Incidental Mutation 'IGL02852:Ttc23'
ID 361959
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ttc23
Ensembl Gene ENSMUSG00000030555
Gene Name tetratricopeptide repeat domain 23
Synonyms 1600012K10Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL02852
Quality Score
Status
Chromosome 7
Chromosomal Location 67295180-67378370 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 67316903 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000032774] [ENSMUST00000107470] [ENSMUST00000107471]
AlphaFold Q8CHY7
Predicted Effect probably benign
Transcript: ENSMUST00000032774
SMART Domains Protein: ENSMUSP00000032774
Gene: ENSMUSG00000030555

DomainStartEndE-ValueType
Blast:TPR 45 78 5e-10 BLAST
SCOP:d1a17__ 50 214 6e-8 SMART
Blast:TPR 87 121 3e-10 BLAST
Blast:TPR 137 170 3e-8 BLAST
Blast:TPR 186 219 1e-6 BLAST
low complexity region 310 323 N/A INTRINSIC
Blast:TPR 398 431 5e-8 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000107470
SMART Domains Protein: ENSMUSP00000103094
Gene: ENSMUSG00000030555

DomainStartEndE-ValueType
Blast:TPR 45 78 4e-10 BLAST
Blast:TPR 87 121 2e-10 BLAST
Blast:TPR 137 170 3e-8 BLAST
Pfam:TPR_12 185 257 5.9e-10 PFAM
low complexity region 268 281 N/A INTRINSIC
Blast:TPR 356 389 5e-8 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000107471
SMART Domains Protein: ENSMUSP00000103095
Gene: ENSMUSG00000030555

