Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra3 |
C |
T |
5: 50,016,867 |
A110T |
probably benign |
Het |
Adra1a |
A |
C |
14: 66,637,935 |
I120L |
probably damaging |
Het |
Ahnak2 |
C |
T |
12: 112,774,405 |
V1078I |
possibly damaging |
Het |
Ccser1 |
A |
G |
6: 61,570,723 |
H590R |
probably benign |
Het |
Cdh12 |
T |
G |
15: 21,583,765 |
L564V |
probably benign |
Het |
Celsr3 |
T |
A |
9: 108,836,622 |
H1900Q |
probably benign |
Het |
Clasp1 |
T |
A |
1: 118,545,434 |
M918K |
probably benign |
Het |
Cmtm6 |
A |
G |
9: 114,731,240 |
E2G |
probably damaging |
Het |
Ctsg |
A |
G |
14: 56,100,541 |
|
probably null |
Het |
Cylc2 |
T |
A |
4: 51,229,256 |
|
probably null |
Het |
Dna2 |
A |
G |
10: 62,971,993 |
|
probably null |
Het |
Dnaic1 |
G |
A |
4: 41,614,323 |
R333H |
probably benign |
Het |
Egln3 |
T |
C |
12: 54,180,628 |
D239G |
probably benign |
Het |
Fam13a |
A |
T |
6: 58,987,284 |
D54E |
probably damaging |
Het |
Fn1 |
A |
G |
1: 71,597,516 |
V2159A |
probably benign |
Het |
Gcnt2 |
T |
A |
13: 40,887,681 |
F105L |
probably benign |
Het |
Gm5788 |
T |
C |
12: 87,494,842 |
M41T |
possibly damaging |
Het |
Gpd1 |
G |
A |
15: 99,722,086 |
S255N |
probably damaging |
Het |
Hacd4 |
A |
G |
4: 88,437,478 |
F57L |
probably benign |
Het |
Helb |
T |
C |
10: 120,105,283 |
D500G |
probably benign |
Het |
Ighv1-26 |
G |
A |
12: 114,788,442 |
S94F |
probably damaging |
Het |
Kirrel |
T |
C |
3: 87,083,439 |
D692G |
possibly damaging |
Het |
Klra7 |
A |
T |
6: 130,230,091 |
|
probably null |
Het |
Lyl1 |
T |
C |
8: 84,704,300 |
V277A |
probably benign |
Het |
Mon2 |
A |
C |
10: 123,023,939 |
W811G |
probably damaging |
Het |
Myo9b |
T |
C |
8: 71,354,801 |
L1627P |
probably benign |
Het |
Neurl1b |
C |
G |
17: 26,438,746 |
H219Q |
probably benign |
Het |
Odf4 |
A |
T |
11: 68,922,423 |
C218S |
possibly damaging |
Het |
Olfr1038-ps |
A |
G |
2: 86,121,938 |
N5S |
possibly damaging |
Het |
Olfr11 |
T |
A |
13: 21,638,609 |
I305F |
probably benign |
Het |
Pde5a |
A |
G |
3: 122,818,030 |
D571G |
probably damaging |
Het |
Pgc |
A |
G |
17: 47,734,186 |
E343G |
probably benign |
Het |
Pik3cd |
A |
G |
4: 149,654,583 |
F667L |
possibly damaging |
Het |
Prf1 |
G |
A |
10: 61,300,155 |
R70H |
possibly damaging |
Het |
Ptprb |
C |
T |
10: 116,353,991 |
Q1565* |
probably null |
Het |
Rapgef4 |
T |
A |
2: 72,205,733 |
N523K |
probably benign |
Het |
Rbm25 |
T |
C |
12: 83,672,877 |
L557P |
probably damaging |
Het |
Rhobtb3 |
C |
T |
13: 75,878,857 |
V466I |
probably benign |
Het |
Rnpep |
A |
G |
1: 135,278,858 |
V166A |
probably benign |
Het |
Sgo2a |
A |
G |
1: 58,017,795 |
K1046R |
probably benign |
Het |
Slc12a2 |
T |
C |
18: 57,904,393 |
V525A |
probably benign |
Het |
Slc1a4 |
A |
T |
11: 20,306,487 |
I448N |
probably damaging |
Het |
Slc29a4 |
C |
T |
5: 142,718,506 |
P305L |
probably benign |
Het |
Slc9a5 |
T |
A |
8: 105,363,253 |
|
probably null |
Het |
Spag16 |
A |
T |
1: 69,887,520 |
N258I |
possibly damaging |
Het |
Sspo |
T |
A |
6: 48,466,699 |
L2076Q |
probably damaging |
Het |
Taok1 |
T |
A |
11: 77,545,326 |
H704L |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,145,120 |
F148L |
probably damaging |
Het |
Tm4sf1 |
A |
G |
3: 57,294,755 |
Y12H |
probably benign |
Het |
Traj6 |
C |
T |
14: 54,212,714 |
T9M |
|
Het |
Ttll4 |
A |
G |
1: 74,687,259 |
N672S |
possibly damaging |
Het |
Ube3a |
T |
A |
7: 59,303,689 |
H790Q |
possibly damaging |
Het |
Usp49 |
G |
A |
17: 47,672,280 |
R70Q |
probably benign |
Het |
Wars |
A |
G |
12: 108,882,875 |
S49P |
probably benign |
Het |
Zbp1 |
T |
A |
2: 173,207,811 |
Q386L |
possibly damaging |
Het |
Zfp369 |
T |
C |
13: 65,279,273 |
F10S |
unknown |
Het |
Zfp512 |
C |
G |
5: 31,473,539 |
I408M |
possibly damaging |
Het |
Zfp952 |
A |
G |
17: 33,003,782 |
I412V |
probably benign |
Het |
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