Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410089E03Rik |
T |
C |
15: 8,221,937 |
S1898P |
probably benign |
Het |
4932438A13Rik |
T |
G |
3: 36,965,937 |
N2108K |
probably damaging |
Het |
Abcb4 |
T |
C |
5: 8,907,267 |
V132A |
possibly damaging |
Het |
Acpp |
A |
T |
9: 104,306,975 |
V292E |
probably damaging |
Het |
Adamts10 |
T |
C |
17: 33,528,896 |
V102A |
possibly damaging |
Het |
Add2 |
A |
G |
6: 86,096,746 |
T206A |
probably benign |
Het |
Alg12 |
A |
T |
15: 88,816,188 |
L15Q |
probably damaging |
Het |
Ankrd27 |
T |
A |
7: 35,608,375 |
D346E |
probably damaging |
Het |
Armc2 |
A |
T |
10: 41,923,794 |
N689K |
probably damaging |
Het |
Best3 |
T |
A |
10: 117,024,555 |
D573E |
probably benign |
Het |
Ccdc80 |
A |
T |
16: 45,095,898 |
Q339L |
probably benign |
Het |
Cdh9 |
T |
C |
15: 16,778,156 |
V19A |
probably benign |
Het |
Cnksr1 |
A |
T |
4: 134,229,675 |
|
probably null |
Het |
Col7a1 |
T |
A |
9: 108,957,277 |
V525E |
unknown |
Het |
Crebrf |
T |
C |
17: 26,742,420 |
S172P |
possibly damaging |
Het |
Csmd1 |
T |
C |
8: 16,009,439 |
I2099V |
probably benign |
Het |
Dcaf4 |
T |
A |
12: 83,539,459 |
M400K |
possibly damaging |
Het |
Dnah11 |
A |
T |
12: 117,995,200 |
F2983I |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,824,437 |
V1005A |
possibly damaging |
Het |
Dyrk2 |
C |
A |
10: 118,868,248 |
G34C |
probably damaging |
Het |
Eif4a1 |
A |
T |
11: 69,668,597 |
|
probably benign |
Het |
Eno4 |
G |
T |
19: 58,964,543 |
D330Y |
probably damaging |
Het |
Faf1 |
G |
A |
4: 109,842,299 |
C347Y |
probably benign |
Het |
Fam169a |
A |
G |
13: 97,097,592 |
Y124C |
probably damaging |
Het |
Fam227a |
G |
T |
15: 79,637,054 |
F269L |
probably benign |
Het |
Fam60a |
A |
G |
6: 148,933,000 |
|
probably null |
Het |
Fancm |
C |
A |
12: 65,075,831 |
D42E |
probably damaging |
Het |
Fat1 |
T |
A |
8: 44,951,280 |
I356N |
possibly damaging |
Het |
Fer1l6 |
A |
T |
15: 58,638,020 |
T1444S |
probably damaging |
Het |
Galr1 |
A |
G |
18: 82,393,940 |
L267P |
probably damaging |
Het |
Gbx1 |
T |
C |
5: 24,504,839 |
H336R |
probably damaging |
Het |
Gimap8 |
A |
T |
6: 48,659,347 |
Q682L |
possibly damaging |
Het |
Gm2396 |
T |
G |
9: 88,931,228 |
|
noncoding transcript |
Het |
Gm5798 |
T |
C |
14: 41,348,657 |
L8S |
probably damaging |
Het |
Hmgcll1 |
C |
T |
9: 76,056,178 |
S39F |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,518,940 |
R1010C |
probably damaging |
Het |
Il3ra |
A |
T |
14: 14,355,381 |
E289D |
probably benign |
Het |
Isoc1 |
T |
A |
18: 58,673,278 |
L220Q |
probably damaging |
Het |
Itga2 |
T |
A |
13: 114,853,766 |
K918* |
probably null |
Het |
Kat6a |
C |
T |
8: 22,938,313 |
T1228I |
probably benign |
Het |
Klhl30 |
T |
A |
1: 91,359,324 |
|
probably null |
Het |
Krtap6-2 |
A |
T |
16: 89,419,918 |
C54S |
unknown |
Het |
Lmf2 |
G |
A |
15: 89,351,800 |
P634S |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,272,019 |
V175A |
possibly damaging |
Het |
Mcm3 |
A |
C |
1: 20,820,256 |
|
probably benign |
Het |
Mon1b |
T |
C |
8: 113,639,227 |
S396P |
probably damaging |
Het |
Mroh2a |
T |
C |
1: 88,256,754 |
V1453A |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,049,340 |
