Incidental Mutation 'R1872:Ttc6'
ID |
210875 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ttc6
|
Ensembl Gene |
ENSMUSG00000046782 |
Gene Name |
tetratricopeptide repeat domain 6 |
Synonyms |
LOC217602, Gm9813, EG639426, 4921506M07Rik, AU024163 |
MMRRC Submission |
039894-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.119)
|
Stock # |
R1872 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
57610899-57784714 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 57751338 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000134273
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000172939]
|
AlphaFold |
G3UYY4 |
Predicted Effect |
probably null
Transcript: ENSMUST00000172939
|
SMART Domains |
Protein: ENSMUSP00000134273 Gene: ENSMUSG00000046782
Domain | Start | End | E-Value | Type |
coiled coil region
|
18 |
42 |
N/A |
INTRINSIC |
low complexity region
|
146 |
162 |
N/A |
INTRINSIC |
low complexity region
|
188 |
212 |
N/A |
INTRINSIC |
low complexity region
|
227 |
238 |
N/A |
INTRINSIC |
low complexity region
|
486 |
495 |
N/A |
INTRINSIC |
low complexity region
|
670 |
685 |
N/A |
INTRINSIC |
low complexity region
|
733 |
740 |
N/A |
INTRINSIC |
TPR
|
889 |
922 |
2e-4 |
SMART |
TPR
|
957 |
989 |
2.36e1 |
SMART |
TPR
|
990 |
1022 |
2.63e1 |
SMART |
TPR
|
1023 |
1056 |
9.39e-1 |
SMART |
TPR
|
1057 |
1090 |
3.78e-5 |
SMART |
Blast:TPR
|
1126 |
1157 |
1e-11 |
BLAST |
SEL1
|
1160 |
1192 |
3.39e1 |
SMART |
TPR
|
1160 |
1194 |
4.44e1 |
SMART |
TPR
|
1195 |
1228 |
7.87e0 |
SMART |
Blast:TPR
|
1229 |
1262 |
1e-11 |
BLAST |
TPR
|
1297 |
1330 |
1.24e0 |
SMART |
SEL1
|
1341 |
1372 |
9.26e-1 |
SMART |
TPR
|
1341 |
1374 |
3.45e-8 |
SMART |
TPR
|
1375 |
1407 |
8.76e-1 |
SMART |
TPR
|
1408 |
1441 |
1.45e-1 |
SMART |
TPR
|
1442 |
1475 |
1.36e1 |
SMART |
TPR
|
1476 |
1509 |
7.34e-3 |
SMART |
TPR
|
1513 |
1546 |
1.01e0 |
SMART |
TPR
|
1547 |
1580 |
2.55e-2 |
SMART |
TPR
|
1581 |
1617 |
2.43e1 |
SMART |
Blast:TPR
|
1618 |
1651 |
4e-12 |
BLAST |
TPR
|
1652 |
1685 |
7.87e0 |
SMART |
TPR
|
1686 |
1718 |
2.35e-1 |
SMART |
SEL1
|
1719 |
1750 |
1.21e2 |
SMART |
TPR
|
1719 |
1752 |
1.65e-5 |
SMART |
TPR
|
1753 |
1786 |
1.66e-1 |
SMART |
TPR
|
1787 |
1820 |
1.45e-1 |
SMART |
TPR
|
1821 |
1854 |
3.27e0 |
SMART |
|
Meta Mutation Damage Score |
0.9484 |
Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.8%
- 10x: 95.4%
- 20x: 93.0%
|
Validation Efficiency |
97% (113/117) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
C |
T |
3: 124,350,493 (GRCm39) |
C133Y |
unknown |
Het |
Abce1 |
A |
G |
8: 80,416,880 (GRCm39) |
M377T |
possibly damaging |
Het |
Adam25 |
A |
T |
8: 41,208,263 (GRCm39) |
R510* |
probably null |
Het |
Adamts12 |
G |
T |
15: 11,217,966 (GRCm39) |
E308* |
probably null |
Het |
Adgrg3 |
C |
A |
8: 95,760,070 (GRCm39) |
N96K |
possibly damaging |
Het |
Afdn |
T |
C |
17: 14,101,578 (GRCm39) |
V1022A |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,051,406 (GRCm39) |
V1391A |
probably damaging |
Het |
Akip1 |
A |
G |
7: 109,310,982 (GRCm39) |
Y174C |
probably damaging |
Het |
Aoc1l1 |
A |
G |
6: 48,952,554 (GRCm39) |
I160V |
probably benign |
Het |
Ap3b2 |
T |
C |
7: 81,113,898 (GRCm39) |
T830A |
unknown |
Het |
Aph1a |
A |
G |
3: 95,802,876 (GRCm39) |
T159A |
probably damaging |
