Incidental Mutation 'R1467:Ttc28'
ID 500248
Institutional Source Beutler Lab
Gene Symbol Ttc28
Ensembl Gene ENSMUSG00000033209
Gene Name tetratricopeptide repeat domain 28
Synonyms TPRBK, 2310015L07Rik
MMRRC Submission 039520-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1467 (G1)
Quality Score 225
Status Not validated
Chromosome 5
Chromosomal Location 111027669-111437646 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 111433254 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Arginine at position 2096 (Q2096R)
Ref Sequence ENSEMBL: ENSMUSP00000136116 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040111] [ENSMUST00000156290]
AlphaFold Q80XJ3
Predicted Effect probably benign
Transcript: ENSMUST00000040111
AA Change: Q2096R

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000136116
Gene: ENSMUSG00000033209
AA Change: Q2096R

DomainStartEndE-ValueType
low complexity region 4 28 N/A INTRINSIC
TPR 52 85 2.84e1 SMART
TPR 86 119 5.03e-1 SMART
TPR 120 153 2.11e-3 SMART
TPR 268 301 8.51e0 SMART
TPR 339 372 1.78e-1 SMART
TPR 379 412 2.82e-4 SMART
TPR 419 452 9.98e-5 SMART
TPR 459 492 1.88e0 SMART
TPR 499 532 1.11e1 SMART
TPR 539 572 2.93e-2 SMART
TPR 579 612 1.21e-3 SMART
TPR 619 652 4.91e-4 SMART
TPR 659 692 7.56e-5 SMART
TPR 699 732 8.29e0 SMART
TPR 739 772 1.63e0 SMART
TPR 779 812 1.24e0 SMART
TPR 819 852 7.98e-4 SMART
TPR 859 892 8.74e0 SMART
TPR 902 935 5.43e-6 SMART
TPR 942 975 4.09e-1 SMART
TPR 982 1015 9.98e-5 SMART
TPR 1022 1055 7.12e-1 SMART
TPR 1062 1095 5.69e0 SMART
TPR 1102 1135 3.14e-2 SMART
TPR 1142 1175 2.84e1 SMART
low complexity region 1259 1277 N/A INTRINSIC
Pfam:CHAT 1415 1738 7.3e-77 PFAM
low complexity region 1972 1990 N/A INTRINSIC
low complexity region 2014 2031 N/A INTRINSIC
low complexity region 2033 2045 N/A INTRINSIC
low complexity region 2155 2171 N/A INTRINSIC
low complexity region 2283 2293 N/A INTRINSIC
low complexity region 2327 2352 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000156290
AA Change: Q2065R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000137609
Gene: ENSMUSG00000033209
AA Change: Q2065R

DomainStartEndE-ValueType
low complexity region 4 28 N/A INTRINSIC
TPR 52 85 2.84e1 SMART
TPR 86 119 5.03e-1 SMART
TPR 120 153 2.11e-3 SMART
TPR 268 301 8.51e0 SMART
TPR 308 341 1.78e-1 SMART
TPR 348 381 2.82e-4 SMART
TPR 388 421 9.98e-5 SMART
TPR 428 461 1.88e0 SMART
TPR 468 501 1.11e1 SMART
TPR 508 541 2.93e-2 SMART
TPR 548 581 1.21e-3 SMART
TPR 588 621 4.91e-4 SMART
TPR 628 661 7.56e-5 SMART
TPR 668 701 8.29e0 SMART
TPR 708 741 1.63e0 SMART
TPR 748 781 1.24e0 SMART
TPR 788 821 7.98e-4 SMART
TPR 828 861 8.74e0 SMART
TPR 871 904 5.43e-6 SMART
TPR 911 944 4.09e-1 SMART
TPR 951 984 9.98e-5 SMART
TPR 991 1024 7.12e-1 SMART
TPR 1031 1064 5.69e0 SMART
TPR 1071 1104 3.14e-2 SMART
TPR 1111 1144 2.84e1 SMART
low complexity region 1228 1246 N/A INTRINSIC
Pfam:CHAT 1384 1707 1.1e-76 PFAM
low complexity region 1941 1959 N/A INTRINSIC
low complexity region 1983 2000 N/A INTRINSIC
low complexity region 2002 2014 N/A INTRINSIC
low complexity region 2124 2140 N/A INTRINSIC
low complexity region 2252 2262 N/A INTRINSIC
low complexity region 2296 2321 N/A INTRINSIC
Meta Mutation Damage Score 0.0603 question?
