Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
T |
A |
5: 77,024,203 (GRCm39) |
I991L |
probably benign |
Het |
Abtb3 |
C |
A |
10: 85,223,520 (GRCm39) |
R110S |
unknown |
Het |
Actg2 |
C |
A |
6: 83,497,745 (GRCm39) |
G96V |
probably damaging |
Het |
Adh5 |
T |
A |
3: 138,156,812 (GRCm39) |
L166* |
probably null |
Het |
Akap13 |
A |
G |
7: 75,260,010 (GRCm39) |
D75G |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,739,947 (GRCm39) |
|
probably benign |
Het |
Arfgap1 |
T |
A |
2: 180,615,913 (GRCm39) |
D197E |
probably benign |
Het |
Aste1 |
T |
C |
9: 105,273,906 (GRCm39) |
|
probably null |
Het |
Atp8b2 |
T |
A |
3: 89,861,878 (GRCm39) |
N78I |
probably damaging |
Het |
Cacna2d3 |
T |
A |
14: 28,691,260 (GRCm39) |
|
probably benign |
Het |
Chrd |
T |
A |
16: 20,558,183 (GRCm39) |
W809R |
probably damaging |
Het |
Col2a1 |
C |
T |
15: 97,896,469 (GRCm39) |
G60D |
unknown |
Het |
Coro7 |
T |
A |
16: 4,497,475 (GRCm39) |
M1L |
probably damaging |
Het |
Cracdl |
A |
T |
1: 37,670,982 (GRCm39) |
F97Y |
probably damaging |
Het |
Dhx40 |
T |
C |
11: 86,688,569 (GRCm39) |
I285V |
probably benign |
Het |
Dop1a |
T |
C |
9: 86,432,222 (GRCm39) |
|
probably null |
Het |
Enox1 |
A |
T |
14: 77,848,764 (GRCm39) |
R358S |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,815,990 (GRCm39) |
V2724A |
probably damaging |
Het |
Fam221a |
A |
C |
6: 49,355,432 (GRCm39) |
Q178P |
probably damaging |
Het |
Fcho1 |
A |
C |
8: 72,163,141 (GRCm39) |
|
probably null |
Het |
Fndc1 |
A |
T |
17: 7,988,567 (GRCm39) |
V1165D |
unknown |
Het |
Gal3st2b |
A |
T |
1: 93,868,341 (GRCm39) |
N189Y |
possibly damaging |
Het |
Ghr |
T |
A |
15: 3,349,966 (GRCm39) |
D404V |
probably damaging |
Het |
Glis3 |
A |
T |
19: 28,508,919 (GRCm39) |
V355D |
probably damaging |
Het |
Gpr12 |
A |
C |
5: 146,520,349 (GRCm39) |
V32G |
possibly damaging |
Het |
Gspt1 |
T |
A |
16: 11,040,525 (GRCm39) |
L593F |
probably damaging |
Het |
H2-Q7 |
A |
T |
17: 35,659,007 (GRCm39) |
T153S |
probably damaging |
Het |
Hars2 |
A |
G |
18: 36,921,009 (GRCm39) |
I194V |
probably damaging |
Het |
Hdac9 |
T |
A |
12: 34,479,548 (GRCm39) |
T202S |
possibly damaging |
Het |
Hoxd13 |
T |
C |
2: 74,499,368 (GRCm39) |
Y239H |
probably damaging |
Het |
Insm2 |
C |
T |
12: 55,646,621 (GRCm39) |
Q122* |
probably null |
Het |
Insyn2b |
T |
A |
11: 34,352,677 (GRCm39) |
C240S |
possibly damaging |
Het |
Ip6k1 |
T |
A |
9: 107,922,651 (GRCm39) |
|
probably null |
Het |
Ippk |
T |
C |
13: 49,615,219 (GRCm39) |
V534A |
probably damaging |
Het |
Itch |
T |
G |
2: 155,051,914 (GRCm39) |
F611C |
probably damaging |
Het |
Itga1 |
A |
T |
13: 115,104,776 (GRCm39) |
N1083K |
probably damaging |
Het |
Itgae |
A |
C |
11: 73,006,969 (GRCm39) |
D405A |
probably damaging |
Het |
Kif18a |
T |
C |
2: 109,125,347 (GRCm39) |
S255P |
probably damaging |
Het |
Klhl24 |
C |
G |
16: 19,926,231 (GRCm39) |
T253R |
probably benign |
Het |
Krt81 |
T |
A |
15: 101,358,609 (GRCm39) |
T307S |
possibly damaging |
Het |
Lbr |
A |
T |
1: 181,656,354 (GRCm39) |
W265R |
probably damaging |
Het |
Lgals3bp |
T |
C |
11: 118,283,999 (GRCm39) |
T527A |
probably benign |
Het |
Lzts1 |
A |
C |
8: 69,593,397 (GRCm39) |
V70G |
probably damaging |
Het |
Map3k6 |
C |
T |
4: 132,979,023 (GRCm39) |
P1154S |
probably benign |
Het |
Masp1 |
T |
C |
16: 23,271,205 (GRCm39) |
D681G |
probably benign |
Het |
Mdga2 |
T |
C |
