Incidental Mutation 'R0109:Vmn1r194'
ID 64219
Institutional Source Beutler Lab
Gene Symbol Vmn1r194
Ensembl Gene ENSMUSG00000069297
Gene Name vomeronasal 1 receptor 194
Synonyms Gm11294
MMRRC Submission 038395-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R0109 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 22428385-22429275 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 22429217 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 278 (Y278C)
Ref Sequence ENSEMBL: ENSMUSP00000089331 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091737]
AlphaFold J3JS27
Predicted Effect probably damaging
Transcript: ENSMUST00000091737
AA Change: Y278C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000089331
Gene: ENSMUSG00000069297
AA Change: Y278C

DomainStartEndE-ValueType
Pfam:V1R 35 296 3.4e-37 PFAM
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 A T 7: 119,917,985 (GRCm39) K1496* probably null Het
Anapc1 C A 2: 128,476,613 (GRCm39) R1335L probably damaging Het
Arhgef10l A T 4: 140,305,605 (GRCm39) S203T probably benign Het
Astn1 C T 1: 158,491,674 (GRCm39) T41I possibly damaging Het
Avil A G 10: 126,849,513 (GRCm39) N603S probably benign Het
Brca1 T C 11: 101,421,916 (GRCm39) D149G possibly damaging Het
Col19a1 A C 1: 24,598,849 (GRCm39) probably null Het
Cps1 T C 1: 67,268,577 (GRCm39) V1435A possibly damaging Het
Cyp2j6 A T 4: 96,406,394 (GRCm39) I459N probably damaging Het
Cyth1 T C 11: 118,073,132 (GRCm39) E242G probably damaging Het
Dclk3 T G 9: 111,296,738 (GRCm39) L94R possibly damaging Het
Dsg3 T C 18: 20,673,191 (GRCm39) V954A probably damaging Het
Dync2h1 T A 9: 7,111,487 (GRCm39) D309V probably damaging Het
Efhd2 A G 4: 141,601,878 (GRCm39) F101L probably benign Het
Fgd5 T A 6: 91,965,216 (GRCm39) M325K possibly damaging Het
Fras1 T C 5: 96,857,936 (GRCm39) S2077P probably benign Het
Frmpd1 A T 4: 45,279,340 (GRCm39) E688D probably benign Het
Hspg2 T C 4: 137,289,512 (GRCm39) V3824A probably benign Het
Kctd16 A G 18: 40,392,204 (GRCm39) E264G probably benign Het
Mapk15 A T 15: 75,867,926 (GRCm39) K153* probably null Het
Miox G A 15: 89,219,784 (GRCm39) V91I probably benign Het
Nfyb G A 10: 82,590,836 (GRCm39) A65V possibly damaging Het
Or4a69 A G 2: 89,313,147 (GRCm39) F111L probably benign Het
Or52d1 T C 7: 103,755,812 (GRCm39) S109P probably damaging Het
Or5b94 C A 19: 12,652,224 (GRCm39) F218L probably benign Het
Parp9 T C 16: 35,768,711 (GRCm39) I64T probably damaging Het
Pfkfb4 T C 9: 108,827,957 (GRCm39) V43A probably benign Het
Pgap1 A T 1: 54,533,984 (GRCm39) V643E probably damaging Het
Pip5k1b T A 19: 24,356,411 (GRCm39) M176L probably benign Het
Ppfia4 A T 1: 134,251,955 (GRCm39) probably null Het
Prdx2 G A 8: 85,696,880 (GRCm39) G4S probably benign Het
Rin3 A G 12: 102,279,340 (GRCm39) I50V possibly damaging Het
Rtl1 G A 12: 109,561,841 (GRCm39) probably benign Het
Sgsm3 G C 15: 80,893,667 (GRCm39) D434H probably damaging Het
Shank2 T C 7: 143,964,314 (GRCm39) S634P possibly damaging Het
