Incidental Mutation 'IGL03310:Trgv7'
ID 416538
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Trgv7
Ensembl Gene ENSMUSG00000076744
Gene Name T cell receptor gamma, variable 7
Synonyms Tcrg-V7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL03310
Quality Score
Status
Chromosome 13
Chromosomal Location 19362212-19362662 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 19362664 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100334 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103553]
AlphaFold A0A0A6YYE8
Predicted Effect probably benign
Transcript: ENSMUST00000103553
SMART Domains Protein: ENSMUSP00000100334
Gene: ENSMUSG00000076744

DomainStartEndE-ValueType
low complexity region 2 14 N/A INTRINSIC
IG 26 117 2.19e0 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000197661
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam10 C T 9: 70,685,371 (GRCm39) R749C probably damaging Het
Atp9a A G 2: 168,481,879 (GRCm39) F872L probably damaging Het
Cacna1e A C 1: 154,317,997 (GRCm39) Y1462D probably damaging Het
Ccna1 T C 3: 54,958,041 (GRCm39) T7A probably benign Het
Ces1d A G 8: 93,901,816 (GRCm39) probably benign Het
Cmtm8 A T 9: 114,619,794 (GRCm39) V117D probably benign Het
Cnot1 A G 8: 96,462,308 (GRCm39) probably benign Het
Col24a1 A T 3: 145,019,744 (GRCm39) probably benign Het
Crispld1 T C 1: 17,815,701 (GRCm39) probably benign Het
Dnaja2 A T 8: 86,275,534 (GRCm39) N140K probably benign Het
Fktn A T 4: 53,720,120 (GRCm39) K6* probably null Het
Fryl C A 5: 73,293,659 (GRCm39) probably benign Het
Gm5117 T A 8: 32,228,836 (GRCm39) noncoding transcript Het
Gucy2c A C 6: 136,728,044 (GRCm39) S319R probably benign Het
Helz2 G A 2: 180,873,597 (GRCm39) A2299V probably benign Het
Hivep2 T C 10: 14,019,411 (GRCm39) S2061P probably damaging Het
Irx4 A G 13: 73,415,850 (GRCm39) N213S possibly damaging Het
Mark3 A G 12: 111,614,104 (GRCm39) T649A probably benign Het
Nav3 C T 10: 109,660,433 (GRCm39) probably null Het
Npr1 C T 3: 90,363,298 (GRCm39) E861K probably benign Het
Or52a5 A C 7: 103,426,634 (GRCm39) V306G probably benign Het
Or5a3 T C 19: 12,400,291 (GRCm39) V206A probably benign Het
Pcdhb10 C T 18: 37,545,374 (GRCm39) T150I probably damaging Het
Sdk2 A G 11: 113,684,151 (GRCm39) C2009R possibly damaging Het
Ttc16 T C 2: 32,652,409 (GRCm39) probably benign Het
Ttc39b T A 4: 83,165,896 (GRCm39) Y230F probably benign Het
Ubr1 A T 2: 120,694,898 (GRCm39) I1678N probably damaging Het
Other mutations in Trgv7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01640:Trgv7 APN 13 19,362,260 (GRCm39) splice site probably benign
IGL02320:Trgv7 APN 13 19,362,249 (GRCm39) missense unknown
IGL03178:Trgv7 APN 13 19,362,211 (GRCm39) utr 5 prime probably benign
R0069:Trgv7 UTSW 13 19,362,592 (GRCm39) missense probably benign 0.19
R3925:Trgv7 UTSW 13 19,362,644 (GRCm39) missense probably damaging 1.00
R5030:Trgv7 UTSW 13 19,362,558 (GRCm39) missense probably damaging 0.97
R5085:Trgv7 UTSW 13 19,362,598 (GRCm39) nonsense probably null
R9456:Trgv7 UTSW 13 19,362,385 (GRCm39) nonsense probably null
Posted On 2016-08-02