Incidental Mutation 'R7244:Mup5'
ID 568707
Institutional Source Beutler Lab
Gene Symbol Mup5
Ensembl Gene ENSMUSG00000058523
Gene Name major urinary protein 5
Synonyms Mup V
MMRRC Submission 045308-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.180) question?
Stock # R7244 (G1)
Quality Score 165.009
Status Validated
Chromosome 4
Chromosomal Location 61749556-61753417 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 61749818 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000080908 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000082287] [ENSMUST00000082287] [ENSMUST00000082287]
AlphaFold P11591
Predicted Effect probably null
Transcript: ENSMUST00000082287
SMART Domains Protein: ENSMUSP00000080908
Gene: ENSMUSG00000058523

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:Lipocalin 34 173 8.3e-38 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000082287
SMART Domains Protein: ENSMUSP00000080908
Gene: ENSMUSG00000058523

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:Lipocalin 34 173 8.3e-38 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000082287
SMART Domains Protein: ENSMUSP00000080908
Gene: ENSMUSG00000058523

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:Lipocalin 34 173 8.3e-38 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 96% (45/47)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrb3 A G 1: 25,170,350 (GRCm39) F983L probably damaging Het
Cc2d1b T A 4: 108,486,799 (GRCm39) M632K probably benign Het
Cdyl2 G A 8: 117,301,999 (GRCm39) R461* probably null Het
Cfap57 G A 4: 118,411,997 (GRCm39) Q1216* probably null Het
Chd1l A T 3: 97,505,066 (GRCm39) V167E probably damaging Het
Col6a1 C A 10: 76,553,242 (GRCm39) G391* probably null Het
Ctsc C A 7: 87,951,430 (GRCm39) Q226K probably benign Het
Cyp2c54 A G 19: 40,035,953 (GRCm39) V319A probably damaging Het
Dnah7b T C 1: 46,316,303 (GRCm39) S3139P probably damaging Het
Edrf1 T C 7: 133,256,079 (GRCm39) S643P probably benign Het
Fam186a A T 15: 99,844,273 (GRCm39) V657D unknown Het
Fkbp11 A G 15: 98,626,073 (GRCm39) probably benign Het
Fsip2 G A 2: 82,823,607 (GRCm39) A6447T possibly damaging Het
H2-T9 C A 17: 36,438,496 (GRCm39) probably null Het
Hydin A G 8: 111,276,307 (GRCm39) D3017G probably damaging Het
Ifi205 G A 1: 173,845,210 (GRCm39) Q191* probably null Het
Mbd4 C T 6: 115,821,564 (GRCm39) D484N probably benign Het
Med24 C T 11: 98,605,223 (GRCm39) probably null Het
Mis18bp1 T C 12: 65,208,404 (GRCm39) N103S probably damaging Het
Mmd2 T C 5: 142,550,587 (GRCm39) H217R probably damaging Het
Mn1 C T 5: 111,566,699 (GRCm39) T223M possibly damaging Het
Ms4a4a A G 19: 11,358,794 (GRCm39) Y84C probably damaging Het
Mybl2 C T 2: 162,924,605 (GRCm39) P658S probably benign Het
Mycbp2 C A 14: 103,446,345 (GRCm39) V1828L probably damaging Het
Myh15 T C 16: 49,017,149 (GRCm39) Y1887H probably damaging Het
Nadk2 A G 15: 9,083,271 (GRCm39) probably null Het
Nsd3 A G 8: 26,156,055 (GRCm39) N541D probably damaging Het