Het |
Ccdc146 |
T |
C |
5: 21,506,288 (GRCm39) |
T718A |
probably benign |
Het |
Cdk5r2 |
T |
C |
1: 74,894,981 (GRCm39) |
L242P |
probably damaging |
Het |
Cep97 |
T |
A |
16: 55,748,229 (GRCm39) |
N67I |
probably damaging |
Het |
Cgas |
T |
C |
9: 78,340,484 (GRCm39) |
D416G |
probably benign |
Het |
Chic2 |
A |
T |
5: 75,172,140 (GRCm39) |
W121R |
possibly damaging |
Het |
Clock |
A |
G |
5: 76,396,309 (GRCm39) |
S147P |
possibly damaging |
Het |
Cntnap5a |
T |
G |
1: 116,016,940 (GRCm39) |
S178A |
probably benign |
Het |
Col11a2 |
C |
A |
17: 34,281,529 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,757,936 (GRCm39) |
H6L |
probably damaging |
Het |
Cpne5 |
T |
C |
17: 29,423,667 (GRCm39) |
N154D |
probably benign |
Het |
Ctsz |
T |
G |
2: 174,269,769 (GRCm39) |
K273Q |
probably benign |
Het |
Cybrd1 |
G |
A |
2: 70,960,104 (GRCm39) |
V101M |
probably benign |
Het |
Cyp2c23 |
T |
A |
19: 43,993,990 (GRCm39) |
K459* |
probably null |
Het |
Cyp4a31 |
A |
T |
4: 115,431,933 (GRCm39) |
H419L |
probably damaging |
Het |
D930020B18Rik |
G |
A |
10: 121,477,879 (GRCm39) |
V35M |
probably damaging |
Het |
Depp1 |
G |
A |
6: 116,628,683 (GRCm39) |
V9M |
possibly damaging |
Het |
Dnah9 |
C |
T |
11: 65,928,316 (GRCm39) |
V2118M |
probably benign |
Het |
Dtna |
T |
C |
18: 23,730,617 (GRCm39) |
|
probably null |
Het |
Ednra |
C |
T |
8: 78,447,025 (GRCm39) |
V18I |
possibly damaging |
Het |
Elac1 |
T |
C |
18: 73,875,717 (GRCm39) |
R105G |
probably benign |
Het |
Exoc2 |
A |
G |
13: 31,006,644 (GRCm39) |
S844P |
probably benign |
Het |
Fam185a |
A |
T |
5: 21,685,328 (GRCm39) |
|
probably null |
Het |
Fam204a |
A |
G |
19: 60,187,881 (GRCm39) |
M233T |
possibly damaging |
Het |
Fat1 |
C |
A |
8: 45,406,341 (GRCm39) |
H1031N |
probably benign |
Het |
Fat1 |
T |
A |
8: 45,491,386 (GRCm39) |
Y3816N |
probably damaging |
Het |
Fbxo38 |
C |
T |
18: 62,650,094 (GRCm39) |
R621Q |
probably benign |
Het |
Fhod3 |
C |
A |
18: 25,263,667 (GRCm39) |
R1524S |
probably damaging |
Het |
Fnip1 |
A |
T |
11: 54,378,561 (GRCm39) |
R192W |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,339,205 (GRCm39) |
H499Q |
probably damaging |
Het |
Gab2 |
C |
T |
7: 96,948,250 (GRCm39) |
T280I |
probably damaging |
Het |
Gdpgp1 |
A |
G |
7: 79,888,172 (GRCm39) |
R68G |
probably benign |
Het |
Gm10382 |
C |
T |
5: 125,466,624 (GRCm39) |
|
probably benign |
Het |
Gmps |
A |
G |
3: 63,908,938 (GRCm39) |
H480R |
probably benign |
Het |
Hecw1 |
G |
A |
13: 14,455,034 (GRCm39) |
R674* |
probably null |
Het |
Herc2 |
T |
A |
7: 55,807,257 (GRCm39) |
F2478L |
probably benign |
Het |
Homer2 |
C |
T |
7: 81,286,150 (GRCm39) |
V21M |
probably damaging |
Het |
Ifna9 |
A |
G |
4: 88,510,492 (GRCm39) |
M44T |
probably damaging |
Het |
Igfl3 |
A |
G |
7: 17,913,821 (GRCm39) |
D57G |
possibly damaging |
Het |
Jcad |
T |
C |
18: 4,673,048 (GRCm39) |
M270T |
probably benign |
Het |
Kdm5b |
T |
C |
1: 134,552,732 (GRCm39) |
L1236P |
probably damaging |
Het |
Kif14 |
T |
A |
1: 136,414,096 (GRCm39) |
L724Q |
probably damaging |
Het |
Lhb |
T |
C |
7: 45,070,757 (GRCm39) |
V45A |
probably damaging |
Het |
Lhpp |
A |
G |
7: 132,235,816 (GRCm39) |
N134D |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,061,078 (GRCm39) |
