Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd5 |
A |
G |
9: 122,208,606 (GRCm39) |
Y332C |
probably damaging |
Het |
Adcyap1r1 |
A |
T |
6: 55,457,055 (GRCm39) |
E262V |
probably damaging |
Het |
Adgre5 |
A |
G |
8: 84,450,658 (GRCm39) |
Y793H |
probably damaging |
Het |
Arhgef33 |
A |
T |
17: 80,654,707 (GRCm39) |
Y78F |
possibly damaging |
Het |
Asl |
G |
A |
5: 130,047,693 (GRCm39) |
A91V |
probably damaging |
Het |
Cd40 |
A |
T |
2: 164,905,061 (GRCm39) |
I126F |
probably benign |
Het |
Ceacam10 |
A |
G |
7: 24,476,705 (GRCm39) |
E2G |
probably damaging |
Het |
Cfap46 |
C |
T |
7: 139,230,805 (GRCm39) |
R941H |
|
Het |
Cntnap3 |
A |
T |
13: 65,006,579 (GRCm39) |
S78T |
probably damaging |
Het |
Cntnap4 |
T |
C |
8: 113,602,181 (GRCm39) |
V1195A |
possibly damaging |
Het |
Cthrc1 |
T |
C |
15: 38,947,874 (GRCm39) |
S198P |
probably damaging |
Het |
Dcaf7 |
T |
G |
11: 105,942,794 (GRCm39) |
|
probably null |
Het |
Dhx16 |
A |
G |
17: 36,193,413 (GRCm39) |
E252G |
probably benign |
Het |
Efcab2 |
C |
T |
1: 178,302,505 (GRCm39) |
T83I |
possibly damaging |
Het |
Efhc1 |
A |
G |
1: 21,049,738 (GRCm39) |
N533D |
probably benign |
Het |
Emilin2 |
A |
G |
17: 71,581,112 (GRCm39) |
V538A |
probably benign |
Het |
Fam171b |
A |
T |
2: 83,683,914 (GRCm39) |
T144S |
probably damaging |
Het |
Fam98a |
A |
G |
17: 75,845,474 (GRCm39) |
F424S |
unknown |
Het |
Gm3573 |
T |
C |
14: 42,011,605 (GRCm39) |
R42G |
possibly damaging |
Het |
Gpr143 |
GTTTTTT |
GTTTTTTT |
X: 151,578,627 (GRCm39) |
|
probably null |
Het |
H2-K2 |
G |
A |
17: 34,218,975 (GRCm39) |
P23S |
probably benign |
Het |
Hormad2 |
G |
A |
11: 4,377,372 (GRCm39) |
P22L |
probably damaging |
Het |
Hoxb1 |
C |
T |
11: 96,256,810 (GRCm39) |
A53V |
probably benign |
Het |
Kalrn |
T |
A |
16: 33,849,197 (GRCm39) |
|
probably null |
Het |
Kdm2a |
C |
T |
19: 4,393,141 (GRCm39) |
D405N |
|
Het |
Kif1a |
C |
T |
1: 93,000,766 (GRCm39) |
E287K |
probably benign |
Het |
Lrrk1 |
A |
T |
7: 65,909,666 (GRCm39) |
*2015K |
probably null |
Het |
Ltbp1 |
G |
T |
17: 75,486,157 (GRCm39) |
G61C |
probably damaging |
Het |
Mthfd2l |
A |
G |
5: 91,107,567 (GRCm39) |
H143R |
probably damaging |
Het |
Myo1d |
C |
A |
11: 80,448,296 (GRCm39) |
G943V |
possibly damaging |
Het |
Ncoa1 |
T |
A |
12: 4,345,643 (GRCm39) |
Q568L |
probably damaging |
Het |
Ncoa3 |
G |
A |
2: 165,899,130 (GRCm39) |
S824N |
probably benign |
Het |
Nfe2l3 |
A |
T |
6: 51,434,925 (GRCm39) |
D495V |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nlrp14 |
A |
G |
7: 106,782,169 (GRCm39) |
I455M |
probably benign |
Het |
Npb |
T |
C |
11: 120,499,375 (GRCm39) |
L14P |
probably damaging |
Het |
Or51f1 |
C |
T |
7: 102,505,636 (GRCm39) |
M284I |
probably benign |
Het |
P2ry12 |
G |
A |
3: 59,125,496 (GRCm39) |
R60C |
possibly damaging |
Het |
Pcdhb17 |
T |
A |
18: 37,619,419 (GRCm39) |
L403* |
probably null |
Het |
Phb2 |
G |
A |
6: 124,690,974 (GRCm39) |
R44H |
probably damaging |
Het |
Plekha5 |
A |
T |
6: 140,372,253 (GRCm39) |
T68S |
probably benign |
Het |
Ptprg |
C |
T |
14: 12,152,027 (GRCm38) |
R447W |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,462,006 (GRCm39) |
Y1190H |
probably damaging |
Het |
Ptpro |
G |
T |
6: 137,371,873 (GRCm39) |
C630F |
probably damaging |
Het |
Rrp15 |
G |
T |
1: 186,453,718 (GRCm39) |
P243Q |
possibly damaging |
Het |
Smurf1 |
A |
G |
5: 144,830,920 (GRCm39) |
F285S |
possibly damaging |
Het |
Spata13 |
C |
T |
14: 60,944,349 (GRCm39) |
P581S |
probably benign |
Het |
Tex44 |
T |
C |
1: 86,354,253 (GRCm39) |
I54T |
unknown |
Het |
Tom1l2 |
A |
G |
11: 60,161,277 (GRCm39) |
V78A |
probably damaging |
Het |
Vps11 |
A |
G |
9: 44,265,738 (GRCm39) |
W514R |
probably damaging |
Het |
Wnk2 |
C |
A |
13: 49,254,445 (GRCm39) |
V357L |
probably benign |
Het |
Zfp970 |
C |
T |
2: 177,167,790 (GRCm39) |
Q455* |
probably null |
Het |
|