Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak6 |
A |
T |
13: 100,790,722 (GRCm39) |
T18S |
probably damaging |
Het |
Aqp7 |
G |
A |
4: 41,035,510 (GRCm39) |
T115I |
probably benign |
Het |
Arhgap19 |
A |
G |
19: 41,773,227 (GRCm39) |
V275A |
possibly damaging |
Het |
Cebpz |
T |
A |
17: 79,242,040 (GRCm39) |
Q538L |
probably damaging |
Het |
Cldn1 |
C |
A |
16: 26,190,167 (GRCm39) |
L70F |
probably damaging |
Het |
Crybg2 |
A |
T |
4: 133,809,938 (GRCm39) |
D1230V |
probably damaging |
Het |
Csmd1 |
C |
T |
8: 16,003,703 (GRCm39) |
C2617Y |
probably damaging |
Het |
D7Ertd443e |
T |
A |
7: 133,951,110 (GRCm39) |
N188Y |
probably benign |
Het |
Ddx51 |
A |
G |
5: 110,802,790 (GRCm39) |
I214M |
probably benign |
Het |
Dlg5 |
A |
G |
14: 24,200,716 (GRCm39) |
V1328A |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,326,216 (GRCm39) |
C3639Y |
probably damaging |
Het |
Dync1i2 |
C |
T |
2: 71,081,326 (GRCm39) |
T511I |
probably benign |
Het |
Fam220a |
A |
T |
5: 143,549,212 (GRCm39) |
E208V |
probably damaging |
Het |
Gm4846 |
T |
C |
1: 166,311,594 (GRCm39) |
S422G |
probably benign |
Het |
Grin2c |
C |
T |
11: 115,141,115 (GRCm39) |
R1001Q |
probably benign |
Het |
H2-T3 |
T |
C |
17: 36,498,301 (GRCm39) |
E248G |
probably damaging |
Het |
Idi2 |
T |
C |
13: 9,008,518 (GRCm39) |
V92A |
probably benign |
Het |
Iqcd |
C |
T |
5: 120,740,571 (GRCm39) |
Q301* |
probably null |
Het |
Klhl26 |
T |
C |
8: 70,904,974 (GRCm39) |
D278G |
probably damaging |
Het |
Mok |
G |
T |
12: 110,774,503 (GRCm39) |
T228K |
probably damaging |
Het |
Or1e22 |
A |
G |
11: 73,377,008 (GRCm39) |
I214T |
probably damaging |
Het |
Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
Pabpc1 |
T |
C |
15: 36,606,074 (GRCm39) |
I101V |
probably benign |
Het |
Ppargc1a |
G |
T |
5: 51,631,562 (GRCm39) |
Q356K |
probably damaging |
Het |
Ptprt |
T |
A |
2: 161,652,524 (GRCm39) |
D608V |
probably damaging |
Het |
Rxfp1 |
C |
T |
3: 79,586,054 (GRCm39) |
C96Y |
probably damaging |
Het |
Scn11a |
A |
C |
9: 119,618,990 (GRCm39) |
V784G |
probably damaging |
Het |
Septin4 |
T |
C |
11: 87,458,723 (GRCm39) |
S366P |
probably benign |
Het |
Slc12a8 |
A |
G |
16: 33,410,679 (GRCm39) |
Y226C |
probably damaging |
Het |
Slc25a33 |
A |
G |
4: 149,846,914 (GRCm39) |
V49A |
possibly damaging |
Het |
Slc25a45 |
T |
C |
19: 5,934,451 (GRCm39) |
S140P |
probably benign |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Spty2d1 |
G |
T |
7: 46,647,845 (GRCm39) |
N361K |
possibly damaging |
Het |
Stk4 |
G |
A |
2: 163,941,674 (GRCm39) |
A297T |
probably benign |
Het |
Thsd7b |
T |
A |
1: 129,688,139 (GRCm39) |
N683K |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,299,829 (GRCm39) |
E141G |
probably benign |
Het |
Tmem125 |
A |
T |
4: 118,399,216 (GRCm39) |
C72S |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,572,437 (GRCm39) |
T26152K |
probably damaging |
Het |
Uhrf1 |
G |
A |
17: 56,627,259 (GRCm39) |
G643D |
possibly damaging |
Het |
Vmn2r50 |
C |
T |
7: 9,774,299 (GRCm39) |
M532I |
possibly damaging |
Het |
|
Other mutations in Chgb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01601:Chgb
|
APN |
2 |
132,635,411 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03031:Chgb
|
APN |
2 |
132,635,434 (GRCm39) |
missense |
probably benign |
0.03 |
R0317:Chgb
|
UTSW |
2 |
132,635,731 (GRCm39) |
missense |
probably benign |
0.06 |
R0513:Chgb
|
UTSW |
2 |
132,627,897 (GRCm39) |
splice site |
probably benign |
|
R0607:Chgb
|
UTSW |
2 |
132,635,255 (GRCm39) |
missense |
probably benign |
|
R1177:Chgb
|
UTSW |
2 |
132,635,390 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1468:Chgb
|
UTSW |
2 |
132,634,720 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Chgb
|
UTSW |
2 |
132,634,720 (GRCm39) |
missense |
probably benign |
0.00 |
R1595:Chgb
|
UTSW |
2 |
132,635,657 (GRCm39) |
missense |
probably benign |
0.22 |
R1994:Chgb
|
UTSW |
2 |
132,628,418 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3861:Chgb
|
UTSW |
2 |
132,635,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R4074:Chgb
|
UTSW |
2 |
132,635,847 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4354:Chgb
|
UTSW |
2 |
132,635,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R4815:Chgb
|
UTSW |
2 |
132,635,219 (GRCm39) |
missense |
probably benign |
0.27 |
R4983:Chgb
|
UTSW |
2 |
132,635,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Chgb
|
UTSW |
2 |
132,635,453 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5946:Chgb
|
UTSW |
2 |
132,634,516 (GRCm39) |
missense |
probably benign |
|
R7116:Chgb
|
UTSW |
2 |
132,623,237 (GRCm39) |
start gained |
probably benign |
|
R8978:Chgb
|
UTSW |
2 |
132,634,498 (GRCm39) |
missense |
probably benign |
0.00 |
R9033:Chgb
|
UTSW |
2 |
132,634,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R9428:Chgb
|
UTSW |
2 |
132,635,154 (GRCm39) |
missense |
probably damaging |
0.99 |
|