12: 66,533,526 (GRCm39) |
N948D |
probably benign |
Het |
Mettl4 |
A |
T |
17: 95,041,061 (GRCm39) |
F364L |
probably damaging |
Het |
Mosmo |
T |
C |
7: 120,277,055 (GRCm39) |
I23T |
probably benign |
Het |
Mtg1 |
G |
A |
7: 139,723,657 (GRCm39) |
V96I |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,036,803 (GRCm39) |
R966S |
possibly damaging |
Het |
Ncapg2 |
A |
G |
12: 116,388,337 (GRCm39) |
|
probably null |
Het |
Nid1 |
G |
A |
13: 13,683,353 (GRCm39) |
V1144I |
probably benign |
Het |
Or4a77 |
T |
C |
2: 89,486,910 (GRCm39) |
I292V |
probably benign |
Het |
Or52a33 |
A |
T |
7: 103,289,167 (GRCm39) |
M60K |
probably damaging |
Het |
Or55b4 |
C |
A |
7: 102,133,979 (GRCm39) |
C116F |
possibly damaging |
Het |
Oscar |
T |
G |
7: 3,614,238 (GRCm39) |
Y167S |
probably damaging |
Het |
Pa2g4 |
T |
C |
10: 128,396,559 (GRCm39) |
T200A |
probably benign |
Het |
Pcdh7 |
A |
G |
5: 57,877,126 (GRCm39) |
D227G |
probably benign |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Plce1 |
G |
A |
19: 38,747,384 (GRCm39) |
G1702R |
probably damaging |
Het |
Plxna2 |
C |
A |
1: 194,476,212 (GRCm39) |
T1144K |
possibly damaging |
Het |
Prl8a8 |
G |
A |
13: 27,695,450 (GRCm39) |
T99I |
probably benign |
Het |
Prr29 |
C |
A |
11: 106,267,085 (GRCm39) |
H83Q |
probably damaging |
Het |
Raly |
T |
A |
2: 154,701,664 (GRCm39) |
I108N |
possibly damaging |
Het |
Ranbp9 |
A |
T |
13: 43,573,098 (GRCm39) |
S475R |
probably benign |
Het |
Rogdi |
C |
A |
16: 4,831,362 (GRCm39) |
|
probably benign |
Het |
Rorc |
C |
T |
3: 94,280,214 (GRCm39) |
Q6* |
probably null |
Het |
Sacs |
T |
C |
14: 61,449,945 (GRCm39) |
L3997S |
probably damaging |
Het |
Scn2a |
A |
T |
2: 65,594,950 (GRCm39) |
Y1933F |
probably benign |
Het |
Sik3 |
T |
C |
9: 46,122,041 (GRCm39) |
L898P |
probably damaging |
Het |
Sipa1l1 |
A |
G |
12: 82,388,180 (GRCm39) |
I135M |
probably damaging |
Het |
Slc26a3 |
C |
A |
12: 31,500,934 (GRCm39) |
Q224K |
probably damaging |
Het |
Sobp |
G |
T |
10: 42,897,436 (GRCm39) |
N716K |
probably benign |
Het |
Spata16 |
A |
G |
3: 26,981,483 (GRCm39) |
D513G |
probably damaging |
Het |
Spata31h1 |
G |
A |
10: 82,125,777 (GRCm39) |
T2411I |
probably damaging |
Het |
Speer4a3 |
A |
T |
5: 26,154,842 (GRCm39) |
S253T |
possibly damaging |
Het |
Stac |
T |
C |
9: 111,401,394 (GRCm39) |
R351G |
possibly damaging |
Het |
Tecta |
T |
A |
9: 42,306,237 (GRCm39) |
T64S |
probably benign |
Het |
Tex15 |
G |
A |
8: 34,060,748 (GRCm39) |
M333I |
probably benign |
Het |
Tmbim4 |
A |
T |
10: 120,056,664 (GRCm39) |
Q72L |
probably benign |
Het |
Trav9n-4 |
T |
C |
14: 53,532,256 (GRCm39) |
S37P |
probably benign |
Het |
Trpv5 |
A |
T |
6: 41,652,894 (GRCm39) |
M93K |
possibly damaging |
Het |
Ulk4 |
T |
C |
9: 121,087,876 (GRCm39) |
E272G |
probably benign |
Het |
Ulk4 |
T |
C |
9: 121,095,583 (GRCm39) |
T79A |
probably benign |
Het |
Upb1 |
A |
G |
10: 75,248,602 (GRCm39) |
N41D |
probably benign |
Het |
Wls |
A |
T |
3: 159,639,965 (GRCm39) |
Y532F |
probably damaging |
Het |
Zdhhc5 |
G |
A |
2: 84,545,355 (GRCm39) |
|
probably benign |
Het |
Zfp109 |
T |
C |
7: 23,928,785 (GRCm39) |
D216G |
probably benign |
Het |
Zfp473 |
G |
A |
7: 44,381,798 (GRCm39) |
A845V |
probably 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 |
|
R5013: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 |
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 |
|