Incidental Mutation 'R5633:Vmn1r91'
ID439976
Institutional Source Beutler Lab
Gene Symbol Vmn1r91
Ensembl Gene ENSMUSG00000095201
Gene Namevomeronasal 1 receptor 91
SynonymsGm8442
MMRRC Submission 043284-MU
Accession Numbers
Is this an essential gene? Not available question?
Stock #R5633 (G1)
Quality Score225
Status Not validated
Chromosome7
Chromosomal Location20101158-20102081 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 20101945 bp
ZygosityHeterozygous
Amino Acid Change Histidine to Leucine at position 263 (H263L)
Ref Sequence ENSEMBL: ENSMUSP00000129283 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165330]
Predicted Effect possibly damaging
Transcript: ENSMUST00000165330
AA Change: H263L

PolyPhen 2 Score 0.564 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000129283
Gene: ENSMUSG00000095201
AA Change: H263L

DomainStartEndE-ValueType
Pfam:TAS2R 8 299 5.1e-18 PFAM
Pfam:V1R 41 298 7.1e-15 PFAM
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency 98% (55/56)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4 T A 4: 144,618,028 C125S probably benign Het
Abcb8 T C 5: 24,403,109 L382P probably damaging Het
Acot3 A G 12: 84,058,950 probably null Het
Acsl6 A T 11: 54,337,189 Q345L probably benign Het
Adcy8 A G 15: 64,699,285 S1170P probably damaging Het
Ankrd28 T G 14: 31,735,065 D182A probably damaging Het
B3galt5 A T 16: 96,315,509 H114L probably benign Het
BC053393 C T 11: 46,574,606 S9L unknown Het
Bcas2 T A 3: 103,178,424 Y207* probably null Het
Best1 A G 19: 9,992,103 L197P probably benign Het
Chil6 C A 3: 106,388,752 C389F probably damaging Het
Chrna4 T C 2: 181,029,460 T168A probably damaging Het
Ckmt1 C G 2: 121,363,629 probably benign Het
Dhcr7 T C 7: 143,847,423 L441P probably damaging Het
Dmtn T C 14: 70,604,979 M365V probably benign Het
Dmxl1 T A 18: 49,877,697 S974T probably damaging Het
Dnajb13 T C 7: 100,507,419 D150G probably benign Het
Eef2k C A 7: 120,873,290 probably benign Het
Elp2 T A 18: 24,615,210 V213E probably damaging Het
Fbxo43 A T 15: 36,162,095 probably null Het
Gm11559 C A 11: 99,864,586 C20* probably null Het
Gnb2 T C 5: 137,529,192 I213V probably benign Het
Gnb5 C T 9: 75,344,514 T306I probably damaging Het
Ica1 A T 6: 8,667,257 I303N possibly damaging Het
Idh1 A G 1: 65,165,136 Y272H probably damaging Het
Ikzf2 G A 1: 69,539,097 Q273* probably null Het
Itpkb A T 1: 180,327,225 probably benign Het
Kntc1 C T 5: 123,819,057 T2143I probably damaging Het
Lin9 T A 1: 180,669,198 L351I probably benign Het
Lmbrd1 C A 1: 24,748,862 D464E possibly damaging Het
Med13 A G 11: 86,278,931 probably benign Het
Mn1 T C 5: 111,420,326 F721L possibly damaging Het
Myo9a T A 9: 59,868,184 L1026Q possibly damaging Het
Olfr773 A T 10: 129,186,849 F191I probably benign Het
P4htm A C 9: 108,579,723 D428E probably damaging Het
Parp8 C T 13: 116,876,580 R602H probably damaging Het
Pkd2 T A 5: 104,498,506 S726R probably damaging Het
Pla2g6 A T 15: 79,299,142 I495N possibly damaging Het
Psmd5 A G 2: 34,856,488 I359T probably benign Het
Rassf6 T C 5: 90,604,118 H292R possibly damaging Het
Rnf145 T C 11: 44,560,088 I413T probably damaging Het
Rpn2 T A 2: 157,283,596 V9D possibly damaging Het
Rpp30 T C 19: 36,086,990 L57P probably damaging Het
Slc41a1 A G 1: 131,846,587 H464R possibly damaging Het
Slc47a1 G T 11: 61,369,261 P163Q probably damaging Het
Smc4 T A 3: 69,008,110 I165K probably damaging Het
Stra6l T A 4: 45,881,455 I439K probably benign Het
Syt9 C T 7: 107,425,296 T132I probably damaging Het
Trpm2 T C 10: 77,938,353 I471V possibly damaging Het
Uap1l1 A G 2: 25,363,349 M358T probably benign Het
Zfp407 T C 18: 84,561,044 D648G probably benign Het
Zpbp2 T C 11: 98,554,758 I150T probably damaging Het
Other mutations in Vmn1r91
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01875:Vmn1r91 APN 7 20101934 nonsense probably null
IGL02125:Vmn1r91 APN 7 20101504 missense probably damaging 0.96
IGL02263:Vmn1r91 APN 7 20101843 missense probably benign 0.00
IGL02338:Vmn1r91 APN 7 20101746 missense probably damaging 0.96
IGL02708:Vmn1r91 APN 7 20101490 missense probably damaging 1.00
R1880:Vmn1r91 UTSW 7 20101773 missense probably damaging 1.00
R2679:Vmn1r91 UTSW 7 20102058 missense probably damaging 0.97
R4730:Vmn1r91 UTSW 7 20101770 missense possibly damaging 0.71
R5362:Vmn1r91 UTSW 7 20101461 missense probably benign 0.05
R5979:Vmn1r91 UTSW 7 20102065 missense probably benign 0.00
R6151:Vmn1r91 UTSW 7 20101435 missense probably benign
R6177:Vmn1r91 UTSW 7 20101479 missense possibly damaging 0.95
R7397:Vmn1r91 UTSW 7 20101770 missense possibly damaging 0.71
R7589:Vmn1r91 UTSW 7 20101877 missense probably benign 0.07
Predicted Primers PCR Primer
(F):5'- GACCAGTGTCTCCATGGTAC -3'
(R):5'- GTGAGCACCACACCTTATTCATAC -3'

Sequencing Primer
(F):5'- ACTTCTCCTCCATAGACATCATCAG -3'
(R):5'- CCACACCTTATTCATACAAAATGTTG -3'
Posted On2016-11-08