Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
A |
C |
5: 144,981,693 (GRCm39) |
E176A |
possibly damaging |
Het |
Abcc2 |
A |
G |
19: 43,792,178 (GRCm39) |
I320V |
probably benign |
Het |
Abtb1 |
C |
T |
6: 88,813,269 (GRCm39) |
A466T |
probably benign |
Het |
Ak6 |
C |
A |
13: 100,792,181 (GRCm39) |
T208K |
probably benign |
Het |
Albfm1 |
G |
T |
5: 90,719,611 (GRCm39) |
V236L |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Anapc15 |
T |
A |
7: 101,550,239 (GRCm39) |
|
probably benign |
Het |
Anxa2r1 |
G |
T |
13: 120,496,765 (GRCm39) |
R35S |
possibly damaging |
Het |
Aopep |
T |
C |
13: 63,215,906 (GRCm39) |
S393P |
probably benign |
Het |
Aspn |
A |
G |
13: 49,710,901 (GRCm39) |
D182G |
probably benign |
Het |
Astn1 |
A |
T |
1: 158,407,864 (GRCm39) |
D607V |
probably damaging |
Het |
Btnl1 |
A |
G |
17: 34,598,725 (GRCm39) |
I114V |
probably null |
Het |
Ccdc159 |
A |
G |
9: 21,840,762 (GRCm39) |
S110G |
probably benign |
Het |
Cdh18 |
A |
C |
15: 22,714,128 (GRCm39) |
|
probably benign |
Het |
Cenpk |
T |
A |
13: 104,385,901 (GRCm39) |
H265Q |
possibly damaging |
Het |
Chd6 |
A |
G |
2: 160,811,412 (GRCm39) |
L1397P |
probably damaging |
Het |
Chia1 |
A |
C |
3: 106,036,256 (GRCm39) |
N279H |
probably benign |
Het |
Cyp8b1 |
T |
C |
9: 121,744,651 (GRCm39) |
E227G |
probably damaging |
Het |
Dmxl2 |
A |
T |
9: 54,311,404 (GRCm39) |
N1772K |
possibly damaging |
Het |
Dnah2 |
A |
G |
11: 69,354,487 (GRCm39) |
S2244P |
probably damaging |
Het |
Fshr |
T |
C |
17: 89,293,148 (GRCm39) |
Y510C |
probably damaging |
Het |
Gm5087 |
T |
C |
14: 13,158,798 (GRCm38) |
|
noncoding transcript |
Het |
Gm7135 |
A |
C |
1: 97,387,351 (GRCm39) |
|
noncoding transcript |
Het |
Hnrnpll |
A |
T |
17: 80,358,291 (GRCm39) |
Y153* |
probably null |
Het |
Htt |
T |
A |
5: 34,987,129 (GRCm39) |
V1116E |
probably damaging |
Het |
Ikzf5 |
A |
T |
7: 130,995,482 (GRCm39) |
|
probably null |
Het |
Kcnb1 |
A |
G |
2: 167,030,153 (GRCm39) |
S131P |
probably damaging |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Kctd21 |
A |
G |
7: 96,996,782 (GRCm39) |
D85G |
probably damaging |
Het |
Kera |
A |
G |
10: 97,445,493 (GRCm39) |
N284S |
probably benign |
Het |
Kif1a |
A |
T |
1: 92,970,381 (GRCm39) |
D952E |
probably benign |
Het |
Klf4 |
A |
G |
4: 55,530,370 (GRCm39) |
V247A |
probably benign |
Het |
Krt1 |
C |
T |
15: 101,754,622 (GRCm39) |
G543S |
unknown |
Het |
Lamc1 |
A |
G |
1: 153,118,442 (GRCm39) |
S910P |
probably benign |
Het |
Lin9 |
T |
A |
1: 180,516,845 (GRCm39) |
N512K |
probably damaging |
Het |
Mroh2a |
A |
T |
1: 88,182,687 (GRCm39) |
N1205I |
possibly damaging |
Het |
Mrps30 |
A |
G |
13: 118,523,250 (GRCm39) |
V174A |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,462,240 (GRCm39) |
E574G |
probably damaging |
Het |
Nphp3 |
G |
A |
9: 103,913,358 (GRCm39) |
G997R |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,958,084 (GRCm39) |
C3748R |
probably damaging |
Het |
Or1j17 |
A |
G |
2: 36,578,083 (GRCm39) |
D23G |
probably benign |
Het |
Or5p69 |
T |
C |
7: 107,966,895 (GRCm39) |
L66P |
probably damaging |
Het |
