Incidental Mutation 'IGL02225:Trbv20'
ID 285327
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Trbv20
Ensembl Gene ENSMUSG00000076476
Gene Name T cell receptor beta, variable 20
Synonyms Gm16911, Tcrb-V15
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL02225
Quality Score
Status
Chromosome 6
Chromosomal Location 41165207-41165911 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 41165241 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100093 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103277]
AlphaFold A0A0B4J1H5
Predicted Effect probably benign
Transcript: ENSMUST00000103277
SMART Domains Protein: ENSMUSP00000100093
Gene: ENSMUSG00000076476

DomainStartEndE-ValueType
Pfam:V-set 15 111 8e-11 PFAM
Pfam:I-set 17 111 1.8e-7 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp4 A G 7: 43,906,165 (GRCm39) probably null Het
Adgrf4 C A 17: 42,974,269 (GRCm39) probably null Het
Aqp9 A T 9: 71,037,829 (GRCm39) probably benign Het
C1s1 A G 6: 124,518,293 (GRCm39) W8R probably benign Het
Cep43 T G 17: 8,401,251 (GRCm39) D257E probably damaging Het
Cfap43 A G 19: 47,800,616 (GRCm39) I345T probably benign Het
Cwh43 T C 5: 73,578,910 (GRCm39) Y306H probably damaging Het
Cyp4a32 A T 4: 115,467,700 (GRCm39) H228L probably benign Het
Ddx24 A G 12: 103,383,630 (GRCm39) L607P probably damaging Het
Dlg3 A G X: 99,850,794 (GRCm39) K232R probably benign Het
Fig4 A G 10: 41,132,448 (GRCm39) S453P probably benign Het
Frem1 A G 4: 82,858,743 (GRCm39) L1556P probably damaging Het
Gjb2 T C 14: 57,337,645 (GRCm39) K188E probably damaging Het
Gp1bb C A 16: 18,439,650 (GRCm39) W148L possibly damaging Het
Grip1 C T 10: 119,885,358 (GRCm39) T375M probably damaging Het
Hnf1b T C 11: 83,752,611 (GRCm39) L82P probably damaging Het
Jakmip1 T C 5: 37,262,200 (GRCm39) V333A probably damaging Het
Magi1 G T 6: 93,671,007 (GRCm39) R1069S probably damaging Het
Myh15 A T 16: 48,911,526 (GRCm39) E319D probably benign Het
Myl4 A G 11: 104,471,228 (GRCm39) I42V probably benign Het
Obsl1 A T 1: 75,480,442 (GRCm39) V394E probably damaging Het
Or1e1c T A 11: 73,265,904 (GRCm39) F110I probably damaging Het
Or52ab7 A T 7: 102,978,373 (GRCm39) I227F probably damaging Het
Or5w14 C T 2: 87,541,743 (GRCm39) C169Y possibly damaging Het
Pcnt C T 10: 76,225,308 (GRCm39) R1732K probably benign Het
Pkd1l3 T C 8: 110,365,310 (GRCm39) Y1144H probably damaging Het
Pogz A G 3: 94,786,327 (GRCm39) K972E probably damaging Het
Sccpdh A G 1: 179,507,264 (GRCm39) T227A probably benign Het
Sec16b A G 1: 157,359,614 (GRCm39) probably benign Het
Slain2 T A 5: 73,098,733 (GRCm39) V163E probably damaging Het
Snx1 G A 9: 66,016,903 (GRCm39) P56L probably benign Het
Snx14 G A 9: 88,295,577 (GRCm39) T196I probably damaging Het
Sspo T C 6: 48,461,268 (GRCm39) F3570L probably benign Het
Tbrg4 C A 11: 6,574,094 (GRCm39) V43F probably damaging Het
Traf3ip3 A G 1: 192,877,408 (GRCm39) I176T probably benign Het
Ubc A T 5: 125,463,197 (GRCm39) V710D probably benign Het
Ugt2b35 T C 5: 87,155,264 (GRCm39) probably benign Het
Zbed5 C T 5: 129,930,974 (GRCm39) probably null Het
Zc3hav1 T C 6: 38,317,276 (GRCm39) Y108C probably damaging Het
Other mutations in Trbv20
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02451:Trbv20 APN 6 41,165,210 (GRCm39) missense unknown
IGL03161:Trbv20 APN 6 41,165,757 (GRCm39) missense probably benign 0.44
R4060:Trbv20 UTSW 6 41,165,195 (GRCm39) unclassified probably benign
R5789:Trbv20 UTSW 6 41,165,725 (GRCm39) missense probably damaging 1.00
R6245:Trbv20 UTSW 6 41,165,840 (GRCm39) missense possibly damaging 0.87
R7556:Trbv20 UTSW 6 41,165,715 (GRCm39) missense probably benign 0.10
R8284:Trbv20 UTSW 6 41,165,782 (GRCm39) missense probably damaging 0.97
R8440:Trbv20 UTSW 6 41,165,892 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16