Incidental Mutation 'IGL01895:Vmn1r19'
ID 179347
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r19
Ensembl Gene ENSMUSG00000115799
Gene Name vomeronasal 1 receptor 19
Synonyms V1rc27
Accession Numbers
Essential gene? Probably non essential (E-score: 0.094) question?
Stock # IGL01895
Quality Score
Status
Chromosome 6
Chromosomal Location 57381449-57382375 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 57382245 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Leucine at position 266 (Q266L)
Ref Sequence ENSEMBL: ENSMUSP00000087264 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089830]
AlphaFold Q8R2C7
Predicted Effect probably benign
Transcript: ENSMUST00000089830
AA Change: Q266L

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000087264
Gene: ENSMUSG00000115799
AA Change: Q266L

DomainStartEndE-ValueType
Pfam:V1R 28 293 6.6e-58 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc6 A T 7: 45,678,482 (GRCm39) I56N possibly damaging Het
Akr1c13 A T 13: 4,255,372 (GRCm39) E321V possibly damaging Het
Atp8b3 A T 10: 80,357,662 (GRCm39) V1119D possibly damaging Het
Cacna1e G T 1: 154,319,646 (GRCm39) F1351L probably damaging Het
Cadps2 A G 6: 23,427,274 (GRCm39) W585R probably damaging Het
Ccdc113 C T 8: 96,263,086 (GRCm39) probably benign Het
Ccer1 A T 10: 97,529,912 (GRCm39) I192F unknown Het
Chd8 T C 14: 52,436,551 (GRCm39) N90S probably benign Het
Clca3a1 A T 3: 144,453,333 (GRCm39) C463* probably null Het
Cplane1 T A 15: 8,258,591 (GRCm39) V2279E possibly damaging Het
Cyp2c65 T A 19: 39,060,676 (GRCm39) C179S possibly damaging Het
Dennd4b A G 3: 90,182,874 (GRCm39) Q35R probably benign Het
Enpep T C 3: 129,063,983 (GRCm39) E928G possibly damaging Het
Fem1c T C 18: 46,638,629 (GRCm39) T458A probably benign Het
Fezf2 A T 14: 12,342,498 (GRCm38) *456R probably null Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Iqcm T G 8: 76,615,188 (GRCm39) L423R probably damaging Het
Kcnc4 C A 3: 107,355,534 (GRCm39) V305L probably benign Het
Kif1a G A 1: 92,953,455 (GRCm39) T1337I possibly damaging Het
Lpxn A G 19: 12,810,450 (GRCm39) D298G probably damaging Het
Lypd8 A G 11: 58,281,046 (GRCm39) T203A possibly damaging Het
Mrps28 C T 3: 8,965,119 (GRCm39) V107M probably damaging Het
Myo15b A G 11: 115,774,324 (GRCm39) E586G possibly damaging Het
Pdzk1 C T 3: 96,776,417 (GRCm39) A459V possibly damaging Het
Rbpj A G 5: 53,808,728 (GRCm39) D285G probably damaging Het
Rimbp3 T C 16: 17,029,300 (GRCm39) L908P probably damaging Het
Samd4b T C 7: 28,101,334 (GRCm39) probably null Het
Slc28a2b A C 2: 122,355,572 (GRCm39) Y588S possibly damaging Het
Stau2 C T 1: 16,416,161 (GRCm39) G401S probably damaging Het
Trpa1 A T 1: 14,957,867 (GRCm39) I697K possibly damaging Het
Ttc17 A C 2: 94,205,491 (GRCm39) V285G possibly damaging Het
Unc5b A G 10: 60,602,864 (GRCm39) F845S probably damaging Het