Y115C |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,638,234 (GRCm39) |
K395* |
probably null |
Het |
Mms22l |
A |
G |
4: 24,598,807 (GRCm39) |
N1134S |
probably damaging |
Het |
Mrc1 |
A |
G |
2: 14,330,192 (GRCm39) |
|
probably null |
Het |
Mrgprg |
G |
A |
7: 143,318,281 (GRCm39) |
S277L |
probably damaging |
Het |
Mrpl49 |
G |
T |
19: 6,107,010 (GRCm39) |
P60T |
possibly damaging |
Het |
Mrps10 |
G |
A |
17: 47,683,377 (GRCm39) |
G104D |
possibly damaging |
Het |
Msantd3 |
A |
G |
4: 48,552,771 (GRCm39) |
Y120C |
probably damaging |
Het |
Mtcl2 |
A |
G |
2: 156,882,181 (GRCm39) |
C624R |
possibly damaging |
Het |
N4bp2 |
C |
T |
5: 65,951,861 (GRCm39) |
|
probably benign |
Het |
Nbea |
A |
G |
3: 55,550,310 (GRCm39) |
V2706A |
probably benign |
Het |
Nfic |
T |
A |
10: 81,256,518 (GRCm39) |
M71L |
possibly damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or12e1 |
A |
G |
2: 87,022,222 (GRCm39) |
T64A |
possibly damaging |
Het |
Or14j4 |
G |
T |
17: 37,920,803 (GRCm39) |
P280T |
probably damaging |
Het |
Or4a15 |
A |
G |
2: 89,192,933 (GRCm39) |
L280P |
probably damaging |
Het |
Or4c105 |
T |
A |
2: 88,648,280 (GRCm39) |
V255E |
probably benign |
Het |
Pak5 |
T |
C |
2: 135,927,508 (GRCm39) |
I655V |
possibly damaging |
Het |
Pip5k1c |
A |
G |
10: 81,142,153 (GRCm39) |
N121S |
probably damaging |
Het |
Plce1 |
A |
T |
19: 38,748,521 (GRCm39) |
I1737F |
probably damaging |
Het |
Prrt1 |
T |
C |
17: 34,849,925 (GRCm39) |
L113P |
probably damaging |
Het |
Ptprq |
T |
A |
10: 107,479,860 (GRCm39) |
T1137S |
probably benign |
Het |
Recql5 |
T |
C |
11: 115,814,135 (GRCm39) |
I223V |
probably benign |
Het |
Reg3g |
A |
T |
6: 78,444,836 (GRCm39) |
Y47* |
probably null |
Het |
Rgs12 |
T |
G |
5: 35,123,165 (GRCm39) |
M316R |
probably damaging |
Het |
Ric1 |
T |
C |
19: 29,580,068 (GRCm39) |
S1290P |
probably benign |
Het |
Rpl36al |
A |
G |
12: 69,229,697 (GRCm39) |
C72R |
probably damaging |
Het |
Rplp0 |
T |
A |
5: 115,701,374 (GRCm39) |
F275L |
possibly damaging |
Het |
Rpp30 |
G |
A |
19: 36,064,793 (GRCm39) |
V89I |
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,539,482 (GRCm39) |
F3253L |
possibly damaging |
Het |
Serpina3n |
A |
T |
12: 104,375,203 (GRCm39) |
N92Y |
probably benign |
Het |
Setd7 |
G |
T |
3: 51,450,252 (GRCm39) |
T58N |
probably benign |
Het |
Sh3tc2 |
T |
A |
18: 62,144,954 (GRCm39) |
L1136Q |
probably damaging |
Het |
Slc35b4 |
G |
A |
6: 34,135,440 (GRCm39) |
Q291* |
probably null |
Het |
Sort1 |
A |
G |
3: 108,248,011 (GRCm39) |
N452S |
probably benign |
Het |
Sympk |
A |
G |
7: 18,763,070 (GRCm39) |
I46V |
probably benign |
Het |
Syngr2 |
T |
C |
11: 117,703,364 (GRCm39) |
V60A |
probably damaging |
Het |
Syt17 |
A |
T |
7: 118,007,341 (GRCm39) |
F318I |
probably benign |
Het |
Tdpoz8 |
T |
A |
3: 92,981,729 (GRCm39) |
L249H |
probably damaging |
Het |
Tgfb1 |
T |
A |
7: 25,391,891 (GRCm39) |
L149M |
probably damaging |
Het |
Ticam1 |
A |
T |
17: 56,578,897 (GRCm39) |
M66K |
probably benign |
Het |
Tmem131 |
G |
T |
1: 36,847,008 (GRCm39) |
D1363E |
probably benign |
Het |
Tns4 |
A |
C |
11: 98,970,926 (GRCm39) |
D261E |
probably damaging |
Het |
Trim30a |
T |
C |
7: 104,078,417 (GRCm39) |
N220D |
probably benign |
Het |
Trmt10a |
T |
C |
3: 137,862,481 (GRCm39) |
L257P |