|
probably null |
Het |
Nlrc5 |
T |
G |
8: 94,521,216 |
|
probably benign |
Het |
Nlrp14 |
GT |
GTT |
7: 107,197,179 |
|
probably null |
Het |
Nwd2 |
T |
G |
5: 63,804,808 |
S578R |
probably damaging |
Het |
Odf3 |
G |
A |
7: 140,848,485 |
|
probably benign |
Het |
Olfr1289 |
G |
A |
2: 111,483,660 |
V105I |
possibly damaging |
Het |
Olfr360 |
A |
G |
2: 37,068,410 |
Y35C |
probably damaging |
Het |
Otoa |
C |
A |
7: 121,102,679 |
P194T |
probably damaging |
Het |
Pde1b |
A |
C |
15: 103,521,374 |
D98A |
probably damaging |
Het |
Pi4ka |
A |
T |
16: 17,377,169 |
C122S |
probably damaging |
Het |
Pole2 |
C |
T |
12: 69,223,150 |
V67M |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,416,755 |
D312E |
probably benign |
Het |
Prkd1 |
T |
C |
12: 50,389,962 |
D453G |
probably damaging |
Het |
Prrc1 |
T |
A |
18: 57,374,554 |
V260E |
probably damaging |
Het |
Reg3g |
A |
T |
6: 78,467,810 |
Y62N |
probably benign |
Het |
Reln |
C |
T |
5: 21,955,238 |
G2111E |
probably damaging |
Het |
Rsph6a |
A |
T |
7: 19,057,740 |
E278V |
possibly damaging |
Het |
Scpep1 |
T |
A |
11: 88,941,296 |
I203F |
probably damaging |
Het |
Sec24d |
T |
C |
3: 123,354,947 |
C747R |
probably damaging |
Het |
Sec31a |
A |
T |
5: 100,368,333 |
N967K |
probably damaging |
Het |
Sell |
T |
C |
1: 164,063,062 |
W5R |
probably benign |
Het |
Siglec1 |
C |
T |
2: 131,069,869 |
V1697M |
probably benign |
Het |
Slc22a26 |
T |
A |
19: 7,791,054 |
I213L |
probably benign |
Het |
Slc2a13 |
G |
A |
15: 91,412,212 |
P300S |
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,815,505 |
Y461H |
possibly damaging |
Het |
Slco3a1 |
G |
C |
7: 74,320,556 |
C434W |
probably null |
Het |
Sp3 |
A |
T |
2: 72,938,289 |
V666D |
probably benign |
Het |
Spidr |
A |
T |
16: 16,118,942 |
W100R |
possibly damaging |
Het |
Stk33 |
T |
A |
7: 109,327,595 |
M286L |
probably damaging |
Het |
Sult1c2 |
T |
A |
17: 53,832,135 |
I183F |
probably benign |
Het |
Svep1 |
G |
T |
4: 58,087,751 |
T1776K |
probably benign |
Het |
Tesk2 |
A |
G |
4: 116,802,993 |
H436R |
probably benign |
Het |
Tex2 |
T |
C |
11: 106,568,404 |
T67A |
probably damaging |
Het |
Timm10 |
T |
C |
2: 84,829,848 |
S44P |
possibly damaging |
Het |
Tmed11 |
C |
A |
5: 108,795,182 |
|
probably null |
Het |
Trim12c |
G |
A |
7: 104,340,948 |
R441C |
probably damaging |
Het |
Trmt2a |
A |
G |
16: 18,252,929 |
K509E |
probably damaging |
Het |
Upk3a |
A |
G |
15: 85,019,423 |
T108A |
probably benign |
Het |
Usp29 |
A |
G |
7: 6,962,159 |
M334V |
probably benign |
Het |
Vash1 |
A |
G |
12: 86,680,142 |
D52G |
probably benign |
Het |
Vmn2r14 |
T |
G |
5: 109,220,380 |
T249P |
probably benign |
Het |
Vmn2r43 |
A |
T |
7: 8,244,849 |
F772I |
probably damaging |
Het |
Vmn2r75 |
G |
T |
7: 86,171,579 |
S49Y |
probably benign |
Het |
Xdh |
T |
C |
17: 73,910,243 |
T677A |
probably damaging |
Het |
Zfp160 |
T |
A |
17: 21,020,081 |
S9T |
probably benign |
Het |
Zfp273 |
A |
T |
13: 67,825,554 |
H267L |
probably damaging |
Het |
Zfp97 |
T |
A |
17: 17,144,776 |
I179K |
probably benign |
Het |
Zfp975 |
T |
C |
7: 42,662,292 |
Y299C |
probably damaging |
Het |
|