Coding Region Coverage
  • 1x: 99.6%
  • 3x: 98.1%
  • 10x: 88.5%
  • 20x: 62.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 98 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010315B03Rik C A 9: 124,058,093 (GRCm39) V9L possibly damaging Het
A630010A05Rik C A 16: 14,436,447 (GRCm39) L167I possibly damaging Het
Abca14 A T 7: 119,815,405 (GRCm39) M218L possibly damaging Het
Abca15 C A 7: 119,939,761 (GRCm39) probably null Het
Acod1 T C 14: 103,292,003 (GRCm39) F176L probably benign Het
Actr5 A G 2: 158,480,617 (GRCm39) H545R probably benign Het
Adcy1 A G 11: 7,088,396 (GRCm39) T472A probably damaging Het
Aldh1l1 A G 6: 90,548,910 (GRCm39) K469R possibly damaging Het
Ambra1 A T 2: 91,716,048 (GRCm39) Q853L probably damaging Het
Apol7e G T 15: 77,601,966 (GRCm39) G188V probably damaging Het
AU018091 A T 7: 3,214,089 (GRCm39) W43R probably benign Het
Baat A G 4: 49,503,101 (GRCm39) V7A probably benign Het
Bcas1 C A 2: 170,229,852 (GRCm39) Q249H possibly damaging Het
Bltp1 T A 3: 37,090,094 (GRCm39) V676D probably damaging Het
Bptf G T 11: 106,945,881 (GRCm39) Q2453K possibly damaging Het
Btg3 A G 16: 78,161,688 (GRCm39) probably null Het
Cacna2d3 T C 14: 29,055,736 (GRCm39) N298S possibly damaging Het
Carf G A 1: 60,167,152 (GRCm39) V127I possibly damaging Het
Catsperg1 T C 7: 28,884,433 (GRCm39) S916G probably damaging Het
Cers1 T C 8: 70,775,819 (GRCm39) S274P possibly damaging Het
Ces4a T A 8: 105,864,667 (GRCm39) V48E possibly damaging Het
Cfap54 T A 10: 92,805,625 (GRCm39) H1495L probably benign Het
Cntnap5a T A 1: 115,612,898 (GRCm39) L11* probably null Het
Cr2 C T 1: 194,839,817 (GRCm39) G913R probably damaging Het
Cul9 A G 17: 46,836,299 (GRCm39) L1155P probably damaging Het
Dlec1 A T 9: 118,971,646 (GRCm39) D1278V probably damaging Het
Dmrt2 A G 19: 25,650,970 (GRCm39) E52G possibly damaging Het
Dsp A G 13: 38,376,688 (GRCm39) K1491R probably benign Het
Ecpas A G 4: 58,832,753 (GRCm39) V869A probably benign Het
Eef1d A T 15: 75,767,770 (GRCm39) D206E probably damaging Het
Erbb2 C T 11: 98,327,001 (GRCm39) Q1137* probably null Het
Ercc2 T A 7: 19,119,811 (GRCm39) D157E probably benign Het
Eri1 A G 8: 35,936,284 (GRCm39) *346Q probably null Het
Espl1 A G 15: 102,228,293 (GRCm39) E1689G probably benign Het
Fap C T 2: 62,347,964 (GRCm39) V539I probably benign Het
Fasn A G 11: 120,701,866 (GRCm39) F1871S probably benign Het
Gabpb1 T G 2: 126,494,247 (GRCm39) Y126S probably damaging Het
Grm1 T C 10: 10,595,702 (GRCm39) Y642C probably damaging Het
Heatr4 T C 12: 84,024,841 (GRCm39) T327A possibly damaging Het
Hmbox1 T C 14: 65,099,027 (GRCm39) D212G possibly damaging Het
Hmcn1 T A 1: 150,565,341 (GRCm39) D2262V probably damaging Het
Hoxb9 A G 11: 96,162,764 (GRCm39) T133A probably benign Het
Insr A T 8: 3,219,720 (GRCm39) V934E probably damaging Het
Ipo9 T C 1: 135,334,281 (GRCm39) E315G possibly damaging Het
Itga10 C T 3: 96,559,545 (GRCm39) Q481* probably null Het
Kntc1 T A 5: 123,925,047 (GRCm39) M1120K probably benign Het
Krt78 A G 15: 101,854,728 (GRCm39) Y1028H possibly damaging Het
