Incidental Mutation 'R5615:Vmn2r61'
ID 458002
Institutional Source Beutler Lab
Gene Symbol Vmn2r61
Ensembl Gene ENSMUSG00000090967
Gene Name vomeronasal 2, receptor 61
Synonyms Gprc2a-rs2, Casr-rs2, EG637873
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # R5615 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 41909477-41950179 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 41949917 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 779 (E779G)
Ref Sequence ENSEMBL: ENSMUSP00000129576 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166131]
AlphaFold L7N2B8
Predicted Effect probably damaging
Transcript: ENSMUST00000166131
AA Change: E779G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129576
Gene: ENSMUSG00000090967
AA Change: E779G

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 77 471 4e-42 PFAM
Pfam:NCD3G 514 567 1.9e-21 PFAM
Pfam:7tm_3 600 835 6.2e-52 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000173044
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.5%
  • 10x: 97.6%
  • 20x: 92.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 A T 1: 71,346,218 (GRCm39) L884H probably damaging Het
Ahr A G 12: 35,553,884 (GRCm39) V745A probably benign Het
Ankrd17 A T 5: 90,431,295 (GRCm39) S830T possibly damaging Het
Aox1 A G 1: 58,136,125 (GRCm39) T1123A probably benign Het
Arhgef11 T C 3: 87,629,792 (GRCm39) probably null Het
Bcas3 T A 11: 85,361,587 (GRCm39) C250S probably damaging Het
Bckdk T C 7: 127,506,489 (GRCm39) I272T probably damaging Het
Cacna1e T C 1: 154,287,916 (GRCm39) K1897E probably damaging Het
Cd180 A T 13: 102,842,711 (GRCm39) I586F probably benign Het
Cep290 A G 10: 100,367,012 (GRCm39) D1121G probably damaging Het
Clasrp A G 7: 19,320,372 (GRCm39) probably benign Het
Col27a1 G T 4: 63,199,351 (GRCm39) K912N probably damaging Het
Dock4 G T 12: 40,699,479 (GRCm39) R231L probably benign Het
Ell G A 8: 71,043,382 (GRCm39) S505N probably benign Het
Ephb6 A G 6: 41,596,225 (GRCm39) T833A probably benign Het
Hemk1 T A 9: 107,208,023 (GRCm39) probably null Het
Hjurp GT GTT 1: 88,194,246 (GRCm39) probably null Het
Hspa12a T C 19: 58,793,082 (GRCm39) I368V possibly damaging Het
Igkv3-3 A T 6: 70,664,214 (GRCm39) T19S probably benign Het
Itpr1 G A 6: 108,465,561 (GRCm39) A2158T possibly damaging Het
Lancl2 T C 6: 57,699,496 (GRCm39) Y104H probably damaging Het
Leng8 G T 7: 4,147,957 (GRCm39) E634* probably null Het
Lrrk1 A T 7: 65,937,363 (GRCm39) C930S probably damaging Het
Lvrn C T 18: 46,983,395 (GRCm39) S46L possibly damaging Het
Mcidas G A 13: 113,133,959 (GRCm39) V148I probably benign Het
Mprip A T 11: 59,649,313 (GRCm39) T1006S probably benign Het
Mrgprb3 T A 7: 48,293,234 (GRCm39) M106L probably benign Het
Mroh2a GCCC GC 1: 88,159,979 (GRCm39) probably null Het
Mtor G A 4: 148,622,733 (GRCm39) V1938I possibly damaging Het
Muc2 A G 7: 141,277,446 (GRCm39) D46G probably damaging Het
Nfkb2 G T 19: 46,296,006 (GRCm39) E170D probably benign Het
Or10ag52 T A 2: 87,044,083 (GRCm39) F282L probably benign Het
Or6c215 A T 10: 129,637,636 (GRCm39) C253S probably damaging Het
Osbp2 C T 11: 3,813,356 (GRCm39) G171D probably benign Het
Otud6b A T 4: 14,818,187 (GRCm39) M238K possibly damaging Het
Pcdhac2 G A 18: 37,279,476 (GRCm39) G819R probably benign Het
Pcdhac2 G T 18: 37,279,477 (GRCm39) G819V probably benign Het
Pcdhga12 T G 18: 37,901,132 (GRCm39) S655A probably damaging Het
Pkd1l3 A G 8: 110,356,842 (GRCm39) I756V probably benign Het
Plekhd1 T A 12: 80,767,364 (GRCm39) S251T probably damaging Het
Ppp2r1a A T 17: 21,179,249 (GRCm39) T96S probably benign Het
