Incidental Mutation 'R9762:Ttc12'
ID 733082
Institutional Source Beutler Lab
Gene Symbol Ttc12
Ensembl Gene ENSMUSG00000040219
Gene Name tetratricopeptide repeat domain 12
Synonyms E330017O07Rik
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.113) question?
Stock # R9762 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 49348263-49397525 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 49368166 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 287 (F287S)
Ref Sequence ENSEMBL: ENSMUSP00000056378 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055096]
AlphaFold Q8BW49
Predicted Effect probably damaging
Transcript: ENSMUST00000055096
AA Change: F287S

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000056378
Gene: ENSMUSG00000040219
AA Change: F287S

DomainStartEndE-ValueType
coiled coil region 1 29 N/A INTRINSIC
low complexity region 88 102 N/A INTRINSIC
TPR 105 138 9.39e-1 SMART
TPR 139 172 1.97e-3 SMART
TPR 173 206 1.09e-5 SMART
low complexity region 356 368 N/A INTRINSIC
low complexity region 602 613 N/A INTRINSIC
Blast:ARM 634 675 1e-7 BLAST
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.4%
  • 20x: 98.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 81 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim1 G T 19: 57,025,691 (GRCm39) R851S probably damaging Het
Acap2 C A 16: 30,929,763 (GRCm39) A407S probably damaging Het
Adam26a A T 8: 44,021,635 (GRCm39) S618R probably benign Het
Adamtsl5 T C 10: 80,180,896 (GRCm39) Y89C probably damaging Het
Aebp2 T A 6: 140,588,021 (GRCm39) S364T probably damaging Het
Ankfy1 A G 11: 72,621,401 (GRCm39) E229G probably benign Het
Arhgap27 G T 11: 103,251,511 (GRCm39) D72E probably benign Het
Arhgap33 T C 7: 30,230,950 (GRCm39) E191G probably null Het
Atp6v0a1 C T 11: 100,946,427 (GRCm39) H807Y possibly damaging Het
Ccdc113 A C 8: 96,272,605 (GRCm39) E237D probably benign Het
Cd200r2 T A 16: 44,729,420 (GRCm39) I25K probably benign Het
Cd300c2 A G 11: 114,887,775 (GRCm39) V209A probably damaging Het
Cdkn2d T A 9: 21,200,383 (GRCm39) E129D probably benign Het
Cfap251 A G 5: 123,460,533 (GRCm39) Y1165C probably damaging Het
Chd9 A T 8: 91,712,741 (GRCm39) N855Y unknown Het
Cntn3 A G 6: 102,254,196 (GRCm39) C249R probably damaging Het
Col12a1 T C 9: 79,527,266 (GRCm39) E2688G possibly damaging Het
Copb2 C T 9: 98,464,901 (GRCm39) T612I probably benign Het
Cplx1 A T 5: 108,673,378 (GRCm39) D29E possibly damaging Het
Cracd A G 5: 77,006,555 (GRCm39) K972R unknown Het
Cstf3 A T 2: 104,494,684 (GRCm39) R645* probably null Het
Ctdp1 A T 18: 80,492,550 (GRCm39) Y648* probably null Het
Daam1 T A 12: 71,990,855 (GRCm39) D156E unknown Het
Dbn1 G A 13: 55,622,824 (GRCm39) P599L probably damaging Het
Diaph1 C A 18: 37,987,589 (GRCm39) V1056F probably damaging Het
