Incidental Mutation 'R4130:Vmn2r44'
ID 315504
Institutional Source Beutler Lab
Gene Symbol Vmn2r44
Ensembl Gene ENSMUSG00000094098
Gene Name vomeronasal 2, receptor 44
Synonyms EG434113
MMRRC Submission 041636-MU
Accession Numbers
Essential gene? Not available question?
Stock # R4130 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 8370459-8386237 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 8370918 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Histidine at position 709 (Q709H)
Ref Sequence ENSEMBL: ENSMUSP00000132467 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166499]
AlphaFold L7N2E1
Predicted Effect probably damaging
Transcript: ENSMUST00000166499
AA Change: Q709H

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000132467
Gene: ENSMUSG00000094098
AA Change: Q709H

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: 99.4%
  • 3x: 98.7%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency 100% (29/29)
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700021A07Rik T C 10: 21,301,441 (GRCm39) noncoding transcript Het
A4gnt A G 9: 99,502,671 (GRCm39) D277G possibly damaging Het
Adam12 C T 7: 133,514,653 (GRCm39) V345I probably damaging Het
Ankrd29 G A 18: 12,387,757 (GRCm39) A275V possibly damaging Het
Arpp21 T A 9: 111,984,376 (GRCm39) probably benign Het
Bbx T C 16: 50,045,221 (GRCm39) K447E probably damaging Het
Bcar1 A G 8: 112,440,797 (GRCm39) L399P possibly damaging Het
Cytl1 T C 5: 37,892,985 (GRCm39) S32P probably damaging Het
Eif4e1b C T 13: 54,935,130 (GRCm39) T219M probably benign Het
F10 A G 8: 13,105,584 (GRCm39) D383G possibly damaging Het
Gm37267 T G 1: 180,336,643 (GRCm39) noncoding transcript Het
Golga2 G A 2: 32,178,178 (GRCm39) R29H probably benign Het
Gpd1 A T 15: 99,617,158 (GRCm39) probably null Het
Lrrk2 G A 15: 91,639,997 (GRCm39) R1514Q probably benign Het
Map1b T C 13: 99,568,188 (GRCm39) E1511G unknown Het
Nup35 G A 2: 80,486,443 (GRCm39) probably benign Het
Or13n4 C T 7: 106,422,792 (GRCm39) G314S probably benign Het
Pdzd9 A T 7: 120,262,092 (GRCm39) D123E possibly damaging Het
Pramel29 T A 4: 143,935,379 (GRCm39) I121F probably damaging Het
Rab3gap2 A G 1: 184,936,494 (GRCm39) D19G possibly damaging Het
Rnf213 T C 11: 119,373,832 (GRCm39) S4972P probably damaging Het
Skap1 A G 11: 96,416,871 (GRCm39) Y52C probably damaging Het
Sphkap T C 1: 83,255,619 (GRCm39) N710S probably damaging Het
Tedc1 T A 12: 113,126,828 (GRCm39) D363E probably benign Het
Wdr5 G T 2: 27,410,441 (GRCm39) 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
R1471:Vmn2r44 UTSW 7 8,380,882 (GRCm39) missense probably damaging 0.99
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
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'- GCTTCATTGAATGCGTCAGG -3'
(R):5'- ATCCTAACAGAGCCACCTGTG -3'

Sequencing Primer
(F):5'- TCAGGCAGATTCTTGGCCAAG -3'
(R):5'- TAACAGAGCCACCTGTGTCTTAC -3'
Posted On 2015-05-14