Incidental Mutation 'R2251:Vstm2a'
ID 241689
Institutional Source Beutler Lab
Gene Symbol Vstm2a
Ensembl Gene ENSMUSG00000048834
Gene Name V-set and transmembrane domain containing 2A
Synonyms Vstm2, 9330184N17Rik
MMRRC Submission 040251-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R2251 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 16207742-16234551 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 16318273 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 231 (Q231K)
Ref Sequence ENSEMBL: ENSMUSP00000105274 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109647]
AlphaFold Q8R0A6
Predicted Effect probably benign
Transcript: ENSMUST00000109647
AA Change: Q231K

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000105274
Gene: ENSMUSG00000048834
AA Change: Q231K

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
IG 33 149 1.32e-12 SMART
low complexity region 266 280 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 94.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700129C05Rik G A 14: 59,380,061 (GRCm39) S79F probably damaging Het
Abl1 T A 2: 31,669,131 (GRCm39) V170E probably damaging Het
Akap13 C T 7: 75,389,225 (GRCm39) T2381M possibly damaging Het
Armc8 T A 9: 99,384,653 (GRCm39) probably null Het
B3gnt3 A T 8: 72,145,462 (GRCm39) M302K probably damaging Het
Casp3 G T 8: 47,090,990 (GRCm39) W214L probably damaging Het
Cnot1 A G 8: 96,489,814 (GRCm39) V463A probably benign Het
Cntn2 T C 1: 132,453,059 (GRCm39) E411G probably damaging Het
Dgkg A T 16: 22,441,010 (GRCm39) M1K probably null Het
Faap20 A C 4: 155,335,010 (GRCm39) E37A possibly damaging Het
Fam186a T C 15: 99,842,978 (GRCm39) T1089A probably benign Het
Fgb T G 3: 82,950,591 (GRCm39) T388P probably damaging Het
Fndc1 G A 17: 7,972,439 (GRCm39) R1498W probably damaging Het
Gch1 T C 14: 47,426,798 (GRCm39) probably benign Het
Gzf1 T C 2: 148,525,856 (GRCm39) M109T probably damaging Het
H2-M10.1 A C 17: 36,636,498 (GRCm39) L102R probably damaging Het
Kpna1 T C 16: 35,841,939 (GRCm39) Y280H possibly damaging Het
Mbtps2 A T X: 156,342,029 (GRCm39) F270L probably benign Het
Mrpl40 T C 16: 18,694,125 (GRCm39) H29R probably benign Het
N4bp2 G A 5: 65,964,071 (GRCm39) V707I probably damaging Het
Nav2 A G 7: 49,103,025 (GRCm39) K608E probably damaging Het
Nfix T C 8: 85,442,799 (GRCm39) D458G probably benign Het
Ngdn T C 14: 55,260,852 (GRCm39) probably null Het
Nr3c1 G T 18: 39,619,804 (GRCm39) T161K probably benign Het
Or2n1e C T 17: 38,585,794 (GRCm39) A44V probably benign Het
Or4g16 A G 2: 111,136,655 (GRCm39) Y35C probably damaging Het
Or52e15 A T 7: 104,645,802 (GRCm39) M103K probably damaging Het
Or5ak20 A G 2: 85,184,202 (GRCm39) S23P possibly damaging Het
Pbld2 G T 10: 62,860,384 (GRCm39) probably benign Het
Pkd1l2 T C 8: 117,784,177 (GRCm39) Y700C probably damaging Het
Plcb2 T C 2: 118,554,246 (GRCm39) N69S probably benign Het
Pwp2 T A 10: 78,016,922 (GRCm39) Q266L probably benign Het
