Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
G |
A |
11: 30,426,228 |
S213L |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,466,184 |
I4030T |
possibly damaging |
Het |
Ap4b1 |
G |
A |
3: 103,812,827 |
R55H |
probably benign |
Het |
Arap3 |
G |
A |
18: 37,990,836 |
R377C |
probably damaging |
Het |
Atp6v1h |
T |
A |
1: 5,089,059 |
M55K |
probably benign |
Het |
B3galt4 |
A |
C |
17: 33,951,213 |
V17G |
probably benign |
Het |
Cd79a |
A |
T |
7: 24,901,266 |
M172L |
probably benign |
Het |
Cry1 |
A |
T |
10: 85,184,362 |
L37H |
possibly damaging |
Het |
D430042O09Rik |
A |
G |
7: 125,752,971 |
|
probably null |
Het |
D5Ertd615e |
A |
T |
5: 45,169,413 |
|
noncoding transcript |
Het |
Dnah17 |
A |
T |
11: 118,119,568 |
L308Q |
probably damaging |
Het |
Dusp2 |
A |
G |
2: 127,337,775 |
T313A |
probably benign |
Het |
Fam110c |
T |
C |
12: 31,074,983 |
S315P |
probably damaging |
Het |
Fcer2a |
G |
A |
8: 3,683,598 |
R198* |
probably null |
Het |
Fryl |
G |
A |
5: 73,054,597 |
T2359M |
probably damaging |
Het |
Gm14221 |
G |
A |
2: 160,568,383 |
|
noncoding transcript |
Het |
Gpc6 |
T |
G |
14: 117,964,830 |
L484R |
probably damaging |
Het |
Igdcc3 |
G |
A |
9: 65,180,073 |
V298M |
probably damaging |
Het |
Impg2 |
T |
A |
16: 56,225,717 |
|
probably benign |
Het |
Iqca |
T |
A |
1: 90,045,642 |
M803L |
probably benign |
Het |
Itga4 |
T |
C |
2: 79,315,970 |
|
probably benign |
Het |
Kidins220 |
T |
C |
12: 25,040,460 |
F1141S |
possibly damaging |
Het |
Kif7 |
A |
G |
7: 79,702,278 |
I912T |
probably damaging |
Het |
Klhl38 |
G |
A |
15: 58,322,458 |
R292W |
probably damaging |
Het |
Lama3 |
A |
G |
18: 12,441,131 |
D590G |
probably benign |
Het |
Map4k4 |
T |
C |
1: 40,014,229 |
|
probably benign |
Het |
Mbd4 |
A |
T |
6: 115,850,797 |
D39E |
probably damaging |
Het |
Mrm2 |
A |
G |
5: 140,331,255 |
V8A |
probably benign |
Het |
Myod1 |
A |
T |
7: 46,377,115 |
E148V |
probably damaging |
Het |
Olfr74 |
A |
C |
2: 87,974,551 |
I38S |
probably benign |
Het |
Pdcd10 |
A |
T |
3: 75,541,168 |
F30I |
possibly damaging |
Het |
Ptcd1 |
T |
A |
5: 145,159,536 |
H249L |
probably damaging |
Het |
Ptcd3 |
A |
T |
6: 71,888,577 |
D451E |
probably benign |
Het |
Rab44 |
C |
A |
17: 29,147,377 |
S680R |
unknown |
Het |
Rad21l |
A |
T |
2: 151,655,164 |
D340E |
probably benign |
Het |
Ranbp2 |
T |
C |
10: 58,478,881 |
F1808L |
possibly damaging |
Het |
Rnf122 |
T |
C |
8: 31,128,602 |
V126A |
probably damaging |
Het |
Slc25a47 |
G |
T |
12: 108,854,216 |
V49L |
probably benign |
Het |
Slc36a2 |
T |
C |
11: 55,184,807 |
|
probably null |
Het |
Sorl1 |
G |
A |
9: 42,043,956 |
R668W |
probably damaging |
Het |
Tbx19 |
T |
A |
1: 165,139,156 |
N383I |
possibly damaging |
Het |
Tenm4 |
A |
G |
7: 96,874,303 |
H1676R |
probably benign |
Het |
Tgm5 |
G |
T |
2: 121,052,808 |
R351S |
probably damaging |
Het |
Tmem106b |
A |
G |
6: 13,071,843 |
S34G |
probably benign |
Het |
Trmo |
C |
T |
4: 46,386,169 |
G119R |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,442,829 |
|
probably benign |
Het |
Wfdc11 |
A |
G |
2: 164,665,445 |
|
probably null |
Het |
Xrn2 |
T |
A |
2: 147,038,179 |
I474K |
probably benign |
Het |
Zfp827 |
A |
G |
8: 79,070,434 |
K383R |
probably damaging |
Het |
|