Incidental Mutation 'IGL01326:Vmn1r31'
ID 74261
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r31
Ensembl Gene ENSMUSG00000115404
Gene Name vomeronasal 1 receptor 31
Synonyms Gm6709
Accession Numbers
Essential gene? Probably non essential (E-score: 0.135) question?
Stock # IGL01326
Quality Score
Status
Chromosome 6
Chromosomal Location 58448952-58449863 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 58449784 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 27 (I27T)
Ref Sequence ENSEMBL: ENSMUSP00000135472 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000176023] [ENSMUST00000176147] [ENSMUST00000176177] [ENSMUST00000177318] [ENSMUST00000226390] [ENSMUST00000228586]
AlphaFold H3BKW5
Predicted Effect probably benign
Transcript: ENSMUST00000176023
SMART Domains Protein: ENSMUSP00000135252
Gene: ENSMUSG00000115404

DomainStartEndE-ValueType
Pfam:V1R 1 58 1.9e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000176147
SMART Domains Protein: ENSMUSP00000135282
Gene: ENSMUSG00000115404

DomainStartEndE-ValueType
Pfam:V1R 1 58 1.9e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000176177
AA Change: I27T

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000135472
Gene: ENSMUSG00000093379
AA Change: I27T

DomainStartEndE-ValueType
Pfam:V1R 28 293 4.7e-56 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000177318
AA Change: I27T

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000135555
Gene: ENSMUSG00000115404
AA Change: I27T

DomainStartEndE-ValueType
Pfam:V1R 28 107 1.9e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204999
Predicted Effect probably benign
Transcript: ENSMUST00000226390
AA Change: I27T

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
Predicted Effect probably benign
Transcript: ENSMUST00000228586
AA Change: I27T

