Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
A |
G |
2: 19,498,905 (GRCm39) |
Y363H |
probably benign |
Het |
4933402N03Rik |
T |
A |
7: 130,740,906 (GRCm39) |
R103S |
probably damaging |
Het |
Aars1 |
A |
G |
8: 111,772,187 (GRCm39) |
D459G |
probably benign |
Het |
Adam25 |
A |
T |
8: 41,207,261 (GRCm39) |
M176L |
probably benign |
Het |
Adcy5 |
A |
G |
16: 35,087,551 (GRCm39) |
I471V |
probably damaging |
Het |
Ano8 |
A |
T |
8: 71,931,388 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
T |
A |
13: 98,083,461 (GRCm39) |
Q1136L |
probably damaging |
Het |
Atp13a3 |
A |
T |
16: 30,178,543 (GRCm39) |
C164* |
probably null |
Het |
Avl9 |
G |
A |
6: 56,734,295 (GRCm39) |
A625T |
probably damaging |
Het |
Avpr1a |
A |
T |
10: 122,285,373 (GRCm39) |
M222L |
probably benign |
Het |
B4galnt4 |
A |
T |
7: 140,651,235 (GRCm39) |
M939L |
probably damaging |
Het |
B4galt6 |
A |
G |
18: 20,822,001 (GRCm39) |
F331S |
probably benign |
Het |
C2cd2 |
G |
T |
16: 97,680,840 (GRCm39) |
Q325K |
possibly damaging |
Het |
Caml |
T |
G |
13: 55,776,409 (GRCm39) |
L216R |
probably damaging |
Het |
Cd200r4 |
A |
G |
16: 44,653,736 (GRCm39) |
T132A |
possibly damaging |
Het |
Ces1h |
A |
C |
8: 94,089,550 (GRCm39) |
V283G |
probably damaging |
Het |
Clptm1 |
A |
T |
7: 19,369,629 (GRCm39) |
V427D |
possibly damaging |
Het |
Drd1 |
T |
A |
13: 54,207,122 (GRCm39) |
N357I |
possibly damaging |
Het |
Foxq1 |
C |
G |
13: 31,743,441 (GRCm39) |
S181W |
probably damaging |
Het |
Gfra2 |
C |
T |
14: 71,215,818 (GRCm39) |
T169M |
possibly damaging |
Het |
Gm42542 |
T |
C |
6: 68,872,634 (GRCm39) |
|
probably null |
Het |
Hoxa13 |
CGG |
CGNGG |
6: 52,260,636 (GRCm38) |
|
probably null |
Het |
Hsd11b1 |
C |
A |
1: 192,922,560 (GRCm39) |
A166S |
probably benign |
Het |
Kcnab3 |
T |
A |
11: 69,219,093 (GRCm39) |
F101L |
probably damaging |
Het |
Klf6 |
C |
A |
13: 5,911,790 (GRCm39) |
H51Q |
probably damaging |
Het |
Krtap4-8 |
G |
A |
11: 99,670,898 (GRCm39) |
P191L |
unknown |
Het |
Lrrk2 |
T |
A |
15: 91,557,561 (GRCm39) |
N26K |
probably benign |
Het |
Mrgprd |
T |
C |
7: 144,876,004 (GRCm39) |
S292P |
probably benign |
Het |
Ms4a8a |
A |
G |
19: 11,053,725 (GRCm39) |
I127T |
possibly damaging |
Het |
Myo7a |
T |
G |
7: 97,744,985 (GRCm39) |
N280T |
possibly damaging |
Het |
Nipal4 |
A |
G |
11: 46,041,304 (GRCm39) |
F297S |
probably damaging |
Het |
Npas1 |
A |
G |
7: 16,195,275 (GRCm39) |
I351T |
possibly damaging |
Het |
Or12k7 |
A |
G |
2: 36,958,341 (GRCm39) |
E8G |
probably benign |
Het |
Or4a72 |
C |
A |
2: 89,405,623 (GRCm39) |
G149V |
probably damaging |
Het |
Or9e1 |
A |
T |
11: 58,732,146 (GRCm39) |
I69F |
probably benign |
Het |
Parp11 |
A |
G |
6: 127,448,598 (GRCm39) |
T72A |
probably damaging |
Het |
Pik3c3 |
T |
C |
18: 30,427,396 (GRCm39) |
V300A |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,928,612 (GRCm39) |
E881G |
possibly damaging |
Het |
Polr2h |
T |
A |
16: 20,539,281 (GRCm39) |
L57* |
probably null |
Het |
Rela |
T |
A |
19: 5,697,046 (GRCm39) |
S418T |
probably benign |
Het |
Rptn |
A |
G |
3: 93,305,180 (GRCm39) |
T838A |
possibly damaging |
Het |
Sez6l2 |
T |
A |
7: 126,560,955 (GRCm39) |
N413K |
possibly damaging |
Het |
Slc6a2 |
A |
G |
8: 93,721,268 (GRCm39) |
I466V |
probably benign |
Het |
Slco4c1 |
A |
T |
1: 96,768,876 (GRCm39) |
C329S |
probably damaging |
Het |
Sppl2c |
A |
G |
11: 104,077,691 (GRCm39) |
M164V |
probably benign |
Het |
Spta1 |
G |
A |
1: 174,007,405 (GRCm39) |
V212M |
probably damaging |
Het |
Sqor |
A |
C |
2: 122,634,288 (GRCm39) |
I142L |
probably benign |
Het |
Suco |
T |
C |
1: 161,680,420 (GRCm39) |
E317G |
probably damaging |
Het |
Tlk2 |
T |
A |
11: 105,145,805 (GRCm39) |
I337N |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,068,182 (GRCm39) |
Y234C |
probably damaging |
Het |
Tmem167 |
A |
C |
13: 90,246,585 (GRCm39) |
K36N |
probably damaging |
Het |
Trim72 |
T |
C |
7: 127,603,963 (GRCm39) |
L103P |
probably damaging |
Het |
Tut4 |
T |
C |
4: 108,408,012 (GRCm39) |
|
probably null |
Het |
Urb1 |
T |
A |
16: 90,566,357 (GRCm39) |
M1477L |
probably benign |
Het |
Vwa2 |
T |
A |
19: 56,898,164 (GRCm39) |
M721K |
possibly damaging |
Het |
Zfp143 |
T |
G |
7: 109,693,575 (GRCm39) |
D636E |
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 |
IGL00987:Tln1
|
APN |
4 |
43,551,297 (GRCm39) |
unclassified |
probably benign |
|
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 |
|
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 |
|