Qser1 A C 2: 104,620,039 (GRCm39) S258A possibly damaging Het
Rsph4a G A 10: 33,785,324 (GRCm39) A412T probably benign Het
Sanbr A T 11: 23,556,759 (GRCm39) L407H probably damaging Het
Sass6 T A 3: 116,401,135 (GRCm39) C159S probably benign Het
Scaf4 T C 16: 90,048,848 (GRCm39) Q322R unknown Het
Sema6d C T 2: 124,498,821 (GRCm39) H244Y probably damaging Het
Sigirr T G 7: 140,672,632 (GRCm39) L163F probably damaging Het
Spata31d1c C A 13: 65,183,078 (GRCm39) L207I possibly damaging Het
Tacstd2 A G 6: 67,512,033 (GRCm39) F220L probably damaging Het
Tdpoz4 A T 3: 93,704,806 (GRCm39) T368S probably benign Het
Tnxb C A 17: 34,902,392 (GRCm39) Q1082K probably damaging Het
Trim41 GCCTAGGCGCCCA G 11: 48,698,192 (GRCm39) probably benign Het
Trpm6 C T 19: 18,807,297 (GRCm39) R1014C probably damaging Het
Ugt1a10 TTCATCA TTCA 1: 88,143,880 (GRCm39) probably benign Het
Vmn2r114 ATTT ATT 17: 23,509,906 (GRCm39) probably null Het
Zfp599 T C 9: 22,165,165 (GRCm39) D70G probably benign Het
Zmym1 A T 4: 126,943,191 (GRCm39) I301N probably damaging Het
Other mutations in Vmn2r61
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Vmn2r61 APN 7 41,950,175 (GRCm39) missense possibly damaging 0.96
IGL00824:Vmn2r61 APN 7 41,916,438 (GRCm39) missense probably benign 0.03
IGL00903:Vmn2r61 APN 7 41,949,935 (GRCm39) missense probably damaging 1.00
IGL01125:Vmn2r61 APN 7 41,909,550 (GRCm39) missense probably damaging 1.00
IGL01393:Vmn2r61 APN 7 41,916,258 (GRCm39) missense probably benign 0.08
IGL01712:Vmn2r61 APN 7 41,909,661 (GRCm39) missense probably damaging 0.98
IGL01822:Vmn2r61 APN 7 41,950,130 (GRCm39) missense probably benign 0.18
IGL01835:Vmn2r61 APN 7 41,950,015 (GRCm39) missense probably benign 0.12
IGL01844:Vmn2r61 APN 7 41,909,639 (GRCm39) missense probably benign 0.00
IGL01953:Vmn2r61 APN 7 41,949,613 (GRCm39) missense probably damaging 1.00
IGL02032:Vmn2r61 APN 7 41,949,466 (GRCm39) missense probably damaging 0.99
IGL02054:Vmn2r61 APN 7 41,926,158 (GRCm39) critical splice donor site probably null
IGL02569:Vmn2r61 APN 7 41,926,070 (GRCm39) missense probably damaging 1.00
IGL02697:Vmn2r61 APN 7 41,924,892 (GRCm39) missense possibly damaging 0.55
IGL02958:Vmn2r61 APN 7 41,949,361 (GRCm39) missense probably benign
IGL03290:Vmn2r61 APN 7 41,915,408 (GRCm39) missense probably benign 0.00
IGL03337:Vmn2r61 APN 7 41,916,509 (GRCm39) missense possibly damaging 0.58
IGL03369:Vmn2r61 APN 7 41,909,517 (GRCm39) missense probably benign
IGL03402:Vmn2r61 APN 7 41,909,679 (GRCm39) missense probably benign
R0026:Vmn2r61 UTSW 7 41,924,898 (GRCm39) missense possibly damaging 0.64
R0319:Vmn2r61 UTSW 7 41,949,941 (GRCm39) missense probably damaging 0.99
R0433:Vmn2r61 UTSW 7 41,915,335 (GRCm39) missense probably benign 0.02
R0555:Vmn2r61 UTSW 7 41,915,442 (GRCm39) missense probably benign 0.02
R0691:Vmn2r61 UTSW 7 41,949,844 (GRCm39) missense probably damaging 1.00
R1701:Vmn2r61 UTSW 7 41,949,935 (GRCm39) missense probably damaging 1.00
R1718:Vmn2r61 UTSW 7 41,950,121 (GRCm39) missense probably benign
R1835:Vmn2r61 UTSW 7 41,916,076 (GRCm39) nonsense probably null
R1920:Vmn2r61 UTSW 7 41,949,710 (GRCm39) missense possibly damaging 0.73
R2069:Vmn2r61 UTSW 7 41,949,425 (GRCm39) missense probably benign 0.06
R2326:Vmn2r61 UTSW 7 41,916,287 (GRCm39) missense probably damaging 1.00
R2402:Vmn2r61 UTSW 7 41,949,529 (GRCm39) missense possibly damaging 0.90
R3103:Vmn2r61 UTSW 7 41,916,067 (GRCm39) missense possibly damaging 0.73
R3107:Vmn2r61 UTSW 7 41,916,491 (GRCm39) missense possibly damaging 0.82
R4426:Vmn2r61 UTSW 7 41,950,159 (GRCm39) missense probably benign
