Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadm |
C |
A |
3: 153,644,250 (GRCm39) |
E110* |
probably null |
Het |
Adad1 |
G |
T |
3: 37,133,951 (GRCm39) |
V289F |
probably damaging |
Het |
Adgra2 |
A |
G |
8: 27,607,440 (GRCm39) |
D717G |
probably benign |
Het |
Arid3b |
T |
C |
9: 57,703,780 (GRCm39) |
I389M |
possibly damaging |
Het |
Axdnd1 |
A |
G |
1: 156,225,023 (GRCm39) |
V47A |
|
Het |
Cachd1 |
T |
A |
4: 100,824,244 (GRCm39) |
L562M |
probably benign |
Het |
Cadm2 |
A |
T |
16: 66,528,357 (GRCm39) |
I326N |
probably benign |
Het |
Ccpg1 |
T |
C |
9: 72,922,787 (GRCm39) |
F799S |
probably damaging |
Het |
Ces1c |
T |
C |
8: 93,833,231 (GRCm39) |
I411M |
probably benign |
Het |
Cgn |
T |
G |
3: 94,669,941 (GRCm39) |
K1066N |
probably damaging |
Het |
Cntn4 |
A |
G |
6: 106,330,684 (GRCm39) |
I101V |
probably benign |
Het |
Cntrl |
A |
G |
2: 35,060,592 (GRCm39) |
E1928G |
probably benign |
Het |
Cxcl12 |
A |
G |
6: 117,148,464 (GRCm39) |
Y28C |
probably damaging |
Het |
Cyp2r1 |
A |
T |
7: 114,153,824 (GRCm39) |
|
probably null |
Het |
D430041D05Rik |
C |
T |
2: 104,087,974 (GRCm39) |
W334* |
probably null |
Het |
Dsp |
G |
A |
13: 38,367,994 (GRCm39) |
R671Q |
possibly damaging |
Het |
Fancm |
A |
G |
12: 65,173,568 (GRCm39) |
K1960R |
probably benign |
Het |
Fgd5 |
T |
A |
6: 92,045,459 (GRCm39) |
Y1331N |
probably damaging |
Het |
Ina |
G |
A |
19: 47,004,100 (GRCm39) |
E303K |
|
Het |
Kctd3 |
C |
A |
1: 188,715,243 (GRCm39) |
V369F |
possibly damaging |
Het |
Kif14 |
T |
C |
1: 136,399,314 (GRCm39) |
|
probably null |
Het |
Kif14 |
T |
C |
1: 136,443,763 (GRCm39) |
V1312A |
probably benign |
Het |
Krt84 |
T |
C |
15: 101,436,826 (GRCm39) |
I403V |
probably benign |
Het |
Krtap9-1 |
A |
C |
11: 99,764,356 (GRCm39) |
T31P |
unknown |
Het |
Lyrm9 |
A |
T |
11: 78,728,967 (GRCm39) |
I60F |
probably damaging |
Het |
Mast1 |
A |
G |
8: 85,639,947 (GRCm39) |
|
probably null |
Het |
Mmp28 |
T |
C |
11: 83,334,752 (GRCm39) |
D334G |
probably damaging |
Het |
Nr1h5 |
T |
C |
3: 102,856,931 (GRCm39) |
T194A |
possibly damaging |
Het |
Nrf1 |
A |
G |
6: 30,090,299 (GRCm39) |
I85M |
probably benign |
Het |
Nrp2 |
C |
T |
1: 62,822,680 (GRCm39) |
R758C |
probably damaging |
Het |
Or5b116 |
A |
T |
19: 13,422,951 (GRCm39) |
T192S |
probably benign |
Het |
Pcdhga4 |
A |
G |
18: 37,819,681 (GRCm39) |
D410G |
probably damaging |
Het |
Pld1 |
T |
C |
3: 28,099,158 (GRCm39) |
V275A |
probably damaging |
Het |
Plxnc1 |
A |
T |
10: 94,679,698 (GRCm39) |
F895I |
probably benign |
Het |
Polr2a |
A |
G |
11: 69,627,000 (GRCm39) |
I1486T |
possibly damaging |
Het |
Ptprz1 |
A |
G |
6: 23,002,256 (GRCm39) |
M1449V |
probably benign |
Het |
Rspo4 |
C |
A |
