Incidental Mutation 'R7589:Vmn1r91'
ID587306
Institutional Source Beutler Lab
Gene Symbol Vmn1r91
Ensembl Gene ENSMUSG00000095201
Gene Namevomeronasal 1 receptor 91
SynonymsGm8442
MMRRC Submission
Accession Numbers
Is this an essential gene? Not available question?
Stock #R7589 (G1)
Quality Score225.009
Status Not validated
Chromosome7
Chromosomal Location20101158-20102081 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 20101877 bp
ZygosityHeterozygous
Amino Acid Change Histidine to Glutamine at position 240 (H240Q)
Ref Sequence ENSEMBL: ENSMUSP00000129283 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165330]
Predicted Effect probably benign
Transcript: ENSMUST00000165330
AA Change: H240Q

PolyPhen 2 Score 0.067 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000129283
Gene: ENSMUSG00000095201
AA Change: H240Q

DomainStartEndE-ValueType
Pfam:TAS2R 8 299 5.1e-18 PFAM
Pfam:V1R 41 298 7.1e-15 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610021A01Rik T G 7: 41,626,972 C700G probably damaging Het
4930486L24Rik T C 13: 60,842,933 K316E probably damaging Het
Akap6 A T 12: 53,142,063 K2087* probably null Het
Alpk2 A T 18: 65,300,073 H1320Q probably damaging Het
Aox1 A T 1: 58,041,484 R31W probably damaging Het
Asnsd1 G T 1: 53,347,967 A167E probably benign Het
Atg14 T C 14: 47,543,090 D409G probably benign Het
Atp13a3 T A 16: 30,344,615 E574D probably benign Het
Bicd1 A T 6: 149,513,667 Y626F possibly damaging Het
Cdc5l C T 17: 45,410,781 R521Q probably benign Het
Dglucy T C 12: 100,841,401 F160L probably damaging Het
Enpp5 G A 17: 44,085,264 G356S probably damaging Het
Fmo9 T A 1: 166,674,428 K209N possibly damaging Het
Gsdmc2 C A 15: 63,825,043 L426F probably damaging Het
Hip1 T C 5: 135,414,311 D956G probably benign Het
Kif28 C T 1: 179,731,400 V248I probably benign Het
Klk10 T C 7: 43,783,627 V149A probably benign Het
Krt40 G T 11: 99,540,157 N255K probably damaging Het
Map4k4 T A 1: 40,021,091 Y1013* probably null Het
Mcur1 T C 13: 43,551,625 Y185C probably damaging Het
Mzt1 T C 14: 99,036,512 probably null Het
Naip5 G T 13: 100,219,697 Q1137K not run Het
Naip5 T C 13: 100,219,696 Q1137R probably benign Het
Nkx1-2 T C 7: 132,599,475 I18V probably damaging Het
Ofcc1 T A 13: 40,255,484 Q155L probably benign Het
Olfr1239 A G 2: 89,418,380 V11A possibly damaging Het
Olfr1282 T C 2: 111,335,374 K235E probably damaging Het
Olfr1377 A T 11: 50,985,030 M110L probably damaging Het
Olfr1411 G A 1: 92,597,059 R180H probably benign Het
Olfr635 T C 7: 103,979,791 Y200H probably damaging Het
Prnp A G 2: 131,936,866 D146G probably benign Het
Rhbdf1 C T 11: 32,212,903 V455I probably benign Het
Rnf6 G A 5: 146,211,429 R260W possibly damaging Het
Rtl1 T C 12: 109,593,845 N520S possibly damaging Het
Setbp1 A T 18: 78,856,492 M1320K probably benign Het
Slc39a8 A G 3: 135,884,362 T338A probably damaging Het
Tcf4 A G 18: 69,682,819 *693W probably null Het
Ttc8 A T 12: 98,976,437 D412V probably damaging Het
Ush2a G T 1: 188,542,849 A1840S probably benign Het
Vmn1r60 A T 7: 5,544,689 S137R Het
Vmn2r107 A T 17: 20,375,372 H729L probably benign Het
Yme1l1 C T 2: 23,160,262 T35I probably benign Het
Zfp292 A G 4: 34,806,777 V2094A probably damaging Het
Zfp934 A T 13: 62,518,316 N202K Het
Other mutations in Vmn1r91
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01875:Vmn1r91 APN 7 20101934 nonsense probably null
IGL02125:Vmn1r91 APN 7 20101504 missense probably damaging 0.96
IGL02263:Vmn1r91 APN 7 20101843 missense probably benign 0.00
IGL02338:Vmn1r91 APN 7 20101746 missense probably damaging 0.96
IGL02708:Vmn1r91 APN 7 20101490 missense probably damaging 1.00
R1880:Vmn1r91 UTSW 7 20101773 missense probably damaging 1.00
R2679:Vmn1r91 UTSW 7 20102058 missense probably damaging 0.97
R4730:Vmn1r91 UTSW 7 20101770 missense possibly damaging 0.71
R5362:Vmn1r91 UTSW 7 20101461 missense probably benign 0.05
R5633:Vmn1r91 UTSW 7 20101945 missense possibly damaging 0.56
R5979:Vmn1r91 UTSW 7 20102065 missense probably benign 0.00
R6151:Vmn1r91 UTSW 7 20101435 missense probably benign
R6177:Vmn1r91 UTSW 7 20101479 missense possibly damaging 0.95
R7397:Vmn1r91 UTSW 7 20101770 missense possibly damaging 0.71
R7872:Vmn1r91 UTSW 7 20101914 missense probably benign 0.26
R7886:Vmn1r91 UTSW 7 20101565 missense probably benign
R7903:Vmn1r91 UTSW 7 20101210 missense possibly damaging 0.88
R7953:Vmn1r91 UTSW 7 20101293 missense possibly damaging 0.68
R8043:Vmn1r91 UTSW 7 20101293 missense possibly damaging 0.68
R8202:Vmn1r91 UTSW 7 20101824 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCAATTAAGGTCACTGGTCCAC -3'
(R):5'- GCACAGAACAAGGATCTTTAGG -3'

Sequencing Primer
(F):5'- AAAGCAACTTGTTCTGTTCCAC -3'
(R):5'- ACTAAAGGGCAGACACTG -3'
Posted On2019-10-24