Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
T |
A |
5: 113,331,685 (GRCm39) |
D843V |
possibly damaging |
Het |
6330409D20Rik |
T |
A |
2: 32,627,623 (GRCm39) |
Q111L |
unknown |
Het |
Abcc5 |
C |
A |
16: 20,241,068 (GRCm39) |
R39L |
probably benign |
Het |
Acbd3 |
C |
A |
1: 180,566,158 (GRCm39) |
Q284K |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,593,462 (GRCm39) |
R4175H |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,300,985 (GRCm39) |
L95P |
probably damaging |
Het |
Apc2 |
T |
G |
10: 80,137,764 (GRCm39) |
D68E |
probably damaging |
Het |
Apob |
A |
T |
12: 8,051,015 (GRCm39) |
I1093F |
possibly damaging |
Het |
Arid2 |
T |
A |
15: 96,260,485 (GRCm39) |
D411E |
probably damaging |
Het |
Astn1 |
T |
A |
1: 158,436,850 (GRCm39) |
Y811N |
probably damaging |
Het |
Ccdc187 |
T |
C |
2: 26,170,630 (GRCm39) |
H616R |
probably benign |
Het |
Ccdc198 |
C |
T |
14: 49,470,356 (GRCm39) |
G197S |
possibly damaging |
Het |
Clca4b |
T |
C |
3: 144,627,762 (GRCm39) |
Y403C |
possibly damaging |
Het |
Dagla |
C |
T |
19: 10,228,451 (GRCm39) |
V656I |
probably benign |
Het |
Dguok |
A |
C |
6: 83,464,061 (GRCm39) |
W166G |
probably damaging |
Het |
Dlg5 |
G |
A |
14: 24,196,388 (GRCm39) |
A1603V |
probably damaging |
Het |
Fanca |
G |
A |
8: 124,039,984 (GRCm39) |
Q138* |
probably null |
Het |
Fbxl19 |
T |
A |
7: 127,347,520 (GRCm39) |
C25* |
probably null |
Het |
Gm49383 |
C |
A |
12: 69,243,643 (GRCm39) |
E79* |
probably null |
Het |
Lcor |
C |
T |
19: 41,570,996 (GRCm39) |
S63L |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,322,268 (GRCm39) |
Y1887C |
probably damaging |
Het |
Mast3 |
T |
C |
8: 71,232,062 (GRCm39) |
D1305G |
probably damaging |
Het |
Mreg |
C |
A |
1: 72,203,257 (GRCm39) |
R107L |
possibly damaging |
Het |
Nbn |
T |
A |
4: 15,981,470 (GRCm39) |
S521T |
probably benign |
Het |
Nxpe2 |
C |
A |
9: 48,231,059 (GRCm39) |
V437L |
probably benign |
Het |
Or2t49 |
T |
C |
11: 58,392,942 (GRCm39) |
M153V |
probably benign |
Het |
Or51s1 |
A |
T |
7: 102,558,926 (GRCm39) |
I40N |
probably damaging |
Het |
Or8c13 |
T |
C |
9: 38,091,186 (GRCm39) |
E311G |
possibly damaging |
Het |
Pcdhb5 |
A |
C |
18: 37,453,953 (GRCm39) |
K111T |
probably benign |
Het |
Pi4kb |
A |
G |
3: 94,906,192 (GRCm39) |
I580V |
probably benign |
Het |
Plaat3 |
T |
C |
19: 7,556,514 (GRCm39) |
L105P |
probably benign |
Het |
Rbm15b |
A |
G |
9: 106,761,646 (GRCm39) |
S841P |
probably benign |
Het |
Reep2 |
A |
G |
18: 34,975,566 (GRCm39) |
N31S |
probably damaging |
Het |
Scmh1 |
C |
T |
4: 120,379,699 (GRCm39) |
H505Y |
probably benign |
Het |
Setd1a |
T |
A |
7: 127,390,669 (GRCm39) |
L1115H |
unknown |
Het |
Slc26a3 |
A |
G |
12: 31,516,430 (GRCm39) |
D596G |
possibly damaging |
Het |
Smg5 |
G |
T |
3: 88,252,714 (GRCm39) |
A167S |
probably damaging |
Het |
Supv3l1 |
T |
C |
10: 62,277,004 (GRCm39) |
T255A |
probably damaging |
Het |
Synrg |
G |
A |
11: 83,899,731 (GRCm39) |
A568T |
probably benign |
Het |
Tmem132a |
G |
T |
19: 10,836,311 (GRCm39) |
P740T |
probably benign |
Het |
Tmem181a |
T |
C |
17: 6,351,680 (GRCm39) |
L353P |
probably damaging |
Het |
Tubgcp3 |
T |
C |
8: 12,704,343 (GRCm39) |
E242G |
probably benign |
Het |
Vmn2r77 |
A |
T |
7: 86,450,680 (GRCm39) |
T189S |
probably benign |
Het |
Zfp638 |
T |
G |
6: 83,905,679 (GRCm39) |
L44W |
probably damaging |
Het |
Zfp715 |
G |
A |
7: 42,947,482 (GRCm39) |
T826I |
possibly damaging |
Het |
Zfp865 |
G |
A |
7: 5,034,058 (GRCm39) |
S681N |
probably benign |
Het |
Zscan5b |
C |
T |
7: 6,236,946 (GRCm39) |
P232S |
possibly damaging |
Het |
|
Other mutations in Calhm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01695:Calhm5
|
APN |
10 |
33,968,198 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01966:Calhm5
|
APN |
10 |
33,972,129 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02090:Calhm5
|
APN |
10 |
33,972,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Calhm5
|
UTSW |
10 |
33,972,013 (GRCm39) |
missense |
probably benign |
0.00 |
R1110:Calhm5
|
UTSW |
10 |
33,972,013 (GRCm39) |
missense |
probably benign |
0.00 |
R5214:Calhm5
|
UTSW |
10 |
33,968,487 (GRCm39) |
missense |
probably damaging |
0.99 |
R5705:Calhm5
|
UTSW |
10 |
33,971,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Calhm5
|
UTSW |
10 |
33,968,198 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6489:Calhm5
|
UTSW |
10 |
33,968,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6863:Calhm5
|
UTSW |
10 |
33,968,451 (GRCm39) |
missense |
probably benign |
0.01 |
R6873:Calhm5
|
UTSW |
10 |
33,968,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Calhm5
|
UTSW |
10 |
33,972,189 (GRCm39) |
missense |
probably benign |
|
R7169:Calhm5
|
UTSW |
10 |
33,968,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R8263:Calhm5
|
UTSW |
10 |
33,972,192 (GRCm39) |
missense |
probably damaging |
0.98 |
R8915:Calhm5
|
UTSW |
10 |
33,968,415 (GRCm39) |
missense |
probably benign |
0.20 |
R9105:Calhm5
|
UTSW |
10 |
33,968,144 (GRCm39) |
missense |
probably benign |
0.00 |
R9438:Calhm5
|
UTSW |
10 |
33,972,049 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Calhm5
|
UTSW |
10 |
33,972,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|