Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot9 |
T |
C |
X: 154,078,177 (GRCm39) |
I241T |
probably benign |
Het |
Atp5mc3 |
T |
A |
2: 73,740,270 (GRCm39) |
R19* |
probably null |
Het |
Celf4 |
T |
C |
18: 25,620,007 (GRCm39) |
D420G |
probably damaging |
Het |
Cideb |
C |
A |
14: 55,992,017 (GRCm39) |
R179L |
possibly damaging |
Het |
Cmtr1 |
G |
A |
17: 29,916,143 (GRCm39) |
R591H |
probably benign |
Het |
Dync1li2 |
A |
T |
8: 105,169,130 (GRCm39) |
S34T |
possibly damaging |
Het |
Eri2 |
A |
G |
7: 119,390,389 (GRCm39) |
Y80H |
probably damaging |
Het |
Eya2 |
A |
G |
2: 165,596,401 (GRCm39) |
E304G |
probably damaging |
Het |
Fam135a |
A |
C |
1: 24,094,979 (GRCm39) |
L130V |
probably damaging |
Het |
Fancb |
A |
T |
X: 163,774,594 (GRCm39) |
K410N |
probably damaging |
Het |
Gabpb2 |
A |
C |
3: 95,107,502 (GRCm39) |
V191G |
probably damaging |
Het |
Gfm1 |
A |
G |
3: 67,345,893 (GRCm39) |
H197R |
possibly damaging |
Het |
Gm11595 |
A |
G |
11: 99,663,365 (GRCm39) |
V105A |
unknown |
Het |
Hectd3 |
T |
A |
4: 116,856,840 (GRCm39) |
D462E |
probably damaging |
Het |
Herc1 |
G |
T |
9: 66,315,334 (GRCm39) |
V1139L |
probably benign |
Het |
Itgal |
T |
C |
7: 126,901,183 (GRCm39) |
F190L |
probably damaging |
Het |
Krt87 |
G |
A |
15: 101,336,327 (GRCm39) |
H109Y |
probably benign |
Het |
Lmf2 |
T |
C |
15: 89,238,771 (GRCm39) |
Y115C |
probably benign |
Het |
Papolg |
T |
A |
11: 23,826,377 (GRCm39) |
Y259F |
possibly damaging |
Het |
Parn |
T |
C |
16: 13,485,467 (GRCm39) |
I10V |
probably benign |
Het |
Pdcd11 |
T |
A |
19: 47,102,989 (GRCm39) |
|
probably benign |
Het |
Phldb2 |
T |
A |
16: 45,583,465 (GRCm39) |
Q1003L |
possibly damaging |
Het |
Pigg |
T |
A |
5: 108,489,944 (GRCm39) |
F850I |
probably damaging |
Het |
Pkp4 |
T |
C |
2: 59,138,701 (GRCm39) |
L317P |
probably damaging |
Het |
Polr2a |
T |
C |
11: 69,634,620 (GRCm39) |
|
probably benign |
Het |
Prdm16 |
G |
A |
4: 154,426,426 (GRCm39) |
T453M |
possibly damaging |
Het |
Rnf144b |
A |
T |
13: 47,360,969 (GRCm39) |
E36D |
possibly damaging |
Het |
Ryr2 |
G |
A |
13: 11,750,388 (GRCm39) |
T1961I |
probably damaging |
Het |
Sash1 |
T |
A |
10: 8,627,177 (GRCm39) |
K305I |
probably damaging |
Het |
Tbc1d7 |
A |
T |
13: 43,312,797 (GRCm39) |
I32N |
probably damaging |
Het |
Thop1 |
T |
C |
10: 80,917,529 (GRCm39) |
F623L |
probably damaging |
Het |
Thsd7b |
G |
A |
1: 129,541,016 (GRCm39) |
G297R |
probably damaging |
Het |
Vmn1r183 |
A |
G |
7: 23,754,649 (GRCm39) |
N151D |
probably damaging |
Het |
|
Other mutations in Tln1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Tln1
|
APN |
4 |
43,542,719 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01345:Tln1
|
APN |
4 |
43,536,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01456:Tln1
|
APN |
4 |
43,543,432 (GRCm39) |
unclassified |
probably benign |
|
IGL01715:Tln1
|
APN |
4 |
43,555,890 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01750:Tln1
|
APN |
4 |
43,545,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Tln1
|
APN |
4 |
43,555,894 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01933:Tln1
|
APN |
4 |
43,539,508 (GRCm39) |
missense |
probably benign |
|
IGL02119:Tln1
|
APN |
4 |
43,546,760 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02148:Tln1
|
APN |
4 |
43,555,388 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Tln1
|
APN |
4 |
43,546,857 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02522:Tln1
|
APN |
4 |
43,540,612 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02691:Tln1
|
APN |
4 |
43,539,544 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02882:Tln1
|
APN |
4 |
43,539,522 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02892:Tln1
|
APN |
4 |
43,555,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Tln1
|
APN |
4 |
