Incidental Mutation 'R4841:Vmn1r173'
ID 371825
Institutional Source Beutler Lab
Gene Symbol Vmn1r173
Ensembl Gene ENSMUSG00000115021
Gene Name vomeronasal 1 receptor 173
Synonyms Gm5892
MMRRC Submission 042454-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.670) question?
Stock # R4841 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 23401767-23402708 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 23402361 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 199 (I199F)
Ref Sequence ENSEMBL: ENSMUSP00000153884 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000174055] [ENSMUST00000226233] [ENSMUST00000227987]
AlphaFold E9Q8V7
Predicted Effect probably damaging
Transcript: ENSMUST00000174055
AA Change: I199F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000134645
Gene: ENSMUSG00000115021
AA Change: I199F

DomainStartEndE-ValueType
transmembrane domain 13 35 N/A INTRINSIC
Pfam:V1R 43 301 5.3e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000226233
AA Change: I199F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000227987
AA Change: I199F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 92.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 89 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600012H06Rik A T 17: 15,164,001 (GRCm39) I43L possibly damaging Het
4933427I04Rik T A 4: 123,754,170 (GRCm39) M28K probably benign Het
A2m A T 6: 121,623,803 (GRCm39) I390F probably benign Het
Abcc8 T C 7: 45,800,252 (GRCm39) K510R probably damaging Het
Adamts6 A G 13: 104,449,295 (GRCm39) D39G probably benign Het
Adgrl3 T C 5: 81,942,118 (GRCm39) S1326P possibly damaging Het
Adgrv1 A G 13: 81,651,120 (GRCm39) probably null Het
Ap3b2 G A 7: 81,127,678 (GRCm39) A166V probably damaging Het
Bbox1 T A 2: 110,134,084 (GRCm39) probably null Het
Bckdk A G 7: 127,504,633 (GRCm39) probably null Het
Cand1 C A 10: 119,049,451 (GRCm39) probably null Het
Capn5 T C 7: 97,780,879 (GRCm39) probably null Het
Ccdc121rt2 A T 5: 112,598,106 (GRCm39) K218* probably null Het
Cd209c G T 8: 3,995,905 (GRCm39) R2S probably benign Het
Ces1g C T 8: 94,060,323 (GRCm39) E99K probably benign Het
Cnmd A G 14: 79,887,762 (GRCm39) I153T possibly damaging Het
Cntrob C G 11: 69,206,220 (GRCm39) L315F possibly damaging Het
Cspg4b G A 13: 113,502,724 (GRCm39) G143D probably benign Het
Ctdp1 A G 18: 80,451,941 (GRCm39) S145P unknown Het
Dmrt2 G A 19: 25,655,031 (GRCm39) G210D probably damaging Het
Dnajc16 A G 4: 141,501,936 (GRCm39) F298S probably damaging Het
Dock5 T C 14: 68,055,012 (GRCm39) D618G probably damaging Het
Drc3 G A 11: 60,261,361 (GRCm39) A171T probably benign Het
Dspp A T 5: 104,325,052 (GRCm39) S472C unknown Het
Dspp G T 5: 104,325,053 (GRCm39) S472I unknown Het
Ecel1 A T 1: 87,081,023 (GRCm39) N322K probably damaging Het
Eftud2 A G 11: 102,745,640 (GRCm39) F362L probably damaging Het
Egfr C T 11: 16,861,607 (GRCm39) H1129Y probably benign Het
Erich3 T A 3: 154,410,480 (GRCm39) F112I possibly damaging Het
Fam107b T C 2: 3,779,580 (GRCm39) L261S probably damaging Het
Fancd2 T C 6: 113,539,391 (GRCm39) S239P probably damaging Het
Fbp2 C A 13: 63,002,727 (GRCm39) Q108H probably benign Het
Fcgbpl1 T A 7: 27,850,147 (GRCm39) C1198S probably damaging Het
