Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,901,315 (GRCm39) |
H970R |
probably benign |
Het |
Anapc1 |
T |
C |
2: 128,471,469 (GRCm39) |
M1496V |
possibly damaging |
Het |
Arhgef4 |
A |
T |
1: 34,763,296 (GRCm39) |
T851S |
probably benign |
Het |
Armh3 |
A |
G |
19: 45,874,394 (GRCm39) |
I593T |
possibly damaging |
Het |
Cacna1d |
A |
G |
14: 29,773,340 (GRCm39) |
S1782P |
probably benign |
Het |
Capn13 |
T |
A |
17: 73,629,074 (GRCm39) |
R578* |
probably null |
Het |
Casp8 |
A |
T |
1: 58,883,533 (GRCm39) |
H280L |
probably damaging |
Het |
Cd274 |
G |
T |
19: 29,361,543 (GRCm39) |
D284Y |
probably damaging |
Het |
Cenpe |
T |
A |
3: 134,976,715 (GRCm39) |
C2441S |
probably damaging |
Het |
Chn2 |
A |
T |
6: 54,267,272 (GRCm39) |
K118* |
probably null |
Het |
Chst12 |
G |
T |
5: 140,510,167 (GRCm39) |
E265* |
probably null |
Het |
Cp |
C |
A |
3: 20,043,379 (GRCm39) |
Q22K |
probably benign |
Het |
Diaph3 |
A |
T |
14: 87,222,306 (GRCm39) |
W404R |
probably damaging |
Het |
Dnajb13 |
T |
G |
7: 100,160,030 (GRCm39) |
E69A |
probably damaging |
Het |
Dzip1l |
A |
G |
9: 99,549,705 (GRCm39) |
E725G |
probably damaging |
Het |
Dzip3 |
T |
A |
16: 48,774,117 (GRCm39) |
K373* |
probably null |
Het |
Fmn1 |
C |
T |
2: 113,195,266 (GRCm39) |
T322I |
unknown |
Het |
Gbp9 |
T |
C |
5: 105,233,028 (GRCm39) |
Y208C |
probably benign |
Het |
Gtf2i |
T |
A |
5: 134,289,425 (GRCm39) |
K418N |
probably damaging |
Het |
Herc3 |
C |
T |
6: 58,832,745 (GRCm39) |
Q137* |
probably null |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Iqcm |
A |
T |
8: 76,472,914 (GRCm39) |
D251V |
probably damaging |
Het |
Itpr3 |
A |
T |
17: 27,308,885 (GRCm39) |
I363F |
possibly damaging |
Het |
Khnyn |
A |
T |
14: 56,124,660 (GRCm39) |
K305* |
probably null |
Het |
Klf17 |
A |
G |
4: 117,617,856 (GRCm39) |
V167A |
possibly damaging |
Het |
Letm2 |
T |
C |
8: 26,071,795 (GRCm39) |
D369G |
probably benign |
Het |
Lrrc31 |
A |
G |
3: 30,744,085 (GRCm39) |
V141A |
possibly damaging |
Het |
Msh5 |
A |
T |
17: 35,261,164 (GRCm39) |
|
probably null |
Het |
Neb |
G |
A |
2: 52,113,224 (GRCm39) |
|
probably benign |
Het |
Or10j5 |
T |
A |
1: 172,785,009 (GRCm39) |
S216T |
possibly damaging |
Het |
Or2t6 |
A |
T |
14: 14,175,593 (GRCm38) |
M163K |
probably damaging |
Het |
Padi6 |
T |
C |
4: 140,469,191 (GRCm39) |
I50V |
probably benign |
Het |
Pcdhb22 |
G |
T |
18: 37,652,179 (GRCm39) |
G216C |
probably damaging |
Het |
Ppy |
A |
G |
11: 101,991,525 (GRCm39) |
Y5H |
probably benign |
Het |
Psmc1 |
T |
C |
12: 100,081,734 (GRCm39) |
L112S |
probably damaging |
Het |
Ptov1 |
A |
G |
7: 44,515,026 (GRCm39) |
I195T |
possibly damaging |
Het |
Rassf10 |
C |
A |
7: 112,553,631 (GRCm39) |
D77E |
probably benign |
Het |
Slc25a45 |
T |
C |
19: 5,934,490 (GRCm39) |
S153P |
possibly damaging |
Het |
Slco1a5 |
G |
A |
6: 142,204,791 (GRCm39) |
R126C |
probably damaging |
Het |
Srebf2 |
T |
C |
15: 82,061,652 (GRCm39) |
V366A |
probably benign |
Het |
St6galnac5 |
T |
C |
3: 152,686,772 (GRCm39) |
S61G |
probably benign |
Het |
Sult6b1 |
A |
T |
17: 79,213,005 (GRCm39) |
V82D |
probably benign |
Het |
Tep1 |
A |
T |
14: 51,088,084 (GRCm39) |
C818S |
possibly damaging |
Het |
Tex15 |
T |
G |
8: 34,072,638 (GRCm39) |
F2728L |
possibly damaging |
Het |
Tm9sf2 |
T |
A |
14: 122,382,558 (GRCm39) |
F190Y |
probably damaging |
Het |
Tmem175 |
T |
C |
5: 108,794,298 (GRCm39) |
L476P |
probably damaging |
Het |
Tmprss11c |
T |
C |
5: 86,385,689 (GRCm39) |
K248R |
probably benign |
Het |
Tnk2 |
T |
A |
16: 32,489,668 (GRCm39) |
F316I |
probably damaging |
Het |
Vmn2r75 |
T |
A |
7: 85,813,372 (GRCm39) |
M477L |
probably benign |
Het |
Vmn2r83 |
A |
C |
10: 79,314,921 (GRCm39) |
I390L |
probably benign |
Het |
Vmn2r88 |
A |
G |
14: 51,648,603 (GRCm39) |
Y49C |
probably damaging |
Het |
Zdhhc4 |
T |
A |
5: 143,302,377 (GRCm39) |
I318F |
probably damaging |
Het |
Zmat4 |
A |
T |
8: 24,238,457 (GRCm39) |
D27V |
probably damaging |
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 |
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 |
R6081: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 |
|