Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
T |
5: 109,887,097 (GRCm39) |
M33K |
probably damaging |
Het |
4930556J24Rik |
T |
C |
11: 3,888,140 (GRCm39) |
Q82R |
unknown |
Het |
Adcy9 |
T |
C |
16: 4,112,545 (GRCm39) |
D714G |
probably benign |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Ahctf1 |
G |
T |
1: 179,609,237 (GRCm39) |
A639E |
probably benign |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Anxa5 |
C |
T |
3: 36,519,436 (GRCm39) |
D18N |
probably damaging |
Het |
Apc |
C |
T |
18: 34,423,164 (GRCm39) |
P299L |
possibly damaging |
Het |
Btnl4 |
C |
A |
17: 34,693,210 (GRCm39) |
W68C |
probably damaging |
Het |
Cmya5 |
T |
A |
13: 93,281,021 (GRCm39) |
|
probably benign |
Het |
Cstf2t |
G |
T |
19: 31,060,523 (GRCm39) |
V20L |
probably benign |
Het |
D630045J12Rik |
A |
T |
6: 38,119,633 (GRCm39) |
V1703E |
probably damaging |
Het |
Dhx32 |
A |
G |
7: 133,323,941 (GRCm39) |
F535S |
probably damaging |
Het |
Diras2 |
T |
C |
13: 52,662,181 (GRCm39) |
D42G |
probably damaging |
Het |
Dppa3 |
T |
A |
6: 122,606,931 (GRCm39) |
D140E |
probably damaging |
Het |
Gpr180 |
C |
T |
14: 118,391,086 (GRCm39) |
T205I |
probably benign |
Het |
Gzme |
T |
G |
14: 56,355,764 (GRCm39) |
T183P |
possibly damaging |
Het |
H2-T23 |
T |
A |
17: 36,342,707 (GRCm39) |
I144F |
possibly damaging |
Het |
Hlx |
T |
C |
1: 184,459,894 (GRCm39) |
S415G |
probably benign |
Het |
Krtap5-3 |
G |
A |
7: 141,755,223 (GRCm39) |
C20Y |
unknown |
Het |
Mcm8 |
G |
T |
2: 132,670,003 (GRCm39) |
R359L |
probably benign |
Het |
Mroh2b |
G |
C |
15: 4,973,859 (GRCm39) |
E1126Q |
probably damaging |
Het |
Nav1 |
C |
T |
1: 135,398,560 (GRCm39) |
R674H |
probably damaging |
Het |
Rnaset2b |
T |
A |
17: 7,256,193 (GRCm39) |
|
probably null |
Het |
Samd12 |
T |
C |
15: 53,583,074 (GRCm39) |
K87E |
probably benign |
Het |
Sec16b |
T |
C |
1: 157,388,324 (GRCm39) |
S564P |
probably benign |
Het |
Speer4a1 |
A |
T |
5: 26,239,960 (GRCm39) |
C263* |
probably null |
Het |
Susd1 |
C |
A |
4: 59,411,359 (GRCm39) |
C158F |
possibly damaging |
Het |
Vmn2r6 |
C |
T |
3: 64,463,953 (GRCm39) |
V294M |
probably benign |
Het |
|
Other mutations in Otx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00574:Otx1
|
APN |
11 |
21,946,794 (GRCm39) |
unclassified |
probably benign |
|
Embarrassed
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R1946:Otx1
|
UTSW |
11 |
21,948,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Otx1
|
UTSW |
11 |
21,946,634 (GRCm39) |
unclassified |
probably benign |
|
R2870:Otx1
|
UTSW |
11 |
21,948,681 (GRCm39) |
intron |
probably benign |
|
R4164:Otx1
|
UTSW |
11 |
21,946,638 (GRCm39) |
unclassified |
probably benign |
|
R4845:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R4993:Otx1
|
UTSW |
11 |
21,948,532 (GRCm39) |
splice site |
probably null |
|
R5061:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5062:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5063:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5069:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5097:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5169:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5170:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5171:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5172:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5198:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5199:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5200:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5201:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5202:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5203:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5204:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5205:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5360:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5381:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5382:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5383:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5415:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5416:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5534:Otx1
|
UTSW |
11 |
21,946,296 (GRCm39) |
unclassified |
probably benign |
|
R5592:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5725:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5727:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5735:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5736:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5841:Otx1
|
UTSW |
11 |
21,948,594 (GRCm39) |
intron |
probably benign |
|
R5940:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5941:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6080:Otx1
|
UTSW |
11 |
21,949,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6093:Otx1
|
UTSW |
11 |
21,949,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6126:Otx1
|
UTSW |
11 |
21,946,457 (GRCm39) |
unclassified |
probably benign |
|
R6131:Otx1
|
UTSW |
11 |
21,949,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6132:Otx1
|
UTSW |
11 |
21,949,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6134:Otx1
|
UTSW |
11 |
21,949,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6187:Otx1
|
UTSW |
11 |
21,949,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6269:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6270:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6271:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6272:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6396:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6619:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6624:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6680:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6681:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6718:Otx1
|
UTSW |
11 |
21,946,412 (GRCm39) |
unclassified |
probably benign |
|
R6831:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6834:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6985:Otx1
|
UTSW |
11 |
21,946,615 (GRCm39) |
nonsense |
probably null |
|
R7631:Otx1
|
UTSW |
11 |
21,949,458 (GRCm39) |
nonsense |
probably null |
|
R8100:Otx1
|
UTSW |
11 |
21,949,392 (GRCm39) |
missense |
probably benign |
0.16 |
R9125:Otx1
|
UTSW |
11 |
21,949,458 (GRCm39) |
nonsense |
probably null |
|
R9541:Otx1
|
UTSW |
11 |
21,947,052 (GRCm39) |
missense |
probably damaging |
1.00 |
X0054:Otx1
|
UTSW |
11 |
21,946,331 (GRCm39) |
unclassified |
probably benign |
|
Z1187:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Otx1
|
UTSW |
11 |
21,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|