Gask1b G A 3: 79,843,912 (GRCm39) R377H probably damaging Het
Gipr C T 7: 18,896,601 (GRCm39) R165H probably damaging Het
Gje1 C T 10: 14,593,082 (GRCm39) G45R probably null Het
Gpat2 C G 2: 127,275,887 (GRCm39) T555S probably benign Het
Grik3 C A 4: 125,584,969 (GRCm39) N612K probably damaging Het
Iqcb1 A G 16: 36,655,952 (GRCm39) E113G probably benign Het
Kat8 A G 7: 127,524,366 (GRCm39) I415V probably benign Het
Kcnk10 A T 12: 98,401,175 (GRCm39) M486K probably benign Het
Kif21b C A 1: 136,072,958 (GRCm39) H119N probably damaging Het
Leng9 T C 7: 4,152,385 (GRCm39) D97G probably damaging Het
Lrguk T C 6: 34,069,802 (GRCm39) V559A probably damaging Het
Lrp1 G T 10: 127,419,805 (GRCm39) R935S probably damaging Het
Lrrcc1 C A 3: 14,627,571 (GRCm39) D503E probably benign Het
Mybph A T 1: 134,126,233 (GRCm39) E349V probably damaging Het
Myzap A G 9: 71,456,037 (GRCm39) S328P probably damaging Het
Nbeal1 T C 1: 60,292,534 (GRCm39) L1062P probably damaging Het
Nepro G A 16: 44,555,160 (GRCm39) S412N probably null Het
Nudt5 T C 2: 5,869,239 (GRCm39) V155A probably benign Het
Or13a25 A T 7: 140,247,502 (GRCm39) I94F probably damaging Het
Or4k51 C G 2: 111,584,679 (GRCm39) F28L probably benign Het
Or5ae2 G T 7: 84,506,328 (GRCm39) L250F probably damaging Het
Or6ae1 A G 7: 139,742,602 (GRCm39) L87P possibly damaging Het
Osbpl3 T A 6: 50,286,356 (GRCm39) N623I probably damaging Het
Pde4dip T A 3: 97,700,844 (GRCm39) H220L probably damaging Het
Pde9a T A 17: 31,662,135 (GRCm39) probably null Het
Pex16 T G 2: 92,209,544 (GRCm39) probably null Het
Pnpla7 A G 2: 24,870,064 (GRCm39) T15A probably benign Het
Polq G T 16: 36,869,145 (GRCm39) probably null Het
Ppfia2 C T 10: 106,690,818 (GRCm39) T553I probably benign Het
Rreb1 G A 13: 38,100,502 (GRCm39) C211Y probably benign Het
Rundc3b A G 5: 8,578,742 (GRCm39) L222P probably damaging Het
Ryr3 T C 2: 112,478,718 (GRCm39) N4405S probably damaging Het
Sardh A G 2: 27,081,967 (GRCm39) V853A probably benign Het
Scfd1 T C 12: 51,436,109 (GRCm39) V86A probably damaging Het
Scube3 G A 17: 28,383,097 (GRCm39) C425Y probably damaging Het
Sfta2 T C 17: 35,960,773 (GRCm39) probably benign Het
Sh3d19 T C 3: 86,031,049 (GRCm39) Y738H probably damaging Het
Shc2 T C 10: 79,458,295 (GRCm39) R463G probably damaging Het
Slc4a10 T C 2: 62,087,939 (GRCm39) V414A possibly damaging Het
Slc9a3 G T 13: 74,313,956 (GRCm39) D755Y probably damaging Het
Snrpb2 C A 2: 142,910,237 (GRCm39) F98L possibly damaging Het
Socs7 T A 11: 97,267,829 (GRCm39) I320N possibly damaging Het
Speer2 A T 16: 69,654,988 (GRCm39) M159K probably benign Het
Sppl2c A C 11: 104,078,478 (GRCm39) H426P probably benign Het
Stxbp5 C A 10: 9,638,635 (GRCm39) V1055L probably benign Het
Synpo A T 18: 60,736,684 (GRCm39) S421T probably damaging Het
Taf6l A G 19: 8,759,770 (GRCm39) V135A possibly damaging Het
Tafa5 C T 15: 87,509,637 (GRCm39) probably benign Het
Trim58 G A 11: 58,542,150 (GRCm39) G370E probably damaging Het
Tshz2 T A 2: 169,728,167 (GRCm39) I452N probably damaging Het
Ttc41 C T 10: 86,566,989 (GRCm39) R552C probably benign Het
Vit T C 17: 78,909,308 (GRCm39) S252P probably benign Het
Vmn2r114 T A 17: 23,529,336 (GRCm39) R255S probably benign Het
Vmn2r17 A G 5: 109,582,246 (GRCm39) N545S probably damaging Het
