Incidental Mutation 'IGL02457:Vmn2r17'
ID 294415
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r17
Ensembl Gene ENSMUSG00000091879
Gene Name vomeronasal 2, receptor 17
Synonyms EG384221
Accession Numbers
Essential gene? Probably non essential (E-score: 0.112) question?
Stock # IGL02457
Quality Score
Status
Chromosome 5
Chromosomal Location 109567879-109601253 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 109601012 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Alanine at position 770 (D770A)
Ref Sequence ENSEMBL: ENSMUSP00000131450 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171841]
AlphaFold E9PYF5
Predicted Effect probably damaging
Transcript: ENSMUST00000171841
AA Change: D770A

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000131450
Gene: ENSMUSG00000091879
AA Change: D770A

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:ANF_receptor 76 465 7e-26 PFAM
Pfam:NCD3G 508 562 3.5e-18 PFAM
Pfam:7tm_3 593 830 4.8e-55 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd16b A G 2: 181,136,127 (GRCm39) D343G probably benign Het
Acot10 T C 15: 20,666,229 (GRCm39) S171G possibly damaging Het
Actr3b T C 5: 26,054,160 (GRCm39) probably null Het
Adamts17 T C 7: 66,677,562 (GRCm39) M492T probably damaging Het
Akap4 A C X: 6,943,707 (GRCm39) N670T probably benign Het
Atrip A G 9: 108,894,299 (GRCm39) S55P possibly damaging Het
Bend3 A T 10: 43,385,946 (GRCm39) E113V probably damaging Het
Ccdc158 A C 5: 92,797,907 (GRCm39) I411S probably damaging Het
Cfap97 G T 8: 46,623,315 (GRCm39) C235F possibly damaging Het
Chil4 T C 3: 106,121,715 (GRCm39) N45D probably benign Het
Cripto C T 9: 110,771,691 (GRCm39) C32Y probably damaging Het
D430041D05Rik A G 2: 104,079,690 (GRCm39) V1131A probably damaging Het
Defb38 T C 8: 19,076,552 (GRCm39) probably benign Het
Dnah10 T A 5: 124,866,860 (GRCm39) W2260R probably damaging Het
Ecsit A G 9: 21,989,500 (GRCm39) S14P probably damaging Het
Eif3l T C 15: 78,962,296 (GRCm39) F106L probably benign Het
Erich5 G T 15: 34,470,999 (GRCm39) G76V probably damaging Het
Evpl A G 11: 116,120,939 (GRCm39) L432P possibly damaging Het
Fbxw10 T C 11: 62,765,808 (GRCm39) F698L probably damaging Het
Frem2 A T 3: 53,428,470 (GRCm39) S2866T probably damaging Het
Fuca1 G A 4: 135,662,073 (GRCm39) V334I probably benign Het
Hprt1 T A X: 52,091,010 (GRCm39) H60Q probably benign Het
Kirrel2 T C 7: 30,152,165 (GRCm39) N481S probably damaging Het
Krt16 A T 11: 100,137,162 (GRCm39) probably benign Het
Lilrb4b T A 10: 51,357,334 (GRCm39) Y57N probably benign Het
Lix1l A G 3: 96,521,792 (GRCm39) Y126C probably damaging Het
Lox T C 18: 52,654,388 (GRCm39) D347G probably damaging Het
Mak16 C T 8: 31,654,753 (GRCm39) R147Q possibly damaging Het
Ndst2 G A 14: 20,779,622 (GRCm39) A206V possibly damaging Het
Or1ak2 A T 2: 36,827,760 (GRCm39) I210F probably damaging Het
Or2q1 T A 6: 42,795,176 (GRCm39) I257N probably damaging Het
Phldb1 T C 9: 44,627,771 (GRCm39) M225V probably benign Het
Pofut1 C T 2: 153,090,516 (GRCm39) Q137* probably null Het
Polr2a T C 11: 69,634,076 (GRCm39) probably benign Het
Prdm5 T A 6: 65,858,100 (GRCm39) L388Q probably damaging Het
Rad51c A G 11: 87,271,681 (GRCm39) S344P possibly damaging Het
Scart1 G A 7: 139,800,308 (GRCm39) G30S probably benign Het
Sdk1 C T 5: 141,938,771 (GRCm39) P398L probably damaging Het
