Incidental Mutation 'R7531:Vmn1r10'
ID583312
Institutional Source Beutler Lab
Gene Symbol Vmn1r10
Ensembl Gene ENSMUSG00000115181
Gene Namevomeronasal 1 receptor 10
SynonymsV1rc1
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.154) question?
Stock #R7531 (G1)
Quality Score225.009
Status Validated
Chromosome6
Chromosomal Location57109454-57115035 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 57113939 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Asparagine at position 172 (I172N)
Ref Sequence ENSEMBL: ENSMUSP00000134901 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000176073] [ENSMUST00000228270]
Predicted Effect possibly damaging
Transcript: ENSMUST00000176073
AA Change: I172N

PolyPhen 2 Score 0.900 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000134901
Gene: ENSMUSG00000115181
AA Change: I172N

DomainStartEndE-ValueType
Pfam:V1R 28 293 4.1e-55 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000228270
AA Change: I172N

PolyPhen 2 Score 0.900 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency 100% (54/54)
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530053A07Rik T C 7: 28,140,231 F490L probably benign Het
Abca12 T A 1: 71,247,173 T2501S probably damaging Het
Abcg3 A G 5: 104,977,641 Y59H probably benign Het
Acsf2 G T 11: 94,573,231 probably null Het
Adam25 T A 8: 40,753,877 I60K probably damaging Het
Agrn A T 4: 156,169,804 V1729E probably damaging Het
Aldh9a1 G A 1: 167,350,326 V31I probably benign Het
Aqp5 T C 15: 99,591,299 F10L possibly damaging Het
Arfgap2 T A 2: 91,273,744 probably null Het
Asb7 T C 7: 66,679,136 H52R probably damaging Het
Aspa G A 11: 73,313,525 Q206* probably null Het
Bpgm A G 6: 34,504,288 I207V possibly damaging Het
Brinp2 A G 1: 158,266,572 S187P possibly damaging Het
Clec4e A G 6: 123,285,574 F128S probably benign Het
Crisp3 A G 17: 40,234,738 F82L probably benign Het
Cry2 A G 2: 92,413,005 L497P probably damaging Het
Dcxr A G 11: 120,727,006 V48A probably benign Het
Ddx11 A T 17: 66,138,219 T379S probably benign Het
Depdc1a A C 3: 159,522,639 T343P probably damaging Het
Dhx36 T C 3: 62,484,968 I546V probably damaging Het
Fam114a2 A G 11: 57,513,716 V74A probably benign Het
Flg2 A T 3: 93,200,870 R68S probably damaging Het
Glb1l3 T C 9: 26,853,654 I154V possibly damaging Het
Gm45844 T C 7: 7,240,186 T22A probably benign Het
Gramd2 A T 9: 59,709,910 I83F probably damaging Het
Hcn4 A G 9: 58,860,137 T994A unknown Het
Hectd1 C T 12: 51,806,367 V124I probably benign Het
Hmcn1 A T 1: 150,686,780 D2342E probably benign Het
Hyal6 A T 6: 24,740,787 H313L possibly damaging Het
Ifnab T A 4: 88,691,286 probably benign Het
Keap1 A G 9: 21,237,327 I128T probably benign Het
Kit T C 5: 75,607,040 S28P probably damaging Het
Krtap5-3 T A 7: 142,202,205 C260S unknown Het
Lepr T A 4: 101,752,175 W320R probably damaging Het
Lmod3 A T 6: 97,248,442 N139K probably benign Het
March1 C G 8: 66,386,337 S10R probably benign Het
Naa35 A T 13: 59,617,941 K380* probably null Het
Npy1r C A 8: 66,704,894 F285L probably damaging Het
Nr1h3 C T 2: 91,184,394 R427H probably damaging Het
Olfr507 T A 7: 108,622,062 N83K probably benign Het
Pate2 A G 9: 35,670,712 probably null Het
Pcmt1 A G 10: 7,680,605 probably null Het
Prg4 T G 1: 150,455,035 E629A unknown Het
Rin2 T G 2: 145,858,499 S199A probably benign Het
Ror1 T A 4: 100,441,191 L587Q probably damaging Het
Rsl1 T A 13: 67,176,502 C31S possibly damaging Het
Scn4a A G 11: 106,348,697 probably null Het
Sema3a T C 5: 13,565,838 Y410H probably damaging Het
Smpd5 T C 15: 76,296,339 V447A probably benign Het
Tax1bp1 A T 6: 52,746,697 D524V probably benign Het
Tesc A T 5: 118,059,458 Y179F probably damaging Het
Tm9sf2 T C 14: 122,142,412 S292P possibly damaging Het
Unc45b A G 11: 82,929,012 D543G probably damaging Het
Usp4 T A 9: 108,372,680 V469E probably damaging Het
Zfyve16 A G 13: 92,522,965 L146S probably damaging Het
Other mutations in Vmn1r10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01062:Vmn1r10 APN 6 57113836 missense possibly damaging 0.70
IGL03255:Vmn1r10 APN 6 57113926 missense probably benign 0.05
IGL03393:Vmn1r10 APN 6 57114057 nonsense probably null
R0310:Vmn1r10 UTSW 6 57113501 missense probably damaging 0.97
R2271:Vmn1r10 UTSW 6 57114103 missense probably damaging 1.00
R2411:Vmn1r10 UTSW 6 57114139 missense probably benign 0.14
R3700:Vmn1r10 UTSW 6 57114302 missense probably benign 0.05
R3731:Vmn1r10 UTSW 6 57113734 missense probably damaging 0.99
R4805:Vmn1r10 UTSW 6 57113617 missense possibly damaging 0.94
R4922:Vmn1r10 UTSW 6 57113826 missense probably damaging 0.99
R5697:Vmn1r10 UTSW 6 57113489 missense probably damaging 1.00
R5936:Vmn1r10 UTSW 6 57114317 missense probably benign 0.01
R6119:Vmn1r10 UTSW 6 57114233 missense probably benign 0.01
R7107:Vmn1r10 UTSW 6 57113630 missense possibly damaging 0.90
R7635:Vmn1r10 UTSW 6 57114041 missense probably benign 0.00
R7860:Vmn1r10 UTSW 6 57113701 missense probably benign 0.19
R7943:Vmn1r10 UTSW 6 57113701 missense probably benign 0.19
Predicted Primers PCR Primer
(F):5'- AGGCTGTCACTATCAGTCCC -3'
(R):5'- TGAAGTCCACCCAGTACATGAC -3'

Sequencing Primer
(F):5'- GGCTGTCACTATCAGTCCCAATAC -3'
(R):5'- AGCAGCACGATGGTCTGG -3'
Posted On2019-10-17