Incidental Mutation 'R5849:Mup3'
ID 453757
Institutional Source Beutler Lab
Gene Symbol Mup3
Ensembl Gene ENSMUSG00000066154
Gene Name major urinary protein 3
Synonyms Mup-3
MMRRC Submission 044066-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R5849 (G1)
Quality Score 225
Status Validated
Chromosome 4
Chromosomal Location 62001713-62005554 bp(-) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) T to G at 62005172 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000103112 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084531] [ENSMUST00000107472] [ENSMUST00000107488]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000084531
SMART Domains Protein: ENSMUSP00000081579
Gene: ENSMUSG00000066154

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:Lipocalin 38 177 2.2e-37 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000107472
SMART Domains Protein: ENSMUSP00000103096
Gene: ENSMUSG00000066154

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:Lipocalin 38 177 2.2e-37 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000107488
SMART Domains Protein: ENSMUSP00000103112
Gene: ENSMUSG00000066154

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:Lipocalin 38 177 2.2e-37 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134190
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.3%
Validation Efficiency 96% (72/75)
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930553M12Rik T C 4: 88,786,596 (GRCm39) I7M unknown Het
Abca8b C A 11: 109,868,639 (GRCm39) G175V probably damaging Het
Agbl1 T C 7: 75,974,846 (GRCm39) S113P probably benign Het
Ak9 A G 10: 41,224,045 (GRCm39) D486G probably benign Het
Aopep A G 13: 63,163,312 (GRCm39) D111G probably benign Het
Arhgap11a T C 2: 113,665,192 (GRCm39) S469G probably null Het
Comtd1 C T 14: 21,898,188 (GRCm39) G48D probably damaging Het
Cyp27a1 T C 1: 74,775,843 (GRCm39) S343P probably damaging Het
Dcun1d1 T A 3: 35,970,333 (GRCm39) probably benign Het
Dennd4c T C 4: 86,744,223 (GRCm39) I1404T possibly damaging Het
Dlgap5 A G 14: 47,626,892 (GRCm39) S766P possibly damaging Het
Ebf1 T A 11: 44,881,331 (GRCm39) probably null Het
Flcn T A 11: 59,695,586 (GRCm39) I4L probably damaging Het
Gm57858 A T 3: 36,087,026 (GRCm39) D189E possibly damaging Het
Grin2c T C 11: 115,151,817 (GRCm39) T48A probably benign Het
Hyal5 T A 6: 24,891,555 (GRCm39) S456R probably benign Het
Igf1r A G 7: 67,839,781 (GRCm39) D696G probably benign Het
Iqgap1 A T 7: 80,452,906 (GRCm39) V13D probably benign Het
Itgal A G 7: 126,916,492 (GRCm39) N728S probably benign Het
Kcnb1 T A 2: 166,947,946 (GRCm39) I301F probably damaging Het
Kcnd3 A G 3: 105,366,111 (GRCm39) probably benign Het
Kdm4a C T 4: 118,019,037 (GRCm39) R393Q probably benign Het
Lcn9 G A 2: 25,713,268 (GRCm39) probably null Het
Madcam1 T A 10: 79,500,824 (GRCm39) M47K probably benign Het
Matn3 A G 12: 9,008,829 (GRCm39) Q314R probably benign Het
Msh3 A T 13: 92,386,386 (GRCm39) D826E possibly damaging Het
Muc4 A T 16: 32,595,213 (GRCm39) T3088S possibly damaging Het
Myo15b A G 11: 115,772,759 (GRCm39) K1807E probably damaging Het
Myrip A G 9: 120,282,759 (GRCm39) D688G probably damaging Het