Sec63 G A 10: 42,677,729 (GRCm39) probably benign Het
Sgo1 A T 17: 53,983,989 (GRCm39) L463Q probably damaging Het
Slc5a6 A G 5: 31,198,002 (GRCm39) L291P probably damaging Het
Smarcb1 T C 10: 75,757,205 (GRCm39) T9A probably benign Het
Sp3 A G 2: 72,801,813 (GRCm39) W67R probably damaging Het
Ssxb9 A C X: 21,041,234 (GRCm39) S23A probably benign Het
Syne1 A G 10: 5,292,167 (GRCm39) L1367S probably damaging Het
Tbc1d23 T A 16: 56,990,754 (GRCm39) I690F probably damaging Het
Tmed5 A T 5: 108,272,416 (GRCm39) S227R probably benign Het
Tnrc6c T A 11: 117,613,803 (GRCm39) S814T probably benign Het
Trbv2 C T 6: 41,024,905 (GRCm39) T107I probably benign Het
Trpm6 T C 19: 18,803,155 (GRCm39) V866A probably damaging Het
Trpm6 A T 19: 18,804,762 (GRCm39) K905* probably null Het
Ttn A G 2: 76,539,654 (GRCm39) V34444A probably benign Het
Vmn1r86 C T 7: 12,836,707 (GRCm39) M56I probably benign Het
Wnk4 T C 11: 101,160,389 (GRCm39) probably benign Het
Xaf1 T C 11: 72,194,257 (GRCm39) M46T possibly damaging Het
Other mutations in Vmn2r17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00325:Vmn2r17 APN 5 109,575,858 (GRCm39) missense probably benign 0.15
IGL01457:Vmn2r17 APN 5 109,600,898 (GRCm39) missense probably benign 0.00
IGL01527:Vmn2r17 APN 5 109,601,006 (GRCm39) missense probably damaging 1.00
IGL01693:Vmn2r17 APN 5 109,600,384 (GRCm39) missense probably damaging 1.00
IGL01738:Vmn2r17 APN 5 109,577,364 (GRCm39) missense probably damaging 1.00
IGL01767:Vmn2r17 APN 5 109,567,903 (GRCm39) missense probably benign 0.01
IGL01932:Vmn2r17 APN 5 109,574,916 (GRCm39) missense probably benign 0.00
IGL01970:Vmn2r17 APN 5 109,575,813 (GRCm39) missense probably damaging 0.97
IGL02009:Vmn2r17 APN 5 109,600,714 (GRCm39) missense possibly damaging 0.67
IGL02365:Vmn2r17 APN 5 109,601,175 (GRCm39) missense probably damaging 1.00
IGL02385:Vmn2r17 APN 5 109,582,247 (GRCm39) missense probably damaging 1.00
IGL02646:Vmn2r17 APN 5 109,600,946 (GRCm39) missense probably damaging 1.00
IGL02741:Vmn2r17 APN 5 109,568,077 (GRCm39) missense probably benign
IGL03213:Vmn2r17 APN 5 109,582,256 (GRCm39) critical splice donor site probably null
IGL03216:Vmn2r17 APN 5 109,600,756 (GRCm39) missense probably damaging 1.00
IGL03342:Vmn2r17 APN 5 109,575,782 (GRCm39) missense probably damaging 1.00
IGL03408:Vmn2r17 APN 5 109,577,238 (GRCm39) splice site probably benign
R0349:Vmn2r17 UTSW 5 109,576,202 (GRCm39) missense probably damaging 1.00
R0418:Vmn2r17 UTSW 5 109,600,747 (GRCm39) missense probably damaging 1.00
R0800:Vmn2r17 UTSW 5 109,575,192 (GRCm39) splice site probably benign
R0836:Vmn2r17 UTSW 5 109,575,822 (GRCm39) missense possibly damaging 0.89
R1715:Vmn2r17 UTSW 5 109,576,110 (GRCm39) missense probably benign 0.00
R1738:Vmn2r17 UTSW 5 109,576,377 (GRCm39) missense probably benign 0.10
R1801:Vmn2r17 UTSW 5 109,576,344 (GRCm39) missense probably damaging 1.00
R2054:Vmn2r17 UTSW 5 109,600,352 (GRCm39) missense probably damaging 0.98
R2060:Vmn2r17 UTSW 5 109,575,075 (GRCm39) missense probably benign 0.00
R2192:Vmn2r17 UTSW 5 109,582,144 (GRCm39) missense possibly damaging 0.81
R2315:Vmn2r17 UTSW 5 109,575,897 (GRCm39) missense probably damaging 1.00
R2374:Vmn2r17 UTSW 5 109,575,104 (GRCm39) missense probably benign
R3612:Vmn2r17 UTSW 5 109,577,463 (GRCm39) missense probably benign 0.00
