Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl3 |
T |
A |
7: 82,206,269 (GRCm39) |
C784S |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,745,989 (GRCm39) |
|
probably benign |
Het |
Apon |
A |
G |
10: 128,090,907 (GRCm39) |
E195G |
probably damaging |
Het |
Camsap1 |
G |
T |
2: 25,855,823 (GRCm39) |
A145E |
probably damaging |
Het |
Capns1 |
G |
T |
7: 29,887,147 (GRCm39) |
F243L |
possibly damaging |
Het |
Catsper2 |
A |
T |
2: 121,237,216 (GRCm39) |
I228N |
probably damaging |
Het |
Ceacam14 |
A |
T |
7: 17,549,402 (GRCm39) |
*264C |
probably null |
Het |
Cel |
A |
C |
2: 28,450,530 (GRCm39) |
V165G |
probably damaging |
Het |
Cldnd1 |
T |
A |
16: 58,550,016 (GRCm39) |
D66E |
possibly damaging |
Het |
Cntnap5b |
T |
A |
1: 100,311,275 (GRCm39) |
C589* |
probably null |
Het |
Dnah3 |
T |
A |
7: 119,620,234 (GRCm39) |
H1554L |
probably damaging |
Het |
Fbxw25 |
T |
A |
9: 109,492,573 (GRCm39) |
M55L |
probably benign |
Het |
Fn1 |
T |
C |
1: 71,636,591 (GRCm39) |
H2187R |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,818,489 (GRCm39) |
T4741A |
possibly damaging |
Het |
Gabpa |
T |
A |
16: 84,653,934 (GRCm39) |
I272N |
possibly damaging |
Het |
Ganab |
T |
C |
19: 8,886,049 (GRCm39) |
S212P |
probably benign |
Het |
Ggt1 |
A |
G |
10: 75,421,495 (GRCm39) |
|
probably null |
Het |
Hpgds |
T |
C |
6: 65,109,169 (GRCm39) |
T81A |
probably benign |
Het |
Insr |
G |
A |
8: 3,252,902 (GRCm39) |
T419I |
probably benign |
Het |
Itgb7 |
A |
G |
15: 102,140,059 (GRCm39) |
|
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,799,289 (GRCm39) |
I951V |
possibly damaging |
Het |
Lrrc4c |
T |
A |
2: 97,460,498 (GRCm39) |
C375S |
probably damaging |
Het |
Muc17 |
G |
T |
5: 137,175,537 (GRCm39) |
C44* |
probably null |
Het |
Mycbpap |
A |
T |
11: 94,394,330 (GRCm39) |
D313E |
probably benign |
Het |
Neo1 |
A |
G |
9: 58,813,931 (GRCm39) |
|
probably null |
Het |
Ntsr2 |
C |
T |
12: 16,709,934 (GRCm39) |
S405F |
probably benign |
Het |
Nup153 |
G |
A |
13: 46,870,682 (GRCm39) |
P21S |
probably benign |
Het |
Obscn |
T |
A |
11: 58,887,703 (GRCm39) |
E7705D |
probably benign |
Het |
Ogn |
A |
G |
13: 49,762,817 (GRCm39) |
D53G |
probably benign |
Het |
Or10d5j |
A |
T |
9: 39,868,125 (GRCm39) |
Y35* |
probably null |
Het |
Or14j10 |
A |
T |
17: 37,935,046 (GRCm39) |
I160K |
probably benign |
Het |
Or5k8 |
G |
A |
16: 58,645,066 (GRCm39) |
T2I |
probably benign |
Het |
Or5p5 |
T |
C |
7: 107,413,883 (GRCm39) |
F33L |
possibly damaging |
Het |
Or9i1b |
A |
T |
19: 13,896,980 (GRCm39) |
I199F |
possibly damaging |
Het |
Pde6a |
G |
A |
18: 61,365,983 (GRCm39) |
R236H |
possibly damaging |
Het |
Pigk |
T |
A |
3: 152,443,837 (GRCm39) |
M85K |
probably damaging |
Het |
Pirb |
A |
C |
7: 3,719,598 (GRCm39) |
I516S |
possibly damaging |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Pum2 |
T |
A |
12: 8,794,706 (GRCm39) |
I737N |
probably damaging |
Het |
Recql5 |
A |
T |
11: 115,818,215 (GRCm39) |
C159S |
probably damaging |
Het |
Rxrg |
A |
G |
1: 167,452,573 (GRCm39) |
N125S |
probably benign |
Het |
Sgip1 |
C |
A |
4: 102,823,477 (GRCm39) |
N699K |
probably damaging |
Het |
Shprh |
G |
A |
10: 11,046,041 (GRCm39) |
|
probably null |
Het |
Smcp |
C |
T |
3: 92,491,454 (GRCm39) |
G131D |
unknown |
Het |
St8sia6 |
A |
G |
2: 13,798,188 (GRCm39) |
L23P |
possibly damaging |
Het |
Stk32c |
T |
A |
7: 138,699,276 (GRCm39) |
T335S |
probably benign |
Het |
Stox1 |