Or8g28 |
A |
T |
9: 39,169,614 (GRCm39) |
M118K |
probably damaging |
Het |
Or9s18 |
T |
A |
13: 65,300,674 (GRCm39) |
V212D |
possibly damaging |
Het |
Orc5 |
G |
T |
5: 22,753,003 (GRCm39) |
F10L |
probably benign |
Het |
Ptch1 |
T |
C |
13: 63,670,978 (GRCm39) |
T851A |
probably benign |
Het |
Ranbp6 |
A |
T |
19: 29,788,263 (GRCm39) |
Y696* |
probably null |
Het |
Rbp3 |
A |
G |
14: 33,678,056 (GRCm39) |
Q668R |
probably benign |
Het |
Rfwd3 |
T |
C |
8: 112,002,990 (GRCm39) |
T611A |
probably benign |
Het |
Rhcg |
T |
A |
7: 79,251,352 (GRCm39) |
D219V |
probably damaging |
Het |
Rmi1 |
A |
G |
13: 58,556,950 (GRCm39) |
R400G |
probably benign |
Het |
Slc25a26 |
G |
T |
6: 94,484,633 (GRCm39) |
V58F |
probably damaging |
Het |
Smarca5 |
T |
A |
8: 81,437,192 (GRCm39) |
K721N |
probably damaging |
Het |
Sp110 |
A |
C |
1: 85,505,050 (GRCm39) |
F434C |
probably benign |
Het |
Speer2 |
A |
T |
16: 69,655,642 (GRCm39) |
Y61* |
probably null |
Het |
Spef2 |
T |
C |
15: 9,647,524 (GRCm39) |
Y961C |
probably damaging |
Het |
Sptb |
C |
A |
12: 76,634,100 (GRCm39) |
|
probably null |
Het |
Svep1 |
T |
G |
4: 58,072,698 (GRCm39) |
N2204H |
probably damaging |
Het |
Tex56 |
G |
A |
13: 35,116,448 (GRCm39) |
G66S |
probably damaging |
Het |
Tmem86a |
C |
A |
7: 46,702,613 (GRCm39) |
P13T |
probably damaging |
Het |
Tmt1a |
A |
T |
15: 100,210,939 (GRCm39) |
Q170L |
probably damaging |
Het |
Tmtc2 |
A |
T |
10: 105,139,511 (GRCm39) |
S672T |
probably benign |
Het |
Tox2 |
G |
A |
2: 163,156,336 (GRCm39) |
S211N |
possibly damaging |
Het |
Trpc6 |
A |
T |
9: 8,677,963 (GRCm39) |
E762D |
probably benign |
Het |
Tshb |
C |
T |
3: 102,685,461 (GRCm39) |
|
probably null |
Het |
Ttc3 |
T |
A |
16: 94,189,131 (GRCm39) |
L163* |
probably null |
Het |
Twsg1 |
G |
T |
17: 66,236,546 (GRCm39) |
D161E |
probably benign |
Het |
Uchl4 |
A |
C |
9: 64,143,080 (GRCm39) |
D187A |
probably damaging |
Het |
Vmn2r104 |
A |
T |
17: 20,268,443 (GRCm39) |
W9R |
probably benign |
Het |
Yju2 |
T |
A |
17: 56,271,598 (GRCm39) |
L173Q |
probably damaging |
Het |
Zfp14 |
G |
A |
7: 29,738,020 (GRCm39) |
Q322* |
probably null |
Het |
Znhit3 |
G |
A |
11: 84,802,316 (GRCm39) |
P145S |
probably damaging |
Het |
|
Other mutations in Cdh22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Cdh22
|
APN |
2 |
164,954,521 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01868:Cdh22
|
APN |
2 |
164,999,278 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01932:Cdh22
|
APN |
2 |
165,012,728 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02268:Cdh22
|
APN |
2 |
164,965,639 (GRCm39) |
splice site |
probably benign |
|
IGL02455:Cdh22
|
APN |
2 |
164,984,175 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03231:Cdh22
|
APN |
2 |
164,958,126 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03264:Cdh22
|
APN |
2 |
164,958,093 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03014:Cdh22
|
UTSW |
2 |
164,954,331 (GRCm39) |
nonsense |
probably null |
|
R0712:Cdh22
|
UTSW |
2 |
165,012,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R0865:Cdh22
|
UTSW |
2 |
