Incidental Mutation 'IGL01914:Vmn2r79'
ID 179873
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r79
Ensembl Gene ENSMUSG00000090362
Gene Name vomeronasal 2, receptor 79
Synonyms EG621430
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # IGL01914
Quality Score
Status
Chromosome 7
Chromosomal Location 86645673-86687176 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 86686571 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 651 (T651S)
Ref Sequence ENSEMBL: ENSMUSP00000132478 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164462]
AlphaFold E9Q067
Predicted Effect probably benign
Transcript: ENSMUST00000164462
AA Change: T651S

PolyPhen 2 Score 0.141 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000132478
Gene: ENSMUSG00000090362
AA Change: T651S

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 75 464 1.9e-31 PFAM
Pfam:NCD3G 506 559 3.1e-21 PFAM
Pfam:7tm_3 592 827 2.8e-53 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atf7 A T 15: 102,459,913 (GRCm39) Y67* probably null Het
Atp6v1b2 C A 8: 69,548,932 (GRCm39) probably benign Het
Cd24a T C 10: 43,458,699 (GRCm39) S79P unknown Het
Col4a2 G A 8: 11,464,754 (GRCm39) E340K possibly damaging Het
Dtna A T 18: 23,730,516 (GRCm39) N301I possibly damaging Het
Ero1a T C 14: 45,544,069 (GRCm39) D45G probably damaging Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
H6pd A T 4: 150,078,920 (GRCm39) probably benign Het
Htt A G 5: 34,987,053 (GRCm39) T1091A probably benign Het
Msto1 T C 3: 88,820,210 (GRCm39) E82G probably benign Het
Mup11 T A 4: 60,615,821 (GRCm39) probably benign Het
Nlrp9a T A 7: 26,256,689 (GRCm39) N13K probably benign Het
Nsun7 C T 5: 66,433,977 (GRCm39) P209L probably damaging Het
Or5ac25 A T 16: 59,182,294 (GRCm39) C96S probably damaging Het
Or5al1 C T 2: 85,990,391 (GRCm39) V108I probably benign Het
Or8j3 G A 2: 86,029,016 (GRCm39) L27F probably benign Het
Pecam1 A G 11: 106,590,693 (GRCm39) I27T possibly damaging Het
Prkcd T C 14: 30,329,383 (GRCm39) E19G possibly damaging Het
Slc4a11 A T 2: 130,529,199 (GRCm39) I417N probably damaging Het
Stat1 T C 1: 52,165,716 (GRCm39) I104T probably benign Het
Stk17b T C 1: 53,800,226 (GRCm39) N251D probably damaging Het
Ttll4 C T 1: 74,718,217 (GRCm39) H23Y probably benign Het
Other mutations in Vmn2r79
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01401:Vmn2r79 APN 7 86,686,481 (GRCm39) missense probably benign 0.01
IGL01675:Vmn2r79 APN 7 86,645,856 (GRCm39) missense probably benign 0.01
IGL01760:Vmn2r79 APN 7 86,651,366 (GRCm39) missense probably benign
IGL01834:Vmn2r79 APN 7 86,686,354 (GRCm39) missense probably benign 0.01
IGL01843:Vmn2r79 APN 7 86,686,485 (GRCm39) missense probably damaging 1.00
IGL01980:Vmn2r79 APN 7 86,686,290 (GRCm39) missense possibly damaging 0.49
IGL02438:Vmn2r79 APN 7 86,651,744 (GRCm39) missense probably damaging 0.98
IGL02740:Vmn2r79 APN 7 86,653,366 (GRCm39) missense probably benign 0.00
IGL03052:Vmn2r79 UTSW 7 86,652,799 (GRCm39) missense probably benign 0.00
PIT4445001:Vmn2r79 UTSW 7 86,651,408 (GRCm39) missense possibly damaging 0.46
R0096:Vmn2r79 UTSW 7 86,686,527 (GRCm39) missense probably damaging 1.00
R0096:Vmn2r79 UTSW 7 86,686,527 (GRCm39) missense probably damaging 1.00
R0270:Vmn2r79 UTSW 7 86,652,594 (GRCm39) missense probably benign 0.00
R0336:Vmn2r79 UTSW 7 86,651,287 (GRCm39) missense probably benign 0.15
R0418:Vmn2r79 UTSW 7 86,651,611 (GRCm39) missense probably benign 0.18
R1070:Vmn2r79 UTSW 7 86,652,681 (GRCm39) missense probably damaging 1.00
R1234:Vmn2r79 UTSW 7 86,653,307 (GRCm39) missense possibly damaging 0.71
R1459:Vmn2r79 UTSW 7 86,687,002 (GRCm39) missense probably benign 0.01
R1513:Vmn2r79 UTSW 7 86,686,652 (GRCm39) missense probably benign 0.01
R1624:Vmn2r79 UTSW 7 86,653,247 (GRCm39) critical splice acceptor site probably null
R1633:Vmn2r79 UTSW 7 86,687,042 (GRCm39) missense possibly damaging 0.52
R1676:Vmn2r79 UTSW 7 86,651,839 (GRCm39) missense probably benign
R1781:Vmn2r79 UTSW 7 86,651,555 (GRCm39) missense probably benign 0.00
R1794:Vmn2r79 UTSW 7 86,650,621 (GRCm39) missense probably benign 0.37
