Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700008P02Rik |
A |
G |
3: 6,620,088 |
L102P |
probably benign |
Het |
Adcy4 |
C |
T |
14: 55,775,178 |
|
probably null |
Het |
Adgrf5 |
A |
T |
17: 43,430,714 |
|
probably benign |
Het |
Atp11a |
A |
G |
8: 12,842,938 |
K643R |
probably benign |
Het |
Cacna2d2 |
C |
T |
9: 107,514,058 |
T428M |
probably damaging |
Het |
Cdh22 |
T |
C |
2: 165,143,673 |
D331G |
possibly damaging |
Het |
Chmp3 |
T |
C |
6: 71,574,238 |
|
probably null |
Het |
Csnk2a1 |
C |
T |
2: 152,258,689 |
T127M |
probably damaging |
Het |
Cyp2c55 |
T |
A |
19: 39,035,434 |
|
probably null |
Het |
Ddias |
G |
T |
7: 92,861,478 |
D105E |
possibly damaging |
Het |
Dnajb11 |
A |
G |
16: 22,869,446 |
D238G |
probably damaging |
Het |
Dock7 |
T |
C |
4: 99,003,920 |
|
probably null |
Het |
Dock9 |
T |
C |
14: 121,626,912 |
K761E |
possibly damaging |
Het |
Entpd7 |
G |
A |
19: 43,691,158 |
R50Q |
probably benign |
Het |
Fam107b |
G |
A |
2: 3,778,474 |
R238Q |
probably damaging |
Het |
Fam186a |
G |
C |
15: 99,941,799 |
T2188S |
possibly damaging |
Het |
Farsa |
A |
G |
8: 84,868,870 |
T465A |
probably damaging |
Het |
Fibp |
T |
C |
19: 5,460,734 |
|
probably null |
Het |
Flywch2 |
G |
A |
17: 23,777,039 |
T128I |
possibly damaging |
Het |
Foxi2 |
A |
T |
7: 135,410,530 |
D49V |
probably damaging |
Het |
Fstl5 |
A |
G |
3: 76,628,975 |
T31A |
probably benign |
Het |
Gabbr2 |
G |
A |
4: 46,846,435 |
T158I |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,120,923 |
R455W |
probably damaging |
Het |
Gm11492 |
A |
G |
11: 87,567,280 |
E160G |
probably damaging |
Het |
Got2 |
T |
G |
8: 95,877,753 |
D69A |
probably damaging |
Het |
Gpr63 |
T |
C |
4: 25,008,470 |
F398S |
possibly damaging |
Het |
Gtf2h4 |
T |
C |
17: 35,670,664 |
M186V |
probably benign |
Het |
Haus2 |
A |
T |
2: 120,615,930 |
Q111L |
probably damaging |
Het |
Hexdc |
T |
C |
11: 121,218,161 |
|
probably null |
Het |
Igf2r |
T |
A |
17: 12,748,751 |
N27I |
probably damaging |
Het |
Itgax |
T |
A |
7: 128,133,139 |
|
probably null |
Het |
Krit1 |
T |
A |
5: 3,832,132 |
I596K |
probably benign |
Het |
Lair1 |
A |
G |
7: 4,055,916 |
|
probably null |
Het |
Lilra6 |
G |
T |
7: 3,911,418 |
T276K |
probably benign |
Het |
Mast4 |
G |
A |
13: 102,739,321 |
R1112* |
probably null |
Het |
Mrgprb1 |
A |
T |
7: 48,447,123 |
I347N |
possibly damaging |
Het |
Mroh2b |
T |
A |
15: 4,925,100 |
C682S |
possibly damaging |
Het |
Mtif3 |
T |
A |
5: 146,955,678 |
R249S |
possibly damaging |
Het |
Mycbp2 |
C |
T |
14: 103,152,157 |
E3406K |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,873,505 |
H1315R |
probably benign |
Het |
Nlrp2 |
A |
G |
7: 5,325,012 |
F681L |
probably benign |
Het |
Olfr1157 |
T |
A |
2: 87,962,722 |
T57S |
possibly damaging |
Het |
Olfr703 |
T |
A |
7: 106,845,019 |
M136K |
probably damaging |
Het |
Pear1 |
T |
C |
3: 87,756,222 |
N390D |
possibly damaging |
Het |
Ranbp17 |
G |
A |
11: 33,479,189 |
A352V |
probably benign |
Het |
Rnf17 |
C |
T |
14: 56,460,001 |
H451Y |
probably damaging |
Het |
Sag |
A |
T |
1: 87,821,305 |
|
probably null |
Het |
Slc22a2 |
T |
C |
17: 12,584,489 |
L70P |
probably damaging |
Het |
Slc32a1 |
C |
T |
2: 158,611,232 |
|
probably benign |
Het |
Spag17 |
A |
T |
3: 100,049,230 |
I881F |
probably benign |
Het |
Tbck |
C |
A |
3: 132,727,134 |
T435K |
probably damaging |
Het |
Tril |
T |
G |
6: 53,819,019 |
D406A |
probably damaging |
Het |
Tshz2 |
G |
A |
2: 169,885,862 |
D324N |
probably damaging |
Het |
Vps13d |
A |
G |
4: 145,075,061 |
V2349A |
possibly damaging |
Het |
Wdr6 |
A |
G |
9: 108,575,206 |
W493R |
probably damaging |
Het |
Wdr72 |
G |
A |
9: 74,151,593 |
V323I |
probably benign |
Het |
Zfp488 |
T |
A |
14: 33,971,153 |
M18L |
probably benign |
Het |
Zic4 |
A |
G |
9: 91,379,036 |
T108A |
probably benign |
Het |
Znrf3 |
T |
C |
11: 5,281,278 |
D745G |
possibly damaging |
Het |
|