Incidental Mutation 'R5610:Arrdc5'
ID 440335
Institutional Source Beutler Lab
Gene Symbol Arrdc5
Ensembl Gene ENSMUSG00000073380
Gene Name arrestin domain containing 5
Synonyms 1700013E09Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5610 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 56601111-56607262 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 56604846 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Histidine at position 147 (R147H)
Ref Sequence ENSEMBL: ENSMUSP00000094906 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097303]
AlphaFold Q497K5
Predicted Effect probably benign
Transcript: ENSMUST00000097303
AA Change: R147H

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000094906
Gene: ENSMUSG00000073380
AA Change: R147H

DomainStartEndE-ValueType
Pfam:Arrestin_N 7 144 3.3e-21 PFAM
Arrestin_C 170 307 7.47e-19 SMART
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik A G 5: 144,982,156 (GRCm39) D247G possibly damaging Het
1700123K08Rik A G 5: 138,562,403 (GRCm39) probably null Het
Abca8b C A 11: 109,868,639 (GRCm39) G175V probably damaging Het
Accsl C A 2: 93,692,118 (GRCm39) probably null Het
Adad2 C T 8: 120,341,500 (GRCm39) R171C probably benign Het
Adgrv1 A C 13: 81,669,236 (GRCm39) L2440R probably damaging Het
Antxr1 A G 6: 87,232,845 (GRCm39) V239A probably damaging Het
Aoc1l2 G A 6: 48,907,953 (GRCm39) V318I probably benign Het
Arhgap28 G A 17: 68,203,235 (GRCm39) Q73* probably null Het
Ash1l T C 3: 88,930,492 (GRCm39) Y1990H probably damaging Het
Bank1 T C 3: 135,772,148 (GRCm39) E494G probably damaging Het
Bicral A T 17: 47,119,418 (GRCm39) I701N probably damaging Het
Bod1l T C 5: 41,979,217 (GRCm39) Y699C probably damaging Het
C3ar1 T G 6: 122,827,537 (GRCm39) T227P probably benign Het
Ccr3 C A 9: 123,829,518 (GRCm39) D284E probably damaging Het
Cdh13 T C 8: 119,578,462 (GRCm39) V163A possibly damaging Het
CK137956 C T 4: 127,840,440 (GRCm39) probably null Het
Cltc T C 11: 86,612,472 (GRCm39) S529G probably benign Het
Cplane2 C T 4: 140,947,177 (GRCm39) P186L probably benign Het
Ddx11 A G 17: 66,457,021 (GRCm39) K783E probably damaging Het
Dnah3 T A 7: 119,538,288 (GRCm39) probably null Het
Eef2k A G 7: 120,486,005 (GRCm39) H408R probably benign Het
Esr1 A G 10: 4,951,221 (GRCm39) K533R probably damaging Het
Fat1 T A 8: 45,406,109 (GRCm39) Y953* probably null Het
Fosl1 T A 19: 5,505,133 (GRCm39) probably null Het
Frmd4b A G 6: 97,283,752 (GRCm39) M373T probably benign Het
Gm1968 A G 16: 29,777,557 (GRCm39) noncoding transcript Het
Gpr26 T C 7: 131,568,694 (GRCm39) V13A possibly damaging Het
Gtf3c1 T C 7: 125,303,117 (GRCm39) N106S possibly damaging Het
Itgb8 T G 12: 119,134,429 (GRCm39) E546A probably damaging Het
Itpr3 C T 17: 27,337,540 (GRCm39) T2450M probably benign Het
Kif1a A T 1: 92,953,450 (GRCm39) Y1245N probably damaging Het
Klrb1f G A 6: 129,031,335 (GRCm39) probably null Het
Lars1 A G 18: 42,390,156 (GRCm39) L37P probably benign Het
Lnpk T C 2: 74,378,369 (GRCm39) T131A probably benign Het
Mob3c C T 4: 115,690,878 (GRCm39) T156I probably benign Het
Nadk T A 4: 155,668,628 (GRCm39) W100R probably damaging Het
Npy6r A T 18: 44,409,061 (GRCm39) I161F probably benign Het
Or4c107 A C 2: 88,789,170 (GRCm39) D120A probably damaging Het
Or6c204 G A 10: 129,022,426 (GRCm39) T288I probably damaging Het