G |
A |
10: 62,499,812 (GRCm39) |
A916V |
possibly damaging |
Het |
Syk |
A |
T |
13: 52,785,753 (GRCm39) |
T297S |
probably benign |
Het |
Tert |
G |
T |
13: 73,796,490 (GRCm39) |
A1074S |
probably benign |
Het |
Tex9 |
A |
T |
9: 72,385,187 (GRCm39) |
D135E |
probably damaging |
Het |
Tmem132a |
G |
A |
19: 10,841,371 (GRCm39) |
H318Y |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,738,249 (GRCm39) |
S4097P |
probably benign |
Het |
Ush2a |
A |
T |
1: 188,553,874 (GRCm39) |
|
probably null |
Het |
Usp36 |
A |
T |
11: 118,156,020 (GRCm39) |
S586T |
probably benign |
Het |
Vsig8 |
A |
G |
1: 172,388,244 (GRCm39) |
S71G |
probably benign |
Het |
Zfp318 |
G |
A |
17: 46,697,662 (GRCm39) |
D173N |
probably damaging |
Het |
Zfp638 |
T |
A |
6: 83,939,076 (GRCm39) |
S936T |
probably damaging |
Het |
Zic2 |
A |
G |
14: 122,713,728 (GRCm39) |
Y214C |
probably damaging |
Het |
|
Other mutations in Atxn10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00975:Atxn10
|
APN |
15 |
85,220,666 (GRCm39) |
start codon destroyed |
probably benign |
0.33 |
IGL01020:Atxn10
|
APN |
15 |
85,259,623 (GRCm39) |
splice site |
probably null |
|
IGL01380:Atxn10
|
APN |
15 |
85,260,896 (GRCm39) |
nonsense |
probably null |
|
IGL01408:Atxn10
|
APN |
15 |
85,260,896 (GRCm39) |
nonsense |
probably null |
|
3-1:Atxn10
|
UTSW |
15 |
85,322,295 (GRCm39) |
splice site |
probably benign |
|
R0190:Atxn10
|
UTSW |
15 |
85,220,730 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0319:Atxn10
|
UTSW |
15 |
85,249,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Atxn10
|
UTSW |
15 |
85,243,675 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1746:Atxn10
|
UTSW |
15 |
85,260,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Atxn10
|
UTSW |
15 |
85,249,513 (GRCm39) |
missense |
probably benign |
0.37 |
R3055:Atxn10
|
UTSW |
15 |
85,271,206 (GRCm39) |
missense |
probably benign |
0.03 |
R4559:Atxn10
|
UTSW |
15 |
85,322,321 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4786:Atxn10
|
UTSW |
15 |
85,271,344 (GRCm39) |
missense |
probably benign |
0.03 |
R4799:Atxn10
|
UTSW |
15 |
85,260,909 (GRCm39) |
splice site |
probably null |
|
R4831:Atxn10
|
UTSW |
15 |
85,271,260 (GRCm39) |
missense |
probably benign |
0.01 |
R5335:Atxn10
|
UTSW |
15 |
85,220,785 (GRCm39) |
splice site |
probably null |
|
R5355:Atxn10
|
UTSW |
15 |
85,346,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R5768:Atxn10
|
UTSW |
15 |
85,277,621 (GRCm39) |
missense |
probably benign |
0.01 |
R6260:Atxn10
|
UTSW |
15 |
85,346,612 (GRCm39) |
missense |
probably benign |
0.38 |
R6277:Atxn10
|
UTSW |
15 |
85,275,893 (GRCm39) |
missense |
probably benign |
0.05 |
R6370:Atxn10
|
UTSW |
15 |
85,277,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Atxn10
|
UTSW |
15 |
85,260,904 (GRCm39) |
critical splice donor site |
probably null |
|
R6957:Atxn10
|
UTSW |
15 |
85,220,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R7859:Atxn10
|
UTSW |
15 |
85,346,526 (GRCm39) |
missense |
probably benign |
0.01 |
R8031:Atxn10
|
UTSW |
15 |
85,277,594 (GRCm39) |
missense |
probably benign |
|
R9062:Atxn10
|
UTSW |
15 |
85,275,918 (GRCm39) |
missense |
probably benign |
|
R9171:Atxn10
|
UTSW |
15 |
85,277,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Atxn10
|
UTSW |
15 |
85,243,687 (GRCm39) |
missense |
probably damaging |
0.98 |
R9429:Atxn10
|
UTSW |
15 |
85,346,565 (GRCm39) |
missense |
probably benign |
0.13 |
|