Dzip3 A T 16: 48,748,707 (GRCm39) D870E probably damaging Het
Efcab12 T C 6: 115,800,331 (GRCm39) T231A possibly damaging Het
Efl1 A C 7: 82,412,596 (GRCm39) D995A probably benign Het
Fam186a T C 15: 99,842,393 (GRCm39) T1284A possibly damaging Het
Fbxo33 T C 12: 59,251,708 (GRCm39) E269G probably benign Het
Foxj3 T A 4: 119,483,540 (GRCm39) M604K unknown Het
Gabra4 A G 5: 71,814,463 (GRCm39) S86P unknown Het
Gnas G A 2: 174,140,639 (GRCm39) W269* probably null Het
Gpc6 T G 14: 118,202,258 (GRCm39) N489K probably damaging Het
Gprin3 T C 6: 59,331,236 (GRCm39) K357R possibly damaging Het
Grip1 G T 10: 119,811,906 (GRCm39) A286S possibly damaging Het
Grm4 A T 17: 27,721,688 (GRCm39) V151E probably damaging Het
Gucy1b1 A T 3: 81,942,065 (GRCm39) S565T possibly damaging Het
Hace1 T C 10: 45,525,014 (GRCm39) V260A probably benign Het
Hepacam2 A G 6: 3,486,940 (GRCm39) I139T probably damaging Het
Hspa4l T C 3: 40,727,057 (GRCm39) I486T probably benign Het
Igkv8-19 T C 6: 70,317,866 (GRCm39) Y120C probably damaging Het
Iglv2 C T 16: 19,079,548 (GRCm39) probably benign Het
Igsf10 A T 3: 59,237,106 (GRCm39) L1025H probably damaging Het
Itpkb A G 1: 180,161,752 (GRCm39) N626S probably benign Het
Jarid2 C T 13: 45,068,253 (GRCm39) R1092W possibly damaging Het
Klc3 C T 7: 19,132,023 (GRCm39) W118* probably null Het
Klhl25 C T 7: 75,516,741 (GRCm39) T549I probably damaging Het
Krtap6-2 T A 16: 89,216,763 (GRCm39) Y68F unknown Het
Mtcl1 T C 17: 66,673,347 (GRCm39) N1121D probably benign Het
Ncbp3 A G 11: 72,961,668 (GRCm39) K314R probably benign Het
Nop2 T C 6: 125,121,272 (GRCm39) W685R probably benign Het
Orc1 T A 4: 108,447,874 (GRCm39) D40E probably benign Het
Pappa2 G T 1: 158,684,948 (GRCm39) N730K probably damaging Het
Parpbp A G 10: 87,960,815 (GRCm39) S224P possibly damaging Het
Pdgfc A G 3: 80,944,792 (GRCm39) R17G probably benign Het
Pfpl G C 19: 12,406,297 (GRCm39) E183Q probably damaging Het
Pik3r6 T A 11: 68,424,358 (GRCm39) L321* probably null Het
Pnp2 T C 14: 51,197,006 (GRCm39) W31R probably damaging Het
Prr12 T C 7: 44,696,954 (GRCm39) Y987C unknown Het
Prr27 C A 5: 87,990,994 (GRCm39) P202Q probably benign Het
Prss23 T C 7: 89,159,683 (GRCm39) I129V probably damaging Het
Rhno1 T C 6: 128,336,119 (GRCm39) T39A probably damaging Het
Rps2 A T 17: 24,940,810 (GRCm39) R279* probably null Het
Ski T C 4: 155,244,344 (GRCm39) K427R probably damaging Het
Slc23a3 ATT ATTT 1: 75,109,925 (GRCm39) probably null Het
Slc26a7 C T 4: 14,546,372 (GRCm39) G319D probably damaging Het
Slc7a6os A G 8: 106,937,523 (GRCm39) V8A probably damaging Het
Smim8 A C 4: 34,771,265 (GRCm39) I43S probably damaging Het
Sox5 T C 6: 143,819,842 (GRCm39) K400R probably damaging Het
Tab1 G A 15: 80,032,943 (GRCm39) V76M probably damaging Het
