Incidental Mutation 'IGL03163:Trcg1'
ID 411500
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Trcg1
Ensembl Gene ENSMUSG00000070298
Gene Name taste receptor cell gene 1
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL03163
Quality Score
Status
Chromosome 9
Chromosomal Location 57143839-57157147 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 57155630 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 761 (L761P)
Ref Sequence ENSEMBL: ENSMUSP00000091357 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034846] [ENSMUST00000093837]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000034846
SMART Domains Protein: ENSMUSP00000034846
Gene: ENSMUSG00000032300

DomainStartEndE-ValueType
low complexity region 265 284 N/A INTRINSIC
low complexity region 293 299 N/A INTRINSIC
low complexity region 334 347 N/A INTRINSIC
low complexity region 649 675 N/A INTRINSIC
low complexity region 692 728 N/A INTRINSIC
low complexity region 785 799 N/A INTRINSIC
low complexity region 933 951 N/A INTRINSIC
low complexity region 963 977 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000093837
AA Change: L761P

PolyPhen 2 Score 0.924 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000091357
Gene: ENSMUSG00000070298
AA Change: L761P

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 302 335 N/A INTRINSIC
Blast:SEA 449 549 5e-21 BLAST
low complexity region 580 594 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn1 T A 12: 80,228,191 (GRCm39) D393V probably benign Het
Amz2 C A 11: 109,319,751 (GRCm39) Q46K probably benign Het
Ankhd1 G A 18: 36,780,681 (GRCm39) R1911H probably damaging Het
Apba3 A G 10: 81,105,057 (GRCm39) probably null Het
Atxn1l T C 8: 110,459,017 (GRCm39) N415S probably damaging Het
Clu C T 14: 66,217,235 (GRCm39) S356F probably benign Het
Cluh T C 11: 74,556,894 (GRCm39) V1029A probably benign Het
Creb3 C T 4: 43,566,315 (GRCm39) L274F probably damaging Het
Dcaf8 T C 1: 172,000,475 (GRCm39) V211A probably damaging Het
Emilin3 G A 2: 160,750,649 (GRCm39) Q320* probably null Het
Fam131c T C 4: 141,110,069 (GRCm39) F156L probably damaging Het
Fbxw21 T A 9: 108,974,552 (GRCm39) I323F probably benign Het
Fmo9 A G 1: 166,502,019 (GRCm39) V202A possibly damaging Het
Gipr C T 7: 18,896,481 (GRCm39) W205* probably null Het
Gm13941 A T 2: 110,928,761 (GRCm39) I99K unknown Het
Gpr22 A T 12: 31,759,171 (GRCm39) V317E possibly damaging Het
Hace1 T C 10: 45,548,701 (GRCm39) I582T probably damaging Het
Iho1 G T 9: 108,282,132 (GRCm39) L519I probably benign Het
Khdrbs1 T C 4: 129,619,508 (GRCm39) E211G probably benign Het
Lonrf1 T C 8: 36,697,484 (GRCm39) D500G probably benign Het
Lrp2 A C 2: 69,331,870 (GRCm39) Y1628* probably null Het
Lrrc40 T C 3: 157,747,224 (GRCm39) I112T possibly damaging Het
Matr3 G A 18: 35,705,644 (GRCm39) D190N probably damaging Het
Or8c16 T C 9: 38,130,710 (GRCm39) V194A probably benign Het
Ptpn13 A T 5: 103,739,212 (GRCm39) D2326V probably damaging Het
Ptpn3 T C 4: 57,222,020 (GRCm39) D557G probably damaging Het
Rangap1 A T 15: 81,600,801 (GRCm39) N194K probably damaging Het
Rasgef1c T C 11: 49,862,200 (GRCm39) V363A possibly damaging Het
Ric8b A G 10: 84,837,686 (GRCm39) N498D probably damaging Het
Scn1a A C 2: 66,148,418 (GRCm39) D22E probably benign Het
Spc25 T G 2: 69,027,548 (GRCm39) I115L probably damaging Het
Sspo A G 6: 48,461,266 (GRCm39) H3569R probably benign Het
Stra6l T C 4: 45,881,455 (GRCm39) I439T probably benign Het
Trappc12 G T 12: 28,796,653 (GRCm39) P293Q probably damaging Het
Usp15 A C 10: 123,007,049 (GRCm39) M144R probably damaging Het
Vmn2r11 T C 5: 109,201,692 (GRCm39) I271V probably benign Het
Zcchc2 T C 1: 105,958,841 (GRCm39) V1104A probably damaging Het
Zftraf1 A T 15: 76,543,474 (GRCm39) L13Q probably damaging Het
Other mutations in Trcg1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01727:Trcg1 APN 9 57,149,877 (GRCm39) missense probably damaging 0.97
IGL01727:Trcg1 APN 9 57,149,556 (GRCm39) missense probably benign
IGL02147:Trcg1 APN 9 57,153,132 (GRCm39) missense probably benign 0.20
IGL02329:Trcg1 APN 9 57,147,676 (GRCm39) missense possibly damaging 0.92
IGL02658:Trcg1 APN 9 57,149,511 (GRCm39) nonsense probably null
IGL02852:Trcg1 APN 9 57,148,595 (GRCm39) missense possibly damaging 0.94
FR4589:Trcg1 UTSW 9 57,149,485 (GRCm39) frame shift probably null
R0555:Trcg1 UTSW 9 57,149,616 (GRCm39) missense probably damaging 1.00
R0747:Trcg1 UTSW 9 57,149,204 (GRCm39) missense probably benign 0.00
R1061:Trcg1 UTSW 9 57,153,156 (GRCm39) missense possibly damaging 0.66
R1521:Trcg1 UTSW 9 57,149,748 (GRCm39) missense probably benign 0.36
R1622:Trcg1 UTSW 9 57,155,955 (GRCm39) missense possibly damaging 0.94
R1652:Trcg1 UTSW 9 57,152,856 (GRCm39) missense probably damaging 0.99
R4677:Trcg1 UTSW 9 57,153,144 (GRCm39) missense possibly damaging 0.94
R4879:Trcg1 UTSW 9 57,154,003 (GRCm39) missense probably damaging 0.99
R5013:Trcg1 UTSW 9 57,149,562 (GRCm39) missense probably damaging 0.99
R5141:Trcg1 UTSW 9 57,148,587 (GRCm39) missense probably damaging 1.00
R5690:Trcg1 UTSW 9 57,149,094 (GRCm39) missense probably benign 0.36
R6416:Trcg1 UTSW 9 57,148,613 (GRCm39) missense possibly damaging 0.46
R6980:Trcg1 UTSW 9 57,152,856 (GRCm39) missense probably damaging 0.99
R7022:Trcg1 UTSW 9 57,148,852 (GRCm39) missense possibly damaging 0.46
R7172:Trcg1 UTSW 9 57,155,618 (GRCm39) missense probably benign 0.01
R7276:Trcg1 UTSW 9 57,149,862 (GRCm39) missense probably damaging 0.99
R7412:Trcg1 UTSW 9 57,148,766 (GRCm39) missense probably benign 0.00
R7546:Trcg1 UTSW 9 57,155,621 (GRCm39) missense probably benign 0.34
R7942:Trcg1 UTSW 9 57,149,499 (GRCm39) missense probably benign
R8087:Trcg1 UTSW 9 57,155,957 (GRCm39) missense probably damaging 0.99
R8094:Trcg1 UTSW 9 57,149,564 (GRCm39) missense probably benign 0.01
R8825:Trcg1 UTSW 9 57,148,754 (GRCm39) missense probably benign 0.19
Posted On 2016-08-02