Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
T |
A |
5: 146,121,681 (GRCm39) |
M73L |
possibly damaging |
Het |
AA986860 |
A |
T |
1: 130,668,806 (GRCm39) |
I58F |
probably damaging |
Het |
Acsl3 |
A |
T |
1: 78,677,528 (GRCm39) |
K507N |
probably damaging |
Het |
Adcy3 |
T |
C |
12: 4,223,512 (GRCm39) |
Y245H |
probably damaging |
Het |
Adgra1 |
T |
C |
7: 139,455,547 (GRCm39) |
S392P |
probably damaging |
Het |
Ahnak |
C |
T |
19: 8,988,921 (GRCm39) |
P3402S |
probably damaging |
Het |
Ambra1 |
T |
A |
2: 91,596,945 (GRCm39) |
I12N |
possibly damaging |
Het |
Atp10b |
A |
G |
11: 43,103,250 (GRCm39) |
T545A |
probably benign |
Het |
Atxn2 |
G |
T |
5: 121,922,069 (GRCm39) |
A638S |
probably benign |
Het |
Cd109 |
T |
C |
9: 78,574,575 (GRCm39) |
S520P |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,709,733 (GRCm39) |
D1821G |
unknown |
Het |
Cyp4a10 |
T |
C |
4: 115,382,505 (GRCm39) |
V265A |
possibly damaging |
Het |
Dmrtb1 |
C |
T |
4: 107,540,809 (GRCm39) |
R184Q |
possibly damaging |
Het |
Dnah7b |
A |
T |
1: 46,280,227 (GRCm39) |
I2719F |
possibly damaging |
Het |
En2 |
T |
C |
5: 28,372,071 (GRCm39) |
S183P |
probably damaging |
Het |
Etfb |
A |
G |
7: 43,105,924 (GRCm39) |
T101A |
probably benign |
Het |
Etl4 |
T |
A |
2: 20,748,360 (GRCm39) |
S364T |
probably damaging |
Het |
Gm17728 |
C |
A |
17: 9,641,121 (GRCm39) |
S77Y |
possibly damaging |
Het |
Golga4 |
A |
G |
9: 118,361,658 (GRCm39) |
E221G |
probably damaging |
Het |
Gpr37 |
T |
C |
6: 25,688,416 (GRCm39) |
N227S |
possibly damaging |
Het |
Insyn2b |
A |
G |
11: 34,352,141 (GRCm39) |
D61G |
probably benign |
Het |
Kctd1 |
A |
T |
18: 15,107,112 (GRCm39) |
N784K |
possibly damaging |
Het |
Klhl22 |
A |
G |
16: 17,594,389 (GRCm39) |
T173A |
probably benign |
Het |
Ly6e |
T |
A |
15: 74,830,168 (GRCm39) |
C41S |
probably damaging |
Het |
Mapkbp1 |
T |
C |
2: 119,845,963 (GRCm39) |
L444P |
possibly damaging |
Het |
Mkx |
A |
T |
18: 6,992,855 (GRCm39) |
I143K |
probably damaging |
Het |
Mlh3 |
A |
G |
12: 85,315,815 (GRCm39) |
F124L |
probably benign |
Het |
Nlrp1a |
A |
T |
11: 71,015,046 (GRCm39) |
L68H |
possibly damaging |
Het |
Obscn |
A |
C |
11: 58,964,457 (GRCm39) |
Y726* |
probably null |
Het |
Or4f59 |
C |
T |
2: 111,872,898 (GRCm39) |
V160I |
probably benign |
Het |
Or8d1 |
T |
G |
9: 38,766,637 (GRCm39) |
V93G |
probably benign |
Het |
Peak1 |
G |
A |
9: 56,166,233 (GRCm39) |
S565L |
probably damaging |
Het |
Pter |
T |
A |
2: 12,983,247 (GRCm39) |
L84Q |
probably damaging |
Het |
Ptpn4 |
A |
G |
1: 119,615,489 (GRCm39) |
L555P |
possibly damaging |
Het |
Sacs |
A |
G |
14: 61,443,955 (GRCm39) |
I2000M |
possibly damaging |
Het |
Scn5a |
T |
C |