probably damaging |
Het |
Troap |
G |
T |
15: 98,973,233 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Vav1 |
A |
C |
17: 57,631,750 (GRCm39) |
K775T |
probably damaging |
Het |
Vmn1r236 |
A |
G |
17: 21,507,673 (GRCm39) |
K264E |
possibly damaging |
Het |
Vmn1r84 |
A |
G |
7: 12,096,555 (GRCm39) |
V46A |
probably benign |
Het |
Wdr59 |
A |
T |
8: 112,185,649 (GRCm39) |
W835R |
probably damaging |
Het |
Zfp513 |
T |
G |
5: 31,357,767 (GRCm39) |
K202T |
probably damaging |
Het |
Zfp7 |
T |
G |
15: 76,775,977 (GRCm39) |
I673S |
probably benign |
Het |
Zmynd11 |
A |
G |
13: 9,748,737 (GRCm39) |
I108T |
possibly damaging |
Het |
|
Other mutations in Ttc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03278:Ttc6
|
APN |
12 |
57,668,812 (GRCm39) |
missense |
probably damaging |
0.99 |
polonius
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
tybalt
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02802:Ttc6
|
UTSW |
12 |
57,622,654 (GRCm39) |
missense |
probably benign |
0.14 |
PIT4802001:Ttc6
|
UTSW |
12 |
57,772,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0698:Ttc6
|
UTSW |
12 |
57,720,002 (GRCm39) |
missense |
probably benign |
0.04 |
R0988:Ttc6
|
UTSW |
12 |
57,735,435 (GRCm39) |
splice site |
probably benign |
|
R1290:Ttc6
|
UTSW |
12 |
57,707,199 (GRCm39) |
missense |
probably benign |
0.00 |
R1338:Ttc6
|
UTSW |
12 |
57,663,155 (GRCm39) |
missense |
probably benign |
0.10 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1481:Ttc6
|
UTSW |
12 |
57,783,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Ttc6
|
UTSW |
12 |
57,696,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1558:Ttc6
|
UTSW |
12 |
57,733,132 (GRCm39) |
missense |
probably benign |
0.14 |
R1570:Ttc6
|
UTSW |
12 |
57,721,549 (GRCm39) |
missense |
probably damaging |
0.98 |
R1619:Ttc6
|
UTSW |
12 |
57,784,454 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1819:Ttc6
|
UTSW |
12 |
57,741,286 (GRCm39) |
critical splice donor site |
probably null |
|
R1826:Ttc6
|
UTSW |
12 |
57,707,033 (GRCm39) |
missense |
probably benign |
0.10 |
R1863:Ttc6
|
UTSW |
12 |
57,760,881 (GRCm39) |
missense |
probably benign |
0.04 |
R1887:Ttc6
|
UTSW |
12 |
57,720,044 (GRCm39) |
missense |
probably benign |
0.04 |
R1937:Ttc6
|
UTSW |
12 |
57,663,109 (GRCm39) |
missense |
probably benign |
0.02 |
R2014:Ttc6
|
UTSW |
12 |
57,623,003 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2056:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2058:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2059:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2152:Ttc6
|
UTSW |
12 |
57,752,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R2179:Ttc6
|
UTSW |
12 |
57,719,904 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2275:Ttc6
|
UTSW |
12 |
57,749,084 (GRCm39) |
missense |
probably benign |
0.01 |
R2432:Ttc6
|
UTSW |
12 |
57,668,821 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2474:Ttc6
|
UTSW |
12 |
57,622,713 (GRCm39) |
missense |
probably benign |
0.37 |
R2853:Ttc6
|
UTSW |
12 |
57,622,967 (GRCm39) |
missense |
probably damaging |
0.96 |
R3848:Ttc6
|
UTSW |
12 |
57,723,932 (GRCm39) |
missense |
probably damaging |
0.97 |
R3853:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3950:Ttc6
|
UTSW |
