Incidental Mutation 'R5642:Rnpep'
ID440706
Institutional Source Beutler Lab
Gene Symbol Rnpep
Ensembl Gene ENSMUSG00000041926
Gene Namearginyl aminopeptidase (aminopeptidase B)
Synonyms
MMRRC Submission 043290-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.231) question?
Stock #R5642 (G1)
Quality Score225
Status Not validated
Chromosome1
Chromosomal Location135262712-135284084 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 135277521 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Isoleucine at position 202 (T202I)
Ref Sequence ENSEMBL: ENSMUSP00000076564 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074357] [ENSMUST00000077340]
Predicted Effect probably damaging
Transcript: ENSMUST00000074357
AA Change: T202I

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000073962
Gene: ENSMUSG00000041926
AA Change: T202I

DomainStartEndE-ValueType
low complexity region 19 30 N/A INTRINSIC
Pfam:Peptidase_M1 31 246 2.5e-33 PFAM
Pfam:Peptidase_M1 243 378 3.1e-36 PFAM
Pfam:Peptidase_MA_2 257 402 4.5e-21 PFAM
Leuk-A4-hydro_C 461 606 1.4e-55 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000077340
AA Change: T202I

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000076564
Gene: ENSMUSG00000041926
AA Change: T202I

DomainStartEndE-ValueType
low complexity region 19 30 N/A INTRINSIC
Pfam:Peptidase_M1 31 417 2.2e-84 PFAM
Leuk-A4-hydro_C 500 645 1.4e-55 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141092
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152169
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188053
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189615
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190632
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 93 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700022I11Rik T C 4: 42,971,831 L388P possibly damaging Het
4930432K21Rik C T 8: 84,167,485 T427I probably damaging Het
4932415D10Rik T A 10: 82,284,483 Q4231L probably damaging Het
Abcc1 A G 16: 14,443,455 E699G probably damaging Het
Ap4e1 T A 2: 127,064,979 V1053D possibly damaging Het
Apobec1 T A 6: 122,581,497 I100F probably damaging Het
Atp6v1g3 G T 1: 138,283,742 K53N probably damaging Het
Bag3 C T 7: 128,546,106 R482W probably damaging Het
Cacna1i A G 15: 80,395,078 T2007A possibly damaging Het
Cd44 T C 2: 102,901,342 D2G probably damaging Het
Cdadc1 T A 14: 59,589,923 I100F possibly damaging Het
Cdh16 A G 8: 104,618,045 F485L probably damaging Het
Cdhr5 T A 7: 141,269,197 K817* probably null Het
Cfap46 G T 7: 139,678,577 P260Q probably damaging Het
Clec11a C T 7: 44,306,408 E72K possibly damaging Het
Cnr2 C A 4: 135,916,765 N51K probably damaging Het
Col3a1 T A 1: 45,331,712 probably benign Het
Cxcr1 G A 1: 74,191,828 T345M probably damaging Het
Cyp2s1 T C 7: 25,816,319 probably null Het
Dalrd3 C T 9: 108,572,290 T474M probably damaging Het
Ddit4 C T 10: 59,951,505 S3N probably benign Het
Ddx41 T C 13: 55,535,895 K108E possibly damaging Het
Ece2 A T 16: 20,643,727 H732L probably benign Het
Etv3 T G 3: 87,536,015 L302R possibly damaging Het
Fam135b A G 15: 71,462,136 S1070P probably damaging Het
Fam160a2 A T 7: 105,389,882 I50N probably damaging Het
Gm11567 T A 11: 99,879,611 I125N unknown Het
Grm3 A G 5: 9,570,536 L236P probably benign Het
Hip1 T A 5: 135,433,085 R97* probably null Het
Hoxa5 T C 6: 52,204,217 Y45C probably damaging Het
Ighg1 T A 12: 113,329,034 H305L probably damaging Het
Inpp5b T A 4: 124,782,436 C362S probably benign Het
Kif1c A G 11: 70,708,447 K391E probably benign Het
Klf9 T C 19: 23,141,882 V43A probably benign Het
Krt28 T A 11: 99,374,494 I116F probably damaging Het
Lct A T 1: 128,295,232 D1439E probably damaging Het
Liph G A 16: 21,965,995 T284M possibly damaging Het
Lrrc75b T C 10: 75,557,221 K98R possibly damaging Het
Lypd4 T C 7: 24,865,179 Q178R probably benign Het
Map1a T A 2: 121,306,043 S2209T probably damaging Het
Map3k21 C T 8: 125,938,824 T584I probably benign Het
Map3k6 T C 4: 133,245,544 V338A probably damaging Het
Mapk8ip3 A T 17: 24,903,311 V699E possibly damaging Het
Marc1 A C 1: 184,810,919 S71A probably damaging Het
Nckap1l T C 15: 103,455,025 S53P probably benign Het
Nt5e T C 9: 88,327,687 M1T probably null Het
Nudt22 T C 19: 6,995,528 H64R probably damaging Het
Olfr1048 T C 2: 86,235,932 N294S probably damaging Het