Lrrc38 A T 4: 143,096,450 (GRCm39) I254F probably damaging Het
Lyrm7 A G 11: 54,741,215 (GRCm39) F40L probably damaging Het
Mfsd4b1 C T 10: 39,878,631 (GRCm39) S422N possibly damaging Het
Mlh3 A T 12: 85,284,374 (GRCm39) L1380* probably null Het
Mrpl24 C A 3: 87,829,744 (GRCm39) A110D probably benign Het
Mrps14 T C 1: 160,024,520 (GRCm39) V17A probably benign Het
Mtcl1 T C 17: 66,755,322 (GRCm39) D340G probably damaging Het
Neb T C 2: 52,120,059 (GRCm39) Y3900C probably damaging Het
Neurod4 T C 10: 130,106,473 (GRCm39) D267G probably benign Het
Nf1 A T 11: 79,319,452 (GRCm39) I536F possibly damaging Het
Nkg7 C T 7: 43,086,857 (GRCm39) P44S probably damaging Het
Or14c40 T C 7: 86,313,185 (GRCm39) V105A possibly damaging Het
Or4a67 T C 2: 88,597,832 (GRCm39) I276V probably benign Het
Pcif1 T C 2: 164,731,058 (GRCm39) Y404H probably benign Het
Pcnx2 A T 8: 126,480,289 (GRCm39) L2006Q possibly damaging Het
Pcnx3 A T 19: 5,724,922 (GRCm39) S821T possibly damaging Het
Pde8b T A 13: 95,170,680 (GRCm39) D662V probably damaging Het
Pkd1l3 C T 8: 110,343,000 (GRCm39) P113S unknown Het
Pkd2l1 G T 19: 44,142,648 (GRCm39) Q465K possibly damaging Het
Plch2 G T 4: 155,068,189 (GRCm39) P1479Q probably benign Het
Plekhm3 A T 1: 64,932,041 (GRCm39) I521N probably damaging Het
Pola2 A T 19: 5,992,093 (GRCm39) Y526* probably null Het
Prss23 T C 7: 89,159,217 (GRCm39) D284G probably damaging Het
Psme2b A G 11: 48,836,467 (GRCm39) F160S probably damaging Het
Rap1gap2 A G 11: 74,327,853 (GRCm39) V139A possibly damaging Het
Rbbp9 G T 2: 144,385,777 (GRCm39) R163S possibly damaging Het
Rdh12 T C 12: 79,260,522 (GRCm39) L206P probably damaging Het
Rhou T C 8: 124,388,029 (GRCm39) W254R possibly damaging Het
Scfd1 A G 12: 51,478,281 (GRCm39) K498E possibly damaging Het
Scn7a A G 2: 66,519,902 (GRCm39) Y1001H probably benign Het
Setx T A 2: 29,048,917 (GRCm39) V1981E probably damaging Het
Sfxn1 T C 13: 54,247,890 (GRCm39) I205T possibly damaging Het
Shld2 G T 14: 33,990,619 (GRCm39) H96N possibly damaging Het
Speer1g C T 5: 11,180,337 (GRCm39) H82Y probably damaging Het
Spock1 G A 13: 57,577,182 (GRCm39) R416C possibly damaging Het
Spred2 A G 11: 19,968,109 (GRCm39) I222V probably benign Het
Stkld1 A T 2: 26,839,407 (GRCm39) T358S probably benign Het
Strip1 T C 3: 107,534,724 (GRCm39) E102G possibly damaging Het
Tars3 T C 7: 65,305,444 (GRCm39) S223P probably damaging Het
Tdpoz1 T A 3: 93,578,637 (GRCm39) E49V probably benign Het
Tert A G 13: 73,776,328 (GRCm39) T360A probably benign Het
Tspear A G 10: 77,717,026 (GRCm39) Y567C probably damaging Het
Ugt2b38 T G 5: 87,560,232 (GRCm39) N361H probably damaging Het
Unc80 C T 1: 66,560,740 (GRCm39) H823Y possibly damaging Het
Vmn2r111 T A 17: 22,790,028 (GRCm39) H326L probably damaging Het
Vmn2r18 A G 5: 151,510,301 (GRCm39) F24S possibly damaging Het
Vmn2r82 A T 10: 79,232,133 (GRCm39) I711F probably benign Het
Vwa8 C T 14: 79,341,134 (GRCm39) Q1537* probably null Het
Wdr64 G A 1: 175,603,288 (GRCm39) V630I probably benign Het
Wnt6 G T 1: 74,821,434 (GRCm39) W84L probably damaging Het
