Incidental Mutation 'R1471:Vmn2r44'
ID 164888
Institutional Source Beutler Lab
Gene Symbol Vmn2r44
Ensembl Gene ENSMUSG00000094098
Gene Name vomeronasal 2, receptor 44
Synonyms EG434113
MMRRC Submission 039524-MU
Accession Numbers
Essential gene? Not available question?
Stock # R1471 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 8370459-8386237 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 8380882 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 337 (V337E)
Ref Sequence ENSEMBL: ENSMUSP00000132467 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166499]
AlphaFold L7N2E1
Predicted Effect probably damaging
Transcript: ENSMUST00000166499
AA Change: V337E

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000132467
Gene: ENSMUSG00000094098
AA Change: V337E

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 469 2.5e-34 PFAM
Pfam:NCD3G 512 565 3.8e-20 PFAM
Pfam:7tm_3 598 833 5.7e-55 PFAM
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 96.8%
  • 20x: 94.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 96 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930486L24Rik C A 13: 61,001,336 (GRCm39) K130N probably damaging Het
Adam6a T A 12: 113,508,013 (GRCm39) S129T probably damaging Het
Adamts10 T A 17: 33,772,112 (GRCm39) F1087I probably damaging Het
Afp T A 5: 90,651,541 (GRCm39) N385K possibly damaging Het
Ahnak T G 19: 8,990,296 (GRCm39) probably benign Het
Akap6 A G 12: 53,188,279 (GRCm39) T1898A probably benign Het
Antxr2 C A 5: 98,123,199 (GRCm39) V283F possibly damaging Het
Asgr1 T C 11: 69,946,919 (GRCm39) V55A possibly damaging Het
Asxl3 A G 18: 22,649,411 (GRCm39) K467E probably damaging Het
Atp5f1a C A 18: 77,868,969 (GRCm39) Q398K probably damaging Het
Atxn2 T A 5: 121,924,437 (GRCm39) D455E probably damaging Het
B4galt6 C T 18: 20,878,410 (GRCm39) A39T possibly damaging Het
C130073F10Rik C T 4: 101,747,535 (GRCm39) E165K probably benign Het
Cabin1 A G 10: 75,530,626 (GRCm39) C1519R probably damaging Het
Casp8ap2 C T 4: 32,639,386 (GRCm39) R147* probably null Het
Ccdc88b A G 19: 6,831,391 (GRCm39) L517P probably benign Het
Cd109 G A 9: 78,561,869 (GRCm39) V220I probably damaging Het
Cd2ap T C 17: 43,131,488 (GRCm39) K369R probably benign Het
Cd300c A G 11: 114,850,614 (GRCm39) V63A probably benign Het
Cnot10 A G 9: 114,420,619 (GRCm39) V741A probably benign Het
Col18a1 G T 10: 76,932,040 (GRCm39) Q350K unknown Het
Crnkl1 T C 2: 145,774,236 (GRCm39) K76E possibly damaging Het
Cryzl2 A G 1: 157,298,291 (GRCm39) K227E probably benign Het
Cts6 G A 13: 61,344,194 (GRCm39) T286I probably benign Het
Cul1 T C 6: 47,491,820 (GRCm39) V392A probably damaging Het
Dcaf7 T A 11: 105,937,573 (GRCm39) F65L probably benign Het
Dgke A C 11: 88,946,320 (GRCm39) V160G possibly damaging Het
Dock8 C A 19: 25,178,400 (GRCm39) Q2098K possibly damaging Het
Efhb T A 17: 53,706,140 (GRCm39) D799V possibly damaging Het
Ephb2 T C 4: 136,386,262 (GRCm39) D829G probably benign Het
Exosc1 A T 19: 41,913,157 (GRCm39) S117R probably damaging Het
Fga T C 3: 82,935,925 (GRCm39) S51P probably benign Het
Fmn1 T C 2: 113,523,439 (GRCm39) F1141L possibly damaging Het
Foxm1 C T 6: 128,350,837 (GRCm39) L713F probably damaging Het
Galnt4 A G 10: 98,944,536 (GRCm39) E87G probably benign Het
Gamt T C 10: 80,096,692 (GRCm39) D15G probably benign Het