12 |
57,696,292 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3954:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3955:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3957:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R4135:Ttc6
|
UTSW |
12 |
57,679,581 (GRCm39) |
intron |
probably benign |
|
R4387:Ttc6
|
UTSW |
12 |
57,689,836 (GRCm39) |
missense |
probably benign |
0.00 |
R4577:Ttc6
|
UTSW |
12 |
57,623,441 (GRCm39) |
missense |
probably benign |
0.22 |
R4747:Ttc6
|
UTSW |
12 |
57,721,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4779:Ttc6
|
UTSW |
12 |
57,776,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Ttc6
|
UTSW |
12 |
57,775,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Ttc6
|
UTSW |
12 |
57,749,142 (GRCm39) |
missense |
probably damaging |
0.96 |
R4898:Ttc6
|
UTSW |
12 |
57,707,026 (GRCm39) |
missense |
probably benign |
0.00 |
R4930:Ttc6
|
UTSW |
12 |
57,720,609 (GRCm39) |
critical splice donor site |
probably null |
|
R4946:Ttc6
|
UTSW |
12 |
57,689,926 (GRCm39) |
missense |
probably benign |
0.01 |
R5257:Ttc6
|
UTSW |
12 |
57,749,061 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5303:Ttc6
|
UTSW |
12 |
57,622,606 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5385:Ttc6
|
UTSW |
12 |
57,689,821 (GRCm39) |
splice site |
probably null |
|
R5402:Ttc6
|
UTSW |
12 |
57,783,817 (GRCm39) |
nonsense |
probably null |
|
R5428:Ttc6
|
UTSW |
12 |
57,736,620 (GRCm39) |
missense |
probably null |
0.98 |
R5436:Ttc6
|
UTSW |
12 |
57,721,380 (GRCm39) |
splice site |
probably null |
|
R5646:Ttc6
|
UTSW |
12 |
57,622,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R5697:Ttc6
|
UTSW |
12 |
57,724,000 (GRCm39) |
missense |
probably benign |
0.22 |
R5792:Ttc6
|
UTSW |
12 |
57,719,990 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5808:Ttc6
|
UTSW |
12 |
57,664,397 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5842:Ttc6
|
UTSW |
12 |
57,783,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Ttc6
|
UTSW |
12 |
57,720,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R6144:Ttc6
|
UTSW |
12 |
57,719,886 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6155:Ttc6
|
UTSW |
12 |
57,784,402 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6283:Ttc6
|
UTSW |
12 |
57,749,048 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6371:Ttc6
|
UTSW |
12 |
57,775,249 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6715:Ttc6
|
UTSW |
12 |
57,721,556 (GRCm39) |
critical splice donor site |
probably null |
|
R6738:Ttc6
|
UTSW |
12 |
57,735,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R6795:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6959:Ttc6
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
R7053:Ttc6
|
UTSW |
12 |
57,707,318 (GRCm39) |
missense |
probably benign |
0.01 |
R7125:Ttc6
|
UTSW |
12 |
57,623,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7259:Ttc6
|
UTSW |
12 |
57,622,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7304:Ttc6
|
UTSW |
12 |
57,622,837 (GRCm39) |
missense |
probably damaging |
0.96 |
R7369:Ttc6
|
UTSW |
12 |
57,719,717 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7409:Ttc6
|
UTSW |
12 |
