Incidental Mutation 'IGL03310:Tcrg-V7'
ID416538
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tcrg-V7
Ensembl Gene ENSMUSG00000076744
Gene NameT cell receptor gamma, variable 7
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock #IGL03310
Quality Score
Status
Chromosome13
Chromosomal Location19178042-19178492 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 19178494 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100334 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103553]
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: 70,778,089 R749C probably damaging Het
Atp9a A G 2: 168,639,959 F872L probably damaging Het
Cacna1e A C 1: 154,442,251 Y1462D probably damaging Het
Ccna1 T C 3: 55,050,620 T7A probably benign Het
Ces1d A G 8: 93,175,188 probably benign Het
Cmtm8 A T 9: 114,790,726 V117D probably benign Het
Cnot1 A G 8: 95,735,680 probably benign Het
Col24a1 A T 3: 145,313,983 probably benign Het
Crispld1 T C 1: 17,745,477 probably benign Het
Dnaja2 A T 8: 85,548,905 N140K probably benign Het
Fktn A T 4: 53,720,120 K6* probably null Het
Fryl C A 5: 73,136,316 probably benign Het
Gm5117 T A 8: 31,738,808 noncoding transcript Het
Gucy2c A C 6: 136,751,046 S319R probably benign Het
Helz2 G A 2: 181,231,804 A2299V probably benign Het
Hivep2 T C 10: 14,143,667 S2061P probably damaging Het
Irx4 A G 13: 73,267,731 N213S possibly damaging Het
Mark3 A G 12: 111,647,670 T649A probably benign Het
Nav3 C T 10: 109,824,572 probably null Het
Npr1 C T 3: 90,455,991 E861K probably benign Het
Olfr1441 T C 19: 12,422,927 V206A probably benign Het
Olfr68 A C 7: 103,777,427 V306G probably benign Het
Pcdhb10 C T 18: 37,412,321 T150I probably damaging Het
Sdk2 A G 11: 113,793,325 C2009R possibly damaging Het
Ttc16 T C 2: 32,762,397 probably benign Het
Ttc39b T A 4: 83,247,659 Y230F probably benign Het
Ubr1 A T 2: 120,864,417 I1678N probably damaging Het
Other mutations in Tcrg-V7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01640:Tcrg-V7 APN 13 19178090 splice site probably benign
IGL02320:Tcrg-V7 APN 13 19178079 missense unknown
IGL03178:Tcrg-V7 APN 13 19178041 utr 5 prime probably benign
R0069:Tcrg-V7 UTSW 13 19178422 missense probably benign 0.19
R3925:Tcrg-V7 UTSW 13 19178474 missense probably damaging 1.00
R5030:Tcrg-V7 UTSW 13 19178388 missense probably damaging 0.97
R5085:Tcrg-V7 UTSW 13 19178428 nonsense probably null
Posted On2016-08-02