43,545,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03102:Tln1
|
APN |
4 |
43,532,861 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03183:Tln1
|
APN |
4 |
43,539,084 (GRCm39) |
splice site |
probably benign |
|
H8786:Tln1
|
UTSW |
4 |
43,544,589 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4576001:Tln1
|
UTSW |
4 |
43,539,998 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4696001:Tln1
|
UTSW |
4 |
43,542,701 (GRCm39) |
critical splice donor site |
probably null |
|
R0206:Tln1
|
UTSW |
4 |
43,549,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Tln1
|
UTSW |
4 |
43,549,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Tln1
|
UTSW |
4 |
43,553,504 (GRCm39) |
missense |
probably benign |
|
R0539:Tln1
|
UTSW |
4 |
43,543,434 (GRCm39) |
critical splice donor site |
probably null |
|
R0548:Tln1
|
UTSW |
4 |
43,542,709 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0561:Tln1
|
UTSW |
4 |
43,550,304 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0606:Tln1
|
UTSW |
4 |
43,547,756 (GRCm39) |
missense |
probably benign |
0.34 |
R0607:Tln1
|
UTSW |
4 |
43,553,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Tln1
|
UTSW |
4 |
43,544,645 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0847:Tln1
|
UTSW |
4 |
43,555,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R0993:Tln1
|
UTSW |
4 |
43,549,825 (GRCm39) |
missense |
probably benign |
0.22 |
R1255:Tln1
|
UTSW |
4 |
43,538,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R1292:Tln1
|
UTSW |
4 |
43,534,578 (GRCm39) |
critical splice donor site |
probably null |
|
R1752:Tln1
|
UTSW |
4 |
43,536,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R2169:Tln1
|
UTSW |
4 |
43,548,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Tln1
|
UTSW |
4 |
43,545,721 (GRCm39) |
missense |
probably benign |
|
R2202:Tln1
|
UTSW |
4 |
43,553,083 (GRCm39) |
splice site |
probably null |
|
R2680:Tln1
|
UTSW |
4 |
43,539,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R3012:Tln1
|
UTSW |
4 |
43,542,525 (GRCm39) |
missense |
probably benign |
|
R3714:Tln1
|
UTSW |
4 |
43,540,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R3735:Tln1
|
UTSW |
4 |
43,549,370 (GRCm39) |
missense |
probably damaging |
0.97 |
R3794:Tln1
|
UTSW |
4 |
43,536,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R3825:Tln1
|
UTSW |
4 |
43,536,413 (GRCm39) |
splice site |
probably benign |
|
R3983:Tln1
|
UTSW |
4 |
43,553,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R4061:Tln1
|
UTSW |
4 |
43,549,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R4249:Tln1
|
UTSW |
4 |
43,536,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R4287:Tln1
|
UTSW |
4 |
43,543,509 (GRCm39) |
missense |
probably benign |
0.01 |
R4471:Tln1
|
UTSW |
4 |
43,551,018 (GRCm39) |
missense |
probably benign |
0.03 |
R4562:Tln1
|
UTSW |
4 |
43,533,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R4654:Tln1
|
UTSW |
4 |
43,535,954 (GRCm39) |
missense |
probably null |
1.00 |
R4737:Tln1
|
UTSW |
4 |
43,540,588 (GRCm39) |
missense |
probably benign |
0.00 |
R4936:Tln1
|
UTSW |
4 |
43,547,522 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5225:Tln1
|
UTSW |
4 |
43,539,406 (GRCm39) |
missense |
probably benign |
0.06 |
R5288:Tln1
|
UTSW |
4 |
43,540,661 (GRCm39) |
missense |
probably benign |
0.06 |
R5421:Tln1
|
UTSW |
4 |
43,533,609 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5445:Tln1
|
UTSW |
4 |
43,543,905 (GRCm39) |
missense |
probably benign |
0.26 |
R5660:Tln1
|
UTSW |
4 |
43,547,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Tln1
|
UTSW |
4 |
43,545,191 (GRCm39) |
missense |
probably benign |
0.13 |
R6012:Tln1
|
UTSW |
4 |
43,539,508 (GRCm39) |
missense |
probably benign |
|
