Incidental Mutation 'R3810:Trgv2'
ID 473958
Institutional Source Beutler Lab
Gene Symbol Trgv2
Ensembl Gene ENSMUSG00000076754
Gene Name T cell receptor gamma variable 2
Synonyms Vgamma2, Tcrg-V2
MMRRC Submission 040880-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # R3810 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 19520743-19521196 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 19521011 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 28 (T28A)
Ref Sequence ENSEMBL: ENSMUSP00000100341 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103563] [ENSMUST00000103564]
AlphaFold A2J008
Predicted Effect possibly damaging
Transcript: ENSMUST00000103563
AA Change: T28A

PolyPhen 2 Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000100341
Gene: ENSMUSG00000076754
AA Change: T28A

DomainStartEndE-ValueType
IGv 34 114 1.66e-9 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000103564
SMART Domains Protein: ENSMUSP00000100342
Gene: ENSMUSG00000076755

DomainStartEndE-ValueType
IGv 34 113 8.44e-11 SMART
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 95.9%
Validation Efficiency 100% (40/40)
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd6 T A 14: 8,045,603 (GRCm38) V173D probably benign Het
Agbl3 G T 6: 34,776,664 (GRCm39) S385I probably damaging Het
Ahcyl2 A G 6: 29,891,260 (GRCm39) I455V probably benign Het
Bpifb2 T A 2: 153,733,871 (GRCm39) D404E probably benign Het
Ctbp1 A G 5: 33,424,389 (GRCm39) probably benign Het
D130040H23Rik T A 8: 69,755,022 (GRCm39) C160S probably damaging Het
Dapk1 T C 13: 60,908,503 (GRCm39) W1039R probably damaging Het
Dock6 T C 9: 21,712,873 (GRCm39) K1995E probably damaging Het
Entpd3 A G 9: 120,391,068 (GRCm39) E440G probably benign Het
Gm20939 G A 17: 95,184,138 (GRCm39) R262K possibly damaging Het
Gm9637 A T 14: 19,402,398 (GRCm38) noncoding transcript Het
Gm9847 T C 12: 14,545,148 (GRCm39) noncoding transcript Het
H2-Q6 A G 17: 35,644,757 (GRCm39) E182G probably damaging Het
Has1 T C 17: 18,067,822 (GRCm39) Y356C probably damaging Het
Hivep2 A G 10: 14,006,101 (GRCm39) T900A probably benign Het
Kcnd3 C T 3: 105,566,082 (GRCm39) A421V probably damaging Het
Klhl35 A G 7: 99,119,448 (GRCm39) D311G probably benign Het
Metap2 A T 10: 93,706,026 (GRCm39) L252* probably null Het
Mrgpra9 T A 7: 46,885,527 (GRCm39) I47F probably damaging Het
Muc5b T C 7: 141,417,863 (GRCm39) L3603P possibly damaging Het
Neurl4 A G 11: 69,794,859 (GRCm39) H323R probably damaging Het
Oas1d A T 5: 121,053,049 (GRCm39) I35F probably damaging Het
Or4c124 G A 2: 89,156,098 (GRCm39) T142M probably benign Het
Or4c12b T A 2: 89,647,395 (GRCm39) S242T probably damaging Het
Or5w18 C T 2: 87,633,396 (GRCm39) S221F possibly damaging Het
Or5w19 T A 2: 87,698,745 (GRCm39) S137T probably damaging Het
Orc6 T A 8: 86,026,613 (GRCm39) S19R probably benign Het
Pcdh12 T C 18: 38,414,290 (GRCm39) E945G probably damaging Het
Plekha6 A G 1: 133,201,717 (GRCm39) M377V probably benign Het
Psmd1 T A 1: 86,060,437 (GRCm39) V828D probably damaging Het
Rbbp5 T C 1: 132,420,325 (GRCm39) V59A probably damaging Het
Secisbp2l C T 2: 125,582,657 (GRCm39) G933D possibly damaging Het
Tas2r130 A G 6: 131,607,792 (GRCm39) M1T probably null Het
Top2b T G 14: 16,409,189 (GRCm38) I777M probably damaging Het
Trpc4ap T A 2: 155,485,355 (GRCm39) I448F probably damaging Het
Ttc21b C T 2: 66,082,577 (GRCm39) probably null Het
Txndc5 T C 13: 38,707,381 (GRCm39) K99E probably benign Het
Uvrag A G 7: 98,628,919 (GRCm39) Y383H probably damaging Het
Vim T C 2: 13,583,563 (GRCm39) probably null Het
Other mutations in Trgv2
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6268:Trgv2 UTSW 13 19,521,001 (GRCm39) missense probably benign 0.30
R6316:Trgv2 UTSW 13 19,520,912 (GRCm39) nonsense probably null
R6968:Trgv2 UTSW 13 19,520,896 (GRCm39) missense probably damaging 1.00
Predicted Primers
Posted On 2017-04-14