Incidental Mutation 'IGL02598:Vmn2r76'
ID 299946
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r76
Ensembl Gene ENSMUSG00000091239
Gene Name vomeronasal 2, receptor 76
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.166) question?
Stock # IGL02598
Quality Score
Status
Chromosome 7
Chromosomal Location 85874414-85895409 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 85877879 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 506 (T506K)
Ref Sequence ENSEMBL: ENSMUSP00000127309 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165771]
AlphaFold E9Q3F5
Predicted Effect probably benign
Transcript: ENSMUST00000165771
AA Change: T506K

PolyPhen 2 Score 0.052 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000127309
Gene: ENSMUSG00000091239
AA Change: T506K

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 78 470 1.2e-29 PFAM
low complexity region 476 489 N/A INTRINSIC
Pfam:NCD3G 513 565 3.7e-22 PFAM
Pfam:7tm_3 598 833 1.4e-52 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933414I15Rik A T 11: 50,834,448 (GRCm39) M1K probably null Het
Abca13 C T 11: 9,381,898 (GRCm39) T3850I probably damaging Het
Abcc4 A T 14: 118,905,781 (GRCm39) L95* probably null Het
Acacb A G 5: 114,384,098 (GRCm39) Y2209C probably damaging Het
Acadm A G 3: 153,644,181 (GRCm39) probably benign Het
Arid2 G A 15: 96,269,417 (GRCm39) V1177M probably damaging Het
Atp8a1 A T 5: 67,840,099 (GRCm39) probably null Het
Catsperd A G 17: 56,954,815 (GRCm39) probably null Het
Cd28 A G 1: 60,802,498 (GRCm39) probably benign Het
Cep164 A G 9: 45,682,002 (GRCm39) Y1934H probably damaging Het
Cep350 T C 1: 155,738,713 (GRCm39) I2377V probably benign Het
Csmd3 T C 15: 47,533,086 (GRCm39) K1581E probably damaging Het
Dab2 A T 15: 6,458,847 (GRCm39) N232I probably damaging Het
Dyrk4 G A 6: 126,860,982 (GRCm39) probably benign Het
Efcab14 T A 4: 115,597,631 (GRCm39) C75* probably null Het
Elovl1 T C 4: 118,288,616 (GRCm39) probably null Het
Eps8l2 T G 7: 140,934,849 (GRCm39) probably benign Het
Grik1 A T 16: 87,744,872 (GRCm39) V460E probably damaging Het
Gtf2f2 A G 14: 76,245,182 (GRCm39) S35P probably benign Het
Ifi203 A G 1: 173,762,568 (GRCm39) probably benign Het
Ifi209 T C 1: 173,472,281 (GRCm39) V374A probably damaging Het
Kics2 G A 10: 121,575,876 (GRCm39) probably benign Het
Lars1 A G 18: 42,360,342 (GRCm39) S705P possibly damaging Het
Lcmt1 A G 7: 123,020,871 (GRCm39) probably benign Het
Limd1 T C 9: 123,345,933 (GRCm39) S571P probably benign Het
Limd1 T A 9: 123,309,236 (GRCm39) Y312N probably benign Het
Lin28b A T 10: 45,296,622 (GRCm39) D125E possibly damaging Het
Lmtk3 T C 7: 45,442,564 (GRCm39) S416P probably damaging Het
Map7d3 T C X: 55,855,146 (GRCm39) T446A probably benign Het
Masp1 T A 16: 23,278,381 (GRCm39) M523L probably benign Het
Mroh4 C A 15: 74,483,092 (GRCm39) probably null Het
Mtmr6 G A 14: 60,537,953 (GRCm39) A651T probably damaging Het
Myocd A G 11: 65,074,296 (GRCm39) S738P probably benign Het
Or10a2 A T 7: 106,673,923 (GRCm39) N296I possibly damaging Het
