Incidental Mutation 'R5977:Vmn1r69'
ID 481184
Institutional Source Beutler Lab
Gene Symbol Vmn1r69
Ensembl Gene ENSMUSG00000091662
Gene Name vomeronasal 1 receptor 69
Synonyms V1re9
MMRRC Submission 044159-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R5977 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 10313683-10315414 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 10314417 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Tryptophan at position 26 (R26W)
Ref Sequence ENSEMBL: ENSMUSP00000154473 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000163658] [ENSMUST00000176284] [ENSMUST00000176707] [ENSMUST00000226160] [ENSMUST00000226190] [ENSMUST00000226228] [ENSMUST00000228478] [ENSMUST00000227853] [ENSMUST00000228638] [ENSMUST00000228296]
AlphaFold Q8VIC1
Predicted Effect probably damaging
Transcript: ENSMUST00000163658
AA Change: R105W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129646
Gene: ENSMUSG00000091662
AA Change: R105W

DomainStartEndE-ValueType
Pfam:V1R 50 307 3.3e-32 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000176284
AA Change: R105W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000176707
AA Change: R105W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000226160
AA Change: R105W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000226190
AA Change: R105W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000226228
AA Change: R105W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226990
Predicted Effect probably damaging
Transcript: ENSMUST00000228478
AA Change: R26W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000227853
AA Change: R26W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000228638
AA Change: R26W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000228296
AA Change: R26W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.3%
Validation Efficiency 97% (72/74)
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik A T 10: 100,451,106 (GRCm39) R446S probably damaging Het
2900092C05Rik A T 7: 12,288,664 (GRCm39) H159L probably benign Het
4933405O20Rik G A 7: 50,249,838 (GRCm39) V291I probably damaging Het
A2ml1 A G 6: 128,558,085 (GRCm39) Y24H probably damaging Het
Adgrv1 C T 13: 81,583,678 (GRCm39) probably null Het
Ankrd52 C T 10: 128,218,566 (GRCm39) H351Y probably damaging Het
Anks6 C A 4: 47,035,748 (GRCm39) A588S probably benign Het
Arl15 T G 13: 114,070,645 (GRCm39) V80G probably damaging Het
Atp8a1 A G 5: 67,904,628 (GRCm39) I532T possibly damaging Het
Birc6 T C 17: 74,910,031 (GRCm39) C1475R probably damaging Het
Carmil1 C T 13: 24,253,719 (GRCm39) R394Q probably damaging Het
Cbfa2t2 T C 2: 154,359,697 (GRCm39) I254T probably damaging Het
Cemip2 A G 19: 21,803,447 (GRCm39) T827A probably benign Het
Col6a3 A G 1: 90,749,571 (GRCm39) V421A possibly damaging Het
Cped1 T C 6: 22,254,607 (GRCm39) V1000A probably damaging Het
Cr1l A T 1: 194,797,076 (GRCm39) Y282* probably null Het
Cryl1 G T 14: 57,620,236 (GRCm39) T43K probably benign Het
Csmd2 C T 4: 127,952,827 (GRCm39) P92L probably damaging Het
Ddx60 G A 8: 62,474,444 (GRCm39) probably null Het
Dhrs7b C T 11: 60,743,328 (GRCm39) R187* probably null Het
Dmtf1 T C 5: 9,190,451 (GRCm39) T88A probably damaging Het
Dnah2 T C 11: 69,411,707 (GRCm39) E305G possibly damaging Het
Dscaml1 A C 9: 45,632,596 (GRCm39) N1154T probably benign Het
Efhc1 A G 1: 21,030,442 (GRCm39) Y125C probably damaging Het
Egflam T A 15: 7,347,726 (GRCm39) Y68F possibly damaging Het
Gcm2 A G 13: 41,256,603 (GRCm39) V382A probably damaging Het
Gm18358 A G 7: 84,739,756 (GRCm39) noncoding transcript Het
Gm3443 T G 19: 21,534,960 (GRCm39) I75S probably benign Het
Gpr182 C A 10: 127,586,748 (GRCm39) V68F possibly damaging Het
Herc1 T A 9: 66,340,604 (GRCm39) M1651K possibly damaging Het
Hey1 A T 3: 8,731,418 (GRCm39) probably null Het
Ighv1-43 A C 12: 114,909,829 (GRCm39) V31G probably benign Het
Il17rc T C 6: 113,459,692 (GRCm39) V450A probably damaging Het
Kbtbd4 T G 2: 90,736,487 (GRCm39) V166G probably benign Het
Marveld2 T C 13: 100,748,197 (GRCm39) N294S possibly damaging Het
Mtdh A G 15: 34,099,720 (GRCm39) K61E probably damaging Het