DomainStartEndE-ValueType
Blast:TPR 45 78 4e-10 BLAST
Blast:TPR 87 121 2e-10 BLAST
Blast:TPR 137 170 3e-8 BLAST
Pfam:TPR_12 185 257 5.9e-10 PFAM
low complexity region 268 281 N/A INTRINSIC
Blast:TPR 356 389 5e-8 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126093
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130681
Predicted Effect noncoding transcript
Transcript: ENSMUST00000133710
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153475
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145348
Predicted Effect probably benign
Transcript: ENSMUST00000208764
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155024
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bcar1 A T 8: 112,441,979 (GRCm39) L287* probably null Het
Birc2 A G 9: 7,854,484 (GRCm39) I402T probably damaging Het
Btrc T A 19: 45,501,095 (GRCm39) L153* probably null Het
C2cd3 T C 7: 100,079,396 (GRCm39) F1245L probably damaging Het
Cabp7 C T 11: 4,688,912 (GRCm39) R186H probably damaging Het
Cdk5r2 T C 1: 74,895,298 (GRCm39) S348P probably benign Het
Cfhr4 T C 1: 139,701,754 (GRCm39) Y120C probably damaging Het
Clca3a2 T C 3: 144,512,104 (GRCm39) D544G probably damaging Het
Col6a6 A C 9: 105,661,272 (GRCm39) I279S probably damaging Het
Csmd1 T A 8: 15,945,728 (GRCm39) T3562S probably damaging Het
Dgkd T C 1: 87,863,135 (GRCm39) S61P probably damaging Het
Dph5 T A 3: 115,722,320 (GRCm39) M266K possibly damaging Het
Gm14226 G A 2: 154,866,841 (GRCm39) S266N possibly damaging Het
Gm28047 A G 15: 102,446,653 (GRCm39) V400A possibly damaging Het
Gucy1a2 A G 9: 3,759,691 (GRCm39) D499G probably benign Het
Hoxb7 C T 11: 96,180,320 (GRCm39) T173M possibly damaging Het
Kcnn3 T A 3: 89,516,923 (GRCm39) I444N probably damaging Het
Kif1b A G 4: 149,375,785 (GRCm39) I27T probably damaging Het
Krtap8-1 A G 16: 89,284,753 (GRCm39) Y15H probably benign Het
Myo18b C T 5: 112,863,377 (GRCm39) V2154I probably benign Het
Pcdhb3 A G 18: 37,435,150 (GRCm39) D372G probably damaging Het
Pfkp G T 13: 6,655,059 (GRCm39) P340Q possibly damaging Het
Plcd3 C T 11: 102,964,631 (GRCm39) R580Q probably damaging Het
Pou5f2 G A 13: 78,173,178 (GRCm39) R40Q probably benign Het
Ppara G T 15: 85,682,079 (GRCm39) M258I probably benign Het
Proc A G 18: 32,258,208 (GRCm39) S246P probably damaging Het
Ptpn21 T C 12: 98,681,454 (GRCm39) probably null Het
Ripor2 T C 13: 24,879,681 (GRCm39) F383S probably damaging Het
Rnf39 T C 17: 37,256,094 (GRCm39) probably benign Het
Sema6c C A 3: 95,077,295 (GRCm39) probably benign Het
Slc16a5 A G 11: 115,360,405 (GRCm39) E196G probably benign Het
Slco1c1 T A 6: 141,493,550 (GRCm39) L313* probably null Het
Slit2 T C 5: 48,402,014 (GRCm39) F789S probably damaging Het
Spta1 A G 1: 174,071,676 (GRCm39) M2219V probably benign Het
Sqle A T 15: 59,197,920 (GRCm39) H380L probably damaging Het
Tek T C 4: 94,743,561 (GRCm39) Y859H probably damaging Het
Trcg1 A T 9: 57,148,595 (GRCm39) T56S possibly damaging Het
Ttn A G 2: 76,774,648 (GRCm39) probably benign Het
Uba1y C T Y: 828,841 (GRCm39) R550* probably null Het
Ubqln4 T C 3: 88,462,778 (GRCm39) V81A probably damaging Het
Ugt2b38 C T 5: 87,559,600 (GRCm39) E431K probably benign Het
Vmn1r85 T G 7: 12,819,010 (GRCm39) I45L possibly damaging Het
Vmn2r68 T G 7: 84,882,595 (GRCm39) S386R probably damaging Het
Washc4 A G 10: 83,419,173 (GRCm39) T902A possibly damaging Het
Zc3h15 G A 2: 83,475,015 (GRCm39) A7T possibly damaging Het
Zdhhc19 A C 16: 32,316,460 (GRCm39) T72P probably damaging Het
Zfp729a A T 13: 67,768,070 (GRCm39) S720T possibly damaging Het
Zfp729b T C 13: 67,740,942 (GRCm39) K441R probably damaging Het
Zfy2 C T Y: 2,106,894 (GRCm39) G580D probably benign Het
Zfy2 T A Y: 2,117,188 (GRCm39) H213L probably benign Het
Other mutations in Ttc23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03257:Ttc23 APN 7 67,361,126 (GRCm39) missense probably damaging 1.00
IGL03365:Ttc23 APN 7 67,312,085 (GRCm39) utr 5 prime probably benign
IGL03404:Ttc23 APN 7 67,328,645 (GRCm39) missense probably damaging 0.99
F5770:Ttc23 UTSW 7 67,359,063 (GRCm39) splice site probably benign
PIT4445001:Ttc23 UTSW 7 67,316,961 (GRCm39) missense probably damaging 1.00
PIT4791001:Ttc23 UTSW 7 67,312,135 (GRCm39) missense probably damaging 1.00
R0295:Ttc23 UTSW 7 67,319,600 (GRCm39) unclassified probably benign
R0316:Ttc23 UTSW 7 67,328,821 (GRCm39) critical splice donor site probably null
R0336:Ttc23 UTSW 7 67,312,231 (GRCm39) missense probably benign 0.01
R1456:Ttc23 UTSW 7 67,316,902 (GRCm39) unclassified probably benign
R1543:Ttc23 UTSW 7 67,328,743 (GRCm39) missense probably benign 0.01
R1662:Ttc23 UTSW 7 67,375,069 (GRCm39) splice site probably null
R1708:Ttc23 UTSW 7 67,316,924 (GRCm39) missense probably damaging 0.99
R1857:Ttc23 UTSW 7 67,328,821 (GRCm39) critical splice donor site probably null
R2292:Ttc23 UTSW 7 67,319,535 (GRCm39) missense probably benign 0.08
R4471:Ttc23 UTSW 7 67,319,904 (GRCm39) missense probably benign 0.37
R6036:Ttc23 UTSW 7 67,361,114 (GRCm39) missense possibly damaging 0.85
R6036:Ttc23 UTSW 7 67,361,114 (GRCm39) missense possibly damaging 0.85
R6841:Ttc23 UTSW 7 67,319,476 (GRCm39) missense possibly damaging 0.91
R7690:Ttc23 UTSW 7 67,319,918 (GRCm39) missense possibly damaging 0.76
R8305:Ttc23 UTSW 7 67,312,135 (GRCm39) missense probably damaging 0.99
R8837:Ttc23 UTSW 7 67,319,494 (GRCm39) missense probably damaging 1.00
R8902:Ttc23 UTSW 7 67,342,761 (GRCm39) missense
R9052:Ttc23 UTSW 7 67,342,687 (GRCm39) nonsense probably null
R9150:Ttc23 UTSW 7 67,375,850 (GRCm39) missense probably damaging 0.99
RF009:Ttc23 UTSW 7 67,375,777 (GRCm39) missense possibly damaging 0.61
X0021:Ttc23 UTSW 7 67,319,879 (GRCm39) missense probably damaging 1.00
Posted On 2015-12-18