Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010111I01Rik |
T |
G |
13: 63,068,111 |
I399S |
possibly damaging |
Het |
Adam15 |
C |
T |
3: 89,345,934 |
|
probably benign |
Het |
Antxr2 |
A |
C |
5: 97,977,595 |
|
probably null |
Het |
Atp8b3 |
A |
C |
10: 80,527,233 |
|
probably benign |
Het |
Brwd1 |
A |
T |
16: 96,013,829 |
M1417K |
probably damaging |
Het |
Camk2d |
A |
T |
3: 126,797,773 |
R297S |
probably damaging |
Het |
Cntnap1 |
A |
T |
11: 101,178,365 |
H215L |
probably damaging |
Het |
Cytip |
T |
C |
2: 58,133,738 |
S357G |
probably damaging |
Het |
Fancg |
A |
G |
4: 43,006,872 |
Y273H |
possibly damaging |
Het |
Fbxo36 |
A |
G |
1: 84,881,164 |
S57G |
probably benign |
Het |
Fgf8 |
A |
T |
19: 45,737,216 |
L141Q |
probably damaging |
Het |
Gm5039 |
T |
C |
12: 88,321,181 |
R101G |
probably benign |
Het |
Gm765 |
T |
C |
6: 98,248,098 |
S75G |
possibly damaging |
Het |
Grm5 |
C |
T |
7: 88,026,442 |
T388M |
probably damaging |
Het |
Hipk1 |
A |
G |
3: 103,758,750 |
L589P |
possibly damaging |
Het |
Kiz |
T |
C |
2: 146,889,600 |
S337P |
probably benign |
Het |
Lrrc37a |
A |
T |
11: 103,497,609 |
I2330K |
unknown |
Het |
Mdfic |
T |
A |
6: 15,770,367 |
I124K |
possibly damaging |
Het |
Mttp |
A |
G |
3: 138,116,000 |
|
probably null |
Het |
Myom1 |
G |
A |
17: 71,072,137 |
S632N |
possibly damaging |
Het |
Nlrp12 |
T |
C |
7: 3,240,464 |
K473E |
probably damaging |
Het |
Nrp2 |
C |
A |
1: 62,718,940 |
C28* |
probably null |
Het |
Olfr1134 |
A |
G |
2: 87,656,792 |
L43P |
probably damaging |
Het |
Olfr1246 |
G |
A |
2: 89,590,293 |
T274I |
probably damaging |
Het |
Olfr48 |
G |
A |
2: 89,844,385 |
A196V |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,340,691 |
M1559L |
possibly damaging |
Het |
Pmm2 |
T |
A |
16: 8,637,804 |
D10E |
possibly damaging |
Het |
Polm |
T |
C |
11: 5,830,137 |
Q300R |
probably benign |
Het |
Prrc2b |
T |
A |
2: 32,221,455 |
N1208K |
probably benign |
Het |
Serpinb3c |
T |
C |
1: 107,271,918 |
D291G |
probably damaging |
Het |
Slc1a2 |
T |
C |
2: 102,748,544 |
F268S |
probably damaging |
Het |
Slc26a4 |
A |
G |
12: 31,549,949 |
Y127H |
probably damaging |
Het |
Slc29a4 |
A |
G |
5: 142,717,751 |
Y260C |
probably damaging |
Het |
Sorbs3 |
C |
T |
14: 70,184,006 |
|
probably null |
Het |
Spen |
T |
C |
4: 141,487,606 |
Y534C |
unknown |
Het |
Tmem237 |
T |
C |
1: 59,120,111 |
|
probably null |
Het |
Tnfrsf21 |
A |
T |
17: 43,085,463 |
N546I |
probably benign |
Het |
Tpgs2 |
T |
A |
18: 25,140,573 |
D177V |
probably damaging |
Het |
Tpx2 |
C |
T |
2: 152,882,320 |
R339* |
probably null |
Het |
Trim12c |
T |
C |
7: 104,348,223 |
Y42C |
probably benign |
Het |
Trip10 |
A |
T |
17: 57,257,272 |
E341V |
probably damaging |
Het |
Trpm8 |
A |
T |
1: 88,330,694 |
|
probably null |
Het |
Ttc37 |
A |
G |
13: 76,111,691 |
K37E |
probably damaging |
Het |
Ubr1 |
T |
A |
2: 120,900,508 |
I1221F |
probably benign |
Het |
Ucp2 |
C |
T |
7: 100,499,322 |
A301V |
probably benign |
Het |
Zfyve1 |
T |
C |
12: 83,558,693 |
I411V |
probably benign |
Het |
|