Incidental Mutation 'R6010:Rbp3'
ID 479725
Institutional Source Beutler Lab
Gene Symbol Rbp3
Ensembl Gene ENSMUSG00000041534
Gene Name retinol binding protein 3, interstitial
Synonyms Irbp, Rbp-3
MMRRC Submission 044187-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.147) question?
Stock # R6010 (G1)
Quality Score 225.009
Status Validated
Chromosome 14
Chromosomal Location 33675960-33686173 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 33676604 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 184 (I184N)
Ref Sequence ENSEMBL: ENSMUSP00000040249 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035695]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000035695
AA Change: I184N

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000040249
Gene: ENSMUSG00000041534
AA Change: I184N

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
TSPc 109 308 5.72e-69 SMART
TSPc 416 616 1.98e-63 SMART
TSPc 720 917 5.34e-69 SMART
TSPc 1019 1216 2.13e-68 SMART
Meta Mutation Damage Score 0.6181 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.7%
  • 20x: 92.9%
Validation Efficiency 100% (65/65)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] 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]
PHENOTYPE: Mice homozygous for disruptions in this gene experience photoreceptor degeneration. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actl7a A G 4: 56,743,870 (GRCm39) I132M possibly damaging Het
Agap2 A T 10: 126,926,779 (GRCm39) I939F probably damaging Het
Ahctf1 A G 1: 179,623,378 (GRCm39) V80A possibly damaging Het
Atxn3 T C 12: 101,914,285 (GRCm39) D67G probably damaging Het
Avl9 G A 6: 56,730,375 (GRCm39) V573M possibly damaging Het
Baz1b G A 5: 135,246,305 (GRCm39) E585K possibly damaging Het
Brms1l T C 12: 55,914,985 (GRCm39) F298S possibly damaging Het
Camk2d G A 3: 126,591,363 (GRCm39) V278I possibly damaging Het
Car10 A G 11: 93,490,149 (GRCm39) I297V possibly damaging Het
Cfap65 C T 1: 74,962,190 (GRCm39) C677Y probably damaging Het
Cfap74 T A 4: 155,538,495 (GRCm39) D872E possibly damaging Het
Cgrrf1 A C 14: 47,091,158 (GRCm39) Q227H probably damaging Het
Chil4 A G 3: 106,121,711 (GRCm39) I46T probably damaging Het
Chpf2 A T 5: 24,796,917 (GRCm39) H621L probably damaging Het
Cluap1 C T 16: 3,755,437 (GRCm39) R351W possibly damaging Het
Cnot6 A T 11: 49,574,066 (GRCm39) Y201* probably null Het
Col15a1 T C 4: 47,245,630 (GRCm39) V127A probably benign Het
Col6a3 C T 1: 90,701,219 (GRCm39) V2566I unknown Het
Cope T A 8: 70,761,162 (GRCm39) M88K probably damaging Het
Cops4 A G 5: 100,691,776 (GRCm39) I358M possibly damaging Het
Coro7 T C 16: 4,487,820 (GRCm39) E130G possibly damaging Het
Csrp3 A G 7: 48,485,213 (GRCm39) probably null Het
Cyp4f39 T C 17: 32,701,160 (GRCm39) F217L probably damaging Het
Dmac1 A G 4: 75,196,473 (GRCm39) S6P unknown Het
Drd4 A T 7: 140,874,709 (GRCm39) I367F probably damaging Het
Efcc1 T A 6: 87,730,711 (GRCm39) probably null Het
Emid1 A T 11: 5,085,389 (GRCm39) M119K possibly damaging Het
Fbn2 C T 18: 58,202,596 (GRCm39) D1237N probably benign Het
Fbxl18 C A 5: 142,858,153 (GRCm39) R761L probably damaging Het
