1.6-1.9 kbp long. The gene is transcribed by photoreceptor and retinoblastoma cells into an approximately 4.3-kilobase mRNA that is translated and processed into a glycosylated protein of 135,000 Da. The amino acid sequence of human IRBP can be divided into four contiguous homology domains with 33-38% identity, suggesting a series of gene duplication events. In the gene, the boundaries of these domains are not defined by exon-intron junctions, as might have been expected. The first three homology domains and part of the fourth are all encoded by the first large exon, which is 3,180 base pairs long. The remainder of the fourth domain is encoded in the last three exons, which are 191, 143, and approximately 740 base pairs long, respectively. [provided by RefSeq, Jul 2008]

Nucleotide sequence of RBP3:[NCBI]
Loading Gene Browser...
Protein Sequence
1MMREWVLLMS VLLCGLAGPT HLFQPSLVLD MAKVLLDNYC
41FPENLLGMQE AIQQAIKSHE ILSISDPQTL ASVLTAGVQS
81 SLNDPRLVI SYEPSTPEPP PQVPALTSLS EEELLAWLQR
121GLRHEVLEGN VGYLRVDSVP GQEVLSMMGE FLVAHVWGNL
161M GTSALVLD LRHCTGGQVS GIPYIISYLH PGNTILHVDT
201IYNRPSNTTT EIWTLPQVLG ERYGADKDVV VLTSSQTRGV
241AE DIAHILK QMRRAIVVGE RTGGGALDLR KLRIGESDFF
281FTVPVSRSLG PLGGGSQTWE GSGVLPCVGT PAEQALEKAL
321AIL TLRSAL PGVVHCLQEV LKDYYTLVDR VPTLLQHLAS
361MDFSTVVSEE DLVTKLNAGL QAASEDPRLL VRAIGPTETP
401SWPA PDAAA EDSPGVAPEL PEDEAIRQAL VDSVFQVSVL
441PGNVGYLRFD SFADASVLGV LAPYVLRQVW EPLQDTEHLI
481MDLRH NPGG PSSAVPLLLS YFQGPEAGPV HLFTTYDRRT
521NITQEHFSHM ELPGPRYSTQ RGVYLLTSHR TATAAEEFAF
561LMQSLG WAT LVGEITAGNL LHTRTVPLLD TPEGSLALTV
601PVLTFIDNHG EAWLGGGVVP DAIVLAEEAL DKAQEVLEFH
641QSLGALV EG TGHLLEAHYA RPEVVGQTSA LLRAKLAQGA
681YRTAVDLESL ASQLTADLQE VSGDHRLLVF HSPGELVVEE
721APPPPPAV P SPEELTYLIE ALFKTEVLPG QLGYLRFDAM
761AELETVKAVG PQLVRLVWQQ LVDTAALVID LRYNPGSYST
801AIPLLCSYF FEAEPRQHLY SVFDRATSKV TEVWTLPQVA
841GQRYGSHKDL YILMSHTSGS AAEAFAHTMQ DLQRATVIGE
881PTAGGALSVG IYQVGSSPL YASMPTQMAM SATTGKAWDL
921AGVEPDITVP MSEALSIAQD IVALRAKVPT VLQTAGKLVA
961DNYASAELGA K MATKLSGL QSRYSRVTSE VALAEILGAD
1001LQMLSGDPHL KAAHIPENAK DRIPGIVPMQ IPSPEVFEEL
1041IKFSFHTNVL ED NIGYLRF DMFGDGELLT QVSRLLVEHI
1081WKKIMHTDAM IIDMRFNIGG PTSSIPILCS YFFDEGPPVL
1121LDKIYSRPDD SVS ELWTHA QVVGERYGSK KSMVILTSSV
1161TAGTAEEFTY IMKRLGRALV IGEVTSGGCQ PPQTYHVDDT
1201NLYLTIPTAR SVGA SDGSS WEGVGVTPHV VVPAEEALAR
1241AKEMLQHNQL RVKRSPGLQD HL
Structure predicted by AlphaFold DB(UniProt: P10745). Color indicates pLDDT confidence (dark blue = high, yellow/orange = low).
SNP variants of RBP3:           Showing partial SNPs
rs3494       rs1870179       rs2070705       rs2070706       rs2234691       rs2234692       rs2376635       rs2854249       rs3740296       rs3758494       rs3758495       rs3781223       rs3781224       rs4922513       rs9421729       rs11204213       rs11598079      

Tissue expression of RBP3:    [UniProt]

Gene expression across tissues
Forward Primer
Forward Tm
Reverse Primer
Reverse Tm
Score
CTGCTGGACAAGATCTACAG
58
ATAGCGTTCACCTACAACC
57
TCTGCTGGACAAGATCTACAG
59
TAGCGTTCACCTACAACCTG
60
TCTGCTGGACAAGATCTACAG
59
TAGCGTTCACCTACAACCT
58
Transcription Factors
Target Gene
Interaction Type
PubMed References
CRX
RBP3
Activation
CRX
RBP3
Repression
CRX
RBP3
Unknown
KLF15
RBP3
Repression
NRL
RBP3
Repression
OTX2
RBP3
Activation
OTX2
RBP3
Unknown
ZNF239
RBP3
Repression

Subcellular localization of RBP3 (and its protein):

[UniProt]     [GenomeNet]