Gm15557 C A 2: 155,784,174 (GRCm39) D154E possibly damaging Het
Gnptab A G 10: 88,281,625 (GRCm39) I1211V probably benign Het
Greb1 A T 12: 16,761,775 (GRCm39) M535K probably damaging Het
Grm8 C A 6: 27,363,308 (GRCm39) A736S possibly damaging Het
Hspa14 T C 2: 3,492,645 (GRCm39) I373M probably benign Het
Ifi207 T A 1: 173,557,629 (GRCm39) T370S unknown Het
Igf1r A G 7: 67,653,585 (GRCm39) N41S probably damaging Het
Ikzf5 A T 7: 130,993,496 (GRCm39) V224D probably damaging Het
Il10 C A 1: 130,949,110 (GRCm39) Y90* probably null Het
Itga4 A G 2: 79,117,376 (GRCm39) D394G probably benign Het
Kif21a A T 15: 90,840,622 (GRCm39) S1165T probably benign Het
Krtap14 A G 16: 88,622,515 (GRCm39) S155P probably damaging Het
Loxl2 A G 14: 69,930,546 (GRCm39) N770S probably benign Het
Man2b1 A G 8: 85,813,474 (GRCm39) D222G probably damaging Het
Mcub T A 3: 129,709,464 (GRCm39) Y283F probably damaging Het
Meis3 T A 7: 15,911,496 (GRCm39) Y64* probably null Het
Mfsd6 T A 1: 52,748,716 (GRCm39) I50F probably benign Het
Micu2 T C 14: 58,182,854 (GRCm39) T165A probably damaging Het
Mtcl1 T C 17: 66,686,143 (GRCm39) E921G probably damaging Het
Muc5b A T 7: 141,396,971 (GRCm39) N215Y unknown Het
Muc6 A G 7: 141,234,176 (GRCm39) F772L possibly damaging Het
Myt1 A G 2: 181,438,904 (GRCm39) D142G probably benign Het
Nol6 C T 4: 41,120,281 (GRCm39) V479I probably benign Het
Nsun7 A G 5: 66,441,572 (GRCm39) K414E probably benign Het
Nup210l A C 3: 90,077,869 (GRCm39) I914L probably benign Het
Obox3 G A 7: 15,360,875 (GRCm39) P88L probably benign Het
Or10ag57 A G 2: 87,218,862 (GRCm39) Y271C probably damaging Het
Or4f4b T C 2: 111,314,351 (GRCm39) L192P probably damaging Het
Or8h8 C T 2: 86,752,922 (GRCm39) probably null Het
Or8w1 T C 2: 87,466,014 (GRCm39) T26A probably benign Het
Pclo T C 5: 14,730,441 (GRCm39) probably benign Het
Pcsk5 T C 19: 17,545,688 (GRCm39) N745D probably damaging Het
Pdzrn3 T A 6: 101,128,473 (GRCm39) N731I possibly damaging Het
Pkdrej T A 15: 85,701,334 (GRCm39) Q1534L probably benign Het
Pramel28 T C 4: 143,691,523 (GRCm39) N400S probably benign Het
Rell1 T A 5: 64,093,428 (GRCm39) D109V probably damaging Het
Rplp0 C T 5: 115,701,403 (GRCm39) T285I probably damaging Het
Sanbr A T 11: 23,565,222 (GRCm39) M255K probably damaging Het
Sema3g C T 14: 30,950,002 (GRCm39) R728C probably damaging Het
Slc15a2 A G 16: 36,574,153 (GRCm39) Y536H probably damaging Het
Slc26a5 T A 5: 22,021,962 (GRCm39) Y488F probably benign Het
Slc5a4a A T 10: 76,022,362 (GRCm39) S566C probably damaging Het
Spink7 C T 18: 62,729,275 (GRCm39) E21K possibly damaging Het
Src C T 2: 157,299,107 (GRCm39) Q35* probably null Het
Srrm2 T A 17: 24,039,770 (GRCm39) V2234E probably damaging Het
Stk36 A T 1: 74,650,314 (GRCm39) Q282L probably benign Het
Tas2r118 T G 6: 23,969,170 (GRCm39) E297A probably damaging Het
Terf1 A G 1: 15,913,194 (GRCm39) Y385C probably damaging Het
Tmc3 T C 7: 83,247,498 (GRCm39) S198P probably damaging Het
Tmprss11b C T 5: 86,808,355 (GRCm39) R407H possibly damaging Het
Tspyl4 G A 10: 34,174,107 (GRCm39) E200K probably damaging Het
Ttc21a T C 9: 119,771,707 (GRCm39) Y169H probably damaging Het
Ugt2b36 C T 5: 87,239,930 (GRCm39) D152N probably damaging Het
Unk T C 11: 115,940,235 (GRCm39) I196T probably benign Het
Uroc1 T G 6: 90,321,153 (GRCm39) V243G probably damaging Het