R3832:Vmn2r17 UTSW 5 109,576,262 (GRCm39) missense probably damaging 1.00
R4273:Vmn2r17 UTSW 5 109,600,832 (GRCm39) missense probably benign 0.44
R4494:Vmn2r17 UTSW 5 109,576,335 (GRCm39) missense probably damaging 1.00
R4597:Vmn2r17 UTSW 5 109,577,428 (GRCm39) missense probably benign 0.01
R4675:Vmn2r17 UTSW 5 109,575,049 (GRCm39) missense probably benign 0.00
R4701:Vmn2r17 UTSW 5 109,575,849 (GRCm39) missense probably damaging 0.99
R4754:Vmn2r17 UTSW 5 109,600,715 (GRCm39) missense probably damaging 0.99
R4841:Vmn2r17 UTSW 5 109,582,246 (GRCm39) missense probably damaging 1.00
R4842:Vmn2r17 UTSW 5 109,582,246 (GRCm39) missense probably damaging 1.00
R4865:Vmn2r17 UTSW 5 109,574,985 (GRCm39) missense probably damaging 1.00
R4902:Vmn2r17 UTSW 5 109,601,220 (GRCm39) missense probably benign 0.14
R4989:Vmn2r17 UTSW 5 109,575,739 (GRCm39) missense probably benign 0.07
R5101:Vmn2r17 UTSW 5 109,576,217 (GRCm39) missense probably damaging 0.99
R5109:Vmn2r17 UTSW 5 109,577,342 (GRCm39) missense probably benign 0.06
R5123:Vmn2r17 UTSW 5 109,575,774 (GRCm39) missense possibly damaging 0.90
R5474:Vmn2r17 UTSW 5 109,582,150 (GRCm39) missense probably damaging 1.00
R5485:Vmn2r17 UTSW 5 109,567,972 (GRCm39) missense probably benign 0.06
R5611:Vmn2r17 UTSW 5 109,576,030 (GRCm39) missense probably damaging 0.97
R5652:Vmn2r17 UTSW 5 109,577,430 (GRCm39) missense probably benign 0.10
R5717:Vmn2r17 UTSW 5 109,575,140 (GRCm39) missense possibly damaging 0.94
R5735:Vmn2r17 UTSW 5 109,600,716 (GRCm39) missense possibly damaging 0.67
R5766:Vmn2r17 UTSW 5 109,575,139 (GRCm39) missense possibly damaging 0.46
R6645:Vmn2r17 UTSW 5 109,576,247 (GRCm39) missense probably damaging 1.00
R6786:Vmn2r17 UTSW 5 109,575,695 (GRCm39) missense probably benign 0.30
R6821:Vmn2r17 UTSW 5 109,577,331 (GRCm39) missense probably damaging 1.00
R6979:Vmn2r17 UTSW 5 109,576,265 (GRCm39) missense possibly damaging 0.46
R6984:Vmn2r17 UTSW 5 109,600,533 (GRCm39) missense probably benign 0.10
R7269:Vmn2r17 UTSW 5 109,576,337 (GRCm39) missense possibly damaging 0.88
R7509:Vmn2r17 UTSW 5 109,575,695 (GRCm39) missense probably benign 0.30
R7736:Vmn2r17 UTSW 5 109,600,757 (GRCm39) missense probably benign 0.05
R7789:Vmn2r17 UTSW 5 109,600,831 (GRCm39) missense possibly damaging 0.77
R7814:Vmn2r17 UTSW 5 109,575,739 (GRCm39) missense probably benign 0.07
R7847:Vmn2r17 UTSW 5 109,568,063 (GRCm39) missense probably damaging 1.00
R7863:Vmn2r17 UTSW 5 109,568,035 (GRCm39) missense probably benign
R7893:Vmn2r17 UTSW 5 109,575,944 (GRCm39) missense probably benign 0.05
R8234:Vmn2r17 UTSW 5 109,601,235 (GRCm39) missense probably benign 0.01
R8382:Vmn2r17 UTSW 5 109,576,387 (GRCm39) missense probably benign 0.01
R8435:Vmn2r17 UTSW 5 109,576,172 (GRCm39) missense probably benign 0.01
R8465:Vmn2r17 UTSW 5 109,600,691 (GRCm39) missense probably damaging 0.99
R8555:Vmn2r17 UTSW 5 109,600,810 (GRCm39) missense probably damaging 0.99
R8900:Vmn2r17 UTSW 5 109,575,863 (GRCm39) missense probably benign 0.25
R9293:Vmn2r17 UTSW 5 109,600,712 (GRCm39) missense probably damaging 1.00
R9308:Vmn2r17 UTSW 5 109,600,505 (GRCm39) missense probably damaging 0.98
R9378:Vmn2r17 UTSW 5 109,575,732 (GRCm39) missense possibly damaging 0.94
R9597:Vmn2r17 UTSW 5 109,575,669 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16