Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
T |
9: 46,220,717 (GRCm39) |
S50T |
probably benign |
Het |
A930011G23Rik |
A |
G |
5: 99,369,289 (GRCm39) |
L529P |
probably damaging |
Het |
Acer2 |
A |
T |
4: 86,818,792 (GRCm39) |
N147Y |
probably damaging |
Het |
Adamtsl1 |
A |
G |
4: 86,150,901 (GRCm39) |
E353G |
probably damaging |
Het |
Alg6 |
T |
C |
4: 99,632,737 (GRCm39) |
F60L |
probably benign |
Het |
Ano6 |
A |
T |
15: 95,811,260 (GRCm39) |
D120V |
probably damaging |
Het |
Armc3 |
A |
G |
2: 19,258,728 (GRCm39) |
D265G |
possibly damaging |
Het |
Aurkc |
A |
T |
7: 7,005,859 (GRCm39) |
Y249F |
probably benign |
Het |
Bmal1 |
G |
A |
7: 112,884,238 (GRCm39) |
R92Q |
probably damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,389,528 (GRCm39) |
I274V |
probably benign |
Het |
Camk2n2 |
C |
A |
16: 20,439,830 (GRCm39) |
G39C |
probably damaging |
Het |
Ccdc39 |
A |
G |
3: 33,880,710 (GRCm39) |
L419P |
possibly damaging |
Het |
Cdh23 |
T |
C |
10: 60,141,388 (GRCm39) |
M3117V |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,704,357 (GRCm39) |
E280G |
probably benign |
Het |
Cherp |
TGCTGGTGGTGGGG |
TG |
8: 73,221,659 (GRCm39) |
|
probably benign |
Het |
Clcn6 |
A |
G |
4: 148,098,646 (GRCm39) |
V494A |
probably damaging |
Het |
Col19a1 |
C |
T |
1: 24,376,996 (GRCm39) |
G450S |
probably damaging |
Het |
Crtac1 |
A |
G |
19: 42,290,612 (GRCm39) |
F363S |
probably damaging |
Het |
Dipk2a |
A |
T |
9: 94,402,594 (GRCm39) |
V356E |
possibly damaging |
Het |
Dnaaf2 |
T |
C |
12: 69,243,715 (GRCm39) |
S449G |
probably benign |
Het |
Dnah7b |
A |
T |
1: 46,273,152 (GRCm39) |
I2427F |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,937,981 (GRCm39) |
D1619E |
probably benign |
Het |
Dock3 |
A |
T |
9: 106,850,995 (GRCm39) |
S836T |
possibly damaging |
Het |
Donson |
A |
T |
16: 91,478,117 (GRCm39) |
|
probably null |
Het |
Drc3 |
G |
A |
11: 60,265,956 (GRCm39) |
R215H |
possibly damaging |
Het |
Entpd2 |
T |
C |
2: 25,289,504 (GRCm39) |
S329P |
possibly damaging |
Het |
Eya2 |
T |
C |
2: 165,603,857 (GRCm39) |
S332P |
probably damaging |
Het |
Fam83f |
T |
A |
15: 80,576,206 (GRCm39) |
Y286N |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,037,283 (GRCm39) |
V3645A |
probably benign |
Het |
G2e3 |
T |
C |
12: 51,419,287 (GRCm39) |
F668L |
possibly damaging |
Het |
Gm14403 |
T |
A |
2: 177,201,040 (GRCm39) |
C329S |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,684,448 (GRCm39) |
T374I |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,634,225 (GRCm39) |
|
probably null |
Het |
Hrnr |
T |
C |
3: 93,230,436 (GRCm39) |
S225P |
unknown |
Het |
Ifi202b |
C |
T |
1: 173,798,918 (GRCm39) |
|
probably null |
Het |
Il10ra |
A |
T |
9: 45,167,368 (GRCm39) |
D394E |
possibly damaging |
Het |
Itga2b |
A |
T |
11: 102,356,735 (GRCm39) |
D275E |
probably benign |
Het |
Jaml |
A |
T |
9: 45,000,026 (GRCm39) |
D108V |
probably damaging |
Het |
Kir3dl1 |
G |
A |
X: 135,427,231 (GRCm39) |
D56N |
probably damaging |
Het |
Lrrtm1 |
T |
C |
6: 77,221,872 (GRCm39) |
V443A |
probably damaging |
Het |
Mkln1 |
T |
A |
6: 31,473,637 (GRCm39) |
S126R |
probably benign |
Het |
Myo19 |
T |
C |
11: 84,788,450 (GRCm39) |
I354T |
probably damaging |
Het |
Nucb1 |
A |
T |
7: 45,151,084 (GRCm39) |
L99Q |
probably damaging |
Het |
Or4f59 |
A |
G |
2: 111,873,128 (GRCm39) |
F83S |
probably damaging |
Het |
Pask |
A |
G |
1: 93,249,778 (GRCm39) |
S541P |
probably benign |
Het |
Pdpr |
A |
T |
8: 111,861,252 (GRCm39) |
I749F |