Zfp11 C A 5: 129,735,254 (GRCm39) R69L probably benign Het
Other mutations in Ttc28
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00516:Ttc28 APN 5 111,373,554 (GRCm39) missense probably damaging 1.00
IGL00963:Ttc28 APN 5 111,434,255 (GRCm39) nonsense probably null
IGL00969:Ttc28 APN 5 111,373,606 (GRCm39) missense probably benign 0.00
IGL01366:Ttc28 APN 5 111,233,037 (GRCm39) critical splice donor site probably null
IGL01528:Ttc28 APN 5 111,249,826 (GRCm39) splice site probably benign
IGL01558:Ttc28 APN 5 111,431,828 (GRCm39) missense probably damaging 0.99
IGL01973:Ttc28 APN 5 111,372,101 (GRCm39) missense possibly damaging 0.88
IGL02040:Ttc28 APN 5 111,040,802 (GRCm39) nonsense probably null
IGL02432:Ttc28 APN 5 111,371,101 (GRCm39) missense probably damaging 1.00
IGL02531:Ttc28 APN 5 111,373,716 (GRCm39) missense probably damaging 1.00
IGL02819:Ttc28 APN 5 111,414,449 (GRCm39) missense probably benign
IGL02830:Ttc28 APN 5 111,434,105 (GRCm39) missense probably benign 0.10
IGL02893:Ttc28 APN 5 111,433,251 (GRCm39) missense possibly damaging 0.87
IGL03387:Ttc28 APN 5 111,381,208 (GRCm39) missense probably benign 0.07
PIT4131001:Ttc28 UTSW 5 111,040,719 (GRCm39) missense probably benign 0.00
R0142:Ttc28 UTSW 5 111,425,323 (GRCm39) missense probably benign 0.40
R0166:Ttc28 UTSW 5 111,373,500 (GRCm39) missense probably benign 0.01
R0328:Ttc28 UTSW 5 111,431,933 (GRCm39) splice site probably benign
R0582:Ttc28 UTSW 5 111,331,162 (GRCm39) missense probably damaging 1.00
R0744:Ttc28 UTSW 5 111,378,947 (GRCm39) missense probably damaging 1.00
R0811:Ttc28 UTSW 5 111,383,366 (GRCm39) missense probably benign 0.24
R0812:Ttc28 UTSW 5 111,383,366 (GRCm39) missense probably benign 0.24
R0828:Ttc28 UTSW 5 111,371,312 (GRCm39) missense probably damaging 1.00
R0833:Ttc28 UTSW 5 111,378,947 (GRCm39) missense probably damaging 1.00
R1013:Ttc28 UTSW 5 111,424,831 (GRCm39) missense probably benign 0.01
R1168:Ttc28 UTSW 5 111,378,977 (GRCm39) missense probably damaging 1.00
R1194:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1195:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1195:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1195:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1196:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1205:Ttc28 UTSW 5 111,433,635 (GRCm39) missense probably benign 0.04
R1386:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1467:Ttc28 UTSW 5 111,433,254 (GRCm39) missense probably benign 0.00
R1537:Ttc28 UTSW 5 111,433,184 (GRCm39) missense probably damaging 0.96
R1539:Ttc28 UTSW 5 111,248,677 (GRCm39) missense possibly damaging 0.77
R1558:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1560:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1561:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1566:Ttc28 UTSW 5 111,373,543 (GRCm39) missense probably damaging 1.00
R1768:Ttc28 UTSW 5 111,425,034 (GRCm39) missense possibly damaging 0.77
R1775:Ttc28 UTSW 5 111,424,677 (GRCm39) missense probably benign 0.00