Gbp10 A C 5: 105,372,205 (GRCm39) L185R probably damaging Het
Gm7247 C T 14: 51,601,805 (GRCm39) S26F probably benign Het
Gucd1 G T 10: 75,256,600 (GRCm39) probably benign Het
Helb G A 10: 119,941,788 (GRCm39) T300M probably damaging Het
Ifna11 A T 4: 88,738,278 (GRCm39) H28L probably benign Het
Kalrn T A 16: 33,830,950 (GRCm39) N723I probably benign Het
Kcnb2 C T 1: 15,780,790 (GRCm39) S554F possibly damaging Het
Med1 A C 11: 98,049,188 (GRCm39) V536G probably damaging Het
Nanog A C 6: 122,690,255 (GRCm39) N195T probably benign Het
Neu1 C T 17: 35,151,031 (GRCm39) S94F probably damaging Het
Nop58 T A 1: 59,740,071 (GRCm39) S154R probably damaging Het
Npl A T 1: 153,388,314 (GRCm39) L239* probably null Het
Nrg1 G A 8: 32,308,600 (GRCm39) T483M probably damaging Het
Nup98 G T 7: 101,829,636 (GRCm39) F391L probably damaging Het
Or4c122 A T 2: 89,079,087 (GRCm39) I305K probably benign Het
Or5ar1 T C 2: 85,671,905 (GRCm39) I77V probably benign Het
Or5d47 A T 2: 87,804,886 (GRCm39) V41E probably damaging Het
Or5g26 T C 2: 85,494,374 (GRCm39) I135V probably benign Het
Pacsin2 A G 15: 83,266,020 (GRCm39) V59A possibly damaging Het
Pcsk9 C T 4: 106,311,469 (GRCm39) R254H possibly damaging Het
Pierce2 A T 9: 72,887,488 (GRCm39) probably null Het
Psme2 C A 14: 55,824,980 (GRCm39) probably null Het
Ptprc T A 1: 138,028,794 (GRCm39) H468L probably benign Het
Serpinb1c A G 13: 33,066,042 (GRCm39) L301P probably damaging Het
Smim6 G T 11: 115,804,219 (GRCm39) G2V probably damaging Het
Snrpb2 A G 2: 142,912,815 (GRCm39) D146G possibly damaging Het
Svep1 T A 4: 58,115,832 (GRCm39) S954C possibly damaging Het
Telo2 G T 17: 25,323,852 (GRCm39) T568N possibly damaging Het
Tpp2 T C 1: 43,990,373 (GRCm39) probably null Het
Upf1 A G 8: 70,789,675 (GRCm39) V720A probably damaging Het
Vmn1r81 T C 7: 11,994,349 (GRCm39) I86M possibly damaging Het
Vps8 T A 16: 21,363,955 (GRCm39) probably benign Het
Wdr70 T C 15: 7,916,900 (GRCm39) probably null Het
Zfp385c A T 11: 100,548,363 (GRCm39) S30T probably benign Het
Zfp607a T A 7: 27,577,254 (GRCm39) L108* probably null Het
Other mutations in Rbp3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01364:Rbp3 APN 14 33,676,145 (GRCm39) missense possibly damaging 0.82
IGL01643:Rbp3 APN 14 33,678,793 (GRCm39) missense probably benign 0.18
IGL01665:Rbp3 APN 14 33,678,088 (GRCm39) missense probably benign 0.02
IGL01809:Rbp3 APN 14 33,677,257 (GRCm39) missense probably damaging 1.00
IGL01975:Rbp3 APN 14 33,680,602 (GRCm39) missense probably damaging 1.00
IGL02349:Rbp3 APN 14 33,677,676 (GRCm39) missense probably damaging 0.97
IGL02447:Rbp3 APN 14 33,676,460 (GRCm39) missense probably damaging 1.00
IGL03192:Rbp3 APN 14 33,680,540 (GRCm39) missense possibly damaging 0.52
IGL03302:Rbp3 APN 14 33,676,616 (GRCm39) missense probably damaging 0.97
Behagt UTSW 14 33,676,411 (GRCm39) missense probably benign 0.00
jagt UTSW 14 33,678,439 (GRCm39) missense probably damaging 0.97
muntre UTSW 14 33,678,313 (GRCm39) missense possibly damaging 0.95
Rotwild UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
P4717OSA:Rbp3 UTSW 14 33,677,456 (GRCm39) missense probably damaging 0.96