Or52e8b A G 7: 104,674,148 (GRCm39) V13A probably benign Het
Or52i2 G T 7: 102,319,046 (GRCm39) probably benign Het
Oxa1l A T 14: 54,598,312 (GRCm39) M1L probably benign Het
Pcdha11 A T 18: 37,144,421 (GRCm39) R171* probably null Het
Pkd1l1 A T 11: 8,821,771 (GRCm39) V1641E Het
Pramel28 A T 4: 143,692,455 (GRCm39) M182K probably benign Het
Prom1 T A 5: 44,178,242 (GRCm39) I497L probably benign Het
Rasgef1b T C 5: 99,706,753 (GRCm39) K41E possibly damaging Het
Rasgrf1 T C 9: 89,876,810 (GRCm39) F725S probably damaging Het
Ryr2 T A 13: 11,612,032 (GRCm39) S3962C probably damaging Het
Sema5b A T 16: 35,480,915 (GRCm39) T829S probably benign Het
Tdp2 A G 13: 25,025,284 (GRCm39) D351G probably benign Het
Tet3 A T 6: 83,347,603 (GRCm39) D1130E probably damaging Het
Tg T C 15: 66,612,563 (GRCm39) C1993R probably damaging Het
Tll1 T C 8: 64,478,222 (GRCm39) I844V probably benign Het
Ttll13 A C 7: 79,903,911 (GRCm39) K280Q probably damaging Het
Vmn2r109 A G 17: 20,760,945 (GRCm39) V804A possibly damaging Het
Vps13c T C 9: 67,797,086 (GRCm39) V491A probably benign Het
Xpo5 G T 17: 46,525,551 (GRCm39) G233C probably damaging Het
Other mutations in Mup5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0167:Mup5 UTSW 4 61,752,019 (GRCm39) critical splice acceptor site probably null
R0485:Mup5 UTSW 4 61,751,229 (GRCm39) splice site probably null
R0547:Mup5 UTSW 4 61,751,237 (GRCm39) missense probably damaging 1.00
R1054:Mup5 UTSW 4 61,750,871 (GRCm39) missense probably benign 0.07
R1597:Mup5 UTSW 4 61,753,317 (GRCm39) missense possibly damaging 0.87
R1721:Mup5 UTSW 4 61,750,607 (GRCm39) nonsense probably null
R1772:Mup5 UTSW 4 61,750,578 (GRCm39) critical splice donor site probably null
R1881:Mup5 UTSW 4 61,752,868 (GRCm39) nonsense probably null
R2104:Mup5 UTSW 4 61,751,962 (GRCm39) missense probably damaging 0.99
R2384:Mup5 UTSW 4 61,753,261 (GRCm39) splice site probably null
R4971:Mup5 UTSW 4 61,751,297 (GRCm39) missense probably benign 0.32
R5246:Mup5 UTSW 4 61,752,874 (GRCm39) missense probably benign 0.04
R5926:Mup5 UTSW 4 61,751,286 (GRCm39) missense probably benign 0.03
R6905:Mup5 UTSW 4 61,751,340 (GRCm39) missense possibly damaging 0.60
R6912:Mup5 UTSW 4 61,752,806 (GRCm39) missense probably benign 0.03
R6957:Mup5 UTSW 4 61,751,273 (GRCm39) missense probably damaging 1.00
R7204:Mup5 UTSW 4 61,751,992 (GRCm39) missense probably damaging 0.96
R7224:Mup5 UTSW 4 61,750,622 (GRCm39) missense probably damaging 1.00
R7570:Mup5 UTSW 4 61,752,911 (GRCm39) nonsense probably null
R8253:Mup5 UTSW 4 61,752,811 (GRCm39) missense probably benign 0.00
R8465:Mup5 UTSW 4 61,752,015 (GRCm39) missense probably benign
R9048:Mup5 UTSW 4 61,750,612 (GRCm39) missense probably benign 0.20
R9571:Mup5 UTSW 4 61,750,787 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- AGAATTGTCATGGGTGTGTCAAAG -3'
(R):5'- GAAACAAGCCTCAGATTCCATTATGG -3'

Sequencing Primer
(F):5'- TGGGTGTGTCAAAGAGAAATTTAAAG -3'
(R):5'- ATGGTCATTTATTCTGACTTTCATCC -3'
Posted On 2019-09-13