Rnf133 T C 6: 23,649,174 (GRCm39) M252V probably benign Het
Scn8a A G 15: 100,914,987 (GRCm39) I1184V probably benign Het
Slc7a2 T C 8: 41,358,658 (GRCm39) Y334H probably benign Het
Smim11 T C 16: 92,107,716 (GRCm39) Y14H probably benign Het
Spata17 A T 1: 186,780,670 (GRCm39) L359Q possibly damaging Het
Spn T C 7: 126,736,331 (GRCm39) K59E probably benign Het
Tap2 A G 17: 34,430,928 (GRCm39) S343G probably damaging Het
Tcp11l2 T C 10: 84,440,933 (GRCm39) probably null Het
Tlr11 T A 14: 50,598,249 (GRCm39) N78K probably benign Het
Tm9sf2 T A 14: 122,377,143 (GRCm39) S224T probably benign Het
Trpm1 G A 7: 63,859,724 (GRCm39) G261D probably damaging Het
Tut4 T A 4: 108,377,405 (GRCm39) D938E probably damaging Het
Usp3 T C 9: 66,469,860 (GRCm39) D87G probably damaging Het
Vmn1r189 T C 13: 22,286,718 (GRCm39) K40E probably damaging Het
Vps45 A T 3: 95,964,352 (GRCm39) D56E probably benign Het
Zfp575 A T 7: 24,285,015 (GRCm39) C209S probably damaging Het
Zfp768 T C 7: 126,943,550 (GRCm39) T193A probably benign Het
Zfp867 T A 11: 59,356,319 (GRCm39) R38* probably null Het
Other mutations in Vstm2a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01024:Vstm2a APN 11 16,231,874 (GRCm39) missense possibly damaging 0.51
popiah UTSW 11 16,213,041 (GRCm39) missense probably damaging 1.00
R0167:Vstm2a UTSW 11 16,208,044 (GRCm39) missense probably damaging 0.99
R0314:Vstm2a UTSW 11 16,318,388 (GRCm39) splice site probably benign
R0480:Vstm2a UTSW 11 16,213,240 (GRCm39) missense probably damaging 1.00
R0533:Vstm2a UTSW 11 16,213,041 (GRCm39) missense probably damaging 1.00
R0613:Vstm2a UTSW 11 16,213,140 (GRCm39) missense probably damaging 1.00
R0788:Vstm2a UTSW 11 16,209,968 (GRCm39) missense probably damaging 1.00
R1750:Vstm2a UTSW 11 16,213,166 (GRCm39) missense possibly damaging 0.49
R1934:Vstm2a UTSW 11 16,359,734 (GRCm39) missense unknown
R2066:Vstm2a UTSW 11 16,211,483 (GRCm39) missense probably benign 0.09
R2101:Vstm2a UTSW 11 16,213,191 (GRCm39) missense probably benign 0.19
R4084:Vstm2a UTSW 11 16,213,098 (GRCm39) missense probably damaging 1.00
R4093:Vstm2a UTSW 11 16,209,884 (GRCm39) missense probably damaging 0.98
R4745:Vstm2a UTSW 11 16,213,061 (GRCm39) missense probably damaging 1.00
R4978:Vstm2a UTSW 11 16,211,460 (GRCm39) missense possibly damaging 0.82
R5533:Vstm2a UTSW 11 16,213,125 (GRCm39) missense possibly damaging 0.49
R5873:Vstm2a UTSW 11 16,208,044 (GRCm39) missense probably damaging 0.99
R5894:Vstm2a UTSW 11 16,211,483 (GRCm39) missense probably benign 0.09
R7094:Vstm2a UTSW 11 16,207,990 (GRCm39) unclassified probably benign
R7753:Vstm2a UTSW 11 16,213,040 (GRCm39) missense probably damaging 1.00
R8313:Vstm2a UTSW 11 16,231,898 (GRCm39) missense probably damaging 1.00
R8336:Vstm2a UTSW 11 16,207,801 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- GGTTCATAGGATGGAGGCCC -3'
(R):5'- GTGGCAAAATTAAATGAAGTCTGACAC -3'

Sequencing Primer
(F):5'- AATGTTGGTAGTGTATCAAAGTAGGC -3'
(R):5'- CCCAGTATGAGACAAAAGAAATCTTC -3'
Posted On 2014-10-16