Olfr108 A T 17: 37,445,772 T84S probably damaging Het
Olfr198 A G 16: 59,202,006 L140P probably damaging Het
Olfr314 A T 11: 58,786,828 Y198F probably damaging Het
Olfr322 T C 11: 58,666,399 I280T possibly damaging Het
Olfr690 A T 7: 105,329,565 V209D probably damaging Het
Otogl T C 10: 107,886,552 I314V probably benign Het
Pan2 G T 10: 128,308,100 E106D probably benign Het
Papss1 T A 3: 131,631,804 Y554* probably null Het
Pcnx T C 12: 81,895,029 V67A possibly damaging Het
Pdpk1 A C 17: 24,106,855 Y122* probably null Het
Pkd1l1 A T 11: 8,879,202 N1463K probably damaging Het
Ptgfrn C A 3: 101,043,362 M878I probably damaging Het
Ranbp3 G A 17: 56,710,703 G453E probably benign Het
Rapgef2 T C 3: 79,094,850 D261G probably damaging Het
Reep2 A G 18: 34,846,218 S199G probably benign Het
Sass6 T A 3: 116,607,496 probably null Het
Sema3e A G 5: 14,162,243 D111G probably damaging Het
Slc29a4 A G 5: 142,711,972 E60G probably damaging Het
Sptlc3 T C 2: 139,546,408 Y107H probably damaging Het
Stx6 T C 1: 155,198,179 I245T probably benign Het
Syne2 T C 12: 75,918,532 S774P probably damaging Het
Tbc1d16 T A 11: 119,158,791 Q293L probably damaging Het
Tbc1d30 T C 10: 121,296,787 D224G probably damaging Het
Tbc1d32 T A 10: 56,150,877 N759Y possibly damaging Het
Tdrd12 G T 7: 35,511,300 A166E probably damaging Het
Tex14 A G 11: 87,514,220 R653G probably benign Het
Them6 A T 15: 74,721,805 R171W probably null Het
Tln2 T C 9: 67,296,358 T489A probably benign Het
Tmem87a A G 2: 120,403,946 F39L probably benign Het
Toporsl T A 4: 52,611,515 C469* probably null Het
Tpr T C 1: 150,423,818 S1147P probably damaging Het
Trp53bp1 T C 2: 121,236,662 M528V probably benign Het
Trpm6 T A 19: 18,830,207 C1039S probably damaging Het
Ttc16 T A 2: 32,775,336 S5C probably damaging Het
Ttn T C 2: 76,787,068 Y14607C probably damaging Het
Usp6nl T C 2: 6,430,464 F345L probably damaging Het
Vmn1r205 C T 13: 22,592,036 G299R probably benign Het
Vmn2r74 G A 7: 85,957,380 H253Y probably benign Het
Vps13d A T 4: 145,170,302 D343E possibly damaging Het
Vwf A G 6: 125,603,418 E543G Het
Wdr92 A G 11: 17,227,263 N207S possibly damaging Het
Zfat A T 15: 68,180,916 V343E probably damaging Het
Zfp316 T C 5: 143,264,091 E139G unknown Het
Zfp943 T A 17: 21,992,832 C300S probably damaging Het
Zkscan16 A G 4: 58,957,748 K677E probably benign Het
Other mutations in Rnpep
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01789:Rnpep APN 1 135268095 missense possibly damaging 0.72
R0001:Rnpep UTSW 1 135272485 splice site probably benign
R0498:Rnpep UTSW 1 135265352 missense probably damaging 1.00
R0597:Rnpep UTSW 1 135272419 missense probably damaging 0.99
R1728:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1728:Rnpep UTSW 1 135283977 missense probably benign
R1729:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1729:Rnpep UTSW 1 135283977 missense probably benign
R1730:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1739:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1739:Rnpep UTSW 1 135283629 missense probably benign
R1762:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1783:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1783:Rnpep UTSW 1 135283977 missense probably benign
R1784:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1785:Rnpep UTSW 1 135263096 missense possibly damaging 0.95
R1785:Rnpep UTSW 1 135283977 missense probably benign
R2101:Rnpep UTSW 1 135271617 missense probably damaging 1.00
R4933:Rnpep UTSW 1 135267026 intron probably benign
R4993:Rnpep UTSW 1 135263032 missense possibly damaging 0.80
R6965:Rnpep UTSW 1 135263120 nonsense probably null
R7143:Rnpep UTSW 1 135283749 missense probably benign 0.41
R7508:Rnpep UTSW 1 135278858 missense probably benign 0.33
R8060:Rnpep UTSW 1 135266920 missense probably damaging 1.00
R8094:Rnpep UTSW 1 135283776 missense probably damaging 1.00
R8191:Rnpep UTSW 1 135272434 missense possibly damaging 0.56
R8300:Rnpep UTSW 1 135283659 missense probably benign 0.00
Z1176:Rnpep UTSW 1 135271755 missense probably benign 0.19
Z1176:Rnpep UTSW 1 135283836 missense probably benign 0.16
Predicted Primers PCR Primer
(F):5'- AGGTCAATCCAACCTTGCC -3'
(R):5'- TCTTCAAGTTAGACAGAGGAGGC -3'

Sequencing Primer
(F):5'- AATCCAACCTTGCCTATCGAGTG -3'
(R):5'- GGGCTGCATAGAAACACTTTGTCTC -3'
Posted On2016-11-08