Or4d5 A T 9: 40,011,861 (GRCm39) F308L probably benign Het
Or52l1 A G 7: 104,830,163 (GRCm39) V134A probably damaging Het
Or5d46 A T 2: 88,170,595 (GRCm39) I229F possibly damaging Het
Or6c3b A T 10: 129,527,142 (GRCm39) I256N possibly damaging Het
Parg G T 14: 31,936,281 (GRCm39) V479L probably damaging Het
Pcdhb10 C A 18: 37,546,834 (GRCm39) H637N possibly damaging Het
Plekhg2 G A 7: 28,059,900 (GRCm39) T1118I possibly damaging Het
Podxl T C 6: 31,501,355 (GRCm39) E400G probably damaging Het
Prss54 C A 8: 96,292,337 (GRCm39) V81F probably damaging Het
Pzp A G 6: 128,464,420 (GRCm39) L1369P probably benign Het
Rfx8 A T 1: 39,735,128 (GRCm39) probably benign Het
Rgs6 C T 12: 83,138,571 (GRCm39) P302S probably benign Het
Rnf148 A C 6: 23,654,456 (GRCm39) I180S probably damaging Het
Sacm1l A G 9: 123,408,061 (GRCm39) D350G probably benign Het
Slc33a1 C T 3: 63,850,753 (GRCm39) G524S probably benign Het
Slc5a7 A G 17: 54,591,221 (GRCm39) V237A probably benign Het
Spink7 T C 18: 62,727,356 (GRCm39) D56G probably damaging Het
Syn3 A G 10: 86,303,063 (GRCm39) S31P probably damaging Het
Tesl1 A T X: 23,773,710 (GRCm39) T404S probably benign Het
Thrb C A 14: 18,008,606 (GRCm38) P110Q possibly damaging Het
Vps45 A G 3: 95,938,354 (GRCm39) L486P probably benign Het
Zan G A 5: 137,444,473 (GRCm39) T1823M unknown Het
Zdhhc6 T A 19: 55,302,959 (GRCm39) Q14L probably benign Het
Zfp990 A T 4: 145,263,533 (GRCm39) N177I possibly damaging Het
Other mutations in Vmn2r76
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00969:Vmn2r76 APN 7 85,877,925 (GRCm39) missense probably benign
IGL01374:Vmn2r76 APN 7 85,874,857 (GRCm39) missense probably benign 0.02
IGL01419:Vmn2r76 APN 7 85,874,910 (GRCm39) missense probably benign 0.32
IGL01627:Vmn2r76 APN 7 85,874,871 (GRCm39) missense probably damaging 1.00
IGL01730:Vmn2r76 APN 7 85,879,406 (GRCm39) missense probably benign 0.02
IGL01957:Vmn2r76 APN 7 85,877,925 (GRCm39) missense probably benign
IGL02214:Vmn2r76 APN 7 85,879,138 (GRCm39) missense probably benign 0.07
IGL02489:Vmn2r76 APN 7 85,878,071 (GRCm39) missense probably benign 0.41
IGL02543:Vmn2r76 APN 7 85,879,356 (GRCm39) missense probably benign 0.06
IGL02579:Vmn2r76 APN 7 85,877,961 (GRCm39) nonsense probably null
IGL02720:Vmn2r76 APN 7 85,874,914 (GRCm39) missense probably benign 0.35
IGL02745:Vmn2r76 APN 7 85,879,495 (GRCm39) missense probably benign 0.06
IGL03393:Vmn2r76 APN 7 85,879,034 (GRCm39) missense probably benign 0.01
R0483:Vmn2r76 UTSW 7 85,874,959 (GRCm39) missense probably damaging 1.00
R0513:Vmn2r76 UTSW 7 85,877,987 (GRCm39) missense probably benign 0.01
R0528:Vmn2r76 UTSW 7 85,879,506 (GRCm39) missense possibly damaging 0.80
R0601:Vmn2r76 UTSW 7 85,875,323 (GRCm39) critical splice acceptor site probably null
R0662:Vmn2r76 UTSW 7 85,879,578 (GRCm39) missense probably benign 0.39
R0883:Vmn2r76 UTSW 7 85,877,904 (GRCm39) missense probably benign 0.00
R1532:Vmn2r76 UTSW 7 85,879,454 (GRCm39) missense probably benign 0.02
R1694:Vmn2r76 UTSW 7 85,879,356 (GRCm39) missense probably benign 0.06