R0234:Rbp3 UTSW 14 33,677,858 (GRCm39) missense probably damaging 0.98
R0234:Rbp3 UTSW 14 33,677,858 (GRCm39) missense probably damaging 0.98
R0432:Rbp3 UTSW 14 33,676,730 (GRCm39) missense probably damaging 1.00
R0469:Rbp3 UTSW 14 33,684,376 (GRCm39) missense possibly damaging 0.95
R0652:Rbp3 UTSW 14 33,680,605 (GRCm39) missense possibly damaging 0.89
R0739:Rbp3 UTSW 14 33,680,604 (GRCm39) missense probably benign 0.28
R0747:Rbp3 UTSW 14 33,678,235 (GRCm39) missense possibly damaging 0.51
R0836:Rbp3 UTSW 14 33,678,595 (GRCm39) missense possibly damaging 0.84
R1102:Rbp3 UTSW 14 33,678,313 (GRCm39) missense possibly damaging 0.95
R1583:Rbp3 UTSW 14 33,676,481 (GRCm39) missense possibly damaging 0.45
R1589:Rbp3 UTSW 14 33,677,749 (GRCm39) missense probably damaging 0.99
R1595:Rbp3 UTSW 14 33,678,155 (GRCm39) missense possibly damaging 0.93
R1720:Rbp3 UTSW 14 33,678,866 (GRCm39) missense probably benign 0.38
R1830:Rbp3 UTSW 14 33,676,601 (GRCm39) missense probably benign 0.31
R1982:Rbp3 UTSW 14 33,676,502 (GRCm39) missense probably damaging 0.99
R1985:Rbp3 UTSW 14 33,678,418 (GRCm39) missense probably benign 0.00
R1985:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2007:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2027:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2100:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2101:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2113:Rbp3 UTSW 14 33,678,014 (GRCm39) missense probably benign 0.00
R2138:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2183:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2248:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2277:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2306:Rbp3 UTSW 14 33,684,520 (GRCm39) missense probably damaging 1.00
R2504:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2696:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2697:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2698:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2920:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2940:Rbp3 UTSW 14 33,677,975 (GRCm39) missense probably damaging 1.00
R2971:Rbp3 UTSW 14 33,676,411 (GRCm39) missense probably benign 0.00
R3111:Rbp3 UTSW 14 33,676,069 (GRCm39) missense probably benign 0.01
R3155:Rbp3 UTSW 14 33,679,071 (GRCm39) missense probably damaging 0.98
R3156:Rbp3 UTSW 14 33,679,071 (GRCm39) missense probably damaging 0.98
R3751:Rbp3 UTSW 14 33,677,969 (GRCm39) missense probably damaging 0.98
R3752:Rbp3 UTSW 14 33,677,969 (GRCm39) missense probably damaging 0.98
R3851:Rbp3 UTSW 14 33,677,464 (GRCm39) missense probably damaging 0.98
R4016:Rbp3 UTSW 14 33,677,347 (GRCm39) missense possibly damaging 0.82
R4276:Rbp3 UTSW 14 33,680,607 (GRCm39) missense probably benign 0.24
R4277:Rbp3 UTSW 14 33,680,607 (GRCm39) missense probably benign 0.24
R4278:Rbp3 UTSW 14 33,680,607 (GRCm39) missense probably benign 0.24
R4382:Rbp3 UTSW 14 33,677,253 (GRCm39) missense probably benign 0.12
R4383:Rbp3 UTSW 14 33,677,253 (GRCm39) missense probably benign 0.12
R4385:Rbp3 UTSW 14 33,677,253 (GRCm39) missense probably benign 0.12
R4625:Rbp3 UTSW 14 33,678,056 (GRCm39) missense probably benign