R1909:Ttc28 UTSW 5 111,431,920 (GRCm39) critical splice donor site probably null
R1911:Ttc28 UTSW 5 111,428,616 (GRCm39) missense possibly damaging 0.93
R1970:Ttc28 UTSW 5 111,383,501 (GRCm39) missense probably benign 0.00
R1990:Ttc28 UTSW 5 111,424,188 (GRCm39) missense probably benign 0.37
R1992:Ttc28 UTSW 5 111,424,188 (GRCm39) missense probably benign 0.37
R2066:Ttc28 UTSW 5 111,373,799 (GRCm39) missense probably benign 0.01
R2112:Ttc28 UTSW 5 111,424,139 (GRCm39) missense probably damaging 0.99
R2158:Ttc28 UTSW 5 111,325,483 (GRCm39) intron probably benign
R2192:Ttc28 UTSW 5 111,371,362 (GRCm39) missense probably damaging 0.99
R2267:Ttc28 UTSW 5 111,373,869 (GRCm39) missense possibly damaging 0.75
R2384:Ttc28 UTSW 5 111,424,074 (GRCm39) missense possibly damaging 0.95
R2989:Ttc28 UTSW 5 111,371,881 (GRCm39) missense probably benign 0.29
R3881:Ttc28 UTSW 5 111,331,106 (GRCm39) missense probably damaging 1.00
R3919:Ttc28 UTSW 5 111,433,245 (GRCm39) missense possibly damaging 0.80
R4455:Ttc28 UTSW 5 111,371,924 (GRCm39) frame shift probably null
R4456:Ttc28 UTSW 5 111,371,924 (GRCm39) frame shift probably null
R4522:Ttc28 UTSW 5 111,428,038 (GRCm39) missense probably benign 0.01
R4548:Ttc28 UTSW 5 111,419,090 (GRCm39) missense possibly damaging 0.86
R4591:Ttc28 UTSW 5 111,371,147 (GRCm39) missense probably damaging 1.00
R4633:Ttc28 UTSW 5 111,371,867 (GRCm39) missense probably damaging 1.00
R4700:Ttc28 UTSW 5 111,424,909 (GRCm39) missense probably damaging 1.00
R4714:Ttc28 UTSW 5 111,433,095 (GRCm39) missense possibly damaging 0.65
R4790:Ttc28 UTSW 5 111,372,083 (GRCm39) missense possibly damaging 0.94
R4803:Ttc28 UTSW 5 111,425,329 (GRCm39) missense possibly damaging 0.90
R4840:Ttc28 UTSW 5 111,433,947 (GRCm39) missense probably damaging 1.00
R4969:Ttc28 UTSW 5 111,424,121 (GRCm39) missense probably damaging 0.96
R5019:Ttc28 UTSW 5 111,249,930 (GRCm39) missense possibly damaging 0.47
R5130:Ttc28 UTSW 5 111,040,722 (GRCm39) missense probably benign
R5150:Ttc28 UTSW 5 111,373,555 (GRCm39) missense probably damaging 1.00
R5214:Ttc28 UTSW 5 111,325,489 (GRCm39) intron probably benign
R5254:Ttc28 UTSW 5 111,419,104 (GRCm39) missense probably benign 0.01
R5518:Ttc28 UTSW 5 111,373,794 (GRCm39) missense probably benign 0.17
R5851:Ttc28 UTSW 5 111,383,335 (GRCm39) splice site probably benign
R5931:Ttc28 UTSW 5 111,232,975 (GRCm39) missense possibly damaging 0.81
R6011:Ttc28 UTSW 5 111,434,309 (GRCm39) missense probably benign
R6176:Ttc28 UTSW 5 111,371,851 (GRCm39) missense probably damaging 1.00
R6221:Ttc28 UTSW 5 111,419,114 (GRCm39) missense probably benign 0.00
R6398:Ttc28 UTSW 5 111,424,142 (GRCm39) missense probably damaging 1.00
R6717:Ttc28 UTSW 5 111,433,302 (GRCm39) missense probably benign
R6770:Ttc28 UTSW 5 111,434,006 (GRCm39) missense probably damaging 1.00
R6901:Ttc28 UTSW 5 111,424,891 (GRCm39) missense possibly damaging 0.88
R7038:Ttc28 UTSW 5 111,414,445 (GRCm39) missense probably benign 0.09
R7073:Ttc28 UTSW 5 111,371,282 (GRCm39) missense possibly damaging 0.96
R7101:Ttc28 UTSW 5 111,232,958 (GRCm39) missense probably damaging 1.00
