Incidental Mutation 'R5436:Ttc6'
ID |
428374 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ttc6
|
Ensembl Gene |
ENSMUSG00000046782 |
Gene Name |
tetratricopeptide repeat domain 6 |
Synonyms |
LOC217602, Gm9813, EG639426, 4921506M07Rik, AU024163 |
MMRRC Submission |
043001-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.119)
|
Stock # |
R5436 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
57610899-57784714 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to A
at 57721380 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 |
0.9755 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.4%
|
Validation Efficiency |
99% (106/107) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449A18Rik |
T |
C |
3: 59,754,114 (GRCm39) |
|
noncoding transcript |
Het |
Abca9 |
G |
A |
11: 110,025,062 (GRCm39) |
L994F |
probably damaging |
Het |
Abl2 |
A |
T |
1: 156,457,450 (GRCm39) |
S239C |
probably damaging |
Het |
Acsl5 |
T |
A |
19: 55,267,997 (GRCm39) |
|
probably null |
Het |
Aff1 |
C |
T |
5: 103,931,736 (GRCm39) |
T126I |
probably damaging |
Het |
Amtn |
T |
C |
5: 88,529,485 (GRCm39) |
L107P |
probably damaging |
Het |
Ankrd45 |
A |
G |
1: 160,986,682 (GRCm39) |
|
probably benign |
Het |
Arl6ip5 |
G |
A |
6: 97,187,887 (GRCm39) |
V36I |
probably damaging |
Het |
Ascc3 |
T |
A |
10: 50,535,079 (GRCm39) |
D657E |
probably damaging |
Het |
Ascl1 |
T |
A |
10: 87,328,808 (GRCm39) |
Q48L |
unknown |
Het |
Asic4 |
T |
A |
1: 75,427,963 (GRCm39) |
V163E |
probably benign |
Het |
Atm |
A |
T |
9: 53,371,104 (GRCm39) |
M2245K |
probably benign |
Het |
Barx2 |
T |
G |
9: 31,824,285 (GRCm39) |
T35P |
probably damaging |
Het |
Bdh1 |
C |
T |
16: 31,275,475 (GRCm39) |
R235C |
probably damaging |
Het |
C8b |
T |
A |
4: 104,657,546 (GRCm39) |
Y404* |
probably null |
Het |
Car5a |
A |
G |
8: 122,643,981 (GRCm39) |
|
probably benign |
Het |
Ccdc13 |
T |
C |
9: 121,628,109 (GRCm39) |
I169M |
probably benign |
Het |
Cd163 |
A |
T |
6: 124,304,923 (GRCm39) |
D1100V |
probably benign |
Het |
Cimap2 |
A |
T |
4: 106,467,690 (GRCm39) |
H315Q |
probably benign |
Het |
Cntfr |
T |
C |
4: 41,663,322 (GRCm39) |
N162D |
probably damaging |
Het |
Cops3 |
T |
G |
11: 59,715,171 (GRCm39) |
D289A |
probably damaging |
Het |
Crbn |
A |
T |
6: 106,772,861 (GRCm39) |
S42R |
probably damaging |
Het |
Cth |
T |
A |
3: 157,600,463 (GRCm39) |
H397L |
probably benign |
Het |
Dact2 |
A |
G |
17: 14,416,010 (GRCm39) |
L730P |
probably damaging |
Het |
Dhx37 |
C |
T |
5: 125,506,867 (GRCm39) |
G210R |
probably benign |
Het |
Dnaaf9 |
C |
A |
2: 130,606,419 (GRCm39) |
K415N |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,038,704 (GRCm39) |
I126V |
probably benign |
Het |
Dnttip2 |
T |
C |
3: 122,072,418 (GRCm39) |
I566T |
probably damaging |
Het |
Ehbp1l1 |
G |
T |