possibly damaging |
Het |
Pgap6 |
T |
A |
17: 26,339,425 (GRCm39) |
F580I |
probably damaging |
Het |
Phyhipl |
T |
C |
10: 70,395,399 (GRCm39) |
D269G |
possibly damaging |
Het |
Pkdcc |
A |
G |
17: 83,523,223 (GRCm39) |
D110G |
probably benign |
Het |
Ppox |
A |
G |
1: 171,107,570 (GRCm39) |
L115P |
probably damaging |
Het |
Ppp1r12c |
A |
G |
7: 4,500,281 (GRCm39) |
L94P |
probably damaging |
Het |
Ppp6r2 |
T |
A |
15: 89,143,276 (GRCm39) |
M141K |
probably benign |
Het |
Prl3d1 |
A |
T |
13: 27,283,995 (GRCm39) |
H188L |
probably benign |
Het |
Psmb3 |
T |
A |
11: 97,604,296 (GRCm39) |
|
probably benign |
Het |
Pxdn |
T |
A |
12: 30,032,333 (GRCm39) |
S150T |
probably benign |
Het |
Ripor3 |
T |
C |
2: 167,823,203 (GRCm39) |
T903A |
probably damaging |
Het |
Rnase4 |
T |
C |
14: 51,342,306 (GRCm39) |
L10S |
probably benign |
Het |
Rnf224 |
T |
C |
2: 25,126,012 (GRCm39) |
T114A |
probably benign |
Het |
Rp1l1 |
A |
T |
14: 64,269,619 (GRCm39) |
E1735V |
probably benign |
Het |
Rrp1b |
T |
A |
17: 32,264,950 (GRCm39) |
Y60N |
probably damaging |
Het |
Rsbn1l |
A |
T |
5: 21,110,814 (GRCm39) |
V508E |
probably damaging |
Het |
Rubcnl |
T |
C |
14: 75,278,381 (GRCm39) |
|
probably null |
Het |
Rxfp4 |
A |
G |
3: 88,559,209 (GRCm39) |
|
probably benign |
Het |
Sdccag8 |
A |
G |
1: 176,653,797 (GRCm39) |
T85A |
probably benign |
Het |
Slc46a1 |
A |
T |
11: 78,357,975 (GRCm39) |
I343F |
possibly damaging |
Het |
Ssh2 |
A |
G |
11: 77,340,639 (GRCm39) |
D597G |
probably damaging |
Het |
Syne2 |
T |
A |
12: 76,044,239 (GRCm39) |
V3942E |
possibly damaging |
Het |
Timd4 |
T |
C |
11: 46,708,573 (GRCm39) |
S200P |
probably benign |
Het |
Tmc5 |
G |
A |
7: 118,265,834 (GRCm39) |
|
probably null |
Het |
Trbv16 |
A |
G |
6: 41,129,013 (GRCm39) |
T66A |
probably benign |
Het |
Ttc3 |
A |
T |
16: 94,240,183 (GRCm39) |
K1103* |
probably null |
Het |
Ttc7b |
A |
G |
12: 100,350,492 (GRCm39) |
V458A |
probably damaging |
Het |
Ubxn10 |
A |
G |
4: 138,448,134 (GRCm39) |
S181P |
probably benign |
Het |
Vmn2r11 |
A |
G |
5: 109,207,114 (GRCm39) |
|
probably null |
Het |
Vmn2r26 |
A |
T |
6: 124,002,925 (GRCm39) |
N112Y |
probably benign |
Het |
Vmn2r5 |
T |
C |
3: 64,411,497 (GRCm39) |
D357G |
probably damaging |
Het |
Zc3h10 |
T |
C |
10: 128,380,670 (GRCm39) |
N229S |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,226,867 (GRCm39) |
*2247W |
probably null |
Het |
Zfyve1 |
C |
A |
12: 83,621,910 (GRCm39) |
V162L |
possibly damaging |
Het |
|
Other mutations in Crb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00785:Crb2
|
APN |
2 |
37,682,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01357:Crb2
|
APN |
2 |
37,685,523 (GRCm39) |
unclassified |
probably benign |
|
IGL01363:Crb2
|
APN |
2 |
37,683,845 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02006:Crb2
|
APN |
2 |
37,676,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02380:Crb2
|
APN |
2 |
37,673,447 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02455:Crb2
|
APN |
2 |
37,684,576 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL03107:Crb2
|
APN |
2 |
37,681,428 (GRCm39) |
missense |
probably benign |
0.10 |
R1350:Crb2
|
UTSW |
2 |
37,682,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R1353:Crb2
|
UTSW |
2 |
37,677,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Crb2
|
UTSW |
2 |
37,673,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Crb2
|
UTSW |
2 |
37,673,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Crb2
|
UTSW |
2 |
37,676,631 (GRCm39) |
