Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
G |
1: 71,303,926 (GRCm39) |
L2117P |
probably damaging |
Het |
Ago3 |
A |
T |
4: 126,262,391 (GRCm39) |
S386R |
probably benign |
Het |
Agxt |
T |
C |
1: 93,069,779 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
A |
T |
1: 179,611,675 (GRCm39) |
I565N |
possibly damaging |
Het |
Ank1 |
C |
T |
8: 23,572,300 (GRCm39) |
T70I |
probably damaging |
Het |
Anxa1 |
A |
G |
19: 20,360,287 (GRCm39) |
V108A |
probably benign |
Het |
Aqp3 |
A |
G |
4: 41,093,819 (GRCm39) |
F225L |
probably damaging |
Het |
Atp11b |
T |
G |
3: 35,888,532 (GRCm39) |
I934R |
possibly damaging |
Het |
Atp13a5 |
A |
T |
16: 29,169,566 (GRCm39) |
L42Q |
probably damaging |
Het |
Bcr |
A |
G |
10: 74,960,898 (GRCm39) |
D443G |
probably benign |
Het |
Cbfa2t3 |
G |
T |
8: 123,365,598 (GRCm39) |
D211E |
possibly damaging |
Het |
Ccdc146 |
A |
T |
5: 21,538,036 (GRCm39) |
L96Q |
probably damaging |
Het |
Cdh16 |
A |
G |
8: 105,343,660 (GRCm39) |
I612T |
probably damaging |
Het |
Clcn2 |
G |
A |
16: 20,525,965 (GRCm39) |
P785S |
probably damaging |
Het |
Dennd5a |
A |
G |
7: 109,513,983 (GRCm39) |
I743T |
possibly damaging |
Het |
Dnah12 |
T |
A |
14: 26,431,326 (GRCm39) |
D381E |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dnajc2 |
G |
A |
5: 21,962,771 (GRCm39) |
R521* |
probably null |
Het |
Dst |
T |
C |
1: 34,289,728 (GRCm39) |
V5776A |
probably damaging |
Het |
Eddm13 |
G |
A |
7: 6,269,332 (GRCm39) |
|
probably benign |
Het |
Eif1ad19 |
T |
A |
12: 87,740,512 (GRCm39) |
K16* |
probably null |
Het |
Ercc4 |
G |
A |
16: 12,941,445 (GRCm39) |
|
probably benign |
Het |
Eya1 |
T |
A |
1: 14,254,582 (GRCm39) |
N417Y |
probably damaging |
Het |
Fam149b |
T |
A |
14: 20,413,439 (GRCm39) |
H219Q |
possibly damaging |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fbxw17 |
C |
T |
13: 50,586,506 (GRCm39) |
R403C |
probably benign |
Het |
Fer1l4 |
T |
C |
2: 155,873,135 (GRCm39) |
Y1315C |
probably damaging |
Het |
Gatd1 |
G |
T |
7: 140,988,861 (GRCm39) |
|
probably benign |
Het |
Gm10330 |
A |
T |
12: 23,829,961 (GRCm39) |
Y73* |
probably null |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
Gsn |
T |
A |
2: 35,188,933 (GRCm39) |
Y440N |
probably damaging |
Het |
Hdc |
C |
T |
2: 126,446,220 (GRCm39) |
E180K |
probably benign |
Het |
Ilk |
A |
G |
7: 105,391,456 (GRCm39) |
D374G |
probably damaging |
Het |
Invs |
G |
A |
4: 48,421,807 (GRCm39) |
R813Q |
probably damaging |
Het |
Itln1 |
T |
A |
1: 171,360,958 (GRCm39) |
K45* |
probably null |
Het |
Ivd |
A |
G |
2: 118,710,946 (GRCm39) |
Y385C |
probably damaging |
Het |
Klk1b4 |
A |
G |
7: 43,860,492 (GRCm39) |
N170S |
probably benign |
Het |
Klk1b9 |
A |
C |
7: 43,445,419 (GRCm39) |
D203A |
probably damaging |
Het |
Lamtor3 |
A |
T |
3: 137,630,909 (GRCm39) |
R27S |
probably damaging |
Het |
Lcn6 |
T |
A |
2: 25,567,082 (GRCm39) |
|
probably null |
Het |
Lrriq1 |
T |
C |
10: 103,025,784 (GRCm39) |
D946G |
probably damaging |
Het |
Morc1 |
A |
G |
16: 48,322,699 (GRCm39) |
D332G |
probably benign |
Het |
Myo15a |
T |
C |
11: 60,382,493 (GRCm39) |
I1523T |
probably damaging |
Het |
Nagpa |
A |
T |
16: 5,013,743 (GRCm39) |
M365K |
probably benign |
Het |
Nckap5l |
G |
T |
15: 99,324,457 (GRCm39) |
P682Q |
probably benign |
Het |
Nfix |
A |
G |
8: 85,498,713 (GRCm39) |
F87L |
possibly damaging |
Het |
Nup155 |
C |
A |