19: 5,766,276 (GRCm39) |
R412S |
possibly damaging |
Het |
Fam110b |
A |
C |
4: 5,799,104 (GRCm39) |
Q174P |
probably benign |
Het |
Fam149a |
A |
T |
8: 45,801,508 (GRCm39) |
S457T |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,871,810 (GRCm39) |
V3527G |
probably benign |
Het |
Fat4 |
A |
G |
3: 38,945,495 (GRCm39) |
M1463V |
probably benign |
Het |
Gak |
T |
A |
5: 108,740,218 (GRCm39) |
I566F |
possibly damaging |
Het |
Gdf10 |
T |
A |
14: 33,654,213 (GRCm39) |
I240N |
probably damaging |
Het |
Gprc6a |
T |
A |
10: 51,502,798 (GRCm39) |
H355L |
probably benign |
Het |
Gxylt1 |
T |
C |
15: 93,145,780 (GRCm39) |
K338R |
probably damaging |
Het |
Hexim2 |
A |
T |
11: 103,029,095 (GRCm39) |
E49V |
probably null |
Het |
Hfm1 |
T |
C |
5: 107,040,638 (GRCm39) |
D709G |
possibly damaging |
Het |
Ighv1-49 |
T |
C |
12: 115,019,081 (GRCm39) |
K19R |
probably damaging |
Het |
Il17a |
T |
A |
1: 20,803,870 (GRCm39) |
Y88* |
probably null |
Het |
Iqsec1 |
A |
T |
6: 90,822,343 (GRCm39) |
|
probably benign |
Het |
Itih2 |
T |
C |
2: 10,110,007 (GRCm39) |
D582G |
probably benign |
Het |
Klc3 |
T |
C |
7: 19,131,884 (GRCm39) |
|
probably null |
Het |
Larp4 |
T |
A |
15: 99,883,995 (GRCm39) |
N78K |
probably damaging |
Het |
Larp4b |
A |
G |
13: 9,218,936 (GRCm39) |
D526G |
possibly damaging |
Het |
Limch1 |
T |
C |
5: 67,131,909 (GRCm39) |
V133A |
possibly damaging |
Het |
Lmbr1l |
G |
A |
15: 98,802,672 (GRCm39) |
R426C |
probably damaging |
Het |
Lox |
T |
A |
18: 52,662,175 (GRCm39) |
D76V |
probably benign |
Het |
Lrrc8d |
T |
A |
5: 105,960,418 (GRCm39) |
I276N |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Marchf10 |
A |
T |
11: 105,292,991 (GRCm39) |
Y139N |
possibly damaging |
Het |
Mrc1 |
T |
G |
2: 14,271,326 (GRCm39) |
I410S |
probably damaging |
Het |
Mrto4 |
A |
T |
4: 139,075,276 (GRCm39) |
C176S |
probably damaging |
Het |
Mtch1 |
G |
T |
17: 29,566,564 (GRCm39) |
D66E |
probably benign |
Het |
Nbas |
T |
G |
12: 13,424,812 (GRCm39) |
L1017R |
probably damaging |
Het |
Nherf4 |
A |
G |
9: 44,159,652 (GRCm39) |
V448A |
possibly damaging |
Het |
Nim1k |
A |
G |
13: 120,189,065 (GRCm39) |
|
probably benign |
Het |
Nlrp6 |
T |
A |
7: 140,502,630 (GRCm39) |
Y245* |
probably null |
Het |
Or11g7 |
T |
G |
14: 50,691,184 (GRCm39) |
V225G |
probably damaging |
Het |
Or2t43 |
T |
A |
11: 58,457,763 (GRCm39) |
H136L |
probably benign |
Het |
Or4c3 |
T |
A |
2: 89,852,009 (GRCm39) |
M134L |
probably benign |
Het |
Or51q1 |
A |
T |
7: 103,628,473 (GRCm39) |
I25F |
probably benign |
Het |
Or5h24 |
C |
T |
16: 58,919,182 (GRCm39) |
V58I |
unknown |
Het |
Or8b1 |
A |
C |
9: 38,399,835 (GRCm39) |
D170A |
probably benign |
Het |
Pcare |
A |
T |
17: 72,057,837 (GRCm39) |
S613R |
probably damaging |
Het |
Pcnx1 |
G |
T |
12: 81,907,180 (GRCm39) |
G12V |
probably damaging |
