Incidental Mutation 'R2848:Vmn1r181'
ID251840
Institutional Source Beutler Lab
Gene Symbol Vmn1r181
Ensembl Gene ENSMUSG00000097425
Gene Namevomeronasal 1 receptor 181
SynonymsV1rd20
MMRRC Submission 040441-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.060) question?
Stock #R2848 (G1)
Quality Score225
Status Not validated
Chromosome7
Chromosomal Location23974615-23988139 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 23984518 bp
ZygosityHeterozygous
Amino Acid Change Serine to Isoleucine at position 136 (S136I)
Ref Sequence ENSEMBL: ENSMUSP00000154403 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000181796] [ENSMUST00000226843] [ENSMUST00000226978] [ENSMUST00000227637] [ENSMUST00000228399] [ENSMUST00000228842]
Predicted Effect possibly damaging
Transcript: ENSMUST00000077386
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000076604
Gene: ENSMUSG00000057946
AA Change: S136I

DomainStartEndE-ValueType
Pfam:TAS2R 8 295 3.6e-12 PFAM
Pfam:7tm_1 30 282 4.6e-7 PFAM
Pfam:V1R 41 295 4.2e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000181796
AA Change: S136I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000137685
Gene: ENSMUSG00000097425
AA Change: S136I

DomainStartEndE-ValueType
Pfam:TAS2R 8 296 3.9e-9 PFAM
Pfam:V1R 41 295 2.7e-13 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000226843
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000226978
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000227637
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000228399
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228531
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228607
Predicted Effect possibly damaging
Transcript: ENSMUST00000228842
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930451I11Rik A T 7: 126,830,722 F101Y possibly damaging Het
A230050P20Rik A T 9: 20,873,572 H225L probably damaging Het
Abca17 G C 17: 24,289,507 T1018R probably damaging Het
Adamts14 T A 10: 61,218,435 Q606L probably damaging Het
Adgrf5 C A 17: 43,422,640 N118K possibly damaging Het
Baz2b A T 2: 59,924,666 Y1073N possibly damaging Het
Celf2 T C 2: 6,604,125 R282G probably damaging Het
Cntnap5c A T 17: 57,876,392 D31V probably damaging Het
Cobl A G 11: 12,378,342 L81P probably damaging Het
Cpsf1 A T 15: 76,602,851 L209Q probably damaging Het
Crocc G A 4: 141,018,756 A1684V probably damaging Het
Cyp4f37 T A 17: 32,629,125 C206S probably damaging Het
Diexf A T 1: 193,128,451 N81K probably benign Het
Dnah3 A G 7: 119,967,938 V2355A probably benign Het
Dnah6 T C 6: 73,129,331 K1756E probably benign Het
Fis1 T C 5: 136,963,117 I55T possibly damaging Het
Gm2381 G A 7: 42,820,407 P98S probably damaging Het
Gpr37 C T 6: 25,666,946 probably benign Het
Grin2a A G 16: 9,761,965 F145L possibly damaging Het
Htr4 T C 18: 62,428,126 S153P probably damaging Het
Igkv9-120 T A 6: 68,050,144 probably benign Het
Il12rb1 G A 8: 70,815,802 W396* probably null Het
Itga8 A T 2: 12,160,404 V798D probably damaging Het
Lfng T A 5: 140,611,867 D149E probably damaging Het
Magi2 A AG 5: 20,602,461 probably null Het
Mgam C A 6: 40,652,715 A86E possibly damaging Het
Myh4 A G 11: 67,248,633 N592S probably benign Het