R7135:Ttc28 UTSW 5 111,427,873 (GRCm39) missense probably damaging 1.00
R7350:Ttc28 UTSW 5 111,373,903 (GRCm39) missense probably damaging 0.97
R7454:Ttc28 UTSW 5 111,433,350 (GRCm39) missense probably benign 0.19
R7461:Ttc28 UTSW 5 111,371,995 (GRCm39) missense probably damaging 1.00
R7596:Ttc28 UTSW 5 111,427,990 (GRCm39) missense probably damaging 1.00
R7613:Ttc28 UTSW 5 111,371,995 (GRCm39) missense probably damaging 1.00
R7625:Ttc28 UTSW 5 111,433,085 (GRCm39) missense possibly damaging 0.65
R7648:Ttc28 UTSW 5 111,331,258 (GRCm39) missense possibly damaging 0.52
R7735:Ttc28 UTSW 5 111,414,544 (GRCm39) splice site probably null
R8030:Ttc28 UTSW 5 111,433,922 (GRCm39) missense possibly damaging 0.81
R8205:Ttc28 UTSW 5 111,373,596 (GRCm39) missense possibly damaging 0.95
R8246:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8247:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8269:Ttc28 UTSW 5 111,425,325 (GRCm39) missense probably benign 0.09
R8292:Ttc28 UTSW 5 111,371,123 (GRCm39) missense probably damaging 1.00
R8346:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8356:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8423:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8424:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8426:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8441:Ttc28 UTSW 5 111,325,507 (GRCm39) nonsense probably null
R8494:Ttc28 UTSW 5 111,383,506 (GRCm39) missense probably damaging 0.96
R8508:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8510:Ttc28 UTSW 5 111,381,207 (GRCm39) missense probably benign 0.33
R8729:Ttc28 UTSW 5 111,383,509 (GRCm39) critical splice donor site probably null
R8845:Ttc28 UTSW 5 111,372,041 (GRCm39) missense probably benign 0.11
R9003:Ttc28 UTSW 5 111,424,896 (GRCm39) missense probably benign 0.00
R9185:Ttc28 UTSW 5 111,371,342 (GRCm39) missense probably benign 0.03
R9187:Ttc28 UTSW 5 111,249,902 (GRCm39) missense probably damaging 1.00
R9245:Ttc28 UTSW 5 111,325,525 (GRCm39) missense unknown
R9251:Ttc28 UTSW 5 111,040,698 (GRCm39) missense possibly damaging 0.47
R9372:Ttc28 UTSW 5 111,331,073 (GRCm39) missense probably benign 0.25
R9466:Ttc28 UTSW 5 111,330,895 (GRCm39) missense probably damaging 0.99
R9563:Ttc28 UTSW 5 111,371,092 (GRCm39) missense probably benign 0.22
R9606:Ttc28 UTSW 5 111,433,140 (GRCm39) missense probably benign 0.00
R9691:Ttc28 UTSW 5 111,431,879 (GRCm39) missense probably benign 0.01
R9709:Ttc28 UTSW 5 111,433,637 (GRCm39) missense probably damaging 0.97
V8831:Ttc28 UTSW 5 111,248,578 (GRCm39) missense probably benign 0.11
Z1088:Ttc28 UTSW 5 111,434,181 (GRCm39) missense probably benign 0.00
Z1176:Ttc28 UTSW 5 111,414,432 (GRCm39) missense possibly damaging 0.59
Z1177:Ttc28 UTSW 5 111,433,605 (GRCm39) missense probably benign 0.10
Z1177:Ttc28 UTSW 5 111,426,452 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTACAGTCTCAGCTCAATCGCCTC -3'
(R):5'- TGGGTGCTACCACACTATCTTCTCG -3'

Sequencing Primer
(F):5'- AGTTTTGTCTCCAAGCCCGAG -3'
(R):5'- GCTCTACTGCCAGGAGATG -3'
Posted On 2017-12-01