missense |
probably benign |
0.01 |
R1734:Crb2
|
UTSW |
2 |
37,683,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Crb2
|
UTSW |
2 |
37,673,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R2918:Crb2
|
UTSW |
2 |
37,673,395 (GRCm39) |
missense |
probably benign |
0.01 |
R3431:Crb2
|
UTSW |
2 |
37,682,229 (GRCm39) |
missense |
probably benign |
0.24 |
R3975:Crb2
|
UTSW |
2 |
37,683,680 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4074:Crb2
|
UTSW |
2 |
37,676,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R4518:Crb2
|
UTSW |
2 |
37,680,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R4521:Crb2
|
UTSW |
2 |
37,685,349 (GRCm39) |
unclassified |
probably benign |
|
R4801:Crb2
|
UTSW |
2 |
37,683,768 (GRCm39) |
missense |
probably benign |
0.09 |
R4802:Crb2
|
UTSW |
2 |
37,683,768 (GRCm39) |
missense |
probably benign |
0.09 |
R4913:Crb2
|
UTSW |
2 |
37,680,257 (GRCm39) |
missense |
probably benign |
|
R4930:Crb2
|
UTSW |
2 |
37,673,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Crb2
|
UTSW |
2 |
37,685,343 (GRCm39) |
unclassified |
probably benign |
|
R4959:Crb2
|
UTSW |
2 |
37,680,482 (GRCm39) |
missense |
probably damaging |
0.99 |
R5215:Crb2
|
UTSW |
2 |
37,683,765 (GRCm39) |
missense |
probably benign |
0.23 |
R5268:Crb2
|
UTSW |
2 |
37,680,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5446:Crb2
|
UTSW |
2 |
37,685,461 (GRCm39) |
missense |
probably benign |
0.16 |
R5875:Crb2
|
UTSW |
2 |
37,677,266 (GRCm39) |
splice site |
probably null |
|
R6179:Crb2
|
UTSW |
2 |
37,680,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Crb2
|
UTSW |
2 |
37,683,838 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6569:Crb2
|
UTSW |
2 |
37,682,163 (GRCm39) |
missense |
probably damaging |
0.99 |
R6828:Crb2
|
UTSW |
2 |
37,666,421 (GRCm39) |
small deletion |
probably benign |
|
R7040:Crb2
|
UTSW |
2 |
37,677,696 (GRCm39) |
missense |
probably benign |
0.32 |
R7153:Crb2
|
UTSW |
2 |
37,677,420 (GRCm39) |
missense |
probably benign |
0.00 |
R7362:Crb2
|
UTSW |
2 |
37,680,211 (GRCm39) |
missense |
probably benign |
0.00 |
R7515:Crb2
|
UTSW |
2 |
37,673,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7519:Crb2
|
UTSW |
2 |
37,683,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R7583:Crb2
|
UTSW |
2 |
37,680,607 (GRCm39) |
missense |
probably benign |
0.00 |
R7819:Crb2
|
UTSW |
2 |
37,681,603 (GRCm39) |
missense |
probably benign |
0.00 |
R8016:Crb2
|
UTSW |
2 |
37,676,568 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8049:Crb2
|
UTSW |
2 |
37,683,252 (GRCm39) |
missense |
probably benign |
0.02 |
R8090:Crb2
|
UTSW |
2 |
37,685,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R8907:Crb2
|
UTSW |
2 |
37,685,395 (GRCm39) |
missense |
probably benign |
0.00 |
R9010:Crb2
|
UTSW |
2 |
37,680,698 (GRCm39) |
missense |
probably benign |
0.01 |
R9291:Crb2
|
UTSW |
2 |
37,682,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R9448:Crb2
|
UTSW |
2 |
37,677,773 (GRCm39) |
missense |
probably benign |
0.01 |
R9706:Crb2
|
UTSW |
2 |
37,681,215 (GRCm39) |
missense |
probably damaging |
0.98 |
R9714:Crb2
|
UTSW |
2 |
37,681,215 (GRCm39) |
missense |
probably damaging |
0.98 |
X0025:Crb2
|
UTSW |
2 |
37,682,221 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Crb2
|
UTSW |
2 |
37,666,383 (GRCm39) |
missense |
probably benign |
|
Z1177:Crb2
|
UTSW |
2 |
37,680,836 (GRCm39) |
missense |
possibly damaging |
0.71 |
Z1177:Crb2
|
UTSW |
2 |
37,677,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|