Incidental Mutation 'R6719:Trgj2'
ID 529506
Institutional Source Beutler Lab
Gene Symbol Trgj2
Ensembl Gene ENSMUSG00000105830
Gene Name T cell receptor gamma joining 2
Synonyms Gm16674
MMRRC Submission 044837-MU
Accession Numbers
Essential gene? Not available question?
Stock # R6719 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 19495415-19495474 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 19495426 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000103561
SMART Domains Protein: ENSMUSP00000100340
Gene: ENSMUSG00000076752

DomainStartEndE-ValueType
IGc1 27 98 9.03e-20 SMART
transmembrane domain 133 155 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000197113
AA Change: V16A
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.4%
  • 20x: 95.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933411K16Rik T C 19: 42,041,151 (GRCm39) I94T possibly damaging Het
Afp T A 5: 90,651,562 (GRCm39) N392K probably benign Het
Asrgl1 C T 19: 9,090,512 (GRCm39) G278D probably damaging Het
Atp2c1 T C 9: 105,301,377 (GRCm39) I611V probably damaging Het
Avl9 A G 6: 56,730,370 (GRCm39) Y571C probably damaging Het
Clrn1 A T 3: 58,753,861 (GRCm39) C167S probably damaging Het
Ctsr C T 13: 61,308,265 (GRCm39) G293D possibly damaging Het
Dmbt1 T A 7: 130,721,332 (GRCm39) S1867T possibly damaging Het
Dock9 A T 14: 121,847,439 (GRCm39) I1025N probably damaging Het
Dppa4 G A 16: 48,108,247 (GRCm39) A11T probably damaging Het
Duox2 T A 2: 122,114,867 (GRCm39) probably null Het
Fat3 A G 9: 15,907,440 (GRCm39) L2854P probably benign Het
Fcer1a A G 1: 173,050,340 (GRCm39) S61P possibly damaging Het
Fyb2 A T 4: 104,867,656 (GRCm39) D669V probably benign Het
Herc2 G T 7: 55,862,574 (GRCm39) C4081F probably damaging Het
Hexim1 T C 11: 103,008,091 (GRCm39) L115P probably benign Het
Kat2a T G 11: 100,602,967 (GRCm39) Q88H probably benign Het
Lrriq1 T C 10: 102,906,977 (GRCm39) Y1581C probably damaging Het
Ltbp4 T G 7: 27,028,188 (GRCm39) D323A probably damaging Het
Mark3 T A 12: 111,581,876 (GRCm39) I115K probably damaging Het
Nudt9 A G 5: 104,209,562 (GRCm39) D271G probably damaging Het
Or2a54 T A 6: 43,092,907 (GRCm39) V77D probably damaging Het
Parvb C T 15: 84,182,180 (GRCm39) R237W probably damaging Het
Pcdha5 T C 18: 37,093,925 (GRCm39) S145P probably damaging Het
Pzp T C 6: 128,501,046 (GRCm39) E104G probably benign Het
Rho T C 6: 115,910,854 (GRCm39) I133T possibly damaging Het
Sall3 G T 18: 81,014,721 (GRCm39) T997K probably damaging Het
Scn8a A T 15: 100,908,896 (GRCm39) probably null Het
Sfxn1 T A 13: 54,260,583 (GRCm39) H310Q probably benign Het
Slc25a18 A G 6: 120,765,215 (GRCm39) D92G probably damaging Het
Slc26a9 T C 1: 131,689,523 (GRCm39) I490T probably benign Het
Terf1 T C 1: 15,908,460 (GRCm39) V351A probably benign Het
Thsd7b A G 1: 130,087,451 (GRCm39) probably null Het
Tti1 A T 2: 157,824,220 (GRCm39) C1078S probably benign Het
Ttll3 A G 6: 113,375,993 (GRCm39) probably benign Het
Tubb1 A C 2: 174,299,187 (GRCm39) T290P probably damaging Het
Ugt2b35 G T 5: 87,155,247 (GRCm39) D361Y probably damaging Het
Zc2hc1c T C 12: 85,337,446 (GRCm39) S368P probably damaging Het
Predicted Primers PCR Primer
(F):5'- TGAGGACTCACACTCAAATTGC -3'
(R):5'- ACTCCAGGGAGAACATTGTATGAG -3'

Sequencing Primer
(F):5'- GGACTCACACTCAAATTGCTTTCAC -3'
(R):5'- ATTGCAAGATATCAGATACCACATG -3'
Posted On 2018-08-01