Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
G |
6: 121,670,998 |
L1150V |
probably damaging |
Het |
AB124611 |
A |
G |
9: 21,544,693 |
D194G |
possibly damaging |
Het |
Adgrv1 |
A |
G |
13: 81,521,183 |
L2418P |
probably benign |
Het |
Ap3m1 |
A |
G |
14: 21,040,084 |
S213P |
probably damaging |
Het |
Apobec2 |
A |
T |
17: 48,432,503 |
L36H |
|
Het |
Arrb1 |
A |
G |
7: 99,588,073 |
D78G |
|
Het |
Astn1 |
A |
G |
1: 158,510,985 |
Q434R |
probably damaging |
Het |
Cadps |
C |
G |
14: 12,705,676 |
D240H |
probably damaging |
Het |
Crxos |
A |
C |
7: 15,897,511 |
I45L |
probably benign |
Het |
Dmxl1 |
C |
G |
18: 49,939,572 |
N2744K |
probably damaging |
Het |
Dnah2 |
A |
G |
11: 69,422,861 |
I4204T |
|
Het |
Ei24 |
A |
G |
9: 36,786,031 |
S134P |
probably damaging |
Het |
Eif2ak3 |
G |
T |
6: 70,883,630 |
V397F |
probably damaging |
Het |
Eif4g2 |
T |
C |
7: 111,073,762 |
I134V |
|
Het |
Fam186a |
A |
G |
15: 99,943,278 |
I1695T |
possibly damaging |
Het |
Gcnt3 |
T |
C |
9: 70,034,657 |
M210V |
probably damaging |
Het |
Gm21671 |
CTTT |
C |
5: 25,950,859 |
|
probably benign |
Het |
Gm4788 |
A |
G |
1: 139,732,347 |
I680T |
probably damaging |
Het |
Gpatch8 |
A |
G |
11: 102,479,473 |
S1080P |
probably benign |
Het |
Gtf3c1 |
A |
G |
7: 125,645,777 |
L1695P |
possibly damaging |
Het |
Haus3 |
A |
G |
5: 34,167,650 |
F222L |
probably damaging |
Het |
Kbtbd8 |
C |
T |
6: 95,122,844 |
Q445* |
probably null |
Het |
Kcnc3 |
A |
G |
7: 44,591,168 |
N95D |
probably damaging |
Het |
Krt40 |
C |
T |
11: 99,539,867 |
|
probably null |
Het |
Lgi1 |
A |
G |
19: 38,301,298 |
T271A |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,791,090 |
P1192L |
probably benign |
Het |
Map3k21 |
A |
G |
8: 125,938,724 |
T551A |
possibly damaging |
Het |
Muc5ac |
T |
C |
7: 141,809,792 |
I2280T |
unknown |
Het |
Mug1 |
C |
A |
6: 121,874,431 |
D762E |
probably damaging |
Het |
Myo1e |
A |
T |
9: 70,359,323 |
N615I |
probably damaging |
Het |
Olfr1280 |
T |
C |
2: 111,315,482 |
M1T |
probably null |
Het |
Olfr564 |
T |
C |
7: 102,804,132 |
L218P |
probably damaging |
Het |
Pld5 |
T |
C |
1: 175,975,538 |
E387G |
possibly damaging |
Het |
Pld5 |
A |
G |
1: 176,074,437 |
V195A |
probably benign |
Het |
Rad54l |
T |
C |
4: 116,123,152 |
|
probably benign |
Het |
Rnf123 |
A |
T |
9: 108,063,028 |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,440,748 |
E2262G |
|
Het |
Rp1 |
C |
A |
1: 4,163,938 |
V910L |
unknown |
Het |
Rpp21 |
A |
T |
17: 36,257,515 |
C23S |
probably benign |
Het |
Scn11a |
T |
C |
9: 119,759,923 |
M1306V |
possibly damaging |
Het |
Scn2b |
C |
T |
9: 45,125,436 |
L81F |
possibly damaging |
Het |
Sco2 |
T |
C |
15: 89,372,160 |
D97G |
probably damaging |
Het |
Slc25a54 |
T |
C |
3: 109,094,232 |
V112A |
probably benign |
Het |
Slc5a11 |
A |
T |
7: 123,265,269 |
K363* |
probably null |
Het |
Smg1 |
G |
T |
7: 118,154,661 |
T2563K |
unknown |
Het |
Snap47 |
A |
T |
11: 59,428,464 |
S283T |
probably damaging |
Het |
Stat1 |
G |
T |
1: 52,139,229 |
R274L |
probably damaging |
Het |
Stoml1 |
A |
G |
9: 58,257,126 |
T166A |
|
Het |
Svs2 |
G |
T |
2: 164,237,589 |
Q133K |
probably benign |
Het |
Tas2r107 |
T |
A |
6: 131,659,459 |
H209L |
probably benign |
Het |
Tmco3 |
T |
A |
8: 13,310,228 |
V477D |
possibly damaging |
Het |
Tmem131 |
A |
T |
1: 36,841,686 |
S168T |
possibly damaging |
Het |
Tmem41a |
T |
C |
16: 21,937,109 |
N149S |
probably damaging |
Het |
Ttll4 |
T |
C |
1: 74,680,066 |
F359L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,954,818 |
M784L |
unknown |
Het |
Ubr1 |
A |
G |
2: 120,873,122 |
|
probably null |
Het |
Ubxn2b |
C |
T |
4: 6,214,646 |
P227S |
probably damaging |
Het |
Upb1 |
C |
T |
10: 75,430,127 |
L263F |
probably benign |
Het |
Usp15 |
T |
A |
10: 123,113,648 |
T935S |
probably benign |
Het |
Zscan4-ps3 |
G |
A |
7: 11,613,237 |
C400Y |
probably damaging |
Het |
|