Incidental Mutation 'IGL01372:Vmn2r71'
ID 76202
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r71
Ensembl Gene ENSMUSG00000091205
Gene Name vomeronasal 2, receptor 71
Synonyms EG233445
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # IGL01372
Quality Score
Status
Chromosome 7
Chromosomal Location 85264670-85273755 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 85270022 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000132337 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172338]
AlphaFold L7N2D8
Predicted Effect probably benign
Transcript: ENSMUST00000172338
SMART Domains Protein: ENSMUSP00000132337
Gene: ENSMUSG00000091205

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 77 468 2.1e-31 PFAM
Pfam:NCD3G 511 563 8.7e-20 PFAM
Pfam:7tm_3 593 831 2e-55 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208273
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208545
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 G A 10: 79,842,089 (GRCm39) D1049N probably benign Het
Ankdd1a A T 9: 65,411,421 (GRCm39) L362Q probably damaging Het
Ankib1 A T 5: 3,822,594 (GRCm39) N37K probably damaging Het
Ankrd55 T A 13: 112,459,677 (GRCm39) D90E probably damaging Het
Atp1a2 T C 1: 172,106,510 (GRCm39) R831G probably damaging Het
Bcar3 A G 3: 122,316,943 (GRCm39) D638G probably damaging Het
Cabp4 T A 19: 4,189,322 (GRCm39) E78D probably benign Het
Cmtm8 A G 9: 114,619,755 (GRCm39) V130A possibly damaging Het
Cyth3 A G 5: 143,678,393 (GRCm39) T66A possibly damaging Het
Dmbt1 A T 7: 130,705,409 (GRCm39) I1171F possibly damaging Het
Dnah10 G A 5: 124,856,218 (GRCm39) G2060D probably damaging Het
Dnah11 T C 12: 118,156,134 (GRCm39) H172R probably damaging Het
Dnah5 C T 15: 28,230,636 (GRCm39) A178V probably benign Het
Efcab6 T G 15: 83,928,505 (GRCm39) M30L possibly damaging Het
Ehbp1l1 T C 19: 5,765,817 (GRCm39) probably benign Het
Eps15 G A 4: 109,179,303 (GRCm39) E230K probably damaging Het
Fam91a1 A G 15: 58,301,911 (GRCm39) I258M probably damaging Het
Gm5581 G A 6: 131,145,366 (GRCm39) noncoding transcript Het
Hrh1 G A 6: 114,456,958 (GRCm39) V80I probably damaging Het
Ldhd G A 8: 112,355,032 (GRCm39) H290Y probably benign Het
Lepr G A 4: 101,592,774 (GRCm39) E130K possibly damaging Het
Mycbpap T C 11: 94,397,282 (GRCm39) I40V possibly damaging Het
Nrap T A 19: 56,317,534 (GRCm39) probably null Het
Opn5 T A 17: 42,891,435 (GRCm39) probably null Het
Or1j14 T A 2: 36,417,463 (GRCm39) I13N probably benign Het
Or5ac24 A G 16: 59,165,524 (GRCm39) I180T probably damaging Het
Otop3 A T 11: 115,235,930 (GRCm39) T521S possibly damaging Het
Pcsk5 T G 19: 17,595,108 (GRCm39) T409P probably damaging Het
Pde9a T A 17: 31,680,685 (GRCm39) F322Y probably benign Het
Pgm5 T A 19: 24,710,985 (GRCm39) I406F probably damaging Het
Prrc2b T C 2: 32,113,942 (GRCm39) S1998P probably damaging Het
Prune2 T C 19: 17,102,433 (GRCm39) Y2531H probably damaging Het
Ptprk T C 10: 28,445,923 (GRCm39) V932A probably benign Het
Rapgef6 T A 11: 54,559,437 (GRCm39) probably benign Het
Rgsl1 T A 1: 153,701,887 (GRCm39) Y224F probably damaging Het
Rps6kl1 A T 12: 85,193,663 (GRCm39) C143S probably damaging Het
S100a7l2 A G 3: 90,995,616 (GRCm39) probably benign Het
Slc5a5 G A 8: 71,343,020 (GRCm39) probably benign Het
Tfb2m A G 1: 179,369,878 (GRCm39) S182P probably damaging Het
Tmc3 A G 7: 83,261,746 (GRCm39) H608R probably damaging Het
Trim37 T A 11: 87,075,772 (GRCm39) H459Q probably benign Het
Xirp2 T C 2: 67,344,334 (GRCm39) S2192P possibly damaging Het
Other mutations in Vmn2r71
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00922:Vmn2r71 APN 7 85,267,901 (GRCm39) missense probably benign
IGL00960:Vmn2r71 APN 7 85,273,582 (GRCm39) missense probably damaging 1.00
IGL01690:Vmn2r71 APN 7 85,264,782 (GRCm39) missense probably damaging 1.00
IGL01909:Vmn2r71 APN 7 85,270,001 (GRCm39) missense probably benign 0.00
IGL01950:Vmn2r71 APN 7 85,264,827 (GRCm39) missense probably damaging 0.98
IGL02570:Vmn2r71 APN 7 85,264,748 (GRCm39) missense possibly damaging 0.95
IGL02650:Vmn2r71 APN 7 85,273,535 (GRCm39) missense probably damaging 1.00