Het |
Pkp1 |
T |
A |
1: 135,846,656 (GRCm39) |
K32M |
probably damaging |
Het |
Poc5 |
T |
C |
13: 96,533,321 (GRCm39) |
W150R |
probably damaging |
Het |
Ppp1r16b |
T |
A |
2: 158,599,253 (GRCm39) |
|
probably benign |
Het |
Prune2 |
T |
A |
19: 16,998,007 (GRCm39) |
M248K |
probably damaging |
Het |
Rb1 |
A |
T |
14: 73,450,580 (GRCm39) |
|
probably null |
Het |
Rhod |
A |
G |
19: 4,476,615 (GRCm39) |
C169R |
probably benign |
Het |
Rif1 |
T |
C |
2: 52,010,983 (GRCm39) |
|
probably benign |
Het |
Rnpc3 |
G |
A |
3: 113,418,648 (GRCm39) |
A100V |
probably damaging |
Het |
Rsf1 |
GCGGC |
GCGGCGGCGTCGGC |
7: 97,229,138 (GRCm39) |
|
probably benign |
Het |
Scnn1a |
A |
T |
6: 125,319,985 (GRCm39) |
D528V |
possibly damaging |
Het |
Sdhaf3 |
C |
A |
6: 7,038,855 (GRCm39) |
T59K |
probably benign |
Het |
Sec31a |
C |
A |
5: 100,511,698 (GRCm39) |
A330S |
probably damaging |
Het |
Sgk3 |
A |
G |
1: 9,952,097 (GRCm39) |
D241G |
probably damaging |
Het |
Skint6 |
T |
G |
4: 112,953,788 (GRCm39) |
I459L |
probably benign |
Het |
Slco1a5 |
A |
T |
6: 142,200,118 (GRCm39) |
V222E |
probably damaging |
Het |
Slit3 |
T |
A |
11: 35,598,738 (GRCm39) |
N1447K |
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,249,038 (GRCm39) |
H628R |
probably damaging |
Het |
St6galnac2 |
A |
G |
11: 116,575,353 (GRCm39) |
|
probably benign |
Het |
Tbc1d31 |
T |
C |
15: 57,816,267 (GRCm39) |
V667A |
probably benign |
Het |
Tbx20 |
A |
T |
9: 24,681,016 (GRCm39) |
Y159N |
probably damaging |
Het |
Tmprss11b |
T |
A |
5: 86,810,092 (GRCm39) |
Q296L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,701,243 (GRCm39) |
|
probably benign |
Het |
Tubgcp4 |
T |
A |
2: 121,018,617 (GRCm39) |
L340H |
probably damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,024,663 (GRCm39) |
F613I |
probably benign |
Het |
Urb1 |
T |
C |
16: 90,589,650 (GRCm39) |
Y377C |
probably damaging |
Het |
Utp15 |
G |
A |
13: 98,397,354 (GRCm39) |
|
probably null |
Het |
Vstm2b |
A |
G |
7: 40,550,707 (GRCm39) |
|
probably null |
Het |
Vwde |
A |
T |
6: 13,190,627 (GRCm39) |
V488D |
probably damaging |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Zfp276 |
A |
T |
8: 123,992,021 (GRCm39) |
|
probably benign |
Het |
Zfp318 |
T |
A |
17: 46,723,975 (GRCm39) |
S1993T |
possibly damaging |
Het |
Zfp959 |
T |
C |
17: 56,204,626 (GRCm39) |
L218P |
probably benign |
Het |
Zxdc |
A |
G |
6: 90,347,542 (GRCm39) |
D301G |
probably 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 |
R1872:Ttc6
|
UTSW |
12 |
57,751,338 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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'- AAACCACTTCAGAGGTGAGTG -3'
(R):5'- AGAGTAGTCATCAATAGCCAGC -3'
Sequencing Primer
(F):5'- GGTCATTTTGCTACTTCAGAGTAAC -3'
(R):5'- GTCATCAATAGCCAGCACTTTG -3'
|
Posted On |
2016-09-01 |