Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810062G17Rik |
C |
A |
3: 36,533,690 (GRCm39) |
|
probably benign |
Het |
Ankib1 |
G |
A |
5: 3,777,573 (GRCm39) |
S439L |
probably benign |
Het |
Cdcp3 |
T |
A |
7: 130,839,823 (GRCm39) |
|
probably null |
Het |
Cpd |
G |
T |
11: 76,688,615 (GRCm39) |
H886N |
probably benign |
Het |
Dhrs7 |
A |
G |
12: 72,706,124 (GRCm39) |
C94R |
probably damaging |
Het |
Dmxl2 |
T |
A |
9: 54,323,277 (GRCm39) |
H1369L |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,272,488 (GRCm39) |
N1068S |
probably benign |
Het |
Dop1a |
T |
A |
9: 86,433,732 (GRCm39) |
D2329E |
possibly damaging |
Het |
Eif1ad |
A |
G |
19: 5,418,212 (GRCm39) |
|
probably benign |
Het |
Fam149a |
T |
C |
8: 45,792,380 (GRCm39) |
R693G |
probably damaging |
Het |
Fbxw18 |
T |
A |
9: 109,522,411 (GRCm39) |
T153S |
probably benign |
Het |
Glg1 |
A |
T |
8: 111,886,481 (GRCm39) |
C1104S |
probably damaging |
Het |
Jak3 |
T |
C |
8: 72,134,341 (GRCm39) |
|
probably benign |
Het |
Kctd6 |
C |
T |
14: 8,222,856 (GRCm38) |
R233C |
possibly damaging |
Het |
Kpna3 |
A |
G |
14: 61,611,737 (GRCm39) |
V300A |
possibly damaging |
Het |
Msh5 |
A |
T |
17: 35,248,857 (GRCm39) |
Y725* |
probably null |
Het |
Myh2 |
T |
C |
11: 67,076,059 (GRCm39) |
S749P |
possibly damaging |
Het |
Or2ag15 |
T |
A |
7: 106,340,908 (GRCm39) |
T78S |
probably benign |
Het |
Or4c110 |
A |
G |
2: 88,831,683 (GRCm39) |
|
probably benign |
Het |
Or5ac17 |
A |
T |
16: 59,036,859 (GRCm39) |
M39K |
probably damaging |
Het |
Or8g19 |
T |
A |
9: 39,056,053 (GRCm39) |
I219N |
possibly damaging |
Het |
Pdcd1 |
A |
G |
1: 93,967,860 (GRCm39) |
|
probably benign |
Het |
Pde5a |
T |
A |
3: 122,588,006 (GRCm39) |
F391I |
probably damaging |
Het |
Ptpn12 |
A |
C |
5: 21,203,666 (GRCm39) |
S371A |
probably damaging |
Het |
Sec16b |
A |
G |
1: 157,365,900 (GRCm39) |
Y254C |
probably damaging |
Het |
Slc2a10 |
G |
A |
2: 165,356,700 (GRCm39) |
C120Y |
probably damaging |
Het |
Spink5 |
G |
A |
18: 44,120,938 (GRCm39) |
|
probably benign |
Het |
Svil |
A |
G |
18: 5,099,045 (GRCm39) |
Q1250R |
probably benign |
Het |
Tph1 |
G |
T |
7: 46,306,294 (GRCm39) |
N222K |
probably benign |
Het |
Vmn2r83 |
A |
T |
10: 79,314,805 (GRCm39) |
D351V |
probably damaging |
Het |
Zfp54 |
A |
G |
17: 21,653,821 (GRCm39) |
D105G |
possibly damaging |
Het |
|
Other mutations in Zfp623 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01524:Zfp623
|
APN |
15 |
75,819,528 (GRCm39) |
missense |
probably benign |
|
IGL01927:Zfp623
|
APN |
15 |
75,819,354 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL03199:Zfp623
|
APN |
15 |
75,819,119 (GRCm39) |
missense |
probably benign |
0.40 |
R0076:Zfp623
|
UTSW |
15 |
75,819,058 (GRCm39) |
missense |
probably benign |
|
R0352:Zfp623
|
UTSW |
15 |
75,820,433 (GRCm39) |
missense |
probably benign |
0.00 |
R0360:Zfp623
|
UTSW |
15 |
75,820,510 (GRCm39) |
missense |
probably benign |
|
R0364:Zfp623
|
UTSW |
15 |
75,820,510 (GRCm39) |
missense |
probably benign |
|
R1783:Zfp623
|
UTSW |
15 |
75,819,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R2219:Zfp623
|
UTSW |
15 |
75,819,379 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5975:Zfp623
|
UTSW |
15 |
75,820,012 (GRCm39) |
missense |
probably benign |
0.43 |
R6161:Zfp623
|
UTSW |
15 |
75,820,470 (GRCm39) |
missense |
probably benign |
0.22 |
R6342:Zfp623
|
UTSW |
15 |
75,819,837 (GRCm39) |
nonsense |
probably null |
|
R6490:Zfp623
|
UTSW |
15 |
75,820,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6513:Zfp623
|
UTSW |
15 |
75,819,317 (GRCm39) |
missense |
probably benign |
|
R7028:Zfp623
|
UTSW |
15 |
75,820,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R7399:Zfp623
|
UTSW |
15 |
75,819,247 (GRCm39) |
missense |
probably damaging |
0.98 |
R7716:Zfp623
|
UTSW |
15 |
75,820,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Zfp623
|
UTSW |
15 |
75,819,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R8445:Zfp623
|
UTSW |
15 |
75,819,402 (GRCm39) |
nonsense |
probably null |
|
R9028:Zfp623
|
UTSW |
15 |
75,819,349 (GRCm39) |
missense |
probably damaging |
0.97 |
R9035:Zfp623
|
UTSW |
15 |
75,820,162 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9310:Zfp623
|
UTSW |
15 |
75,819,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|