Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd4 |
T |
A |
14: 54,499,133 (GRCm39) |
M38K |
probably benign |
Het |
Ackr1 |
T |
A |
1: 173,159,582 (GRCm39) |
R312S |
probably benign |
Het |
Akap9 |
T |
C |
5: 4,094,845 (GRCm39) |
V2213A |
probably benign |
Het |
Alox5 |
T |
A |
6: 116,390,835 (GRCm39) |
R439W |
probably damaging |
Het |
Atrn |
A |
T |
2: 130,864,920 (GRCm39) |
|
probably null |
Het |
Casd1 |
A |
G |
6: 4,601,209 (GRCm39) |
N14S |
probably damaging |
Het |
Cry2 |
T |
C |
2: 92,242,974 (GRCm39) |
S542G |
probably benign |
Het |
Cyb5rl |
A |
G |
4: 106,925,935 (GRCm39) |
Y39C |
probably damaging |
Het |
Dmpk |
A |
T |
7: 18,822,048 (GRCm39) |
K335N |
probably benign |
Het |
Dnai1 |
A |
G |
4: 41,625,221 (GRCm39) |
D395G |
probably benign |
Het |
Dock4 |
C |
T |
12: 40,884,837 (GRCm39) |
|
probably null |
Het |
Eif1ad5 |
A |
T |
12: 87,940,508 (GRCm39) |
I71L |
noncoding transcript |
Het |
Fmo4 |
T |
C |
1: 162,632,757 (GRCm39) |
D198G |
probably damaging |
Het |
Foxc2 |
G |
A |
8: 121,844,777 (GRCm39) |
R475Q |
probably damaging |
Het |
Gpat3 |
T |
C |
5: 101,005,076 (GRCm39) |
|
probably null |
Het |
Hcn4 |
A |
G |
9: 58,751,433 (GRCm39) |
D353G |
unknown |
Het |
Hectd4 |
T |
A |
5: 121,477,607 (GRCm39) |
N2843K |
possibly damaging |
Het |
Hmcn1 |
C |
T |
1: 150,469,761 (GRCm39) |
V4973M |
possibly damaging |
Het |
Il20rb |
C |
T |
9: 100,341,263 (GRCm39) |
S281N |
probably benign |
Het |
Kcnh4 |
A |
T |
11: 100,643,093 (GRCm39) |
N391K |
possibly damaging |
Het |
Kitl |
A |
G |
10: 99,887,708 (GRCm39) |
T6A |
probably damaging |
Het |
Krt36 |
A |
G |
11: 99,995,027 (GRCm39) |
Y182H |
probably damaging |
Het |
Lrp1b |
T |
G |
2: 41,202,668 (GRCm39) |
I1262L |
|
Het |
Mtf1 |
A |
G |
4: 124,738,039 (GRCm39) |
E644G |
probably benign |
Het |
Mtx2 |
A |
G |
2: 74,699,706 (GRCm39) |
Y159C |
probably damaging |
Het |
Nags |
C |
T |
11: 102,039,824 (GRCm39) |
S504F |
probably damaging |
Het |
Ncam1 |
A |
T |
9: 49,456,523 (GRCm39) |
F475L |
probably damaging |
Het |
Nipal2 |
G |
T |
15: 34,600,178 (GRCm39) |
T213N |
possibly damaging |
Het |
Or52m1 |
T |
A |
7: 102,289,678 (GRCm39) |
L75Q |
probably damaging |
Het |
Or8h8 |
A |
G |
2: 86,753,313 (GRCm39) |
S188P |
probably damaging |
Het |
Pkm |
T |
C |
9: 59,577,882 (GRCm39) |
V233A |
possibly damaging |
Het |
Pros1 |
T |
A |
16: 62,748,540 (GRCm39) |
I671N |
possibly damaging |
Het |
Rasd1 |
T |
C |
11: 59,855,118 (GRCm39) |
I121V |
probably damaging |
Het |
Relch |
T |
C |
1: 105,681,235 (GRCm39) |
S1180P |
possibly damaging |
Het |
Samhd1 |
A |
G |
2: 156,958,270 (GRCm39) |
|
probably null |
Het |
Serpinb9f |
A |
T |
13: 33,509,898 (GRCm39) |
Y30F |
probably benign |
Het |
Slc5a10 |
T |
C |
11: 61,564,107 (GRCm39) |
I543V |
probably benign |
Het |
Stat5a |
A |
G |
11: 100,770,129 (GRCm39) |
I469V |
possibly damaging |
Het |
Sugct |
T |
C |