Muc5ac T C 7: 141,350,104 (GRCm39) S616P possibly damaging Het
Myh15 T C 16: 48,973,866 (GRCm39) L1292P probably damaging Het
Nek8 C T 11: 78,058,651 (GRCm39) V550M probably benign Het
Nup155 T A 15: 8,159,721 (GRCm39) probably null Het
Or2y17 G A 11: 49,231,592 (GRCm39) V78M probably damaging Het
Or7c70 A T 10: 78,683,572 (GRCm39) M59K possibly damaging Het
Or8b36 ATTGCTGTTT ATTGCTGTTTGCTGTTT 9: 37,937,836 (GRCm39) probably null Het
Papln G A 12: 83,831,143 (GRCm39) W1099* probably null Het
Pcdhb17 A G 18: 37,618,720 (GRCm39) Y170C probably damaging Het
Pramel12 T C 4: 143,144,229 (GRCm39) Y192H probably benign Het
Prss39 T G 1: 34,541,783 (GRCm39) C287G probably damaging Het
Pyroxd2 A G 19: 42,723,911 (GRCm39) V338A probably damaging Het
Rab19 T A 6: 39,360,860 (GRCm39) F3I probably benign Het
Relt A G 7: 100,512,355 (GRCm39) probably benign Het
Sbf2 T A 7: 109,977,193 (GRCm39) H647L probably benign Het
Scube1 C T 15: 83,513,689 (GRCm39) C327Y probably damaging Het
Sec14l4 A C 11: 3,990,055 (GRCm39) Q118P possibly damaging Het
Shisa9 C G 16: 12,085,292 (GRCm39) D300E probably benign Het
Smg1 A G 7: 117,740,580 (GRCm39) probably benign Het
Sncaip A G 18: 53,002,393 (GRCm39) T305A probably benign Het
Sorcs3 T C 19: 48,784,889 (GRCm39) V1104A probably damaging Het
Ugt1a6b C T 1: 88,143,982 (GRCm39) R201C probably damaging Het
Unc119b A G 5: 115,268,612 (GRCm39) V91A probably benign Het
Uvssa A G 5: 33,547,204 (GRCm39) K257E probably damaging Het
Vmn1r199 A C 13: 22,567,416 (GRCm39) M237L probably benign Het
Vmn2r54 A G 7: 12,366,143 (GRCm39) F264L probably damaging Het
Vmn2r7 C T 3: 64,623,464 (GRCm39) W285* probably null Het
Vmn2r78 T A 7: 86,569,541 (GRCm39) S145T possibly damaging Het
Vmn2r78 T A 7: 86,604,115 (GRCm39) N764K probably benign Het
Wdr5b T G 16: 35,862,374 (GRCm39) H164Q probably damaging Het
Zcchc7 G A 4: 44,894,982 (GRCm39) V236I possibly damaging Het
Zfp729b G A 13: 67,739,740 (GRCm39) R842C probably benign Het
Other mutations in Vmn1r69
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00155:Vmn1r69 APN 7 10,313,879 (GRCm39) missense probably benign 0.00
IGL01972:Vmn1r69 APN 7 10,314,586 (GRCm39) nonsense probably null
IGL02339:Vmn1r69 APN 7 10,314,645 (GRCm39) nonsense probably null
IGL02424:Vmn1r69 APN 7 10,314,585 (GRCm39) missense probably benign 0.00
IGL02602:Vmn1r69 APN 7 10,313,901 (GRCm39) missense probably benign 0.14
IGL03271:Vmn1r69 APN 7 10,314,596 (GRCm39) missense probably benign 0.11
R0034:Vmn1r69 UTSW 7 10,314,738 (GRCm39) intron probably benign
R0052:Vmn1r69 UTSW 7 10,314,327 (GRCm39) missense probably benign 0.00
R0096:Vmn1r69 UTSW 7 10,313,985 (GRCm39) missense probably damaging 1.00
R0539:Vmn1r69 UTSW 7 10,314,874 (GRCm39) splice site probably benign
R0604:Vmn1r69 UTSW 7 10,314,581 (GRCm39) missense probably benign 0.00
R1681:Vmn1r69 UTSW 7 10,314,179 (GRCm39) missense probably benign 0.06
R1884:Vmn1r69 UTSW 7 10,314,678 (GRCm39) missense probably benign 0.00
R3741:Vmn1r69 UTSW 7 10,314,069 (GRCm39) missense possibly damaging 0.47
R4655:Vmn1r69 UTSW 7 10,314,026 (GRCm39) missense probably benign 0.03
R4735:Vmn1r69 UTSW 7 10,314,926 (GRCm39) utr 5 prime probably benign
R4758:Vmn1r69 UTSW 7 10,314,473 (GRCm39) missense probably benign 0.00
R5582:Vmn1r69 UTSW 7 10,314,435 (GRCm39) missense probably damaging 1.00
R5966:Vmn1r69 UTSW 7 10,314,717 (GRCm39) missense probably benign 0.00
R6458:Vmn1r69 UTSW 7 10,314,365 (GRCm39) missense probably benign
R6987:Vmn1r69 UTSW 7 10,314,491 (GRCm39) start codon destroyed probably null 0.99
R7133:Vmn1r69 UTSW 7 10,314,995 (GRCm39) intron probably benign
R7532:Vmn1r69 UTSW 7 10,314,281 (GRCm39) missense probably damaging 0.98
R7878:Vmn1r69 UTSW 7 10,314,717 (GRCm39) missense probably benign 0.00
R9100:Vmn1r69 UTSW 7 10,314,064 (GRCm39) missense probably damaging 0.98
R9558:Vmn1r69 UTSW 7 10,314,185 (GRCm39) missense probably benign
Z1176:Vmn1r69 UTSW 7 10,314,023 (GRCm39) missense possibly damaging 0.64
Predicted Primers PCR Primer
(F):5'- CATTTTGCCCTACAATGTAGCAG -3'
(R):5'- TGGATTTCCGGAATCTGGC -3'

Sequencing Primer
(F):5'- GCAGTATTTAAAATCACGGTCTCTTG -3'
(R):5'- CACAAACTACAATTGGAATTCTGGG -3'
Posted On 2017-06-26