Sik2 A G 9: 50,810,775 (GRCm39) M447T possibly damaging Het
Sla2 A G 2: 156,725,507 (GRCm39) probably null Het
Spata16 T A 3: 26,967,416 (GRCm39) F389I probably damaging Het
Srebf1 G A 11: 60,092,630 (GRCm39) A793V probably benign Het
Tmed11 T A 5: 108,925,278 (GRCm39) D178V probably damaging Het
Traf7 A G 17: 24,732,900 (GRCm39) F110L probably benign Het
Ttn T A 2: 76,555,908 (GRCm39) I30366F probably damaging Het
Ubqlnl C T 7: 103,799,399 (GRCm39) V33M probably damaging Het
Vmn2r100 C A 17: 19,742,382 (GRCm39) P252Q possibly damaging Het
Vmn2r114 A T 17: 23,529,549 (GRCm39) Y184* probably null Het
Vmn2r53 C T 7: 12,315,993 (GRCm39) A609T probably damaging Het
Vps13b A G 15: 35,572,265 (GRCm39) T961A probably benign Het
Xirp2 T A 2: 67,349,622 (GRCm39) N3272K probably damaging Het
Zfp217 C T 2: 169,957,382 (GRCm39) A539T probably benign Het
Zfp454 T A 11: 50,774,602 (GRCm39) T24S possibly damaging Het
Other mutations in Vmn1r194
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01890:Vmn1r194 APN 13 22,428,776 (GRCm39) missense probably benign 0.01
IGL02140:Vmn1r194 APN 13 22,428,706 (GRCm39) missense probably benign 0.08
R0066:Vmn1r194 UTSW 13 22,428,641 (GRCm39) missense probably benign 0.33
R0066:Vmn1r194 UTSW 13 22,428,641 (GRCm39) missense probably benign 0.33
R0109:Vmn1r194 UTSW 13 22,429,217 (GRCm39) missense probably damaging 1.00
R1276:Vmn1r194 UTSW 13 22,429,031 (GRCm39) missense probably damaging 1.00
R1426:Vmn1r194 UTSW 13 22,429,236 (GRCm39) missense probably damaging 0.99
R1620:Vmn1r194 UTSW 13 22,429,133 (GRCm39) missense probably damaging 1.00
R4593:Vmn1r194 UTSW 13 22,428,461 (GRCm39) missense possibly damaging 0.60
R4844:Vmn1r194 UTSW 13 22,429,223 (GRCm39) missense probably benign 0.02
R5011:Vmn1r194 UTSW 13 22,429,058 (GRCm39) missense probably benign 0.00
R5110:Vmn1r194 UTSW 13 22,429,170 (GRCm39) missense probably benign 0.07
R5588:Vmn1r194 UTSW 13 22,428,512 (GRCm39) missense possibly damaging 0.75
R5810:Vmn1r194 UTSW 13 22,428,597 (GRCm39) nonsense probably null
R6648:Vmn1r194 UTSW 13 22,428,694 (GRCm39) missense probably benign 0.11
R7660:Vmn1r194 UTSW 13 22,428,767 (GRCm39) missense not run
R7663:Vmn1r194 UTSW 13 22,428,911 (GRCm39) missense not run
R7879:Vmn1r194 UTSW 13 22,428,772 (GRCm39) missense probably benign 0.06
R8344:Vmn1r194 UTSW 13 22,429,247 (GRCm39) missense probably benign 0.01
R8830:Vmn1r194 UTSW 13 22,429,006 (GRCm39) missense possibly damaging 0.88
R9245:Vmn1r194 UTSW 13 22,428,731 (GRCm39) missense probably benign 0.44
R9291:Vmn1r194 UTSW 13 22,428,875 (GRCm39) missense probably benign 0.20
R9624:Vmn1r194 UTSW 13 22,428,671 (GRCm39) missense probably damaging 1.00
Z1176:Vmn1r194 UTSW 13 22,428,596 (GRCm39) missense probably benign 0.08
Predicted Primers PCR Primer
(F):5'- GTTGCCATCCAAGCACACAGTTAAG -3'
(R):5'- AGCTATATGCCCTCCACACAGTCTC -3'

Sequencing Primer
(F):5'- CTGGAGCAGTGGATACATCTC -3'
(R):5'- TCCACACAGTCTCCAAAATATTAAGG -3'
Posted On 2013-08-06