Vmn2r106 T C 17: 20,499,227 (GRCm39) N228S probably benign Het
Vps13d A G 4: 144,882,836 (GRCm39) F919S possibly damaging Het
Zbtb38 C T 9: 96,570,461 (GRCm39) V208I probably benign Het
Zfp990 A T 4: 145,263,427 (GRCm39) T142S probably damaging Het
Zfp990 C A 4: 145,263,428 (GRCm39) T142N probably damaging Het
Other mutations in Vmn1r19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00948:Vmn1r19 APN 6 57,382,247 (GRCm39) missense probably benign 0.03
IGL01287:Vmn1r19 APN 6 57,382,179 (GRCm39) missense probably damaging 1.00
IGL01516:Vmn1r19 APN 6 57,381,857 (GRCm39) missense probably benign 0.03
IGL02676:Vmn1r19 APN 6 57,382,025 (GRCm39) missense possibly damaging 0.94
IGL03040:Vmn1r19 APN 6 57,382,347 (GRCm39) missense unknown
IGL03087:Vmn1r19 APN 6 57,381,476 (GRCm39) missense probably benign 0.01
PIT4802001:Vmn1r19 UTSW 6 57,382,037 (GRCm39) missense probably damaging 1.00
R0319:Vmn1r19 UTSW 6 57,381,600 (GRCm39) missense possibly damaging 0.93
R1368:Vmn1r19 UTSW 6 57,381,656 (GRCm39) missense probably benign 0.01
R1997:Vmn1r19 UTSW 6 57,382,033 (GRCm39) missense probably damaging 1.00
R2920:Vmn1r19 UTSW 6 57,381,909 (GRCm39) missense probably benign 0.03
R3857:Vmn1r19 UTSW 6 57,382,098 (GRCm39) missense possibly damaging 0.68
R4090:Vmn1r19 UTSW 6 57,381,720 (GRCm39) missense probably damaging 1.00
R4547:Vmn1r19 UTSW 6 57,381,774 (GRCm39) missense possibly damaging 0.56
R4823:Vmn1r19 UTSW 6 57,382,219 (GRCm39) nonsense probably null
R4951:Vmn1r19 UTSW 6 57,381,927 (GRCm39) missense probably benign 0.36
R5077:Vmn1r19 UTSW 6 57,382,026 (GRCm39) missense probably benign 0.00
R5459:Vmn1r19 UTSW 6 57,381,475 (GRCm39) nonsense probably null
R5625:Vmn1r19 UTSW 6 57,382,281 (GRCm39) missense probably damaging 1.00
R5690:Vmn1r19 UTSW 6 57,381,780 (GRCm39) missense probably benign 0.10
R5761:Vmn1r19 UTSW 6 57,382,338 (GRCm39) missense unknown
R6124:Vmn1r19 UTSW 6 57,381,602 (GRCm39) missense probably benign 0.02
R6373:Vmn1r19 UTSW 6 57,382,317 (GRCm39) missense unknown
R6476:Vmn1r19 UTSW 6 57,381,578 (GRCm39) missense probably damaging 0.99
R6938:Vmn1r19 UTSW 6 57,381,992 (GRCm39) missense possibly damaging 0.94
R7027:Vmn1r19 UTSW 6 57,381,475 (GRCm39) nonsense probably null
R7359:Vmn1r19 UTSW 6 57,382,080 (GRCm39) missense probably damaging 0.99
R7568:Vmn1r19 UTSW 6 57,381,813 (GRCm39) missense possibly damaging 0.69
R7893:Vmn1r19 UTSW 6 57,381,664 (GRCm39) missense probably damaging 1.00
R8481:Vmn1r19 UTSW 6 57,381,932 (GRCm39) missense probably damaging 0.99
R8487:Vmn1r19 UTSW 6 57,382,166 (GRCm39) missense probably benign 0.03
R8812:Vmn1r19 UTSW 6 57,381,436 (GRCm39) start gained probably benign
R8907:Vmn1r19 UTSW 6 57,381,991 (GRCm39) missense probably benign
R8976:Vmn1r19 UTSW 6 57,381,719 (GRCm39) missense probably benign 0.01
R9277:Vmn1r19 UTSW 6 57,382,322 (GRCm39) missense unknown
Posted On 2014-05-07