Incidental Mutation 'IGL02883:Vmn1r128'
ID 362860
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r128
Ensembl Gene ENSMUSG00000095758
Gene Name vomeronasal 1 receptor 128
Synonyms Gm8509
Accession Numbers
Essential gene? Not available question?
Stock # IGL02883
Quality Score
Status
Chromosome 7
Chromosomal Location 21349373-21350296 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 21349515 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Lysine to Arginine at position 48 (K48R)
Ref Sequence ENSEMBL: ENSMUSP00000129433 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000169165]
AlphaFold L7N2B4
Predicted Effect probably benign
Transcript: ENSMUST00000169165
AA Change: K48R

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000129433
Gene: ENSMUSG00000095758
AA Change: K48R

DomainStartEndE-ValueType
Pfam:TAS2R 8 299 3.6e-16 PFAM
Pfam:7tm_1 31 288 3.8e-6 PFAM
Pfam:V1R 41 296 8.4e-15 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810055G02Rik C A 19: 3,716,972 (GRCm38) S186R possibly damaging Het
Acap2 A G 16: 31,096,345 (GRCm38) probably benign Het
Cacna1h G T 17: 25,380,532 (GRCm38) R1726S probably damaging Het
Cdca2 T C 14: 67,707,497 (GRCm38) S133G probably damaging Het
Cep295nl A T 11: 118,333,909 (GRCm38) S36R probably benign Het
Crispld1 A G 1: 17,746,789 (GRCm38) N190S possibly damaging Het
Crtam A G 9: 40,994,501 (GRCm38) V44A probably benign Het
Crtc1 C T 8: 70,406,125 (GRCm38) G112S probably benign Het
Cyp17a1 T C 19: 46,669,351 (GRCm38) N254S probably benign Het
Dmrta1 T C 4: 89,688,774 (GRCm38) S156P probably benign Het
Eno2 A C 6: 124,766,209 (GRCm38) V188G probably damaging Het
Fam20a A T 11: 109,675,127 (GRCm38) I427N probably damaging Het
Fat2 T C 11: 55,256,618 (GRCm38) K3933E probably benign Het
Gm15448 A G 7: 3,822,180 (GRCm38) S488P possibly damaging Het
Igkv8-30 T C 6: 70,117,617 (GRCm38) M1V probably null Het
Ist1 G A 8: 109,683,668 (GRCm38) probably benign Het
Kank4 T C 4: 98,773,453 (GRCm38) E765G possibly damaging Het
Kat14 T C 2: 144,393,529 (GRCm38) L92S probably damaging Het
Kcnu1 G A 8: 25,849,827 (GRCm38) V58I probably benign Het
Lrba T A 3: 86,354,206 (GRCm38) V1489E probably damaging Het
Lrba T A 3: 86,445,413 (GRCm38) I1956N probably damaging Het
Mdn1 G A 4: 32,763,199 (GRCm38) V5100I probably benign Het
Mkrn2os C A 6: 115,586,709 (GRCm38) G122* probably null Het
Nme3 T C 17: 24,896,906 (GRCm38) Y78H probably benign Het
Pkd1l2 G A 8: 117,065,745 (GRCm38) T436I probably benign Het
Ppp2r5c T G 12: 110,522,563 (GRCm38) V56G possibly damaging Het
Pramef25 T C 4: 143,949,848 (GRCm38) T229A possibly damaging Het
Prdm10 G A 9: 31,327,348 (GRCm38) V179M probably damaging Het
Rab11fip2 A G 19: 59,906,998 (GRCm38) V344A probably damaging Het
Selp G A 1: 164,130,102 (GRCm38) A267T probably benign Het
Sf3a1 T A 11: 4,179,192 (GRCm38) W718R probably damaging Het
Taar9 T C 10: 24,109,480 (GRCm38) N19D probably benign Het
Tas2r113 T G 6: 132,893,419 (GRCm38) S137A probably damaging Het
Traf4 A T 11: 78,161,621 (GRCm38) I66N possibly damaging Het
Ucp3 A T 7: 100,480,642 (GRCm38) T164S probably benign Het
Uggt1 A T 1: 36,177,615 (GRCm38) N96K probably benign Het
Uqcc1 T A 2: 155,911,829 (GRCm38) Q42L possibly damaging Het
Other mutations in Vmn1r128
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00972:Vmn1r128 APN 7 21,350,076 (GRCm38) missense probably benign 0.01
IGL02169:Vmn1r128 APN 7 21,350,238 (GRCm38) missense probably damaging 0.99
R1740:Vmn1r128 UTSW 7 21,349,944 (GRCm38) missense probably benign 0.00
R2969:Vmn1r128 UTSW 7 21,350,121 (GRCm38) missense probably damaging 1.00
R4583:Vmn1r128 UTSW 7 21,349,719 (GRCm38) missense possibly damaging 0.79
R4867:Vmn1r128 UTSW 7 21,350,014 (GRCm38) missense possibly damaging 0.53
R5266:Vmn1r128 UTSW 7 21,349,403 (GRCm38) missense probably benign 0.14
R5631:Vmn1r128 UTSW 7 21,349,375 (GRCm38) start codon destroyed probably null 1.00
R6267:Vmn1r128 UTSW 7 21,350,296 (GRCm38) makesense probably null
R7376:Vmn1r128 UTSW 7 21,349,743 (GRCm38) missense probably damaging 1.00
R8351:Vmn1r128 UTSW 7 21,349,672 (GRCm38) missense probably damaging 1.00
R8440:Vmn1r128 UTSW 7 21,349,820 (GRCm38) missense probably benign 0.22
R8773:Vmn1r128 UTSW 7 21,349,997 (GRCm38) missense probably benign 0.41
R8889:Vmn1r128 UTSW 7 21,349,815 (GRCm38) missense possibly damaging 0.61
R9182:Vmn1r128 UTSW 7 21,349,758 (GRCm38) missense possibly damaging 0.72
R9200:Vmn1r128 UTSW 7 21,349,391 (GRCm38) missense possibly damaging 0.89
R9665:Vmn1r128 UTSW 7 21,349,437 (GRCm38) missense probably damaging 1.00
Posted On 2015-12-18