Incidental Mutation 'IGL01923:Vmn2r27'
ID 180178
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r27
Ensembl Gene ENSMUSG00000072778
Gene Name vomeronasal 2, receptor27
Synonyms EG232367
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # IGL01923
Quality Score
Status
Chromosome 6
Chromosomal Location 124168555-124208743 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 124177484 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 507 (I507L)
Ref Sequence ENSEMBL: ENSMUSP00000098528 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100968]
AlphaFold D3YUK6
Predicted Effect probably benign
Transcript: ENSMUST00000100968
AA Change: I507L

PolyPhen 2 Score 0.199 (Sensitivity: 0.92; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000098528
Gene: ENSMUSG00000072778
AA Change: I507L

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:ANF_receptor 81 475 1.1e-27 PFAM
Pfam:NCD3G 519 570 1.3e-18 PFAM
Pfam:7tm_3 603 838 2.6e-50 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrd1 T A 5: 129,255,143 (GRCm39) S597T possibly damaging Het
Btnl9 T C 11: 49,071,409 (GRCm39) D138G probably benign Het
Cep135 T A 5: 76,788,829 (GRCm39) *1141K probably null Het
Ctnnd2 A T 15: 30,480,974 (GRCm39) Q74L probably damaging Het
Cyp2j13 A T 4: 95,950,294 (GRCm39) W236R probably benign Het
Dixdc1 A T 9: 50,606,803 (GRCm39) I271N possibly damaging Het
Dlec1 A G 9: 118,957,182 (GRCm39) probably null Het
Dnah9 C A 11: 66,016,061 (GRCm39) probably benign Het
Dop1a A T 9: 86,404,920 (GRCm39) Y275F probably damaging Het
Dysf T A 6: 84,187,811 (GRCm39) *2105R probably null Het
Eif4a1 A T 11: 69,563,129 (GRCm39) D25E possibly damaging Het
Fras1 T A 5: 96,883,139 (GRCm39) I2557N probably damaging Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Gm12253 G T 11: 58,325,727 (GRCm39) probably null Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Hsd17b7 A G 1: 169,787,035 (GRCm39) V254A probably benign Het
Kif21a T A 15: 90,840,633 (GRCm39) D143V probably damaging Het
Lrrc9 T C 12: 72,557,186 (GRCm39) V1417A possibly damaging Het
Macf1 C T 4: 123,274,237 (GRCm39) A4926T possibly damaging Het
Mef2a A C 7: 66,914,620 (GRCm39) S91R probably damaging Het
Myh7 A G 14: 55,222,916 (GRCm39) probably null Het
Or6c65 T A 10: 129,603,973 (GRCm39) F203I probably benign Het
Pbx2 A G 17: 34,813,024 (GRCm39) D160G probably damaging Het
Pcdhb17 T C 18: 37,619,790 (GRCm39) F527L probably benign Het
Ppm1b T C 17: 85,301,489 (GRCm39) L123P probably damaging Het
Ppm1k T A 6: 57,499,813 (GRCm39) K154N probably benign Het
Ppp2r1a T G 17: 21,185,731 (GRCm39) *590G probably null Het
Raver1 A T 9: 20,990,536 (GRCm39) L589Q probably damaging Het
Rrbp1 A G 2: 143,832,081 (GRCm39) S29P probably damaging Het
Senp5 A G 16: 31,784,634 (GRCm39) Y673H probably damaging Het
Serpina3j T A 12: 104,281,473 (GRCm39) probably benign Het
