Incidental Mutation 'IGL01015:Vmn1r122'
ID 53670
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r122
Ensembl Gene ENSMUSG00000094001
Gene Name vomeronasal 1 receptor 122
Synonyms Gm5729
Accession Numbers
Essential gene? Not available question?
Stock # IGL01015
Quality Score
Status
Chromosome 7
Chromosomal Location 20867136-20868053 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 20867761 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 98 (V98E)
Ref Sequence ENSEMBL: ENSMUSP00000131706 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164409]
AlphaFold K7N726
Predicted Effect probably damaging
Transcript: ENSMUST00000164409
AA Change: V98E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000131706
Gene: ENSMUSG00000094001
AA Change: V98E

DomainStartEndE-ValueType
Pfam:TAS2R 8 297 1.2e-17 PFAM
Pfam:7tm_1 31 288 1.6e-6 PFAM
Pfam:V1R 41 296 2.5e-18 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ano4 A G 10: 88,870,961 (GRCm39) Y238H probably damaging Het
Apol7a T C 15: 77,274,055 (GRCm39) probably benign Het
Cacna1d A T 14: 29,773,699 (GRCm39) probably benign Het
Col12a1 A G 9: 79,541,023 (GRCm39) V2368A probably damaging Het
Creb3l4 A G 3: 90,150,138 (GRCm39) M1T probably null Het
Dpys T C 15: 39,710,045 (GRCm39) D128G probably damaging Het
Ero1b A G 13: 12,616,623 (GRCm39) probably null Het
Fcgbpl1 T C 7: 27,854,743 (GRCm39) C1790R probably damaging Het
Fcgr4 A G 1: 170,853,358 (GRCm39) S188G possibly damaging Het
Fry A G 5: 150,346,252 (GRCm39) D1587G probably benign Het
Gm43638 T A 5: 87,634,473 (GRCm39) R45* probably null Het
Gm7647 T A 5: 95,111,746 (GRCm39) C152S probably benign Het
Golga3 T G 5: 110,335,583 (GRCm39) M299R probably benign Het
Iqub A T 6: 24,501,005 (GRCm39) probably benign Het
Irak3 A T 10: 119,978,695 (GRCm39) Y493* probably null Het
Jakmip1 G T 5: 37,242,750 (GRCm39) E13* probably null Het
Morc3 G A 16: 93,659,534 (GRCm39) C446Y probably damaging Het
Mroh2b G A 15: 4,971,024 (GRCm39) D1010N probably damaging Het
Or14c44 A G 7: 86,061,998 (GRCm39) T184A probably damaging Het
Or2y16 T A 11: 49,335,201 (GRCm39) N174K probably damaging Het
Or5m9 A T 2: 85,876,996 (GRCm39) M57L possibly damaging Het
Pkhd1 G A 1: 20,593,482 (GRCm39) H1544Y possibly damaging Het
Rps2-ps10 C T 18: 61,392,896 (GRCm39) probably benign Het
Smco1 T C 16: 32,092,887 (GRCm39) V186A probably damaging Het
Snx1 C T 9: 66,001,713 (GRCm39) E314K possibly damaging Het
Timd2 T C 11: 46,567,170 (GRCm39) Y255C probably benign Het
Tnc A T 4: 63,935,571 (GRCm39) I455K probably benign Het
Tsc22d1 A G 14: 76,656,181 (GRCm39) I31V possibly damaging Het
Tyk2 A G 9: 21,031,996 (GRCm39) S360P probably benign Het
Uroc1 G T 6: 90,335,883 (GRCm39) probably benign Het
Other mutations in Vmn1r122
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01322:Vmn1r122 APN 7 20,868,036 (GRCm39) missense probably benign 0.07
IGL01397:Vmn1r122 APN 7 20,867,707 (GRCm39) missense possibly damaging 0.91
IGL02894:Vmn1r122 APN 7 20,867,649 (GRCm39) missense probably benign
R1837:Vmn1r122 UTSW 7 20,867,291 (GRCm39) missense probably benign 0.34
R3040:Vmn1r122 UTSW 7 20,867,371 (GRCm39) missense probably benign
R4111:Vmn1r122 UTSW 7 20,867,438 (GRCm39) missense probably damaging 1.00
R4868:Vmn1r122 UTSW 7 20,867,227 (GRCm39) missense probably benign 0.01
R5239:Vmn1r122 UTSW 7 20,868,023 (GRCm39) missense possibly damaging 0.69
R6851:Vmn1r122 UTSW 7 20,867,845 (GRCm39) missense probably benign
R7010:Vmn1r122 UTSW 7 20,867,896 (GRCm39) missense probably damaging 0.97
R7184:Vmn1r122 UTSW 7 20,867,820 (GRCm39) missense probably benign 0.14
R7922:Vmn1r122 UTSW 7 20,867,587 (GRCm39) missense possibly damaging 0.89
R8539:Vmn1r122 UTSW 7 20,867,281 (GRCm39) missense possibly damaging 0.94
R9344:Vmn1r122 UTSW 7 20,867,271 (GRCm39) missense probably benign 0.07
Posted On 2013-06-28