Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
A |
C |
7: 29,262,777 (GRCm39) |
|
noncoding transcript |
Het |
Araf |
A |
G |
X: 20,720,148 (GRCm39) |
|
probably benign |
Het |
Arrb2 |
T |
A |
11: 70,330,300 (GRCm39) |
V308E |
probably damaging |
Het |
Asap3 |
A |
G |
4: 135,956,768 (GRCm39) |
|
probably benign |
Het |
Astn2 |
G |
A |
4: 65,910,516 (GRCm39) |
|
probably benign |
Het |
Cactin |
T |
A |
10: 81,158,808 (GRCm39) |
I258N |
probably benign |
Het |
Calhm6 |
T |
C |
10: 34,002,400 (GRCm39) |
T228A |
probably benign |
Het |
Catsperg1 |
T |
C |
7: 28,910,345 (GRCm39) |
|
probably benign |
Het |
Ccna1 |
C |
T |
3: 54,955,915 (GRCm39) |
D146N |
probably benign |
Het |
Chrna3 |
T |
C |
9: 54,922,821 (GRCm39) |
Y329C |
probably damaging |
Het |
Ctps2 |
G |
A |
X: 161,693,005 (GRCm39) |
G56D |
probably damaging |
Het |
Cyp4b1 |
T |
C |
4: 115,504,754 (GRCm39) |
D44G |
probably benign |
Het |
D3Ertd751e |
A |
G |
3: 41,708,155 (GRCm39) |
|
probably null |
Het |
Daxx |
T |
C |
17: 34,131,216 (GRCm39) |
V381A |
probably damaging |
Het |
Dhx37 |
T |
A |
5: 125,496,401 (GRCm39) |
I714F |
possibly damaging |
Het |
Dnah7b |
T |
C |
1: 46,234,478 (GRCm39) |
V1470A |
probably damaging |
Het |
Efl1 |
T |
C |
7: 82,332,247 (GRCm39) |
I297T |
probably damaging |
Het |
Fnd3c2 |
A |
T |
X: 105,289,092 (GRCm39) |
H442Q |
probably damaging |
Het |
Glp2r |
A |
C |
11: 67,630,992 (GRCm39) |
V126G |
possibly damaging |
Het |
Gm5699 |
G |
T |
1: 31,037,843 (GRCm39) |
|
noncoding transcript |
Het |
Gpt2 |
A |
G |
8: 86,242,862 (GRCm39) |
D298G |
probably damaging |
Het |
Gse1 |
G |
T |
8: 121,302,001 (GRCm39) |
|
probably benign |
Het |
Hand1 |
T |
C |
11: 57,722,420 (GRCm39) |
T65A |
probably benign |
Het |
Ints8 |
G |
A |
4: 11,208,834 (GRCm39) |
Q955* |
probably null |
Het |
Lrguk |
C |
T |
6: 34,069,726 (GRCm39) |
P534S |
probably damaging |
Het |
Lrp6 |
A |
G |
6: 134,518,886 (GRCm39) |
F60L |
probably benign |
Het |
Mamld1 |
T |
C |
X: 70,162,258 (GRCm39) |
I423T |
possibly damaging |
Het |
Mrpl22 |
G |
A |
11: 58,063,888 (GRCm39) |
S36N |
possibly damaging |
Het |
Mug2 |
A |
G |
6: 122,049,712 (GRCm39) |
E915G |
probably damaging |
Het |
Oosp2 |
T |
C |
19: 11,628,847 (GRCm39) |
T85A |
probably benign |
Het |
Or5b94 |
T |
C |
19: 12,652,223 (GRCm39) |
F218S |
possibly damaging |
Het |
Or5p68 |
C |
T |
7: 107,945,813 (GRCm39) |
R125Q |
probably damaging |
Het |
Pde4c |
T |
A |
8: 71,200,701 (GRCm39) |
|
probably benign |
Het |
Pdxdc1 |
T |
C |
16: 13,693,945 (GRCm39) |
E159G |
possibly damaging |
Het |
Poln |
T |
C |
5: 34,286,721 (GRCm39) |
E149G |
probably damaging |
Het |
Ppm1k |
A |
T |
6: 57,501,997 (GRCm39) |
S55R |
possibly damaging |
Het |
Ptges2 |
T |
A |
2: 32,287,719 (GRCm39) |
I149N |
probably damaging |
Het |
Pus7l |
A |
G |
15: 94,427,369 (GRCm39) |
V471A |
possibly damaging |
Het |
Raet1e |
A |
T |
10: 22,056,666 (GRCm39) |
M81L |
probably benign |
Het |
Sipa1l3 |
A |
G |
7: 29,098,956 (GRCm39) |
S438P |
probably damaging |
Het |
Skint5 |
T |
A |
4: 113,799,750 (GRCm39) |
K126* |
probably null |
Het |
Stfa2 |
T |
C |
16: 36,225,569 (GRCm39) |
T37A |
probably damaging |
Het |
Ttll12 |
A |
G |
15: 83,465,897 (GRCm39) |
I433T |
possibly damaging |
Het |
Vmn2r32 |
C |
T |
7: 7,467,116 (GRCm39) |
G804D |
probably damaging |
Het |
Zc3h14 |
A |
G |
12: 98,740,560 (GRCm39) |
T84A |
probably benign |
Het |
|
Other mutations in Pou5f2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01018:Pou5f2
|
APN |
13 |
78,174,057 (GRCm39) |
intron |
probably benign |
|
IGL01726:Pou5f2
|
APN |
13 |
78,173,300 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02549:Pou5f2
|
APN |
13 |
78,173,709 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02850:Pou5f2
|
APN |
13 |
78,173,178 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02852:Pou5f2
|
APN |
13 |
78,173,178 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02951:Pou5f2
|
APN |
13 |
78,173,237 (GRCm39) |
missense |
probably benign |
|
R0631:Pou5f2
|
UTSW |
13 |
78,173,873 (GRCm39) |
missense |
probably benign |
0.00 |
R1502:Pou5f2
|
UTSW |
13 |
78,173,370 (GRCm39) |
missense |
probably benign |
0.14 |
R2014:Pou5f2
|
UTSW |
13 |
78,173,972 (GRCm39) |
missense |
probably benign |
0.00 |
R2055:Pou5f2
|
UTSW |
13 |
78,173,940 (GRCm39) |
missense |
probably benign |
0.06 |
R4082:Pou5f2
|
UTSW |
13 |
78,174,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R5193:Pou5f2
|
UTSW |
13 |
78,173,083 (GRCm39) |
missense |
probably benign |
0.15 |
R5487:Pou5f2
|
UTSW |
13 |
78,173,118 (GRCm39) |
missense |
probably benign |
0.09 |
R6880:Pou5f2
|
UTSW |
13 |
78,173,613 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7108:Pou5f2
|
UTSW |
13 |
78,173,384 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7117:Pou5f2
|
UTSW |
13 |
78,173,392 (GRCm39) |
missense |
probably benign |
0.09 |
R8334:Pou5f2
|
UTSW |
13 |
78,173,392 (GRCm39) |
missense |
probably benign |
0.09 |
R8836:Pou5f2
|
UTSW |
13 |
78,173,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R9290:Pou5f2
|
UTSW |
13 |
78,173,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R9584:Pou5f2
|
UTSW |
13 |
78,173,592 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Pou5f2
|
UTSW |
13 |
78,173,216 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Pou5f2
|
UTSW |
13 |
78,173,820 (GRCm39) |
missense |
probably benign |
0.00 |
|