Serpinc1 A G 1: 160,817,116 (GRCm39) E70G probably damaging Het
Sp140l2 A G 1: 85,231,907 (GRCm39) probably benign Het
Stag3 A G 5: 138,287,492 (GRCm39) Q139R probably damaging Het
Sva T A 6: 42,019,104 (GRCm39) H91Q probably benign Het
Tmem263 C T 10: 84,950,295 (GRCm39) Q29* probably null Het
Tpp1 T C 7: 105,400,857 (GRCm39) N57D probably benign Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Wdr11 A T 7: 129,234,046 (GRCm39) probably null Het
Zfp236 C T 18: 82,700,344 (GRCm39) E42K probably damaging Het
Other mutations in Vmn2r27
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01285:Vmn2r27 APN 6 124,169,370 (GRCm39) missense possibly damaging 0.86
IGL01388:Vmn2r27 APN 6 124,200,791 (GRCm39) missense possibly damaging 0.55
IGL01954:Vmn2r27 APN 6 124,169,207 (GRCm39) missense probably damaging 1.00
IGL02105:Vmn2r27 APN 6 124,174,308 (GRCm39) splice site probably benign
IGL02586:Vmn2r27 APN 6 124,201,434 (GRCm39) nonsense probably null
IGL03130:Vmn2r27 APN 6 124,169,276 (GRCm39) missense possibly damaging 0.82
IGL03330:Vmn2r27 APN 6 124,207,139 (GRCm39) nonsense probably null
R0124:Vmn2r27 UTSW 6 124,208,578 (GRCm39) missense probably benign
R0234:Vmn2r27 UTSW 6 124,208,578 (GRCm39) missense probably benign
R0234:Vmn2r27 UTSW 6 124,208,578 (GRCm39) missense probably benign
R0384:Vmn2r27 UTSW 6 124,200,871 (GRCm39) missense probably benign 0.01
R0582:Vmn2r27 UTSW 6 124,201,249 (GRCm39) missense probably benign 0.02
R0733:Vmn2r27 UTSW 6 124,169,147 (GRCm39) missense probably benign 0.18
R0738:Vmn2r27 UTSW 6 124,200,661 (GRCm39) missense possibly damaging 0.48
R0835:Vmn2r27 UTSW 6 124,177,583 (GRCm39) missense probably damaging 0.99
R1183:Vmn2r27 UTSW 6 124,177,491 (GRCm39) missense probably benign
R1401:Vmn2r27 UTSW 6 124,168,591 (GRCm39) nonsense probably null
R1484:Vmn2r27 UTSW 6 124,177,474 (GRCm39) missense probably damaging 0.96
R1536:Vmn2r27 UTSW 6 124,177,649 (GRCm39) missense probably damaging 1.00
R1539:Vmn2r27 UTSW 6 124,168,730 (GRCm39) missense probably damaging 1.00
R1565:Vmn2r27 UTSW 6 124,208,593 (GRCm39) missense probably benign
R1595:Vmn2r27 UTSW 6 124,208,574 (GRCm39) missense probably benign 0.00
R1614:Vmn2r27 UTSW 6 124,200,893 (GRCm39) missense probably benign 0.01
R1742:Vmn2r27 UTSW 6 124,177,636 (GRCm39) missense possibly damaging 0.48
R1816:Vmn2r27 UTSW 6 124,207,330 (GRCm39) nonsense probably null
R1822:Vmn2r27 UTSW 6 124,208,593 (GRCm39) missense probably benign
R1824:Vmn2r27 UTSW 6 124,208,593 (GRCm39) missense probably benign
R1870:Vmn2r27 UTSW 6 124,201,170 (GRCm39) missense probably benign 0.11
R1942:Vmn2r27 UTSW 6 124,200,722 (GRCm39) missense probably damaging 1.00
R1962:Vmn2r27 UTSW 6 124,200,793 (GRCm39) missense possibly damaging 0.70
R2069:Vmn2r27 UTSW 6 124,201,442 (GRCm39) missense probably damaging 1.00