57,743,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R7429:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7430:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7492:Ttc6
|
UTSW |
12 |
57,719,922 (GRCm39) |
missense |
probably benign |
0.02 |
R7535:Ttc6
|
UTSW |
12 |
57,623,305 (GRCm39) |
missense |
probably benign |
0.00 |
R7866:Ttc6
|
UTSW |
12 |
57,721,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R7901:Ttc6
|
UTSW |
12 |
57,735,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7945:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7965:Ttc6
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8062:Ttc6
|
UTSW |
12 |
57,783,764 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8119:Ttc6
|
UTSW |
12 |
57,752,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8142:Ttc6
|
UTSW |
12 |
57,744,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8154:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Ttc6
|
UTSW |
12 |
57,720,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8335:Ttc6
|
UTSW |
12 |
57,707,077 (GRCm39) |
missense |
probably benign |
0.00 |
R8343:Ttc6
|
UTSW |
12 |
57,707,282 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8696:Ttc6
|
UTSW |
12 |
57,784,492 (GRCm39) |
missense |
probably benign |
0.20 |
R8875:Ttc6
|
UTSW |
12 |
57,776,194 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8875:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R8876:Ttc6
|
UTSW |
12 |
57,784,489 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8924:Ttc6
|
UTSW |
12 |
57,697,790 (GRCm39) |
nonsense |
probably null |
|
R8944:Ttc6
|
UTSW |
12 |
57,689,826 (GRCm39) |
missense |
|
|
R8956:Ttc6
|
UTSW |
12 |
57,775,196 (GRCm39) |
nonsense |
probably null |
|
R9009:Ttc6
|
UTSW |
12 |
57,744,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Ttc6
|
UTSW |
12 |
57,752,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Ttc6
|
UTSW |
12 |
57,783,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:Ttc6
|
UTSW |
12 |
57,622,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R9304:Ttc6
|
UTSW |
12 |
57,776,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R9309:Ttc6
|
UTSW |
12 |
57,753,649 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9331:Ttc6
|
UTSW |
12 |
57,720,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Ttc6
|
UTSW |
12 |
57,784,404 (GRCm39) |
nonsense |
probably null |
|
R9430:Ttc6
|
UTSW |
12 |
57,733,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Ttc6
|
UTSW |
12 |
57,664,299 (GRCm39) |
missense |
probably benign |
|
R9688:Ttc6
|
UTSW |
12 |
57,720,602 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9732:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
probably benign |
0.36 |
R9740:Ttc6
|
UTSW |
12 |
57,736,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Ttc6
|
UTSW |
12 |
57,701,559 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Ttc6
|
UTSW |
12 |
57,622,904 (GRCm39) |
missense |
probably damaging |
0.96 |
X0058:Ttc6
|
UTSW |
12 |
57,753,637 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Ttc6
|
UTSW |
12 |
57,744,161 (GRCm39) |
missense |
probably benign |
0.08 |
|
Predicted Primers |
PCR Primer
(F):5'- TGCATAAACATATTCTTCCAGGC -3'
(R):5'- AGGAGGCAAAATCCATGTGA -3'
Sequencing Primer
(F):5'- GCTTTTGAATCATTTACAAAAGCCG -3'
(R):5'- ATCTGTAATCTCTTGAGAGGCAG -3'
|
Posted On |
2014-06-30 |