Incidental Mutation 'IGL01322:Vmn1r34'
ID 74078
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r34
Ensembl Gene ENSMUSG00000091012
Gene Name vomeronasal 1 receptor 34
Synonyms Gm5991
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # IGL01322
Quality Score
Status
Chromosome 6
Chromosomal Location 66613807-66614736 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 66613899 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 280 (Q280*)
Ref Sequence ENSEMBL: ENSMUSP00000153720 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074381] [ENSMUST00000226262] [ENSMUST00000226910] [ENSMUST00000226999] [ENSMUST00000227332] [ENSMUST00000228498] [ENSMUST00000228647]
AlphaFold G3XA52
Predicted Effect probably null
Transcript: ENSMUST00000074381
AA Change: Q280*
SMART Domains Protein: ENSMUSP00000132900
Gene: ENSMUSG00000091012
AA Change: Q280*

DomainStartEndE-ValueType
Pfam:V1R 28 293 2.2e-54 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000226262
AA Change: Q280*
Predicted Effect probably null
Transcript: ENSMUST00000226910
AA Change: Q280*
Predicted Effect probably null
Transcript: ENSMUST00000226999
AA Change: Q280*
Predicted Effect probably null
Transcript: ENSMUST00000227332
AA Change: Q280*
Predicted Effect probably null
Transcript: ENSMUST00000228498
AA Change: Q280*
Predicted Effect probably null
Transcript: ENSMUST00000228647
AA Change: Q280*
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T A 7: 120,038,422 (GRCm39) L368Q probably damaging Het
Abca2 T A 2: 25,336,794 (GRCm39) probably null Het
Ano7 T A 1: 93,323,230 (GRCm39) V497D probably benign Het
B4gat1 T C 19: 5,090,037 (GRCm39) Y345H probably damaging Het
Bckdha T A 7: 25,358,132 (GRCm39) R12W possibly damaging Het
Bcl7c T A 7: 127,306,608 (GRCm39) N93Y probably damaging Het
Cc2d2a C A 5: 43,846,345 (GRCm39) T368K probably benign Het
Chek1 G A 9: 36,629,717 (GRCm39) Q210* probably null Het
Chrdl2 A G 7: 99,666,248 (GRCm39) Y56C probably damaging Het
Cspg4 T A 9: 56,805,872 (GRCm39) F2228I probably damaging Het
Dnah7a T C 1: 53,473,205 (GRCm39) M3474V probably benign Het
Dph7 T C 2: 24,855,629 (GRCm39) S143P possibly damaging Het
Ehbp1 T A 11: 22,039,636 (GRCm39) K821N probably damaging Het
Eomes T C 9: 118,313,898 (GRCm39) S648P probably benign Het
Fam20a A G 11: 109,573,738 (GRCm39) V215A probably damaging Het
Fer1l4 T A 2: 155,862,259 (GRCm39) probably null Het
Frem2 A G 3: 53,448,459 (GRCm39) V2319A probably benign Het
Gtf3c4 T C 2: 28,723,584 (GRCm39) D575G probably benign Het
Ifit1bl2 A G 19: 34,596,404 (GRCm39) V404A probably benign Het
Kcnf1 T C 12: 17,225,349 (GRCm39) M291V probably benign Het
Klra1 T A 6: 130,341,224 (GRCm39) I250F probably benign Het
Klra4 T A 6: 130,038,985 (GRCm39) T136S probably benign Het
Mcrs1 A T 15: 99,141,266 (GRCm39) I399N probably damaging Het
Neo1 T C 9: 58,814,368 (GRCm39) E866G possibly damaging Het
Notch3 T C 17: 32,363,445 (GRCm39) D1206G probably damaging Het
Or10ab4 A G 7: 107,654,188 (GRCm39) probably benign Het
Or14c43 T A 7: 86,115,480 (GRCm39) I287N probably damaging Het