R6038:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6038:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6039:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6039:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6052:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6145:Tln1
|
UTSW |
4 |
43,538,030 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6157:Tln1
|
UTSW |
4 |
43,534,744 (GRCm39) |
missense |
probably benign |
0.06 |
R6242:Tln1
|
UTSW |
4 |
43,533,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6454:Tln1
|
UTSW |
4 |
43,533,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R6467:Tln1
|
UTSW |
4 |
43,543,165 (GRCm39) |
missense |
probably benign |
0.42 |
R6548:Tln1
|
UTSW |
4 |
43,547,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R6576:Tln1
|
UTSW |
4 |
43,555,419 (GRCm39) |
splice site |
probably null |
|
R6722:Tln1
|
UTSW |
4 |
43,547,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Tln1
|
UTSW |
4 |
43,550,217 (GRCm39) |
missense |
probably benign |
0.02 |
R7000:Tln1
|
UTSW |
4 |
43,556,302 (GRCm39) |
missense |
probably damaging |
0.96 |
R7137:Tln1
|
UTSW |
4 |
43,540,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Tln1
|
UTSW |
4 |
43,542,602 (GRCm39) |
missense |
probably benign |
0.01 |
R7294:Tln1
|
UTSW |
4 |
43,534,399 (GRCm39) |
missense |
probably benign |
0.02 |
R7312:Tln1
|
UTSW |
4 |
43,545,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7547:Tln1
|
UTSW |
4 |
43,545,206 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7836:Tln1
|
UTSW |
4 |
43,554,309 (GRCm39) |
missense |
probably benign |
0.01 |
R7874:Tln1
|
UTSW |
4 |
43,555,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R7874:Tln1
|
UTSW |
4 |
43,538,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Tln1
|
UTSW |
4 |
43,535,737 (GRCm39) |
critical splice donor site |
probably null |
|
R8105:Tln1
|
UTSW |
4 |
43,538,231 (GRCm39) |
missense |
probably benign |
0.32 |
R8212:Tln1
|
UTSW |
4 |
43,555,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R8416:Tln1
|
UTSW |
4 |
43,540,116 (GRCm39) |
missense |
probably benign |
0.01 |
R8419:Tln1
|
UTSW |
4 |
43,536,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Tln1
|
UTSW |
4 |
43,553,041 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8708:Tln1
|
UTSW |
4 |
43,534,769 (GRCm39) |
splice site |
probably benign |
|
R8725:Tln1
|
UTSW |
4 |
43,555,911 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8727:Tln1
|
UTSW |
4 |
43,555,911 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8830:Tln1
|
UTSW |
4 |
43,556,383 (GRCm39) |
missense |
probably benign |
|
R8865:Tln1
|
UTSW |
4 |
43,538,281 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9049:Tln1
|
UTSW |
4 |
43,549,786 (GRCm39) |
nonsense |
probably null |
|
R9050:Tln1
|
UTSW |
4 |
43,549,786 (GRCm39) |
nonsense |
probably null |
|
R9145:Tln1
|
UTSW |
4 |
43,536,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Tln1
|
UTSW |
4 |
43,536,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R9337:Tln1
|
UTSW |
4 |
43,532,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Tln1
|
UTSW |
4 |
43,546,895 (GRCm39) |
missense |
probably damaging |
0.97 |
R9358:Tln1
|
UTSW |
4 |
43,532,084 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9487:Tln1
|
UTSW |
4 |
43,542,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R9631:Tln1
|
UTSW |
4 |
43,545,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Tln1
|
UTSW |
4 |
43,545,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9666:Tln1
|
UTSW |
4 |
43,542,957 (GRCm39) |
missense |
probably damaging |
0.96 |
RF021:Tln1
|
UTSW |
4 |
43,555,890 (GRCm39) |
missense |
probably damaging |
1.00 |
X0052:Tln1
|
UTSW |
4 |
43,533,125 (GRCm39) |
critical splice donor site |
probably null |
|
X0063:Tln1
|
UTSW |
4 |
43,548,015 (GRCm39) |
nonsense |
probably null |
|
Z1176:Tln1
|
UTSW |
4 |
43,543,211 (GRCm39) |
missense |
probably benign |
0.31 |
|