Naa16 A G 14: 79,335,883 C816R probably damaging Het
Nek8 A G 11: 78,168,141 S513P probably damaging Het
Ociad1 A G 5: 73,294,351 probably null Het
Olfr1288 T C 2: 111,479,354 M190T probably benign Het
Olfr350 A G 2: 36,850,799 Y251C probably damaging Het
Olfr721-ps1 C T 14: 14,407,398 P57S probably damaging Het
Osbpl8 T A 10: 111,269,436 S251T probably benign Het
Pcdh7 G A 5: 57,720,276 G391E probably damaging Het
Pcdhga10 T A 18: 37,748,200 V338E possibly damaging Het
Pde4b C T 4: 102,601,545 A466V probably damaging Het
Peg10 C T 6: 4,756,912 probably benign Het
Poteg A T 8: 27,481,676 N406I probably benign Het
Ppargc1a A G 5: 51,473,809 F493L probably benign Het
Ptpra C A 2: 130,544,999 H603Q probably benign Het
Rnf10 T C 5: 115,249,112 D439G probably benign Het
Syt3 G A 7: 44,393,442 V383I probably benign Het
Tectb C G 19: 55,180,999 probably benign Het
Try5 C T 6: 41,313,476 V25I probably benign Het
Ttn G T 2: 76,919,207 Q3833K probably benign Het
Usp53 G A 3: 122,934,491 P814L probably benign Het
Vmn2r114 A T 17: 23,290,974 M844K probably benign Het
Vwa8 G T 14: 78,947,142 R360L probably benign Het
Xlr4b A T X: 73,215,332 Q25L probably null Het
Zfp532 T A 18: 65,656,626 H1045Q possibly damaging Het
Zfp985 G A 4: 147,583,011 W112* probably null Het
Other mutations in Vmn1r181
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01443:Vmn1r181 APN 7 23984581 missense possibly damaging 0.91
IGL02055:Vmn1r181 APN 7 23984553 missense probably damaging 1.00
IGL02444:Vmn1r181 APN 7 23984523 missense probably damaging 1.00
IGL03012:Vmn1r181 APN 7 23984602 missense probably damaging 0.98
IGL03026:Vmn1r181 APN 7 23984575 missense possibly damaging 0.94
R0255:Vmn1r181 UTSW 7 23984334 missense probably benign 0.02
R1481:Vmn1r181 UTSW 7 23984712 missense probably damaging 1.00
R2847:Vmn1r181 UTSW 7 23984518 missense possibly damaging 0.88
R2849:Vmn1r181 UTSW 7 23984518 missense possibly damaging 0.88
R3441:Vmn1r181 UTSW 7 23984883 missense probably benign 0.05
R3757:Vmn1r181 UTSW 7 23984484 missense possibly damaging 0.90
R3945:Vmn1r181 UTSW 7 23984152 missense probably damaging 0.98
R3983:Vmn1r181 UTSW 7 23984809 missense probably benign 0.23
R4780:Vmn1r181 UTSW 7 23984583 missense possibly damaging 0.64
R4999:Vmn1r181 UTSW 7 23984365 missense probably damaging 0.99
R5463:Vmn1r181 UTSW 7 23984362 missense probably benign 0.02
R5672:Vmn1r181 UTSW 7 23984316 missense probably damaging 1.00
R6229:Vmn1r181 UTSW 7 23984155 missense probably damaging 1.00
R6315:Vmn1r181 UTSW 7 23984758 missense probably benign 0.23
R6316:Vmn1r181 UTSW 7 23984758 missense probably benign 0.23
R6317:Vmn1r181 UTSW 7 23984758 missense probably benign 0.23
R6324:Vmn1r181 UTSW 7 23984758 missense probably benign 0.23
R6326:Vmn1r181 UTSW 7 23984758 missense probably benign 0.23
R6988:Vmn1r181 UTSW 7 23984847 missense probably damaging 1.00
R7446:Vmn1r181 UTSW 7 23984931 missense probably benign 0.01
X0067:Vmn1r181 UTSW 7 23984901 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- ACATAGCTGTGGCCAATGC -3'
(R):5'- GTGGCATCATGGGCAAATCG -3'

Sequencing Primer
(F):5'- CATGGCTTTTGCTCCAAGAAG -3'
(R):5'- GTCTGTTATCTGTGGACCAG -3'
Posted On2014-12-04