Or4z4 A C 19: 12,076,769 (GRCm39) V78G probably benign Het
Or5ae1 T A 7: 84,565,590 (GRCm39) V201E probably damaging Het
Or5b95 A C 19: 12,658,113 (GRCm39) I214L probably benign Het
Or6c210 A G 10: 129,495,995 (GRCm39) T107A probably benign Het
Pnkd A G 1: 74,390,716 (GRCm39) N336D probably damaging Het
Prag1 T C 8: 36,571,088 (GRCm39) V557A probably benign Het
Ptgfr A C 3: 151,541,323 (GRCm39) S62A probably benign Het
Smc2 A G 4: 52,450,842 (GRCm39) Y220C probably damaging Het
Sufu G A 19: 46,439,382 (GRCm39) E246K probably damaging Het
Sult2a1 T A 7: 13,566,604 (GRCm39) R124* probably null Het
Sult4a1 T A 15: 83,970,817 (GRCm39) Y196F possibly damaging Het
Trim15 G A 17: 37,175,975 (GRCm39) R191W probably damaging Het
Ttn A G 2: 76,773,319 (GRCm39) V2361A possibly damaging Het
Usp16 T C 16: 87,263,164 (GRCm39) V122A possibly damaging Het
Vmn1r122 T A 7: 20,868,036 (GRCm39) K6N probably benign Het
Vmn2r45 T A 7: 8,484,332 (GRCm39) H491L possibly damaging Het
Wdpcp T C 11: 21,661,949 (GRCm39) L407P probably damaging Het
Zfp157 T C 5: 138,445,840 (GRCm39) I65T probably benign Het
Other mutations in Vmn1r34
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00974:Vmn1r34 APN 6 66,614,639 (GRCm39) missense possibly damaging 0.64
IGL01866:Vmn1r34 APN 6 66,614,373 (GRCm39) missense probably benign 0.03
IGL02389:Vmn1r34 APN 6 66,614,042 (GRCm39) missense probably damaging 1.00
IGL03356:Vmn1r34 APN 6 66,613,970 (GRCm39) missense probably benign 0.00
R0508:Vmn1r34 UTSW 6 66,614,392 (GRCm39) missense probably benign 0.19
R0601:Vmn1r34 UTSW 6 66,614,648 (GRCm39) missense possibly damaging 0.94
R1381:Vmn1r34 UTSW 6 66,613,922 (GRCm39) missense probably damaging 1.00
R1605:Vmn1r34 UTSW 6 66,613,932 (GRCm39) missense probably benign 0.01
R1765:Vmn1r34 UTSW 6 66,614,480 (GRCm39) missense probably damaging 0.99
R2022:Vmn1r34 UTSW 6 66,614,385 (GRCm39) missense possibly damaging 0.90
R3878:Vmn1r34 UTSW 6 66,614,552 (GRCm39) missense possibly damaging 0.82
R4023:Vmn1r34 UTSW 6 66,614,688 (GRCm39) missense probably benign
R4024:Vmn1r34 UTSW 6 66,614,688 (GRCm39) missense probably benign
R4025:Vmn1r34 UTSW 6 66,614,688 (GRCm39) missense probably benign
R4026:Vmn1r34 UTSW 6 66,614,688 (GRCm39) missense probably benign
R4385:Vmn1r34 UTSW 6 66,614,123 (GRCm39) missense probably damaging 0.99
R5274:Vmn1r34 UTSW 6 66,614,123 (GRCm39) missense probably damaging 1.00
R6182:Vmn1r34 UTSW 6 66,614,312 (GRCm39) missense probably damaging 0.97
R6629:Vmn1r34 UTSW 6 66,614,499 (GRCm39) missense probably benign 0.00
R7143:Vmn1r34 UTSW 6 66,614,648 (GRCm39) missense probably benign 0.12
R7689:Vmn1r34 UTSW 6 66,613,994 (GRCm39) nonsense probably null
R7956:Vmn1r34 UTSW 6 66,614,777 (GRCm39) start gained probably benign
R8031:Vmn1r34 UTSW 6 66,614,165 (GRCm39) missense probably damaging 1.00
R9570:Vmn1r34 UTSW 6 66,614,718 (GRCm39) missense probably benign 0.00
X0066:Vmn1r34 UTSW 6 66,614,459 (GRCm39) missense probably benign 0.02
Z1176:Vmn1r34 UTSW 6 66,614,109 (GRCm39) nonsense probably null
Posted On 2013-10-07