Pcdhga3 A G 18: 37,808,276 (GRCm39) E243G possibly damaging Het
Pdss2 A G 10: 43,315,828 (GRCm39) T361A probably benign Het
Pkd1l2 G T 8: 117,769,059 (GRCm39) Q1198K probably benign Het
Prdx1 T A 4: 116,550,124 (GRCm39) I102N probably damaging Het
Prss1 G A 6: 41,438,147 (GRCm39) V25I probably benign Het
Pspc1 A G 14: 57,015,388 (GRCm39) Y77H probably damaging Het
Rnf5 T C 17: 34,820,712 (GRCm39) probably benign Het
Ryr1 C A 7: 28,811,399 (GRCm39) M235I probably benign Het
Sec24c A G 14: 20,741,893 (GRCm39) Y776C probably damaging Het
Sharpin A G 15: 76,234,253 (GRCm39) probably null Het
Slc12a4 C A 8: 106,676,845 (GRCm39) V482L possibly damaging Het
Slc38a1 C T 15: 96,514,022 (GRCm39) probably null Het
Smtn G T 11: 3,479,582 (GRCm39) T495N probably damaging Het
Sncaip A G 18: 53,001,991 (GRCm39) T171A probably benign Het
Sprr2e T C 3: 92,260,399 (GRCm39) *77R probably null Het
Syngap1 T A 17: 27,178,754 (GRCm39) D443E possibly damaging Het
Taldo1 T C 7: 140,972,205 (GRCm39) V24A probably damaging Het
Tfap2c T A 2: 172,391,778 (GRCm39) N8K probably benign Het
Tmem229a T C 6: 24,955,580 (GRCm39) Y58C probably damaging Het
Tubgcp3 T C 8: 12,689,577 (GRCm39) Y563C probably damaging Het
Ubr1 T A 2: 120,722,593 (GRCm39) D1342V probably benign Het
Usp7 C T 16: 8,534,374 (GRCm39) probably null Het
Wbp1 C T 6: 83,097,216 (GRCm39) G75D probably damaging Het
Zfp180 G T 7: 23,804,315 (GRCm39) V245F probably benign Het
Zfp414 C T 17: 33,849,012 (GRCm39) T33I probably damaging Het
Zfp646 T A 7: 127,478,530 (GRCm39) C236S probably damaging Het
Other mutations in Arrdc5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00588:Arrdc5 APN 17 56,601,262 (GRCm39) missense probably damaging 1.00
IGL01830:Arrdc5 APN 17 56,601,652 (GRCm39) missense probably damaging 0.99
IGL01861:Arrdc5 APN 17 56,607,144 (GRCm39) missense possibly damaging 0.78
IGL02210:Arrdc5 APN 17 56,607,026 (GRCm39) missense probably damaging 1.00
IGL03379:Arrdc5 APN 17 56,601,589 (GRCm39) nonsense probably null
R0256:Arrdc5 UTSW 17 56,601,382 (GRCm39) missense probably damaging 0.99
R0638:Arrdc5 UTSW 17 56,607,020 (GRCm39) missense possibly damaging 0.94
R1491:Arrdc5 UTSW 17 56,601,222 (GRCm39) missense probably damaging 0.99
R1672:Arrdc5 UTSW 17 56,607,144 (GRCm39) missense possibly damaging 0.78
R2094:Arrdc5 UTSW 17 56,604,856 (GRCm39) missense probably benign 0.44
R4326:Arrdc5 UTSW 17 56,601,420 (GRCm39) missense possibly damaging 0.92
R4327:Arrdc5 UTSW 17 56,601,420 (GRCm39) missense possibly damaging 0.92
R5254:Arrdc5 UTSW 17 56,604,897 (GRCm39) missense probably benign 0.19
R5363:Arrdc5 UTSW 17 56,607,138 (GRCm39) missense probably damaging 0.99
R5740:Arrdc5 UTSW 17 56,604,838 (GRCm39) missense probably benign 0.39
R6054:Arrdc5 UTSW 17 56,601,420 (GRCm39) missense possibly damaging 0.92
R7101:Arrdc5 UTSW 17 56,601,522 (GRCm39) missense probably damaging 1.00
R7439:Arrdc5 UTSW 17 56,604,931 (GRCm39) missense probably benign 0.05
R8878:Arrdc5 UTSW 17 56,601,342 (GRCm39) missense probably benign 0.00
Z1176:Arrdc5 UTSW 17 56,607,189 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AATGCCCAGGTCTCACCATG -3'
(R):5'- TTACAGATAATTGGTTAAGGGCAGG -3'

Sequencing Primer
(F):5'- CAAAGCGCTGGAGTTGATTC -3'
(R):5'- AGGCAGCCACACCTTTG -3'
Posted On 2016-11-08