IGL02901:Vmn2r71 APN 7 85,268,470 (GRCm39) missense probably benign 0.00
IGL03128:Vmn2r71 APN 7 85,268,795 (GRCm39) missense probably damaging 1.00
IGL03328:Vmn2r71 APN 7 85,273,499 (GRCm39) missense probably damaging 1.00
R0533:Vmn2r71 UTSW 7 85,268,426 (GRCm39) frame shift probably null
R0707:Vmn2r71 UTSW 7 85,268,640 (GRCm39) missense probably benign
R0841:Vmn2r71 UTSW 7 85,267,749 (GRCm39) missense possibly damaging 0.62
R0865:Vmn2r71 UTSW 7 85,268,516 (GRCm39) missense probably benign 0.01
R0883:Vmn2r71 UTSW 7 85,272,842 (GRCm39) missense probably benign 0.19
R0939:Vmn2r71 UTSW 7 85,272,889 (GRCm39) missense possibly damaging 0.70
R1597:Vmn2r71 UTSW 7 85,273,352 (GRCm39) missense possibly damaging 0.46
R1646:Vmn2r71 UTSW 7 85,270,476 (GRCm39) missense probably damaging 0.99
R1719:Vmn2r71 UTSW 7 85,270,435 (GRCm39) missense probably damaging 1.00
R1860:Vmn2r71 UTSW 7 85,264,782 (GRCm39) missense probably damaging 1.00
R2013:Vmn2r71 UTSW 7 85,269,845 (GRCm39) missense probably benign 0.38
R2014:Vmn2r71 UTSW 7 85,269,845 (GRCm39) missense probably benign 0.38
R2015:Vmn2r71 UTSW 7 85,269,845 (GRCm39) missense probably benign 0.38
R2050:Vmn2r71 UTSW 7 85,273,681 (GRCm39) missense probably damaging 1.00
R2084:Vmn2r71 UTSW 7 85,267,945 (GRCm39) missense probably benign 0.03
R2221:Vmn2r71 UTSW 7 85,273,301 (GRCm39) missense probably benign 0.40
R2223:Vmn2r71 UTSW 7 85,273,301 (GRCm39) missense probably benign 0.40
R2245:Vmn2r71 UTSW 7 85,273,388 (GRCm39) missense probably damaging 1.00
R3115:Vmn2r71 UTSW 7 85,272,866 (GRCm39) missense probably damaging 0.97
R3122:Vmn2r71 UTSW 7 85,264,828 (GRCm39) nonsense probably null
R3609:Vmn2r71 UTSW 7 85,268,870 (GRCm39) missense probably damaging 1.00
R4093:Vmn2r71 UTSW 7 85,270,442 (GRCm39) missense probably benign 0.00
R4305:Vmn2r71 UTSW 7 85,273,360 (GRCm39) missense probably damaging 1.00
R4306:Vmn2r71 UTSW 7 85,273,360 (GRCm39) missense probably damaging 1.00
R4334:Vmn2r71 UTSW 7 85,269,042 (GRCm39) missense probably benign 0.01
R4569:Vmn2r71 UTSW 7 85,273,402 (GRCm39) missense possibly damaging 0.66
R4622:Vmn2r71 UTSW 7 85,269,817 (GRCm39) missense probably benign 0.00
R4915:Vmn2r71 UTSW 7 85,270,476 (GRCm39) missense probably damaging 0.99
R4956:Vmn2r71 UTSW 7 85,268,436 (GRCm39) missense probably benign 0.19
R5005:Vmn2r71 UTSW 7 85,273,352 (GRCm39) missense probably damaging 1.00
R5045:Vmn2r71 UTSW 7 85,273,597 (GRCm39) missense probably benign 0.00
R5153:Vmn2r71 UTSW 7 85,268,430 (GRCm39) missense possibly damaging 0.94
R5236:Vmn2r71 UTSW 7 85,272,877 (GRCm39) missense probably damaging 1.00
R5373:Vmn2r71 UTSW 7 85,267,750 (GRCm39) missense possibly damaging 0.79
R5405:Vmn2r71 UTSW 7 85,268,622 (GRCm39) missense probably benign
R5831:Vmn2r71 UTSW 7 85,272,922 (GRCm39) missense probably benign 0.16
R6061:Vmn2r71 UTSW 7 85,268,482 (GRCm39) missense probably benign
R6518:Vmn2r71 UTSW 7 85,270,436 (GRCm39) missense probably damaging 1.00
R6751:Vmn2r71 UTSW 7 85,269,095 (GRCm39) critical splice donor site probably null
R6920:Vmn2r71 UTSW 7 85,273,108 (GRCm39) missense probably damaging 1.00
R7358:Vmn2r71 UTSW 7 85,273,468 (GRCm39) missense possibly damaging 0.81
R7453:Vmn2r71 UTSW 7 85,273,297 (GRCm39) missense probably benign 0.21
R7560:Vmn2r71 UTSW 7 85,273,115 (GRCm39) missense probably benign 0.06
R7871:Vmn2r71 UTSW 7 85,272,869 (GRCm39) missense possibly damaging 0.81
R8267:Vmn2r71 UTSW 7 85,264,704 (GRCm39) missense probably benign 0.02
R8377:Vmn2r71 UTSW 7 85,264,707 (GRCm39) missense probably benign
R9278:Vmn2r71 UTSW 7 85,269,788 (GRCm39) missense probably benign 0.19
R9319:Vmn2r71 UTSW 7 85,273,694 (GRCm39) missense probably damaging 1.00
R9329:Vmn2r71 UTSW 7 85,267,950 (GRCm39) missense probably benign 0.00
R9368:Vmn2r71 UTSW 7 85,273,442 (GRCm39) missense probably damaging 1.00
R9636:Vmn2r71 UTSW 7 85,268,388 (GRCm39) missense possibly damaging 0.80
R9756:Vmn2r71 UTSW 7 85,268,573 (GRCm39) nonsense probably null
X0025:Vmn2r71 UTSW 7 85,267,873 (GRCm39) missense probably benign
Z1186:Vmn2r71 UTSW 7 85,273,094 (GRCm39) missense probably damaging 1.00
Posted On 2013-10-07