2: 151,711,746 (GRCm39) |
T156N |
probably damaging |
Het |
Sacs |
A |
G |
14: 61,444,520 (GRCm39) |
I2189V |
probably benign |
Het |
Stat5b |
A |
C |
11: 100,674,601 (GRCm39) |
F711V |
possibly damaging |
Het |
Stk11ip |
C |
A |
1: 75,506,108 (GRCm39) |
Q543K |
probably benign |
Het |
Tarbp1 |
G |
A |
8: 127,183,232 (GRCm39) |
T529M |
probably damaging |
Het |
Thada |
A |
T |
17: 84,736,624 (GRCm39) |
C886S |
possibly damaging |
Het |
Tmem19 |
A |
G |
10: 115,179,608 (GRCm39) |
F296S |
probably benign |
Het |
Tnfsf13b |
A |
G |
8: 10,057,078 (GRCm39) |
N79S |
not run |
Het |
Vdac3 |
C |
A |
8: 23,069,073 (GRCm39) |
G214C |
probably damaging |
Het |
Vmn2r18 |
A |
C |
5: 151,485,329 (GRCm39) |
F722V |
probably damaging |
Het |
Vmn2r45 |
A |
G |
7: 8,486,409 (GRCm39) |
L293S |
possibly damaging |
Het |
Vmn2r88 |
C |
G |
14: 51,650,503 (GRCm39) |
A72G |
probably benign |
Het |
Xpot |
A |
G |
10: 121,454,996 (GRCm39) |
|
probably null |
Het |
Zfp532 |
A |
G |
18: 65,756,561 (GRCm39) |
T165A |
probably benign |
Het |
|
Other mutations in Zfp526 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02255:Zfp526
|
APN |
7 |
24,924,958 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02983:Zfp526
|
APN |
7 |
24,923,840 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03123:Zfp526
|
APN |
7 |
24,924,049 (GRCm39) |
missense |
probably benign |
|
R0456:Zfp526
|
UTSW |
7 |
24,925,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1269:Zfp526
|
UTSW |
7 |
24,923,788 (GRCm39) |
missense |
probably benign |
|
R1542:Zfp526
|
UTSW |
7 |
24,925,687 (GRCm39) |
missense |
probably benign |
0.12 |
R1668:Zfp526
|
UTSW |
7 |
24,924,967 (GRCm39) |
missense |
probably benign |
0.15 |
R1742:Zfp526
|
UTSW |
7 |
24,923,939 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1870:Zfp526
|
UTSW |
7 |
24,924,594 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3791:Zfp526
|
UTSW |
7 |
24,925,628 (GRCm39) |
missense |
probably damaging |
0.98 |
R4755:Zfp526
|
UTSW |
7 |
24,925,064 (GRCm39) |
missense |
probably benign |
0.00 |
R4833:Zfp526
|
UTSW |
7 |
24,925,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Zfp526
|
UTSW |
7 |
24,925,109 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5853:Zfp526
|
UTSW |
7 |
24,924,601 (GRCm39) |
nonsense |
probably null |
|
R6061:Zfp526
|
UTSW |
7 |
24,925,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R6186:Zfp526
|
UTSW |
7 |
24,925,561 (GRCm39) |
missense |
probably benign |
|
R7270:Zfp526
|
UTSW |
7 |
24,925,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R8084:Zfp526
|
UTSW |
7 |
24,924,737 (GRCm39) |
missense |
probably damaging |
0.99 |
R9016:Zfp526
|
UTSW |
7 |
24,925,264 (GRCm39) |
missense |
probably damaging |
1.00 |
|