R1696:Vmn2r76 UTSW 7 85,880,464 (GRCm39) missense possibly damaging 0.56
R2135:Vmn2r76 UTSW 7 85,880,219 (GRCm39) missense probably benign 0.02
R2151:Vmn2r76 UTSW 7 85,879,692 (GRCm39) missense probably benign
R2181:Vmn2r76 UTSW 7 85,874,743 (GRCm39) missense probably benign 0.00
R2268:Vmn2r76 UTSW 7 85,879,707 (GRCm39) missense probably benign 0.03
R2877:Vmn2r76 UTSW 7 85,875,201 (GRCm39) missense probably benign 0.00
R3155:Vmn2r76 UTSW 7 85,874,959 (GRCm39) missense probably damaging 1.00
R3746:Vmn2r76 UTSW 7 85,874,763 (GRCm39) missense probably benign 0.11
R3799:Vmn2r76 UTSW 7 85,875,244 (GRCm39) missense probably benign 0.00
R3825:Vmn2r76 UTSW 7 85,880,415 (GRCm39) missense probably benign 0.10
R4058:Vmn2r76 UTSW 7 85,879,508 (GRCm39) missense probably benign 0.00
R4237:Vmn2r76 UTSW 7 85,879,740 (GRCm39) missense probably benign 0.00
R4404:Vmn2r76 UTSW 7 85,877,511 (GRCm39) missense probably benign 0.16
R4796:Vmn2r76 UTSW 7 85,879,652 (GRCm39) missense possibly damaging 0.95
R4838:Vmn2r76 UTSW 7 85,874,733 (GRCm39) missense probably damaging 1.00
R5175:Vmn2r76 UTSW 7 85,877,915 (GRCm39) missense probably benign 0.00
R5268:Vmn2r76 UTSW 7 85,875,267 (GRCm39) missense probably damaging 1.00
R5381:Vmn2r76 UTSW 7 85,874,496 (GRCm39) missense probably damaging 1.00
R5531:Vmn2r76 UTSW 7 85,874,657 (GRCm39) missense probably damaging 1.00
R5566:Vmn2r76 UTSW 7 85,875,286 (GRCm39) missense probably damaging 1.00
R5646:Vmn2r76 UTSW 7 85,875,261 (GRCm39) missense probably damaging 0.98
R5664:Vmn2r76 UTSW 7 85,895,202 (GRCm39) critical splice donor site probably null
R5818:Vmn2r76 UTSW 7 85,879,142 (GRCm39) missense probably benign 0.00
R6093:Vmn2r76 UTSW 7 85,877,469 (GRCm39) nonsense probably null
R6651:Vmn2r76 UTSW 7 85,878,059 (GRCm39) missense possibly damaging 0.64
R6741:Vmn2r76 UTSW 7 85,879,560 (GRCm39) missense probably benign
R6750:Vmn2r76 UTSW 7 85,875,114 (GRCm39) missense probably damaging 1.00
R7082:Vmn2r76 UTSW 7 85,874,440 (GRCm39) missense probably benign 0.01
R7136:Vmn2r76 UTSW 7 85,877,975 (GRCm39) missense probably benign 0.06
R7524:Vmn2r76 UTSW 7 85,879,374 (GRCm39) missense probably benign 0.00
R7524:Vmn2r76 UTSW 7 85,874,577 (GRCm39) missense probably benign 0.22
R7611:Vmn2r76 UTSW 7 85,879,388 (GRCm39) missense probably benign 0.04
R7833:Vmn2r76 UTSW 7 85,877,892 (GRCm39) missense probably benign
R8002:Vmn2r76 UTSW 7 85,879,271 (GRCm39) missense probably benign 0.05
R8021:Vmn2r76 UTSW 7 85,874,958 (GRCm39) missense probably damaging 1.00
R8023:Vmn2r76 UTSW 7 85,879,028 (GRCm39) missense probably benign 0.00
R8250:Vmn2r76 UTSW 7 85,875,231 (GRCm39) missense possibly damaging 0.82
R8428:Vmn2r76 UTSW 7 85,874,479 (GRCm39) missense possibly damaging 0.63
R8874:Vmn2r76 UTSW 7 85,877,999 (GRCm39) missense probably damaging 1.00
R9139:Vmn2r76 UTSW 7 85,879,170 (GRCm39) missense probably benign 0.02
R9357:Vmn2r76 UTSW 7 85,880,428 (GRCm39) missense probably benign 0.43
Z1176:Vmn2r76 UTSW 7 85,895,271 (GRCm39) missense probably benign 0.39
Posted On 2015-04-16