R1823:Vmn2r79 UTSW 7 86,687,080 (GRCm39) missense probably damaging 1.00
R2013:Vmn2r79 UTSW 7 86,653,289 (GRCm39) missense possibly damaging 0.50
R2018:Vmn2r79 UTSW 7 86,651,634 (GRCm39) missense probably benign 0.07
R2019:Vmn2r79 UTSW 7 86,651,634 (GRCm39) missense probably benign 0.07
R2177:Vmn2r79 UTSW 7 86,645,839 (GRCm39) missense possibly damaging 0.94
R2984:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R3719:Vmn2r79 UTSW 7 86,651,245 (GRCm39) missense probably benign 0.05
R3798:Vmn2r79 UTSW 7 86,651,402 (GRCm39) missense possibly damaging 0.88
R3969:Vmn2r79 UTSW 7 86,652,801 (GRCm39) missense probably damaging 1.00
R4182:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4183:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4245:Vmn2r79 UTSW 7 86,651,624 (GRCm39) missense possibly damaging 0.73
R4301:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4391:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4393:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4394:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4396:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4397:Vmn2r79 UTSW 7 86,651,099 (GRCm39) missense possibly damaging 0.85
R4592:Vmn2r79 UTSW 7 86,653,319 (GRCm39) missense possibly damaging 0.86
R4697:Vmn2r79 UTSW 7 86,687,168 (GRCm39) missense probably damaging 0.98
R4897:Vmn2r79 UTSW 7 86,650,675 (GRCm39) missense probably benign
R5016:Vmn2r79 UTSW 7 86,686,548 (GRCm39) missense probably benign 0.00
R5058:Vmn2r79 UTSW 7 86,651,423 (GRCm39) missense probably damaging 0.98
R5177:Vmn2r79 UTSW 7 86,651,177 (GRCm39) missense probably damaging 0.97
R6078:Vmn2r79 UTSW 7 86,653,319 (GRCm39) missense possibly damaging 0.86
R6079:Vmn2r79 UTSW 7 86,653,319 (GRCm39) missense possibly damaging 0.86
R6138:Vmn2r79 UTSW 7 86,653,319 (GRCm39) missense possibly damaging 0.86
R6257:Vmn2r79 UTSW 7 86,651,778 (GRCm39) missense probably benign 0.27
R6260:Vmn2r79 UTSW 7 86,686,365 (GRCm39) missense probably benign 0.00
R6307:Vmn2r79 UTSW 7 86,686,976 (GRCm39) missense probably damaging 1.00
R6323:Vmn2r79 UTSW 7 86,650,522 (GRCm39) missense probably benign 0.05
R6374:Vmn2r79 UTSW 7 86,651,498 (GRCm39) missense probably benign 0.02
R6530:Vmn2r79 UTSW 7 86,651,252 (GRCm39) missense possibly damaging 0.91
R6546:Vmn2r79 UTSW 7 86,652,741 (GRCm39) missense probably benign 0.01
R6682:Vmn2r79 UTSW 7 86,653,370 (GRCm39) missense possibly damaging 0.69
R6858:Vmn2r79 UTSW 7 86,686,580 (GRCm39) missense probably benign
R6965:Vmn2r79 UTSW 7 86,651,100 (GRCm39) missense probably benign 0.10
R7130:Vmn2r79 UTSW 7 86,651,474 (GRCm39) missense probably damaging 0.99
R7156:Vmn2r79 UTSW 7 86,686,851 (GRCm39) missense probably damaging 0.98
R7604:Vmn2r79 UTSW 7 86,652,592 (GRCm39) critical splice acceptor site probably null
R7691:Vmn2r79 UTSW 7 86,687,111 (GRCm39) missense probably damaging 0.96
R8055:Vmn2r79 UTSW 7 86,686,541 (GRCm39) missense possibly damaging 0.94
R8070:Vmn2r79 UTSW 7 86,651,336 (GRCm39) missense probably benign
R8073:Vmn2r79 UTSW 7 86,651,462 (GRCm39) missense probably benign 0.00
R8145:Vmn2r79 UTSW 7 86,686,862 (GRCm39) missense probably benign 0.02
R8263:Vmn2r79 UTSW 7 86,686,726 (GRCm39) missense possibly damaging 0.89
R8350:Vmn2r79 UTSW 7 86,686,741 (GRCm39) nonsense probably null
R8400:Vmn2r79 UTSW 7 86,651,308 (GRCm39) missense probably benign 0.00
R8814:Vmn2r79 UTSW 7 86,651,714 (GRCm39) missense probably benign 0.00
R8862:Vmn2r79 UTSW 7 86,645,712 (GRCm39) missense probably benign 0.23
R9146:Vmn2r79 UTSW 7 86,650,681 (GRCm39) nonsense probably null
R9276:Vmn2r79 UTSW 7 86,687,045 (GRCm39) missense probably damaging 1.00
R9361:Vmn2r79 UTSW 7 86,652,822 (GRCm39) critical splice donor site probably null
R9676:Vmn2r79 UTSW 7 86,686,452 (GRCm39) missense probably damaging 1.00
U15987:Vmn2r79 UTSW 7 86,653,319 (GRCm39) missense possibly damaging 0.86
X0054:Vmn2r79 UTSW 7 86,653,270 (GRCm39) missense probably benign 0.01
Z1088:Vmn2r79 UTSW 7 86,651,549 (GRCm39) missense probably damaging 1.00
Z1176:Vmn2r79 UTSW 7 86,686,377 (GRCm39) missense probably benign
Z1176:Vmn2r79 UTSW 7 86,651,526 (GRCm39) missense probably benign 0.00
Posted On 2014-05-07