Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
C |
G |
7: 120,216,226 |
N232K |
probably benign |
Het |
Acaca |
T |
A |
11: 84,280,468 |
V5E |
probably damaging |
Het |
Adam18 |
A |
T |
8: 24,629,675 |
D529E |
probably benign |
Het |
Adgrb3 |
T |
C |
1: 25,420,602 |
T798A |
probably benign |
Het |
Alyref |
T |
C |
11: 120,596,046 |
T130A |
probably benign |
Het |
Arhgap24 |
A |
G |
5: 102,897,124 |
S591G |
probably benign |
Het |
Carmil1 |
C |
T |
13: 24,036,564 |
G655E |
probably damaging |
Het |
Cdc42bpg |
T |
A |
19: 6,314,488 |
|
probably null |
Het |
Clec12a |
T |
A |
6: 129,353,403 |
L48H |
probably damaging |
Het |
Coq2 |
C |
A |
5: 100,661,904 |
|
probably benign |
Het |
Crb2 |
C |
A |
2: 37,793,826 |
F1113L |
possibly damaging |
Het |
Ctla4 |
A |
T |
1: 60,912,713 |
M134L |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 74,277,038 |
|
probably null |
Homo |
Efhb |
A |
G |
17: 53,452,604 |
V290A |
possibly damaging |
Het |
Epha8 |
T |
C |
4: 136,931,899 |
N843S |
probably damaging |
Het |
Eva1a |
A |
T |
6: 82,092,105 |
I138F |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,289,310 |
I1402F |
probably damaging |
Het |
Fat3 |
A |
T |
9: 15,999,170 |
H1845Q |
possibly damaging |
Het |
Gimap8 |
T |
A |
6: 48,656,451 |
F401L |
probably benign |
Het |
Gm12394 |
C |
A |
4: 42,792,489 |
G548W |
probably damaging |
Het |
Gpr162 |
C |
T |
6: 124,861,189 |
R166Q |
possibly damaging |
Het |
Hdac4 |
G |
A |
1: 91,984,711 |
P348S |
possibly damaging |
Het |
Hist1h2ae |
A |
G |
13: 23,570,945 |
V55A |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,361,800 |
V849A |
probably benign |
Het |
Inpp5b |
T |
A |
4: 124,792,252 |
N696K |
probably damaging |
Het |
Kdm5d |
G |
T |
Y: 927,056 |
R598L |
probably damaging |
Homo |
Kidins220 |
T |
C |
12: 25,057,191 |
S1548P |
probably benign |
Het |
Kif2b |
C |
A |
11: 91,576,366 |
V364L |
probably damaging |
Het |
Kitl |
A |
G |
10: 100,087,394 |
M1V |
probably null |
Het |
Klra9 |
G |
T |
6: 130,179,032 |
Y253* |
probably null |
Het |
Map6 |
T |
C |
7: 99,268,038 |
I6T |
probably damaging |
Het |
Mastl |
T |
C |
2: 23,120,929 |
T768A |
probably damaging |
Het |
Mettl16 |
T |
C |
11: 74,805,338 |
V335A |
probably benign |
Het |
Mpl |
T |
C |
4: 118,448,700 |
|
probably null |
Het |
Myo5c |
C |
T |
9: 75,286,578 |
T1205I |
probably benign |
Het |
Nav2 |
C |
A |
7: 49,594,366 |
L2114I |
probably damaging |
Het |
Neb |
T |
A |
2: 52,194,469 |
K5330* |
probably null |
Het |
Nfe2l1 |
C |
T |
11: 96,827,335 |
E125K |
possibly damaging |
Het |
Olfr1317 |
T |
A |
2: 112,142,380 |
L145* |
probably null |
Het |
Onecut3 |
A |
G |
10: 80,496,088 |
K361E |
probably damaging |
Het |
Osbpl6 |
A |
G |
2: 76,564,830 |
N370S |
possibly damaging |
Het |
Otud4 |
T |
A |
8: 79,672,997 |
M780K |
probably benign |
Het |
P2rx4 |
A |
G |
5: 122,727,241 |
T310A |
possibly damaging |
Het |
Pcdha11 |
G |
T |
18: 37,013,162 |
D769Y |
probably damaging |
Het |
Pcgf6 |
C |
T |
19: 47,049,088 |
R124H |
probably benign |
Het |
Pibf1 |
T |
A |
14: 99,137,210 |
Y362N |
probably damaging |
Het |
Ppm1g |
T |
C |
5: 31,203,124 |
E422G |
probably benign |
Het |
Prmt8 |
T |
C |
6: 127,732,643 |
I85V |
possibly damaging |
Het |
Prss27 |
A |
T |
17: 24,045,014 |
K225* |
probably null |
Het |
Rai1 |
A |
T |
11: 60,186,603 |
T498S |
probably benign |
Het |
Sbf2 |
C |
A |
7: 110,462,863 |
G23V |
probably damaging |
Het |
Sdha |
C |
T |
13: 74,334,293 |
|
probably null |
Het |
Sgo2a |
C |
T |
1: 58,002,933 |
Q140* |
probably null |
Het |
Sh3rf3 |
A |
G |
10: 58,984,144 |
D259G |
probably damaging |
Het |
Slc27a3 |
C |
A |
3: 90,385,470 |
D631Y |
probably damaging |
Het |
Slc7a10 |
T |
C |
7: 35,186,590 |
S37P |
possibly damaging |
Het |
Slco6d1 |
A |
G |
1: 98,421,467 |
T88A |
probably benign |
Het |
Smad4 |
A |
T |
18: 73,677,746 |
S56T |
possibly damaging |
Het |
Smarcd1 |
A |
G |
15: 99,707,885 |
I346V |
possibly damaging |
Het |
Spast |
C |
T |
17: 74,368,840 |
P260S |
probably benign |
Het |
Sprr2i |
A |
T |
3: 92,408,710 |
|
probably benign |
Het |
Sptbn5 |
A |
G |
2: 120,047,135 |
|
probably benign |
Het |
Taar9 |
A |
T |
10: 24,109,240 |
Y99N |
probably damaging |
Het |
Trappc10 |
A |
T |
10: 78,209,450 |
M468K |
possibly damaging |
Het |
Trim66 |
T |
C |
7: 109,460,738 |
R814G |
probably benign |
Het |
Tspan31 |
A |
G |
10: 127,068,358 |
C157R |
probably damaging |
Het |
Vmn2r90 |
A |
G |
17: 17,733,236 |
D554G |
possibly damaging |
Het |
Vmn2r91 |
A |
T |
17: 18,085,265 |
D70V |
probably damaging |
Het |
Wdr60 |
A |
T |
12: 116,246,727 |
Y314* |
probably null |
Het |
Zfp346 |
G |
T |
13: 55,113,704 |
K102N |
probably damaging |
Het |
Zmym4 |
G |
A |
4: 126,895,306 |
P1002S |
probably damaging |
Het |
|