R4712:Rbp3 UTSW 14 33,682,615 (GRCm39) missense probably damaging 0.97
R4812:Rbp3 UTSW 14 33,676,731 (GRCm39) missense probably damaging 0.99
R4918:Rbp3 UTSW 14 33,677,368 (GRCm39) missense probably damaging 1.00
R4971:Rbp3 UTSW 14 33,676,427 (GRCm39) missense probably damaging 0.98
R5262:Rbp3 UTSW 14 33,676,807 (GRCm39) missense probably damaging 1.00
R5387:Rbp3 UTSW 14 33,678,370 (GRCm39) missense possibly damaging 0.95
R5468:Rbp3 UTSW 14 33,678,584 (GRCm39) missense possibly damaging 0.93
R5837:Rbp3 UTSW 14 33,676,230 (GRCm39) missense probably benign 0.00
R5994:Rbp3 UTSW 14 33,676,857 (GRCm39) missense probably damaging 1.00
R6041:Rbp3 UTSW 14 33,678,439 (GRCm39) missense probably damaging 0.97
R6266:Rbp3 UTSW 14 33,676,418 (GRCm39) missense probably benign
R6357:Rbp3 UTSW 14 33,678,991 (GRCm39) missense probably damaging 0.99
R6457:Rbp3 UTSW 14 33,677,224 (GRCm39) nonsense probably null
R6777:Rbp3 UTSW 14 33,676,230 (GRCm39) missense probably benign 0.00
R7158:Rbp3 UTSW 14 33,677,513 (GRCm39) missense probably benign 0.00
R7183:Rbp3 UTSW 14 33,677,161 (GRCm39) missense probably benign 0.02
R7256:Rbp3 UTSW 14 33,684,540 (GRCm39) missense possibly damaging 0.93
R7654:Rbp3 UTSW 14 33,677,797 (GRCm39) missense probably benign
R7756:Rbp3 UTSW 14 33,676,732 (GRCm39) missense probably benign 0.15
R7758:Rbp3 UTSW 14 33,676,732 (GRCm39) missense probably benign 0.15
R7784:Rbp3 UTSW 14 33,676,115 (GRCm39) missense probably benign 0.41
R7845:Rbp3 UTSW 14 33,678,421 (GRCm39) missense probably benign 0.24
R8176:Rbp3 UTSW 14 33,677,605 (GRCm39) missense possibly damaging 0.67
R8281:Rbp3 UTSW 14 33,678,320 (GRCm39) missense probably benign 0.00
R8393:Rbp3 UTSW 14 33,678,156 (GRCm39) missense possibly damaging 0.93
R8552:Rbp3 UTSW 14 33,677,621 (GRCm39) missense probably benign 0.01
R8717:Rbp3 UTSW 14 33,678,395 (GRCm39) missense probably damaging 0.99
R8730:Rbp3 UTSW 14 33,677,795 (GRCm39) missense probably benign
R8773:Rbp3 UTSW 14 33,684,492 (GRCm39) missense possibly damaging 0.71
R8836:Rbp3 UTSW 14 33,680,588 (GRCm39) missense possibly damaging 0.95
R8843:Rbp3 UTSW 14 33,676,522 (GRCm39) missense probably benign
R8880:Rbp3 UTSW 14 33,678,796 (GRCm39) missense probably benign 0.16
R8941:Rbp3 UTSW 14 33,678,486 (GRCm39) missense possibly damaging 0.92
R8971:Rbp3 UTSW 14 33,677,792 (GRCm39) missense probably damaging 1.00
R8998:Rbp3 UTSW 14 33,684,360 (GRCm39) nonsense probably null
R8999:Rbp3 UTSW 14 33,684,360 (GRCm39) nonsense probably null
R9436:Rbp3 UTSW 14 33,677,234 (GRCm39) missense possibly damaging 0.94
R9525:Rbp3 UTSW 14 33,676,402 (GRCm39) missense probably benign 0.00
R9563:Rbp3 UTSW 14 33,677,477 (GRCm39) missense probably damaging 1.00
R9564:Rbp3 UTSW 14 33,677,477 (GRCm39) missense probably damaging 1.00
R9723:Rbp3 UTSW 14 33,677,474 (GRCm39) missense possibly damaging 0.92
Z1177:Rbp3 UTSW 14 33,676,495 (GRCm39) missense possibly damaging 0.58
Predicted Primers PCR Primer
(F):5'- ACAGAGGAACATCCGCCATG -3'
(R):5'- CCGCATCTGCTTCAGGATGTAG -3'

Sequencing Primer
(F):5'- GAACATCCGCCATGAGGTTCTTG -3'
(R):5'- ATGTAGGCAATGTCCTCTGCGAC -3'
Posted On 2017-06-26