Taf2 A C 15: 54,894,440 (GRCm39) probably null Het
Taf5 G A 19: 47,059,434 (GRCm39) V193M probably damaging Het
Tm2d1 A T 4: 98,246,261 (GRCm39) S180R probably damaging Het
Ubqln4 G A 3: 88,473,185 (GRCm39) probably null Het
Ubr3 T C 2: 69,839,497 (GRCm39) V1537A probably benign Het
Ugt8a A G 3: 125,708,900 (GRCm39) L70P probably damaging Het
Vps26a A T 10: 62,316,433 (GRCm39) N51K probably benign Het
Xkr5 T A 8: 18,990,749 (GRCm39) T173S probably benign Het
Zfp354c A G 11: 50,706,239 (GRCm39) C279R probably damaging Het
Zfp65 T A 13: 67,856,478 (GRCm39) H267L probably damaging Het
Other mutations in Ttc12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00326:Ttc12 APN 9 49,382,506 (GRCm39) splice site probably null
IGL01300:Ttc12 APN 9 49,359,222 (GRCm39) splice site probably benign
IGL02100:Ttc12 APN 9 49,351,482 (GRCm39) missense probably damaging 1.00
IGL03106:Ttc12 APN 9 49,369,362 (GRCm39) missense possibly damaging 0.75
I2288:Ttc12 UTSW 9 49,381,558 (GRCm39) missense possibly damaging 0.62
R1238:Ttc12 UTSW 9 49,369,487 (GRCm39) splice site probably benign
R1712:Ttc12 UTSW 9 49,356,499 (GRCm39) missense probably benign
R1725:Ttc12 UTSW 9 49,369,415 (GRCm39) missense probably benign 0.08
R1824:Ttc12 UTSW 9 49,368,184 (GRCm39) missense probably damaging 1.00
R1916:Ttc12 UTSW 9 49,371,698 (GRCm39) missense probably damaging 1.00
R2226:Ttc12 UTSW 9 49,353,135 (GRCm39) critical splice donor site probably null
R4498:Ttc12 UTSW 9 49,383,705 (GRCm39) missense probably damaging 1.00
R5920:Ttc12 UTSW 9 49,364,633 (GRCm39) missense possibly damaging 0.48
R6020:Ttc12 UTSW 9 49,354,422 (GRCm39) missense probably damaging 0.96
R6687:Ttc12 UTSW 9 49,349,718 (GRCm39) missense probably benign 0.08
R6755:Ttc12 UTSW 9 49,364,646 (GRCm39) missense probably benign 0.00
R6975:Ttc12 UTSW 9 49,349,718 (GRCm39) missense probably benign 0.08
R7349:Ttc12 UTSW 9 49,359,267 (GRCm39) missense possibly damaging 0.94
R7357:Ttc12 UTSW 9 49,349,687 (GRCm39) missense probably benign 0.02
R7451:Ttc12 UTSW 9 49,383,179 (GRCm39) missense probably benign 0.00
R7725:Ttc12 UTSW 9 49,351,602 (GRCm39) missense probably benign 0.00
R7842:Ttc12 UTSW 9 49,349,724 (GRCm39) missense possibly damaging 0.80
R7943:Ttc12 UTSW 9 49,381,620 (GRCm39) missense possibly damaging 0.53
R8029:Ttc12 UTSW 9 49,381,551 (GRCm39) missense possibly damaging 0.83
R8862:Ttc12 UTSW 9 49,351,515 (GRCm39) missense probably benign 0.10
R8965:Ttc12 UTSW 9 49,349,718 (GRCm39) missense probably benign 0.08
R9116:Ttc12 UTSW 9 49,364,757 (GRCm39) missense probably benign
R9342:Ttc12 UTSW 9 49,351,680 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- ATGGTGCAAAAGGCTCTGAG -3'
(R):5'- TCTGAAAGCAACCCACTGAG -3'

Sequencing Primer
(F):5'- TCTGAGCTCAAGGGGGTTCAC -3'
(R):5'- GTGACAGATGACAATTACATTTCTGG -3'
Posted On 2022-11-14