R2075:Vmn2r27 UTSW 6 124,177,510 (GRCm39) missense possibly damaging 0.85
R2379:Vmn2r27 UTSW 6 124,201,342 (GRCm39) missense possibly damaging 0.89
R3748:Vmn2r27 UTSW 6 124,207,351 (GRCm39) missense probably benign 0.35
R4384:Vmn2r27 UTSW 6 124,201,115 (GRCm39) missense probably benign 0.05
R4392:Vmn2r27 UTSW 6 124,207,135 (GRCm39) missense probably benign 0.01
R4758:Vmn2r27 UTSW 6 124,208,596 (GRCm39) missense possibly damaging 0.87
R5018:Vmn2r27 UTSW 6 124,201,141 (GRCm39) missense probably benign 0.02
R5235:Vmn2r27 UTSW 6 124,169,013 (GRCm39) missense probably damaging 0.99
R5718:Vmn2r27 UTSW 6 124,169,103 (GRCm39) missense possibly damaging 0.66
R5859:Vmn2r27 UTSW 6 124,177,647 (GRCm39) missense probably damaging 1.00
R5958:Vmn2r27 UTSW 6 124,208,686 (GRCm39) missense probably benign 0.00
R6044:Vmn2r27 UTSW 6 124,208,731 (GRCm39) missense probably benign
R6086:Vmn2r27 UTSW 6 124,168,958 (GRCm39) missense probably damaging 1.00
R6396:Vmn2r27 UTSW 6 124,201,125 (GRCm39) nonsense probably null
R6546:Vmn2r27 UTSW 6 124,169,369 (GRCm39) missense possibly damaging 0.49
R6746:Vmn2r27 UTSW 6 124,177,552 (GRCm39) missense possibly damaging 0.47
R6976:Vmn2r27 UTSW 6 124,201,312 (GRCm39) nonsense probably null
R7091:Vmn2r27 UTSW 6 124,200,904 (GRCm39) missense possibly damaging 0.85
R7145:Vmn2r27 UTSW 6 124,168,711 (GRCm39) missense probably benign
R7176:Vmn2r27 UTSW 6 124,168,995 (GRCm39) missense probably benign 0.01
R7382:Vmn2r27 UTSW 6 124,174,276 (GRCm39) missense probably damaging 1.00
R7482:Vmn2r27 UTSW 6 124,201,220 (GRCm39) missense probably damaging 1.00
R7853:Vmn2r27 UTSW 6 124,168,980 (GRCm39) missense probably damaging 1.00
R7859:Vmn2r27 UTSW 6 124,201,201 (GRCm39) missense probably benign 0.00
R7959:Vmn2r27 UTSW 6 124,169,040 (GRCm39) missense probably benign
R8266:Vmn2r27 UTSW 6 124,168,937 (GRCm39) missense probably benign 0.00
R8353:Vmn2r27 UTSW 6 124,169,404 (GRCm39) missense probably damaging 0.99
R8394:Vmn2r27 UTSW 6 124,168,776 (GRCm39) missense possibly damaging 0.71
R8463:Vmn2r27 UTSW 6 124,169,168 (GRCm39) missense probably damaging 1.00
R8477:Vmn2r27 UTSW 6 124,201,200 (GRCm39) missense probably benign 0.11
R8705:Vmn2r27 UTSW 6 124,207,188 (GRCm39) missense probably damaging 1.00
R8752:Vmn2r27 UTSW 6 124,201,018 (GRCm39) missense probably benign 0.00
R9109:Vmn2r27 UTSW 6 124,174,224 (GRCm39) missense possibly damaging 0.95
R9140:Vmn2r27 UTSW 6 124,169,207 (GRCm39) missense probably damaging 1.00
R9157:Vmn2r27 UTSW 6 124,201,244 (GRCm39) missense probably benign 0.09
R9431:Vmn2r27 UTSW 6 124,168,856 (GRCm39) missense probably damaging 1.00
R9477:Vmn2r27 UTSW 6 124,168,910 (GRCm39) missense probably damaging 0.99
R9758:Vmn2r27 UTSW 6 124,168,637 (GRCm39) missense possibly damaging 0.89
Z1177:Vmn2r27 UTSW 6 124,168,860 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07