Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm4 |
A |
G |
7: 119,310,395 (GRCm39) |
D460G |
probably damaging |
Het |
Ankrd9 |
T |
C |
12: 110,943,933 (GRCm39) |
M1V |
probably null |
Het |
Anks1 |
T |
C |
17: 28,273,681 (GRCm39) |
I977T |
probably damaging |
Het |
Bcar1 |
T |
C |
8: 112,437,839 (GRCm39) |
D767G |
possibly damaging |
Het |
Bcl6 |
A |
T |
16: 23,793,641 (GRCm39) |
I102N |
probably damaging |
Het |
Cacna2d2 |
G |
A |
9: 107,392,078 (GRCm39) |
G473D |
probably damaging |
Het |
Cdh23 |
G |
T |
10: 60,140,903 (GRCm39) |
H3148Q |
probably damaging |
Het |
Col6a4 |
A |
G |
9: 105,940,141 (GRCm39) |
V1263A |
possibly damaging |
Het |
Crtc2 |
T |
C |
3: 90,166,455 (GRCm39) |
|
probably benign |
Het |
D130043K22Rik |
G |
A |
13: 25,067,738 (GRCm39) |
G825S |
possibly damaging |
Het |
Dera |
T |
A |
6: 137,757,815 (GRCm39) |
|
probably null |
Het |
Dnah17 |
G |
T |
11: 117,963,793 (GRCm39) |
Y2506* |
probably null |
Het |
Enam |
T |
A |
5: 88,652,418 (GRCm39) |
L1309* |
probably null |
Het |
Fbxo15 |
G |
A |
18: 84,982,317 (GRCm39) |
|
probably null |
Het |
Fgfbp1 |
T |
C |
5: 44,136,828 (GRCm39) |
K155E |
probably damaging |
Het |
Foxj2 |
C |
T |
6: 122,815,540 (GRCm39) |
|
probably benign |
Het |
Fuca1 |
A |
G |
4: 135,666,530 (GRCm39) |
|
probably benign |
Het |
Gad1-ps |
T |
A |
10: 99,281,184 (GRCm39) |
|
noncoding transcript |
Het |
Insr |
A |
T |
8: 3,209,578 (GRCm39) |
F1168L |
probably damaging |
Het |
Isx |
T |
A |
8: 75,619,333 (GRCm39) |
V175E |
possibly damaging |
Het |
Kansl3 |
T |
C |
1: 36,407,070 (GRCm39) |
|
probably benign |
Het |
Lin9 |
T |
C |
1: 180,494,932 (GRCm39) |
I218T |
probably damaging |
Het |
Llgl2 |
C |
A |
11: 115,736,205 (GRCm39) |
A126D |
possibly damaging |
Het |
Ltbp2 |
T |
C |
12: 84,876,083 (GRCm39) |
E488G |
possibly damaging |
Het |
Maml3 |
A |
G |
3: 51,597,639 (GRCm39) |
V369A |
possibly damaging |
Het |
Mthfsl |
A |
G |
9: 88,597,708 (GRCm39) |
I14T |
probably damaging |
Het |
Myo3b |
A |
G |
2: 70,119,923 (GRCm39) |
|
probably benign |
Het |
Nfkbil1 |
T |
C |
17: 35,439,722 (GRCm39) |
R264G |
possibly damaging |
Het |
Or4c3d |
A |
G |
2: 89,882,038 (GRCm39) |
L210P |
probably damaging |
Het |
Pde5a |
G |
T |
3: 122,542,031 (GRCm39) |
A174S |
probably benign |
Het |
Plch1 |
A |
T |
3: 63,606,382 (GRCm39) |
I1173N |
probably damaging |
Het |
Ppfia1 |
C |
A |
7: 144,035,512 (GRCm39) |
R1171L |
probably damaging |
Het |
Prom1 |
T |
C |
5: 44,172,131 (GRCm39) |
D595G |
probably damaging |
Het |
Ptprz1 |
T |
C |
6: 23,042,742 (GRCm39) |
|
probably benign |
Het |
Samsn1 |
A |
G |
16: 75,680,763 (GRCm39) |
|
probably null |
Het |
Sbno2 |
T |
A |
10: 79,908,202 (GRCm39) |
T66S |
probably benign |
Het |
Serpina1c |
T |
A |
12: 103,862,338 (GRCm39) |
I326F |
probably damaging |
Het |
Slc12a1 |
T |
C |
2: 125,030,190 (GRCm39) |
|
probably null |
Het |
Slc18a2 |
A |
G |
19: 59,264,988 (GRCm39) |
E324G |
probably benign |
Het |
Slc40a1 |