Zbtb44 T G 9: 30,964,701 (GRCm39) V37G probably damaging Het
Zfp865 A G 7: 5,034,640 (GRCm39) Y875C probably damaging Het
Other mutations in Vmn1r173
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01490:Vmn1r173 APN 7 23,402,132 (GRCm39) missense probably benign 0.01
IGL01637:Vmn1r173 APN 7 23,402,373 (GRCm39) missense probably damaging 0.96
IGL01878:Vmn1r173 APN 7 23,401,877 (GRCm39) missense probably damaging 1.00
IGL02036:Vmn1r173 APN 7 23,402,321 (GRCm39) missense probably benign 0.04
IGL02039:Vmn1r173 APN 7 23,402,321 (GRCm39) missense probably benign 0.04
IGL02171:Vmn1r173 APN 7 23,402,321 (GRCm39) missense probably benign 0.04
IGL02209:Vmn1r173 APN 7 23,402,586 (GRCm39) missense probably benign 0.25
PIT4515001:Vmn1r173 UTSW 7 23,401,911 (GRCm39) nonsense probably null
R0157:Vmn1r173 UTSW 7 23,401,822 (GRCm39) missense probably damaging 0.99
R0226:Vmn1r173 UTSW 7 23,402,508 (GRCm39) missense possibly damaging 0.65
R0482:Vmn1r173 UTSW 7 23,402,216 (GRCm39) missense probably damaging 0.99
R0792:Vmn1r173 UTSW 7 23,402,160 (GRCm39) missense probably benign 0.01
R1242:Vmn1r173 UTSW 7 23,402,650 (GRCm39) missense probably damaging 1.00
R1390:Vmn1r173 UTSW 7 23,402,323 (GRCm39) missense possibly damaging 0.82
R1641:Vmn1r173 UTSW 7 23,402,533 (GRCm39) missense probably benign 0.06
R1867:Vmn1r173 UTSW 7 23,402,660 (GRCm39) missense unknown
R2325:Vmn1r173 UTSW 7 23,402,537 (GRCm39) nonsense probably null
R3863:Vmn1r173 UTSW 7 23,401,977 (GRCm39) missense probably damaging 1.00
R4407:Vmn1r173 UTSW 7 23,402,441 (GRCm39) missense probably damaging 1.00
R4717:Vmn1r173 UTSW 7 23,402,637 (GRCm39) missense probably damaging 1.00
R4842:Vmn1r173 UTSW 7 23,402,361 (GRCm39) missense probably damaging 1.00
R5966:Vmn1r173 UTSW 7 23,402,112 (GRCm39) missense probably benign 0.00
R6022:Vmn1r173 UTSW 7 23,402,260 (GRCm39) missense probably benign 0.07
R6114:Vmn1r173 UTSW 7 23,402,254 (GRCm39) missense possibly damaging 0.53
R6657:Vmn1r173 UTSW 7 23,402,320 (GRCm39) missense probably damaging 0.98
R7165:Vmn1r173 UTSW 7 23,402,076 (GRCm39) missense probably benign 0.00
R7195:Vmn1r173 UTSW 7 23,401,884 (GRCm39) missense probably damaging 0.99
R7201:Vmn1r173 UTSW 7 23,401,583 (GRCm39) start gained probably benign
R7533:Vmn1r173 UTSW 7 23,402,071 (GRCm39) missense probably benign 0.05
R7951:Vmn1r173 UTSW 7 23,402,680 (GRCm39) missense unknown
R8351:Vmn1r173 UTSW 7 23,401,957 (GRCm39) nonsense probably null
R8374:Vmn1r173 UTSW 7 23,401,920 (GRCm39) missense probably damaging 0.98
R8427:Vmn1r173 UTSW 7 23,401,959 (GRCm39) missense probably damaging 0.99
R8451:Vmn1r173 UTSW 7 23,401,957 (GRCm39) nonsense probably null
R8923:Vmn1r173 UTSW 7 23,401,768 (GRCm39) start codon destroyed probably null 1.00
R9126:Vmn1r173 UTSW 7 23,402,008 (GRCm39) missense probably benign 0.23
R9506:Vmn1r173 UTSW 7 23,401,963 (GRCm39) missense probably damaging 0.99
R9557:Vmn1r173 UTSW 7 23,402,209 (GRCm39) missense probably damaging 1.00
X0022:Vmn1r173 UTSW 7 23,402,012 (GRCm39) missense probably benign 0.06
Predicted Primers PCR Primer
(F):5'- GGAAATACCTCCACATTTGTGC -3'
(R):5'- GGGAAACTTGCAGCCAAAATTTC -3'

Sequencing Primer
(F):5'- AATACCTCCACATTTGTGCACTATTC -3'
(R):5'- GCAGCCAAAATTTCATTGACATGC -3'
Posted On 2016-03-01