R4426:Vmn2r61 UTSW 7 41,950,157 (GRCm39) missense probably benign
R4484:Vmn2r61 UTSW 7 41,950,120 (GRCm39) missense probably benign
R4748:Vmn2r61 UTSW 7 41,916,565 (GRCm39) missense probably damaging 0.96
R4835:Vmn2r61 UTSW 7 41,916,459 (GRCm39) missense possibly damaging 0.52
R4863:Vmn2r61 UTSW 7 41,950,132 (GRCm39) missense probably benign 0.03
R4923:Vmn2r61 UTSW 7 41,916,520 (GRCm39) missense probably damaging 1.00
R4968:Vmn2r61 UTSW 7 41,949,478 (GRCm39) missense probably benign 0.14
R5114:Vmn2r61 UTSW 7 41,949,953 (GRCm39) missense possibly damaging 0.92
R5297:Vmn2r61 UTSW 7 41,909,646 (GRCm39) missense probably benign
R5497:Vmn2r61 UTSW 7 41,924,906 (GRCm39) missense possibly damaging 0.95
R5508:Vmn2r61 UTSW 7 41,916,242 (GRCm39) missense possibly damaging 0.52
R5587:Vmn2r61 UTSW 7 41,949,911 (GRCm39) missense probably damaging 1.00
R5615:Vmn2r61 UTSW 7 41,916,677 (GRCm39) missense probably benign 0.00
R5782:Vmn2r61 UTSW 7 41,949,253 (GRCm39) missense probably damaging 1.00
R6136:Vmn2r61 UTSW 7 41,916,455 (GRCm39) missense probably damaging 1.00
R6207:Vmn2r61 UTSW 7 41,909,616 (GRCm39) missense probably benign 0.01
R6265:Vmn2r61 UTSW 7 41,915,915 (GRCm39) missense probably benign 0.01
R6272:Vmn2r61 UTSW 7 41,949,242 (GRCm39) missense probably damaging 1.00
R6355:Vmn2r61 UTSW 7 41,916,659 (GRCm39) missense probably benign 0.00
R6469:Vmn2r61 UTSW 7 41,915,283 (GRCm39) nonsense probably null
R6554:Vmn2r61 UTSW 7 41,926,139 (GRCm39) missense probably damaging 1.00
R6699:Vmn2r61 UTSW 7 41,949,580 (GRCm39) missense probably benign
R6768:Vmn2r61 UTSW 7 41,949,748 (GRCm39) missense probably damaging 1.00
R6824:Vmn2r61 UTSW 7 41,949,403 (GRCm39) missense probably benign 0.10
R6930:Vmn2r61 UTSW 7 41,949,364 (GRCm39) missense probably benign 0.02
R7053:Vmn2r61 UTSW 7 41,916,557 (GRCm39) missense probably damaging 0.96
R7238:Vmn2r61 UTSW 7 41,916,629 (GRCm39) missense possibly damaging 0.73
R7332:Vmn2r61 UTSW 7 41,909,534 (GRCm39) missense probably benign 0.00
R7359:Vmn2r61 UTSW 7 41,915,407 (GRCm39) missense probably benign 0.11
R7553:Vmn2r61 UTSW 7 41,916,205 (GRCm39) missense not run
R7710:Vmn2r61 UTSW 7 41,916,472 (GRCm39) missense probably damaging 1.00
R7732:Vmn2r61 UTSW 7 41,916,097 (GRCm39) missense probably benign
R7839:Vmn2r61 UTSW 7 41,916,032 (GRCm39) missense probably damaging 0.97
R7916:Vmn2r61 UTSW 7 41,949,935 (GRCm39) missense probably damaging 1.00
R8026:Vmn2r61 UTSW 7 41,916,141 (GRCm39) missense probably benign 0.02
R8440:Vmn2r61 UTSW 7 41,916,080 (GRCm39) missense probably benign 0.02
R8499:Vmn2r61 UTSW 7 41,949,700 (GRCm39) missense probably damaging 0.99
R8771:Vmn2r61 UTSW 7 41,916,194 (GRCm39) missense probably damaging 0.99
R8847:Vmn2r61 UTSW 7 41,950,010 (GRCm39) missense probably damaging 1.00
R8986:Vmn2r61 UTSW 7 41,915,325 (GRCm39) nonsense probably null
R9290:Vmn2r61 UTSW 7 41,915,385 (GRCm39) missense probably benign 0.27
R9311:Vmn2r61 UTSW 7 41,950,092 (GRCm39) missense possibly damaging 0.92
R9324:Vmn2r61 UTSW 7 41,916,619 (GRCm39) missense probably benign 0.00
R9476:Vmn2r61 UTSW 7 41,949,593 (GRCm39) missense probably damaging 1.00
R9521:Vmn2r61 UTSW 7 41,916,626 (GRCm39) missense probably damaging 0.99
R9619:Vmn2r61 UTSW 7 41,926,136 (GRCm39) missense probably damaging 0.98
R9729:Vmn2r61 UTSW 7 41,949,917 (GRCm39) missense probably damaging 1.00
Z1088:Vmn2r61 UTSW 7 41,949,388 (GRCm39) missense possibly damaging 0.93
Z1176:Vmn2r61 UTSW 7 41,916,166 (GRCm39) missense probably benign 0.00
Z1176:Vmn2r61 UTSW 7 41,909,585 (GRCm39) missense possibly damaging 0.46
Predicted Primers
Posted On 2017-02-16