Incidental Mutation 'IGL03059:Trgc1'
ID 409358
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Trgc1
Ensembl Gene ENSMUSG00000076749
Gene Name T cell receptor gamma, constant 1
Synonyms Cgamma1, Tcrg-C1, Gm17004
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # IGL03059
Quality Score
Status
Chromosome 13
Chromosomal Location 19398273-19400788 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 19400072 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 123 (K123*)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000103558
AA Change: K123*
SMART Domains Protein: ENSMUSP00000100338
Gene: ENSMUSG00000076749
AA Change: K123*

DomainStartEndE-ValueType
IGc1 27 98 1.35e-18 SMART
transmembrane domain 138 160 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous null mice lack dendritic epidermal T cells. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahsg T C 16: 22,717,755 (GRCm39) V244A possibly damaging Het
Aoc1l3 A T 6: 48,964,349 (GRCm39) Y119F probably benign Het
Ccdc187 C A 2: 26,184,253 (GRCm39) R48M probably null Het
Cnga2 G A X: 71,051,878 (GRCm39) R251H probably damaging Het
Cop1 A C 1: 159,134,279 (GRCm39) K174Q probably damaging Het
Cul9 T C 17: 46,849,913 (GRCm39) D512G probably damaging Het
Flt4 G A 11: 49,533,134 (GRCm39) A1140T probably damaging Het
Galnt3 C T 2: 65,923,954 (GRCm39) R438H probably damaging Het
Gatm G A 2: 122,440,181 (GRCm39) A86V probably damaging Het
Klhl28 C T 12: 64,998,340 (GRCm39) A385T probably benign Het
Klhl40 T A 9: 121,607,203 (GRCm39) V121E probably damaging Het
L1cam T A X: 72,910,630 (GRCm39) H30L probably benign Het
Lss A T 10: 76,367,860 (GRCm39) probably benign Het
Mrnip A T 11: 50,090,596 (GRCm39) Q253H probably damaging Het
Mroh9 A T 1: 162,852,205 (GRCm39) F828Y possibly damaging Het
Mst1 T C 9: 107,962,012 (GRCm39) C668R probably damaging Het
Nadk A G 4: 155,671,253 (GRCm39) E143G probably benign Het
Nap1l4 C T 7: 143,080,902 (GRCm39) probably null Het
Nme8 A G 13: 19,836,414 (GRCm39) I254T possibly damaging Het
Or14c41 A G 7: 86,234,779 (GRCm39) I99V probably benign Het
Or1ab2 T A 8: 72,863,842 (GRCm39) L144Q probably damaging Het
Or2y12 A G 11: 49,426,021 (GRCm39) Y3C probably benign Het
Pkd1l2 G A 8: 117,792,484 (GRCm39) T436I probably benign Het
Pkd1l3 C T 8: 110,374,999 (GRCm39) L1491F probably damaging Het
Plec G T 15: 76,059,968 (GRCm39) T3488N probably damaging Het
Plk2 T G 13: 110,535,668 (GRCm39) S497A probably benign Het
Polr1a G A 6: 71,913,496 (GRCm39) V617I probably benign Het
Prelid3a C A 18: 67,609,909 (GRCm39) Y112* probably null Het
Rnf113a2 C A 12: 84,464,250 (GRCm39) S47R possibly damaging Het
Rtel1 A G 2: 180,991,976 (GRCm39) N410D probably benign Het
Ryr3 C T 2: 112,630,392 (GRCm39) A2140T probably damaging Het
Slc22a29 A G 19: 8,147,354 (GRCm39) L336P probably benign Het
Sphkap T A 1: 83,234,963 (GRCm39) Q1621L probably damaging Het
Ttn T A 2: 76,739,863 (GRCm39) S3559C probably benign Het
Ubr4 C T 4: 139,207,987 (GRCm39) R4923W probably damaging Het
Vac14 T C 8: 111,437,084 (GRCm39) L599P probably damaging Het
Wdr5 T C 2: 27,409,746 (GRCm39) probably benign Het
Other mutations in Trgc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03027:Trgc1 APN 13 19,398,563 (GRCm39) nonsense probably null
IGL03307:Trgc1 APN 13 19,398,528 (GRCm39) unclassified probably benign
R5687:Trgc1 UTSW 13 19,400,729 (GRCm39) missense unknown
R6786:Trgc1 UTSW 13 19,400,646 (GRCm39) missense unknown
R7840:Trgc1 UTSW 13 19,400,691 (GRCm39) missense
R8166:Trgc1 UTSW 13 19,400,772 (GRCm39) missense
Posted On 2016-08-02