Nup153 A G 13: 46,840,452 (GRCm39) F1052S probably damaging Het
Oplah T A 15: 76,181,547 (GRCm39) probably benign Het
Or4f14d A T 2: 111,960,223 (GRCm39) I311K probably benign Het
Or52r1c T A 7: 102,734,728 (GRCm39) M1K probably null Het
Or6z3 A T 7: 6,463,993 (GRCm39) I162F possibly damaging Het
Or9g19 A T 2: 85,600,768 (GRCm39) I208F probably benign Het
Pacsin2 A G 15: 83,274,719 (GRCm39) F120L possibly damaging Het
Ppp1r36 C A 12: 76,485,931 (GRCm39) P363Q probably damaging Het
Rai1 C A 11: 60,081,347 (GRCm39) H1804N possibly damaging Het
Rictor G A 15: 6,823,487 (GRCm39) E1555K probably benign Het
Rnf214 G A 9: 45,779,386 (GRCm39) P455S probably damaging Het
Rnf220 T C 4: 117,134,809 (GRCm39) T188A possibly damaging Het
S1pr4 C T 10: 81,335,157 (GRCm39) V106M possibly damaging Het
Sall2 C A 14: 52,551,704 (GRCm39) S495I probably benign Het
Sars2 A G 7: 28,443,683 (GRCm39) E95G possibly damaging Het
Sema3f G A 9: 107,559,815 (GRCm39) T693M probably damaging Het
Slfn2 C A 11: 82,960,402 (GRCm39) T127K probably benign Het
Snrpe T A 1: 133,536,652 (GRCm39) I43L probably benign Het
Srsf1 T C 11: 87,938,684 (GRCm39) I7T possibly damaging Het
Ssbp1 T A 6: 40,453,837 (GRCm39) probably benign Het
Stbd1 T G 5: 92,752,854 (GRCm39) F115V probably benign Het
Stk11ip T A 1: 75,503,999 (GRCm39) probably null Het
Taf1b T A 12: 24,550,524 (GRCm39) N36K probably damaging Het
Tanc1 A T 2: 59,630,248 (GRCm39) M743L probably benign Het
Tnfsf12 C A 11: 69,577,793 (GRCm39) R208L probably damaging Het
Trafd1 T C 5: 121,511,534 (GRCm39) D428G probably damaging Het
Trim24 A G 6: 37,934,664 (GRCm39) E793G probably damaging Het
Tspan32 T C 7: 142,569,324 (GRCm39) C100R probably damaging Het
Ttn T C 2: 76,576,586 (GRCm39) D16442G probably damaging Het
Ube3c T A 5: 29,863,407 (GRCm39) L894Q probably damaging Het
Wfs1 C G 5: 37,130,608 (GRCm39) G213R probably damaging Het
Zfp384 G A 6: 125,001,062 (GRCm39) A45T possibly damaging Het
Zfp865 G T 7: 5,034,086 (GRCm39) K690N probably damaging Het
Other mutations in Mup3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01383:Mup3 APN 4 62,004,196 (GRCm39) missense probably damaging 0.98
IGL02233:Mup3 APN 4 62,003,016 (GRCm39) missense probably damaging 1.00
IGL03088:Mup3 APN 4 62,005,079 (GRCm39) missense probably damaging 0.99
R0432:Mup3 UTSW 4 62,003,519 (GRCm39) missense probably benign 0.13
R0619:Mup3 UTSW 4 62,004,198 (GRCm39) missense probably benign 0.02
R0884:Mup3 UTSW 4 62,005,411 (GRCm39) missense possibly damaging 0.68
R5568:Mup3 UTSW 4 62,002,809 (GRCm39) missense possibly damaging 0.93
R5909:Mup3 UTSW 4 62,004,244 (GRCm39) missense probably benign 0.01
R7851:Mup3 UTSW 4 62,003,494 (GRCm39) missense possibly damaging 0.65
R7919:Mup3 UTSW 4 62,002,829 (GRCm39) missense probably damaging 0.98
R8975:Mup3 UTSW 4 62,003,472 (GRCm39) missense probably benign 0.01
R9029:Mup3 UTSW 4 62,003,540 (GRCm39) missense probably damaging 1.00
Z1088:Mup3 UTSW 4 62,005,426 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TATCTCTCTGCAACCCCAAGTG -3'
(R):5'- ATAGTAATTCAGAATGGGCTTTGGG -3'

Sequencing Primer
(F):5'- GGCATGAGACCATACCAGGTTTTC -3'
(R):5'- CTTTGGGGCAGAGACAGTATAC -3'
Posted On 2017-02-10