9: 119,321,189 (GRCm39) |
I1458V |
probably benign |
Het |
Slc38a4 |
T |
C |
15: 96,906,874 (GRCm39) |
D288G |
probably benign |
Het |
Slc8a2 |
T |
G |
7: 15,868,440 (GRCm39) |
V224G |
probably damaging |
Het |
Sptbn4 |
T |
C |
7: 27,127,681 (GRCm39) |
E173G |
probably benign |
Het |
Tas1r1 |
T |
A |
4: 152,112,848 (GRCm39) |
H735L |
probably benign |
Het |
Trps1 |
G |
T |
15: 50,685,701 (GRCm39) |
Q155K |
probably damaging |
Het |
Tspyl5 |
T |
C |
15: 33,686,892 (GRCm39) |
H351R |
probably damaging |
Het |
Ttf2 |
A |
T |
3: 100,876,817 (GRCm39) |
D21E |
probably benign |
Het |
Ttll7 |
A |
G |
3: 146,635,859 (GRCm39) |
R398G |
possibly damaging |
Het |
Tubgcp6 |
A |
T |
15: 89,006,579 (GRCm39) |
Y148N |
probably damaging |
Het |
Vmn1r8 |
T |
A |
6: 57,013,325 (GRCm39) |
H125Q |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,468,223 (GRCm39) |
T2794A |
possibly damaging |
Het |
Zfp27 |
T |
C |
7: 29,594,208 (GRCm39) |
I586V |
probably benign |
Het |
Zfyve16 |
T |
C |
13: 92,660,770 (GRCm39) |
D13G |
probably damaging |
Het |
|
Other mutations in Rpp40 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01072:Rpp40
|
APN |
13 |
36,086,017 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01550:Rpp40
|
APN |
13 |
36,090,183 (GRCm39) |
splice site |
probably null |
|
IGL03028:Rpp40
|
APN |
13 |
36,088,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R0006:Rpp40
|
UTSW |
13 |
36,080,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Rpp40
|
UTSW |
13 |
36,082,970 (GRCm39) |
missense |
probably benign |
0.06 |
R0098:Rpp40
|
UTSW |
13 |
36,082,970 (GRCm39) |
missense |
probably benign |
0.06 |
R0144:Rpp40
|
UTSW |
13 |
36,085,352 (GRCm39) |
missense |
probably benign |
0.00 |
R0799:Rpp40
|
UTSW |
13 |
36,086,034 (GRCm39) |
missense |
probably benign |
|
R1852:Rpp40
|
UTSW |
13 |
36,080,897 (GRCm39) |
missense |
probably benign |
0.06 |
R2129:Rpp40
|
UTSW |
13 |
36,082,604 (GRCm39) |
nonsense |
probably null |
|
R4042:Rpp40
|
UTSW |
13 |
36,082,549 (GRCm39) |
missense |
probably benign |
0.00 |
R4044:Rpp40
|
UTSW |
13 |
36,082,549 (GRCm39) |
missense |
probably benign |
0.00 |
R4118:Rpp40
|
UTSW |
13 |
36,080,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Rpp40
|
UTSW |
13 |
36,082,681 (GRCm39) |
missense |
probably benign |
0.00 |
R5181:Rpp40
|
UTSW |
13 |
36,080,695 (GRCm39) |
splice site |
probably null |
|
R7023:Rpp40
|
UTSW |
13 |
36,082,889 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7916:Rpp40
|
UTSW |
13 |
36,086,034 (GRCm39) |
missense |
probably benign |
0.03 |
R9194:Rpp40
|
UTSW |
13 |
36,080,898 (GRCm39) |
missense |
probably benign |
0.02 |
Z1191:Rpp40
|
UTSW |
13 |
36,080,739 (GRCm39) |
missense |
probably benign |
0.33 |
|