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adh1 G A 3: 137,992,672 (GRCm39) V263M probably damaging Het
Akap13 T A 7: 75,375,096 (GRCm39) H1909Q probably benign Het
Atg2b C T 12: 105,588,403 (GRCm39) A1936T probably damaging Het
Atp8b3 G T 10: 80,360,210 (GRCm39) L954M probably damaging Het
C8a T C 4: 104,713,617 (GRCm39) Y171C probably damaging Het
Cd6 A G 19: 10,768,466 (GRCm39) S508P probably benign Het
Cdk4 A G 10: 126,900,492 (GRCm39) D86G possibly damaging Het
Cdr2l G T 11: 115,281,796 (GRCm39) R100S probably benign Het
Cndp1 T A 18: 84,640,357 (GRCm39) T283S probably benign Het
Cr2 T C 1: 194,823,529 (GRCm39) Y1023C probably null Het
Csmd3 A G 15: 47,713,181 (GRCm39) F1494L probably benign Het
Eeig2 A G 3: 108,887,101 (GRCm39) V299A possibly damaging Het
Eng G T 2: 32,562,394 (GRCm39) G231W probably benign Het
Erp44 A G 4: 48,218,126 (GRCm39) V181A probably benign Het
Fkbp15 A G 4: 62,241,487 (GRCm39) S553P probably damaging Het
Glg1 A G 8: 111,909,205 (GRCm39) V495A probably damaging Het
Gm9631 A T 11: 121,836,454 (GRCm39) D28E possibly damaging Het
Gnptab G T 10: 88,268,927 (GRCm39) L543F probably damaging Het
H4c3 A T 13: 23,882,353 (GRCm39) I27N probably damaging Het
Khdrbs2 T G 1: 32,696,558 (GRCm39) L329R possibly damaging Het
Kidins220 C A 12: 25,088,498 (GRCm39) H1080Q probably damaging Het
Maml1 G A 11: 50,156,715 (GRCm39) P487S probably benign Het
Me1 C T 9: 86,480,771 (GRCm39) probably null Het
Morc2a C T 11: 3,631,775 (GRCm39) R569C probably benign Het
Mrc1 A G 2: 14,271,335 (GRCm39) Q413R probably damaging Het
Mrgprx1 A T 7: 47,671,517 (GRCm39) C77S probably benign Het
Mtarc2 T C 1: 184,566,048 (GRCm39) probably benign Het
Myo1d A T 11: 80,575,147 (GRCm39) probably benign Het
Nr4a1 T G 15: 101,171,940 (GRCm39) L538R probably damaging Het
Olfm1 T C 2: 28,119,564 (GRCm39) Y385H probably damaging Het
Or4a39 A T 2: 89,236,675 (GRCm39) F249L possibly damaging Het
Or5m9 A G 2: 85,877,627 (GRCm39) E267G probably damaging Het
Pkd1 T A 17: 24,795,148 (GRCm39) Y2278* probably null Het
Plcg2 T C 8: 118,300,738 (GRCm39) probably benign Het
Prkdc G T 16: 15,647,556 (GRCm39) C3660F probably benign Het
Ptpn11 T C 5: 121,281,199 (GRCm39) D493G probably damaging Het
Rad23b T A 4: 55,383,601 (GRCm39) F278I possibly damaging Het
Saxo2 T C 7: 82,297,613 (GRCm39) I9V probably benign Het
Scn7a T C 2: 66,582,604 (GRCm39) I98V probably benign Het
Serac1 T A 17: 6,124,528 (GRCm39) probably benign Het
Simc1 T C 13: 54,672,473 (GRCm39) C274R probably benign Het
Sirt3 A G 7: 140,444,006 (GRCm39) probably benign Het
Tctn3 A G 19: 40,585,880 (GRCm39) L555P probably damaging Het
Ttc14 A G 3: 33,855,507 (GRCm39) I151V probably benign Het
Ush2a T A 1: 187,995,518 (GRCm39) Y96* probably null Het
Usp42 T C 5: 143,706,970 (GRCm39) T270A possibly damaging Het
Vmn2r93 G A 17: 18,536,906 (GRCm39) A530T possibly damaging Het
Other mutations in Vmn1r31
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01386:Vmn1r31 APN 6 58,449,587 (GRCm39) missense probably benign 0.22
IGL01785:Vmn1r31 APN 6 58,449,709 (GRCm39) missense possibly damaging 0.95
IGL02527:Vmn1r31 APN 6 58,449,778 (GRCm39) missense probably benign 0.01
PIT4791001:Vmn1r31 UTSW 6 58,449,028 (GRCm39) missense probably damaging 0.97
R0107:Vmn1r31 UTSW 6 58,449,728 (GRCm39) missense probably benign 0.05
R1250:Vmn1r31 UTSW 6 58,449,643 (GRCm39) missense probably benign 0.01
R1616:Vmn1r31 UTSW 6 58,449,043 (GRCm39) missense probably damaging 0.97
R1883:Vmn1r31 UTSW 6 58,449,029 (GRCm39) missense probably damaging 0.97
R1884:Vmn1r31 UTSW 6 58,449,029 (GRCm39) missense probably damaging 0.97
R2942:Vmn1r31 UTSW 6 58,449,583 (GRCm39) missense possibly damaging 0.87
R4589:Vmn1r31 UTSW 6 58,449,596 (GRCm39) missense probably damaging 1.00
R4672:Vmn1r31 UTSW 6 58,449,056 (GRCm39) missense probably damaging 0.97
R4676:Vmn1r31 UTSW 6 58,448,998 (GRCm39) missense probably damaging 0.97
R4702:Vmn1r31 UTSW 6 58,448,953 (GRCm39) makesense probably null
R4703:Vmn1r31 UTSW 6 58,448,953 (GRCm39) makesense probably null
R4705:Vmn1r31 UTSW 6 58,448,953 (GRCm39) makesense probably null
R6341:Vmn1r31 UTSW 6 58,448,995 (GRCm39) missense probably benign 0.35
R6549:Vmn1r31 UTSW 6 58,449,648 (GRCm39) missense possibly damaging 0.92
R7238:Vmn1r31 UTSW 6 58,449,858 (GRCm39) missense
R7609:Vmn1r31 UTSW 6 58,449,455 (GRCm39) missense probably damaging 0.97
R8438:Vmn1r31 UTSW 6 58,449,646 (GRCm39) missense
R8936:Vmn1r31 UTSW 6 58,449,083 (GRCm39) missense unknown
R9103:Vmn1r31 UTSW 6 58,449,073 (GRCm39) missense unknown
Z1176:Vmn1r31 UTSW 6 58,449,376 (GRCm39) missense unknown
Posted On 2013-10-07