Usp34 C A 11: 23,438,862 (GRCm39) Q3475K probably benign Het
Vmn2r117 T A 17: 23,697,447 (GRCm39) I82L probably benign Het
Zbtb14 C A 17: 69,695,497 (GRCm39) F398L probably damaging Het
Zfp362 T C 4: 128,680,993 (GRCm39) T111A probably benign Het
Zfp598 T C 17: 24,899,046 (GRCm39) V615A probably benign Het
Other mutations in Vmn2r44
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01650:Vmn2r44 APN 7 8,383,103 (GRCm39) critical splice donor site probably null
IGL01723:Vmn2r44 APN 7 8,380,915 (GRCm39) missense probably damaging 0.97
IGL01767:Vmn2r44 APN 7 8,383,237 (GRCm39) missense probably benign 0.00
IGL02161:Vmn2r44 APN 7 8,380,814 (GRCm39) missense possibly damaging 0.94
IGL02299:Vmn2r44 APN 7 8,380,815 (GRCm39) missense probably benign
IGL02418:Vmn2r44 APN 7 8,380,864 (GRCm39) missense probably damaging 1.00
IGL02829:Vmn2r44 APN 7 8,380,879 (GRCm39) missense possibly damaging 0.94
IGL02851:Vmn2r44 APN 7 8,386,050 (GRCm39) missense probably damaging 1.00
IGL03080:Vmn2r44 APN 7 8,386,244 (GRCm39) utr 5 prime probably benign
R1789:Vmn2r44 UTSW 7 8,383,122 (GRCm39) missense possibly damaging 0.64
R1932:Vmn2r44 UTSW 7 8,370,981 (GRCm39) missense probably benign 0.04
R2354:Vmn2r44 UTSW 7 8,373,639 (GRCm39) missense probably damaging 0.99
R4009:Vmn2r44 UTSW 7 8,380,987 (GRCm39) missense possibly damaging 0.82
R4130:Vmn2r44 UTSW 7 8,370,918 (GRCm39) missense probably damaging 1.00
R4790:Vmn2r44 UTSW 7 8,370,949 (GRCm39) missense probably damaging 1.00
R4854:Vmn2r44 UTSW 7 8,383,300 (GRCm39) missense possibly damaging 0.94
R4887:Vmn2r44 UTSW 7 8,380,985 (GRCm39) missense probably benign 0.19
R4888:Vmn2r44 UTSW 7 8,380,985 (GRCm39) missense probably benign 0.19
R5484:Vmn2r44 UTSW 7 8,383,123 (GRCm39) missense possibly damaging 0.69
R6110:Vmn2r44 UTSW 7 8,381,005 (GRCm39) missense probably damaging 1.00
R6357:Vmn2r44 UTSW 7 8,373,657 (GRCm39) missense probably benign 0.01
R6526:Vmn2r44 UTSW 7 8,381,098 (GRCm39) missense probably benign 0.01
R7083:Vmn2r44 UTSW 7 8,381,369 (GRCm39) missense probably benign 0.44
R7087:Vmn2r44 UTSW 7 8,381,366 (GRCm39) missense probably benign 0.02
R7115:Vmn2r44 UTSW 7 8,370,527 (GRCm39) nonsense probably null
R7125:Vmn2r44 UTSW 7 8,370,941 (GRCm39) missense probably damaging 1.00
R7258:Vmn2r44 UTSW 7 8,380,848 (GRCm39) missense probably damaging 1.00
R7359:Vmn2r44 UTSW 7 8,370,538 (GRCm39) missense probably benign 0.30
R7494:Vmn2r44 UTSW 7 8,386,122 (GRCm39) nonsense probably null
R7766:Vmn2r44 UTSW 7 8,371,219 (GRCm39) missense probably damaging 1.00
R7777:Vmn2r44 UTSW 7 8,381,314 (GRCm39) missense possibly damaging 0.81
R8184:Vmn2r44 UTSW 7 8,371,227 (GRCm39) nonsense probably null
R8674:Vmn2r44 UTSW 7 8,380,822 (GRCm39) missense probably damaging 1.00
R8752:Vmn2r44 UTSW 7 8,370,805 (GRCm39) missense probably damaging 1.00
R8897:Vmn2r44 UTSW 7 8,381,242 (GRCm39) missense probably damaging 1.00
R8915:Vmn2r44 UTSW 7 8,370,650 (GRCm39) missense probably damaging 1.00
R8928:Vmn2r44 UTSW 7 8,381,101 (GRCm39) missense probably damaging 1.00
R9163:Vmn2r44 UTSW 7 8,371,091 (GRCm39) missense probably benign 0.00
Z1177:Vmn2r44 UTSW 7 8,370,976 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- GTGAGAACTGGCTCCTTTCCCATTG -3'
(R):5'- GAACTGGATTGGCCTTGTCATCCC -3'

Sequencing Primer
(F):5'- GCTGCAAATTCATCTCATGGAGTG -3'
(R):5'- TGTCATCCCAGATGATGATCAAGG -3'
Posted On 2014-03-28