Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
G |
A |
5: 8,934,327 |
|
probably null |
Het |
Angptl7 |
C |
G |
4: 148,500,077 |
Q71H |
probably damaging |
Het |
Arhgap30 |
A |
T |
1: 171,402,254 |
N176Y |
probably damaging |
Het |
Armc9 |
T |
A |
1: 86,274,534 |
S805T |
probably damaging |
Het |
Atxn1 |
T |
G |
13: 45,566,931 |
H496P |
probably damaging |
Het |
Cabin1 |
C |
T |
10: 75,721,363 |
G1147D |
probably damaging |
Het |
Cabin1 |
A |
G |
10: 75,739,421 |
S597P |
probably damaging |
Het |
Catsperd |
T |
C |
17: 56,662,744 |
S613P |
probably damaging |
Het |
Cdh2 |
A |
G |
18: 16,650,409 |
Y88H |
probably damaging |
Het |
Cntn1 |
C |
A |
15: 92,228,668 |
P47Q |
probably damaging |
Het |
Col11a2 |
T |
C |
17: 34,042,190 |
L38P |
possibly damaging |
Het |
Col5a2 |
T |
G |
1: 45,376,695 |
I1431L |
possibly damaging |
Het |
Dhcr7 |
T |
A |
7: 143,837,791 |
I39N |
probably damaging |
Het |
Diexf |
A |
T |
1: 193,114,954 |
M530K |
probably damaging |
Het |
Dnajc13 |
C |
T |
9: 104,167,387 |
|
probably benign |
Het |
Folr2 |
T |
C |
7: 101,840,290 |
|
probably null |
Het |
Galnt11 |
T |
C |
5: 25,265,338 |
I595T |
probably damaging |
Het |
Gm884 |
T |
C |
11: 103,613,460 |
T2561A |
possibly damaging |
Het |
Gp5 |
G |
A |
16: 30,309,508 |
A116V |
possibly damaging |
Het |
Gpn3 |
T |
C |
5: 122,382,240 |
|
probably benign |
Het |
Gprin3 |
T |
C |
6: 59,354,659 |
N221S |
probably benign |
Het |
Hfm1 |
T |
C |
5: 106,874,213 |
E989G |
possibly damaging |
Het |
Ints1 |
T |
C |
5: 139,758,092 |
|
probably null |
Het |
Josd2 |
T |
C |
7: 44,471,168 |
S110P |
probably damaging |
Het |
Kat14 |
C |
A |
2: 144,375,953 |
T123K |
probably damaging |
Het |
Lamtor1 |
C |
T |
7: 101,909,764 |
T48I |
probably damaging |
Het |
Lrrc24 |
A |
G |
15: 76,718,346 |
L113P |
probably damaging |
Het |
Mog |
T |
C |
17: 37,020,541 |
E89G |
probably damaging |
Het |
Mon2 |
A |
G |
10: 123,038,459 |
|
probably null |
Het |
Mtx1 |
T |
C |
3: 89,213,898 |
Y143C |
probably benign |
Het |
Nacad |
T |
C |
11: 6,598,507 |
E1409G |
possibly damaging |
Het |
Ndst3 |
T |
C |
3: 123,607,027 |
H410R |
probably damaging |
Het |
Nkx6-2 |
T |
C |
7: 139,581,570 |
E233G |
possibly damaging |
Het |
Oas1h |
A |
G |
5: 120,862,783 |
E152G |
probably damaging |
Het |
Olfr936 |
A |
G |
9: 39,046,862 |
S186P |
probably damaging |
Het |
Ovgp1 |
T |
C |
3: 105,979,953 |
F222L |
possibly damaging |
Het |
Pkhd1 |
T |
C |
1: 20,288,205 |
S2716G |
probably null |
Het |
Pla2g4e |
T |
C |
2: 120,171,237 |
T644A |
probably benign |
Het |
Plxnd1 |
A |
G |
6: 115,955,765 |
I1918T |
probably damaging |
Het |
Prrxl1 |
G |
T |
14: 32,608,249 |
Q136H |
probably damaging |
Het |
Psmg1 |
A |
T |
16: 95,989,612 |
|
probably benign |
Het |
Ptprd |
G |
A |
4: 76,128,899 |
R364C |
probably damaging |
Het |
Rgs22 |
T |
C |
15: 36,025,942 |
I945V |
possibly damaging |
Het |
Rgs7bp |
T |
C |
13: 104,951,564 |
N234S |
probably benign |
Het |
Rrp7a |
T |
C |
15: 83,119,809 |
|
probably benign |
Het |
Scg2 |
T |
A |
1: 79,436,476 |
R177* |
probably null |
Het |
Sema4c |
C |
A |
1: 36,550,311 |
C578F |
probably damaging |
Het |
Slc1a5 |
T |
A |
7: 16,797,743 |
|
probably benign |
Het |
Slc5a3 |
A |
G |
16: 92,078,683 |
T543A |
possibly damaging |
Het |
Slx4ip |
T |
A |
2: 137,046,767 |
F123I |
probably benign |
Het |
Smtn |
C |
T |
11: 3,522,916 |
R737H |
probably damaging |
Het |
Stox2 |
A |
G |
8: 47,413,265 |
I14T |
possibly damaging |
Het |
Stradb |
T |
C |
1: 58,980,440 |
F43L |
probably benign |
Het |
Szt2 |
T |
C |
4: 118,388,669 |
D1029G |
probably benign |
Het |
Taar6 |
T |
C |
10: 23,984,715 |
Y311C |
probably damaging |
Het |
Tcea3 |
A |
T |
4: 136,268,093 |
N249I |
probably damaging |
Het |
Tecta |
A |
G |
9: 42,330,277 |
M2134T |
probably benign |
Het |
Tg |
G |
A |
15: 66,764,337 |
G591D |
probably damaging |
Het |
Tm4sf20 |
T |
A |
1: 82,768,363 |
I19F |
probably benign |
Het |
Top2a |
T |
C |
11: 98,997,850 |
K1262E |
probably benign |
Het |
Ube2r2 |
A |
G |
4: 41,190,742 |
|
probably benign |
Het |
Usp29 |
T |
C |
7: 6,961,928 |
S257P |
possibly damaging |
Het |
Usp40 |
T |
C |
1: 87,952,355 |
N1038S |
probably benign |
Het |
Vmn1r121 |
C |
T |
7: 21,097,613 |
E301K |
probably benign |
Het |
Vmn2r49 |
T |
A |
7: 9,989,032 |
H105L |
probably benign |
Het |
Zgrf1 |
C |
T |
3: 127,561,868 |
Q248* |
probably null |
Het |
|