A |
T |
1: 45,950,495 (GRCm39) |
M319K |
probably damaging |
Het |
Slc44a5 |
T |
C |
3: 153,956,608 (GRCm39) |
Y287H |
possibly damaging |
Het |
Stx4a |
A |
G |
7: 127,441,672 (GRCm39) |
E63G |
possibly damaging |
Het |
Sv2a |
T |
C |
3: 96,098,032 (GRCm39) |
F545S |
probably benign |
Het |
Svop |
T |
C |
5: 114,203,589 (GRCm39) |
D65G |
probably benign |
Het |
Tex30 |
A |
T |
1: 44,126,182 (GRCm39) |
S182R |
probably benign |
Het |
Tmem121b |
T |
C |
6: 120,469,298 (GRCm39) |
D473G |
probably damaging |
Het |
Tnfrsf19 |
C |
A |
14: 61,210,941 (GRCm39) |
|
probably benign |
Het |
Tnrc6a |
T |
C |
7: 122,769,679 (GRCm39) |
S490P |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,115,746 (GRCm39) |
T82A |
probably benign |
Het |
Vps16 |
A |
G |
2: 130,283,573 (GRCm39) |
D589G |
possibly damaging |
Het |
Zscan29 |
A |
C |
2: 120,997,170 (GRCm39) |
S184A |
probably damaging |
Het |
|
Other mutations in H2-Eb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00508:H2-Eb2
|
APN |
17 |
34,553,341 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00965:H2-Eb2
|
APN |
17 |
34,544,771 (GRCm39) |
splice site |
probably null |
|
IGL01380:H2-Eb2
|
APN |
17 |
34,554,783 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02057:H2-Eb2
|
APN |
17 |
34,554,741 (GRCm39) |
splice site |
probably benign |
|
IGL02190:H2-Eb2
|
APN |
17 |
34,553,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R0469:H2-Eb2
|
UTSW |
17 |
34,553,218 (GRCm39) |
nonsense |
probably null |
|
R0510:H2-Eb2
|
UTSW |
17 |
34,553,218 (GRCm39) |
nonsense |
probably null |
|
R1169:H2-Eb2
|
UTSW |
17 |
34,552,331 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1334:H2-Eb2
|
UTSW |
17 |
34,553,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R1598:H2-Eb2
|
UTSW |
17 |
34,553,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:H2-Eb2
|
UTSW |
17 |
34,553,278 (GRCm39) |
missense |
probably benign |
0.15 |
R2103:H2-Eb2
|
UTSW |
17 |
34,553,278 (GRCm39) |
missense |
probably benign |
0.15 |
R4191:H2-Eb2
|
UTSW |
17 |
34,563,529 (GRCm39) |
unclassified |
probably benign |
|
R4194:H2-Eb2
|
UTSW |
17 |
34,552,300 (GRCm39) |
missense |
probably benign |
|
R4461:H2-Eb2
|
UTSW |
17 |
34,552,497 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4774:H2-Eb2
|
UTSW |
17 |
34,553,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R4882:H2-Eb2
|
UTSW |
17 |
34,553,230 (GRCm39) |
missense |
probably benign |
|
R5663:H2-Eb2
|
UTSW |
17 |
34,552,382 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6913:H2-Eb2
|
UTSW |
17 |
34,552,523 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7139:H2-Eb2
|
UTSW |
17 |
34,553,395 (GRCm39) |
missense |
probably benign |
0.30 |
R7457:H2-Eb2
|
UTSW |
17 |
34,553,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R9173:H2-Eb2
|
UTSW |
17 |
34,552,491 (GRCm39) |
missense |
probably benign |
0.37 |
Z1176:H2-Eb2
|
UTSW |
17 |
34,553,283 (GRCm39) |
missense |
possibly damaging |
0.55 |
|