15: 8,153,722 (GRCm39) |
T421K |
probably benign |
Het |
Or5ac25 |
A |
T |
16: 59,182,067 (GRCm39) |
N171K |
probably damaging |
Het |
Or5ae2 |
T |
C |
7: 84,505,646 (GRCm39) |
V23A |
probably damaging |
Het |
Or7c74 |
A |
G |
2: 37,160,937 (GRCm39) |
|
noncoding transcript |
Het |
Or8k53 |
A |
T |
2: 86,177,647 (GRCm39) |
F154L |
probably benign |
Het |
Pate14 |
T |
C |
9: 36,549,120 (GRCm39) |
N47D |
probably benign |
Het |
Pds5a |
A |
C |
5: 65,792,680 (GRCm39) |
V751G |
probably benign |
Het |
Podnl1 |
G |
T |
8: 84,852,965 (GRCm39) |
C45F |
probably damaging |
Het |
Psme2b |
C |
T |
11: 48,836,654 (GRCm39) |
E98K |
probably benign |
Het |
Ptprk |
T |
A |
10: 28,427,713 (GRCm39) |
I764N |
probably damaging |
Het |
Rbm33 |
A |
T |
5: 28,547,409 (GRCm39) |
Q193L |
probably benign |
Het |
Rnasel |
C |
A |
1: 153,629,677 (GRCm39) |
H64Q |
probably damaging |
Het |
Ryr1 |
G |
A |
7: 28,802,234 (GRCm39) |
|
probably null |
Het |
Scamp3 |
A |
G |
3: 89,088,216 (GRCm39) |
|
probably benign |
Het |
Sema6b |
C |
T |
17: 56,439,497 (GRCm39) |
|
probably null |
Het |
Six4 |
A |
C |
12: 73,150,400 (GRCm39) |
I715R |
probably benign |
Het |
Slc28a2 |
T |
C |
2: 122,288,371 (GRCm39) |
M554T |
possibly damaging |
Het |
Snhg11 |
T |
C |
2: 158,218,872 (GRCm39) |
|
probably benign |
Het |
Spdya |
A |
T |
17: 71,869,499 (GRCm39) |
Y98F |
possibly damaging |
Het |
Tex22 |
G |
A |
12: 113,052,104 (GRCm39) |
C54Y |
probably damaging |
Het |
Tmem198b |
C |
T |
10: 128,637,942 (GRCm39) |
R207H |
probably damaging |
Het |
Trbv13-1 |
C |
T |
6: 41,093,189 (GRCm39) |
Q42* |
probably null |
Het |
Trcg1 |
T |
C |
9: 57,149,562 (GRCm39) |
L378P |
probably damaging |
Het |
Trpv5 |
T |
G |
6: 41,636,647 (GRCm39) |
D433A |
probably damaging |
Het |
Ube3b |
A |
G |
5: 114,545,702 (GRCm39) |
N654D |
probably damaging |
Het |
Vmn1r17 |
A |
G |
6: 57,337,828 (GRCm39) |
V130A |
probably benign |
Het |
Vwa7 |
A |
T |
17: 35,241,709 (GRCm39) |
Y448F |
probably damaging |
Het |
Zan |
A |
C |
5: 137,382,099 (GRCm39) |
D5149E |
unknown |
Het |
Zfp106 |
A |
G |
2: 120,341,015 (GRCm39) |
W1832R |
probably damaging |
Het |
Zfp189 |
G |
A |
4: 49,530,438 (GRCm39) |
G514S |
probably damaging |
Het |
Zhx1 |
G |
A |
15: 57,917,538 (GRCm39) |
T236I |
possibly damaging |
Het |
|
Other mutations in Tert |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01286:Tert
|
APN |
13 |
73,776,416 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01585:Tert
|
APN |
13 |
73,782,463 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03167:Tert
|
APN |
13 |
73,788,119 (GRCm39) |
missense |
probably damaging |
1.00 |
galileo
|
UTSW |
13 |
73,775,725 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Tert
|
UTSW |
13 |
73,796,421 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4342:Tert
|
UTSW |
13 |
73,796,419 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4589:Tert
|
UTSW |
13 |
73,796,423 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4377001:Tert
|
UTSW |
13 |
73,776,380 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0372:Tert
|
UTSW |
13 |
73,797,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Tert
|
UTSW |
13 |
73,775,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0829:Tert
|
UTSW |
13 |
73,792,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Tert
|
UTSW |
13 |
73,790,178 (GRCm39) |
missense |
probably benign |
0.41 |
R1236:Tert
|
UTSW |