13: 17,032,459 (GRCm39) |
E431G |
probably benign |
Het |
Tecr |
C |
A |
8: 84,299,880 (GRCm39) |
R133L |
possibly damaging |
Het |
Tiparp |
A |
G |
3: 65,439,002 (GRCm39) |
N106S |
probably benign |
Het |
Triml1 |
T |
C |
8: 43,594,285 (GRCm39) |
S49G |
probably benign |
Het |
Trpm3 |
T |
A |
19: 22,692,640 (GRCm39) |
S244T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,553,324 (GRCm39) |
D31055G |
probably damaging |
Het |
Vcp |
A |
T |
4: 42,985,242 (GRCm39) |
I369N |
probably damaging |
Het |
Vmn2r110 |
A |
C |
17: 20,804,691 (GRCm39) |
N76K |
probably benign |
Het |
Vmn2r12 |
T |
C |
5: 109,234,074 (GRCm39) |
T713A |
probably benign |
Het |
Vmn2r17 |
A |
T |
5: 109,601,235 (GRCm39) |
K844N |
probably benign |
Het |
|
Other mutations in Gipr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01481:Gipr
|
APN |
7 |
18,893,431 (GRCm39) |
unclassified |
probably benign |
|
IGL02214:Gipr
|
APN |
7 |
18,891,471 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02525:Gipr
|
APN |
7 |
18,893,690 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03163:Gipr
|
APN |
7 |
18,896,481 (GRCm39) |
nonsense |
probably null |
|
PIT4449001:Gipr
|
UTSW |
7 |
18,894,543 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4480001:Gipr
|
UTSW |
7 |
18,896,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Gipr
|
UTSW |
7 |
18,897,996 (GRCm39) |
missense |
probably benign |
0.02 |
R1896:Gipr
|
UTSW |
7 |
18,897,996 (GRCm39) |
missense |
probably benign |
0.02 |
R3409:Gipr
|
UTSW |
7 |
18,893,719 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3949:Gipr
|
UTSW |
7 |
18,891,354 (GRCm39) |
missense |
probably benign |
0.00 |
R4781:Gipr
|
UTSW |
7 |
18,891,300 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4841:Gipr
|
UTSW |
7 |
18,896,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Gipr
|
UTSW |
7 |
18,896,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5087:Gipr
|
UTSW |
7 |
18,893,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R5297:Gipr
|
UTSW |
7 |
18,891,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Gipr
|
UTSW |
7 |
18,894,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Gipr
|
UTSW |
7 |
18,897,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R6957:Gipr
|
UTSW |
7 |
18,898,529 (GRCm39) |
missense |
probably benign |
0.01 |
R7035:Gipr
|
UTSW |
7 |
18,896,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R7254:Gipr
|
UTSW |
7 |
18,897,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R7720:Gipr
|
UTSW |
7 |
18,896,884 (GRCm39) |
missense |
probably benign |
0.02 |
R9098:Gipr
|
UTSW |
7 |
18,897,495 (GRCm39) |
missense |
unknown |
|
R9372:Gipr
|
UTSW |
7 |
18,896,863 (GRCm39) |
missense |
probably benign |
0.01 |
R9776:Gipr
|
UTSW |
7 |
18,891,487 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Gipr
|
UTSW |
7 |
18,891,490 (GRCm39) |
missense |
probably benign |
0.39 |
|