Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610507B11Rik |
T |
A |
11: 78,273,245 |
H1137Q |
probably damaging |
Het |
A130051J06Rik |
C |
T |
15: 95,790,760 |
|
probably benign |
Het |
A630001G21Rik |
T |
A |
1: 85,723,385 |
R110W |
probably benign |
Het |
Abca4 |
T |
C |
3: 122,135,266 |
|
probably null |
Het |
Abcc3 |
T |
C |
11: 94,351,068 |
N1379S |
probably damaging |
Het |
Actrt3 |
A |
C |
3: 30,598,127 |
F273V |
probably benign |
Het |
Adam22 |
T |
C |
5: 8,367,217 |
D75G |
probably benign |
Het |
Armc4 |
G |
T |
18: 7,211,496 |
Q793K |
probably benign |
Het |
Ash1l |
C |
A |
3: 89,054,498 |
D2392E |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 89,058,626 |
I2445T |
probably damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,524,652 |
I762V |
probably benign |
Het |
Ccdc127 |
T |
A |
13: 74,357,068 |
|
probably benign |
Het |
Ccdc91 |
C |
G |
6: 147,575,503 |
L230V |
unknown |
Het |
Cdk13 |
A |
G |
13: 17,719,655 |
I1129T |
probably damaging |
Het |
Cnot1 |
C |
T |
8: 95,744,296 |
R1308H |
possibly damaging |
Het |
Crhr2 |
T |
C |
6: 55,103,222 |
H144R |
probably damaging |
Het |
Dnmt1 |
T |
C |
9: 20,912,595 |
N993S |
possibly damaging |
Het |
Eif4g1 |
T |
A |
16: 20,689,011 |
V1182D |
probably damaging |
Het |
Eml2 |
G |
A |
7: 19,201,163 |
V432I |
probably damaging |
Het |
Fam234a |
T |
A |
17: 26,214,653 |
Q399L |
possibly damaging |
Het |
Fyb |
A |
T |
15: 6,580,869 |
K308* |
probably null |
Het |
Gfral |
C |
T |
9: 76,197,046 |
R228Q |
probably benign |
Het |
Gm10309 |
A |
T |
17: 86,498,993 |
|
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,772,555 |
R100C |
unknown |
Het |
Gm5501 |
G |
A |
18: 9,917,417 |
|
noncoding transcript |
Het |
Gm6309 |
A |
T |
5: 146,168,182 |
V307D |
probably benign |
Het |
Gm9871 |
T |
A |
6: 101,796,187 |
|
noncoding transcript |
Het |
Greb1l |
G |
A |
18: 10,542,427 |
E1341K |
probably damaging |
Het |
Herc3 |
T |
A |
6: 58,894,543 |
V70E |
possibly damaging |
Het |
Hes7 |
A |
G |
11: 69,121,589 |
E41G |
probably damaging |
Het |
Ifi27l2b |
T |
C |
12: 103,455,787 |
D106G |
unknown |
Het |
Igfbp6 |
A |
T |
15: 102,148,181 |
Y184F |
probably damaging |
Het |
Isyna1 |
A |
G |
8: 70,594,702 |
Y25C |
probably damaging |
Het |
Kcng3 |
G |
T |
17: 83,631,134 |
T162K |
possibly damaging |
Het |
Krt36 |
T |
C |
11: 100,104,161 |
D195G |
possibly damaging |
Het |
Lrwd1 |
A |
T |
5: 136,132,239 |
|
probably null |
Het |
Lsg1 |
C |
T |
16: 30,561,775 |
A615T |
probably benign |
Het |
Myo5a |
A |
T |
9: 75,151,931 |
E480D |
probably damaging |
Het |
Myrf |
T |
A |
19: 10,216,723 |
D690V |
probably damaging |
Het |
N4bp1 |
T |
C |
8: 86,851,684 |
I684M |
probably damaging |
Het |
Nlrc3 |
C |
T |
16: 3,963,725 |
A607T |
probably damaging |
Het |
Nuak1 |
A |
T |
10: 84,409,720 |
I87N |
probably damaging |
Het |
Olfr1131 |
T |
C |
2: 87,629,131 |
|
probably null |
Het |
Olfr490 |
T |
G |
7: 108,286,392 |
T245P |
probably damaging |
Het |
Olfr878 |
A |
T |
9: 37,919,351 |
E236D |
probably damaging |
Het |
Osbpl9 |
T |
A |
4: 109,062,566 |
R689* |
probably null |
Het |
Ppargc1b |
T |
A |
18: 61,307,568 |
M744L |
probably benign |
Het |
Prss40 |
A |
T |
1: 34,552,517 |
|
probably benign |
Het |
Ptprd |
T |
A |
4: 76,054,602 |
|
probably null |
Het |
Rft1 |
T |
C |
14: 30,663,226 |
|
probably benign |
Het |
Rftn2 |
C |
T |
1: 55,214,286 |
V53I |
probably damaging |
Het |
Rnaset2a |
T |
C |
17: 8,132,047 |
Y167C |
probably damaging |
Het |
Schip1 |
T |
C |
3: 68,408,227 |
|
probably benign |
Het |
Scn5a |
A |
C |
9: 119,530,052 |
L643R |
possibly damaging |
Het |
Shroom3 |
T |
A |
5: 92,943,018 |
M1128K |
probably benign |
Het |
Skint8 |
C |
A |
4: 111,950,193 |
L359M |
probably damaging |
Het |
Slc14a2 |
A |
G |
18: 78,209,042 |
L18P |
probably benign |
Het |
Slc22a3 |
C |
T |
17: 12,423,804 |
V509M |
probably damaging |
Het |
Slc7a5 |
A |
C |
8: 121,883,642 |
F478V |
probably benign |
Het |
Smc1b |
T |
A |
15: 85,096,658 |
N803I |
probably benign |
Het |
Snf8 |
T |
A |
11: 96,041,725 |
N115K |
probably damaging |
Het |
Stox2 |
T |
A |
8: 47,413,137 |
K57* |
probably null |
Het |
Tmem248 |
T |
A |
5: 130,229,588 |
F41I |
probably damaging |
Het |
Tmprss7 |
T |
C |
16: 45,686,430 |
S90G |
probably damaging |
Het |
Top3b |
T |
C |
16: 16,885,836 |
V285A |
probably damaging |
Het |
Tsen15 |
T |
C |
1: 152,371,783 |
T153A |
probably damaging |
Het |
Wdr24 |
T |
C |
17: 25,828,340 |
|
probably null |
Het |
Zbtb2 |
G |
A |
10: 4,369,456 |
T190I |
probably benign |
Het |
Zranb3 |
T |
C |
1: 127,963,876 |
S788G |
probably benign |
Het |
|