13 |
73,784,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R1331:Tert
|
UTSW |
13 |
73,796,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Tert
|
UTSW |
13 |
73,790,472 (GRCm39) |
splice site |
probably benign |
|
R1467:Tert
|
UTSW |
13 |
73,776,328 (GRCm39) |
missense |
probably benign |
0.10 |
R1467:Tert
|
UTSW |
13 |
73,776,328 (GRCm39) |
missense |
probably benign |
0.10 |
R1521:Tert
|
UTSW |
13 |
73,790,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Tert
|
UTSW |
13 |
73,796,104 (GRCm39) |
missense |
probably benign |
|
R3162:Tert
|
UTSW |
13 |
73,775,528 (GRCm39) |
missense |
possibly damaging |
0.45 |
R3162:Tert
|
UTSW |
13 |
73,775,528 (GRCm39) |
missense |
possibly damaging |
0.45 |
R4428:Tert
|
UTSW |
13 |
73,775,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4430:Tert
|
UTSW |
13 |
73,775,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:Tert
|
UTSW |
13 |
73,775,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4630:Tert
|
UTSW |
13 |
73,797,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R4696:Tert
|
UTSW |
13 |
73,775,939 (GRCm39) |
missense |
probably benign |
0.25 |
R4751:Tert
|
UTSW |
13 |
73,776,182 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4926:Tert
|
UTSW |
13 |
73,796,508 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5011:Tert
|
UTSW |
13 |
73,794,428 (GRCm39) |
critical splice donor site |
probably null |
|
R5061:Tert
|
UTSW |
13 |
73,782,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Tert
|
UTSW |
13 |
73,775,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Tert
|
UTSW |
13 |
73,796,490 (GRCm39) |
missense |
probably benign |
0.07 |
R5396:Tert
|
UTSW |
13 |
73,787,362 (GRCm39) |
missense |
probably damaging |
0.97 |
R5445:Tert
|
UTSW |
13 |
73,792,403 (GRCm39) |
missense |
probably benign |
0.00 |
R5680:Tert
|
UTSW |
13 |
73,790,470 (GRCm39) |
splice site |
probably null |
|
R5688:Tert
|
UTSW |
13 |
73,787,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R6092:Tert
|
UTSW |
13 |
73,776,700 (GRCm39) |
missense |
probably benign |
0.34 |
R6973:Tert
|
UTSW |
13 |
73,776,107 (GRCm39) |
missense |
probably benign |
0.02 |
R7069:Tert
|
UTSW |
13 |
73,776,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R7317:Tert
|
UTSW |
13 |
73,790,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R7747:Tert
|
UTSW |
13 |
73,775,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Tert
|
UTSW |
13 |
73,797,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R7846:Tert
|
UTSW |
13 |
73,776,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R7994:Tert
|
UTSW |
13 |
73,797,074 (GRCm39) |
missense |
probably benign |
0.20 |
R8042:Tert
|
UTSW |
13 |
73,775,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R8044:Tert
|
UTSW |
13 |
73,783,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Tert
|
UTSW |
13 |
73,776,566 (GRCm39) |
missense |
probably benign |
|
R9181:Tert
|
UTSW |
13 |
73,785,294 (GRCm39) |
intron |
probably benign |
|
R9412:Tert
|
UTSW |
13 |
73,797,046 (GRCm39) |
missense |
probably benign |
0.03 |
R9745:Tert
|
UTSW |
13 |
73,784,609 (GRCm39) |
missense |
probably damaging |
0.96 |
R9790:Tert
|
UTSW |
13 |
73,775,648 (GRCm39) |
missense |
probably benign |
0.21 |
R9791:Tert
|
UTSW |
13 |
73,775,648 (GRCm39) |
missense |
probably benign |
0.21 |
R9792:Tert
|
UTSW |
13 |
73,792,442 (GRCm39) |
missense |
probably benign |
0.05 |
|