165,022,976 (GRCm39) |
missense |
probably damaging |
0.98 |
R1192:Cdh22
|
UTSW |
2 |
164,977,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R1700:Cdh22
|
UTSW |
2 |
165,012,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1844:Cdh22
|
UTSW |
2 |
164,985,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Cdh22
|
UTSW |
2 |
165,022,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Cdh22
|
UTSW |
2 |
164,958,314 (GRCm39) |
splice site |
probably benign |
|
R2270:Cdh22
|
UTSW |
2 |
164,985,767 (GRCm39) |
splice site |
probably null |
|
R2271:Cdh22
|
UTSW |
2 |
164,985,767 (GRCm39) |
splice site |
probably null |
|
R2272:Cdh22
|
UTSW |
2 |
164,985,767 (GRCm39) |
splice site |
probably null |
|
R4021:Cdh22
|
UTSW |
2 |
164,985,593 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4022:Cdh22
|
UTSW |
2 |
164,999,173 (GRCm39) |
missense |
probably benign |
0.14 |
R4613:Cdh22
|
UTSW |
2 |
164,985,576 (GRCm39) |
missense |
probably benign |
|
R5038:Cdh22
|
UTSW |
2 |
164,984,197 (GRCm39) |
missense |
probably benign |
0.16 |
R5057:Cdh22
|
UTSW |
2 |
164,958,063 (GRCm39) |
missense |
probably damaging |
0.98 |
R5649:Cdh22
|
UTSW |
2 |
164,958,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Cdh22
|
UTSW |
2 |
164,988,550 (GRCm39) |
missense |
probably damaging |
0.98 |
R6297:Cdh22
|
UTSW |
2 |
164,985,564 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6445:Cdh22
|
UTSW |
2 |
165,012,612 (GRCm39) |
missense |
probably damaging |
0.97 |
R7294:Cdh22
|
UTSW |
2 |
164,984,013 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7310:Cdh22
|
UTSW |
2 |
164,954,214 (GRCm39) |
nonsense |
probably null |
|
R7595:Cdh22
|
UTSW |
2 |
164,954,383 (GRCm39) |
missense |
probably benign |
0.00 |
R7601:Cdh22
|
UTSW |
2 |
164,954,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R8047:Cdh22
|
UTSW |
2 |
165,012,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8308:Cdh22
|
UTSW |
2 |
164,954,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R8480:Cdh22
|
UTSW |
2 |
164,988,646 (GRCm39) |
missense |
probably benign |
|
R8526:Cdh22
|
UTSW |
2 |
164,954,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R8771:Cdh22
|
UTSW |
2 |
164,988,689 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8927:Cdh22
|
UTSW |
2 |
164,965,504 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8928:Cdh22
|
UTSW |
2 |
164,965,504 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9158:Cdh22
|
UTSW |
2 |
165,012,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R9433:Cdh22
|
UTSW |
2 |
164,954,329 (GRCm39) |
missense |
probably benign |
0.32 |
R9498:Cdh22
|
UTSW |
2 |
164,954,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R9638:Cdh22
|
UTSW |
2 |
164,988,687 (GRCm39) |
missense |
probably damaging |
0.97 |
R9657:Cdh22
|
UTSW |
2 |
164,965,715 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Cdh22
|
UTSW |
2 |
164,954,350 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Cdh22
|
UTSW |
2 |
164,958,104 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cdh22
|
UTSW |
2 |
164,988,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|