" d="M482.414,245.296c3.539,4.293,4.455,10.009,0.202,11 c-4.244,0.996-4.983-10.983-8.293-8.438c-5.271,4.08,9.834,12.271,5.144,17.287c-3.717,3.607-6.172-5.75-10.839-1.976 c-4.673,3.776,6.781,7.299,2.831,11.326c-4.354,4.045-6.979-1.449-9.837-5.517c-1.193-1.742-2.059-3.851-3.595-2.748 c-1.516,1.078-1.854,1.795-0.938,3.666c2.374,4.854,9.235,10.119,5.156,12.535c-5.636,3.346-5.044-8.871-9.426-7.574 c-4.388,1.291,2.557,10.66-1.245,11.141c-4.089,0.545-3.483-10.239-6.979-8.575c-2.522,1.206-0.929,3.071-0.938,4.899 c0.004,1.32-0.964,3.6-2.372,4.062c-3.593,1.171-8.544-1.065-10.251-3.59c-6.04-8.93,0.396-15.997,4.639-7.015 c3.023,4.642,5.182,0.834,2.839-2.219c-1.032-1.354-4.309-5.901-0.781-7.252c2.904-1.113,4.271,1.941,5.985,4.592 c2.61,4.016,5.485,0.117,3.031-3.414c-1.828-2.633-2.74-3.803,3.156-7.42c6.405-4.369,6.52,3.869,10.077,0.646 c2.309-1.832-4.783-5.149,0.06-8.995c2.896-2.293,5.18,6.207,7.961,3.516c3.523-2.737-7.717-7.369,0.117-11.736 C473.413,240.77,480.519,242.891,482.414,245.296z"/> Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
  • plasma membrane
  • cytoplasm
  • extracellular
  • golgi
  • vesicle
  • cytoskeleton
  • endoplasmic reticulum
  • nucleus
  • endosome
  • lysosome
  • mitochondrion

Gene Ontology (GO) terms for RBP3:

GO ID
Protein
Source DB
GO:0001523
P10745 (UniProtKB)
TAS
GO:0001523
P10745 (UniProtKB)
TAS
GO:0005501
P10745 (UniProtKB)
TAS
GO:0005501
P10745 (UniProtKB)
TAS
GO:0005501
P10745 (UniProtKB)
TAS
GO:0005501
P10745 (UniProtKB)
TAS
GO:0005576
P10745 (UniProtKB)
TAS
GO:0005576
P10745 (UniProtKB)
TAS
GO:0005576
P10745 (UniProtKB)
TAS
GO:0005576
P10745 (UniProtKB)
TAS
GO:0005615
P10745 (UniProtKB)
IDA
GO:0006508
P10745 (UniProtKB)
IEA
GO:0006629
P10745 (UniProtKB)
TAS
GO:0006810
P10745 (UniProtKB)
IEA
GO:0007601
P10745 (UniProtKB)
IEA
GO:0008236
P10745 (UniProtKB)
IEA
GO:0016918
P10745 (UniProtKB)
IEA
GO:0019841
P10745 (UniProtKB)
IEA
GO:0033165
P10745 (UniProtKB)
IEA
GO:1903561
P10745 (UniProtKB)
IDA
Reactome
Loading…
Interacting Gene Interaction Source/Score
Disease Score NofPmids NofSnps Source
Disease Score NofPmids NofSnps Source
Retinitis Pigmentosa 0.243724241 5 0 BeFree_CTD_human_GAD_ORPHANET
RETINITIS PIGMENTOSA 66 0.24 1 1 CLINVAR_UNIPROT
Uveitis 0.121900093 8 0 BeFree_CTD_human
Autoimmune Diseases 0.120271442 3 0 BeFree_CTD_human
Retinal Dystrophies 0.002909916 2 0 BeFree_GAD
Multiple Endocrine Neoplasia Type 2a 0.002714419 10 0 BeFree
Retinoblastoma 0.002171535 8 0 BeFree
Retinal Degeneration 0.000814326 3 0 BeFree
Pheochromocytoma 0.000542884 2 0 BeFree
Autosomal recessive retinitis pigmentosa 0.000542884 2 0 BeFree
Digital PCR Quantification of a Circulating RBP3 and CRX RNA Signature Establishes a Liquid Biopsy Framework for Precision Monitoring of Retinoblastoma.
Mendes TB, Oliveira ID, Tesser Gamba F, Lima FT, Morales BFSC, Macedo CRPD, Teixeira LF, Toledo SRC Int J Mol Sci IF: 3.226 2026-05-08
Inherited Retinal Disease as a Predisposing Factor for Paclitaxel Maculopathy.
Meshkin RS, Eliott D, Yuan AE, McKay KM J Vitreoretin Dis 2026-01-23
HTRA1-dependent proteolysis induces age-related retinal degeneration and exacerbates choroidal neovascularization.
Katschke KJ, Truong T, Pham V, Xi H, Tang W, Gu X, Teotia P, Hofmann JW, Chaney SY, Kirchhofer D, van Lookeren Campagne M, Jeanne M Dis Model Mech IF: 3.6 2025-10-01
Inherited Retinal Diseases with High Myopia: A Review.
Liu C, Sheri N, Benson MD Genes (Basel) IF: 3.600 2025-10-11
Effect of pre-hatch incubator lights on the ontogeny of CNS opsins and photoreceptors in the Pekin duck.
Vostrizansky A, Barce A, Gum Z, Shafer DJ, Jeffrey D, Fraley GS, Rivera PD Poult Sci IF: 4.5 2022-04-00
Exome Sequencing and Epigenetic Analysis of Twins Who Are Discordant for Congenital Cataract.
Wei Tanwei, Sun Hui, Hu Bo, Yang Jie, Qiao Chen, Yan Ming Twin Res Hum Genet IF: 1.3 2015-10-26
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy.
Arno Gavin, Hull Sarah, Robson Anthony G, Holder Graham E, Cheetham Michael E, Webster Andrew R, Plagnol Vincent, Moore Anthony T Invest Ophthalmol Vis Sci IF: 5.5 2015-08-25

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