Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
C |
6: 121,621,172 (GRCm39) |
F292S |
probably benign |
Het |
Aadacl2fm3 |
A |
T |
3: 59,772,760 (GRCm39) |
D88V |
probably damaging |
Het |
Abca13 |
T |
C |
11: 9,242,646 (GRCm39) |
V1503A |
probably damaging |
Het |
AI661453 |
C |
T |
17: 47,777,627 (GRCm39) |
|
probably benign |
Het |
Ano2 |
T |
C |
6: 125,844,134 (GRCm39) |
|
probably null |
Het |
Atg16l2 |
A |
G |
7: 100,940,757 (GRCm39) |
V453A |
probably damaging |
Het |
BC034090 |
A |
G |
1: 155,101,662 (GRCm39) |
S563P |
probably benign |
Het |
Bhmt-ps1 |
A |
G |
4: 26,369,591 (GRCm39) |
|
noncoding transcript |
Het |
Birc6 |
C |
A |
17: 74,959,700 (GRCm39) |
P3855Q |
probably damaging |
Het |
Cd151 |
A |
T |
7: 141,049,197 (GRCm39) |
K8M |
probably damaging |
Het |
Cd163 |
T |
C |
6: 124,304,890 (GRCm39) |
V1089A |
possibly damaging |
Het |
Chd3 |
A |
T |
11: 69,248,400 (GRCm39) |
|
probably null |
Het |
Cnot6l |
T |
A |
5: 96,281,971 (GRCm39) |
E9V |
probably damaging |
Het |
Col22a1 |
A |
G |
15: 71,794,806 (GRCm39) |
|
probably benign |
Het |
Cyp2c68 |
A |
G |
19: 39,729,484 (GRCm39) |
M1T |
probably null |
Het |
Dbp |
T |
C |
7: 45,357,879 (GRCm39) |
V149A |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,839,285 (GRCm39) |
V1241A |
probably benign |
Het |
Galnt10 |
T |
C |
11: 57,662,295 (GRCm39) |
S314P |
probably damaging |
Het |
Glce |
C |
T |
9: 61,977,292 (GRCm39) |
|
probably null |
Het |
Gm5093 |
C |
G |
17: 46,750,680 (GRCm39) |
D116H |
probably damaging |
Het |
Golim4 |
A |
G |
3: 75,785,951 (GRCm39) |
|
probably null |
Het |
Helz2 |
A |
T |
2: 180,877,317 (GRCm39) |
I1107N |
probably damaging |
Het |
Hoxc9 |
T |
C |
15: 102,890,304 (GRCm39) |
S74P |
probably benign |
Het |
Ikbkb |
T |
A |
8: 23,163,419 (GRCm39) |
N297I |
probably benign |
Het |
Il20ra |
T |
A |
10: 19,625,000 (GRCm39) |
I93N |
probably damaging |
Het |
Itch |
C |
A |
2: 155,034,065 (GRCm39) |
N412K |
probably damaging |
Het |
Kcna5 |
T |
A |
6: 126,511,724 (GRCm39) |
T135S |
probably damaging |
Het |
Lncpint |
G |
A |
6: 31,157,974 (GRCm39) |
|
noncoding transcript |
Het |
Lrrc39 |
A |
T |
3: 116,373,293 (GRCm39) |
|
probably null |
Het |
Mad2l1 |
T |
A |
6: 66,516,797 (GRCm39) |
V163E |
possibly damaging |
Het |
Moxd1 |
C |
T |
10: 24,120,256 (GRCm39) |
T128M |
probably damaging |
Het |
Mpeg1 |
C |
T |
19: 12,439,823 (GRCm39) |
S427F |
probably damaging |
Het |
Nckap5 |
T |
C |
1: 125,953,798 (GRCm39) |
Y854C |
possibly damaging |
Het |
Ncln |
C |
T |
10: 81,325,727 (GRCm39) |
E373K |
probably damaging |
Het |
Neurod4 |
T |
C |
10: 130,106,540 (GRCm39) |
T245A |
possibly damaging |
Het |
Nsun5 |
T |
C |
5: 135,399,067 (GRCm39) |
L39P |
probably damaging |
Het |
Or2ad1 |
G |
T |
13: 21,327,162 (GRCm39) |
Q22K |
probably benign |
Het |
Or4c105 |
A |
T |
2: 88,648,336 (GRCm39) |
T274S |
possibly damaging |
Het |
Or4f7 |
A |
G |
2: 111,644,906 (GRCm39) |
L55S |
probably damaging |
Het |
Pde8b |
T |
C |
13: 95,162,678 (GRCm39) |
T815A |
probably benign |
Het |
Pofut2 |
C |
T |
10: 77,104,398 (GRCm39) |
R392W |
probably damaging |
Het |
Ppip5k2 |
G |
A |
1: 97,639,507 (GRCm39) |
T1186I |
probably benign |
Het |
Rhot2 |
A |
C |
17: 26,060,374 (GRCm39) |
S277R |
probably benign |
Het |
Satb1 |
T |
G |
17: 52,111,391 (GRCm39) |
|
probably null |
Het |
Sec31b |
T |
C |
19: 44,524,634 (GRCm39) |
I88V |
probably damaging |
Het |
Selenon |
T |
A |
4: 134,267,997 (GRCm39) |
E483V |
probably damaging |
Het |
Serpinc1 |
A |
G |
1: 160,820,981 (GRCm39) |
T22A |
possibly damaging |
Het |
Sf3a2 |
G |
A |
10: 80,640,040 (GRCm39) |
|
probably benign |
Het |
Sf3b1 |
A |
G |
1: 55,040,580 (GRCm39) |
Y561H |
possibly damaging |
Het |
Smarcc1 |
T |
A |
9: 109,947,708 (GRCm39) |
|
probably benign |
Het |
Stard3nl |
C |
T |
13: 19,556,819 (GRCm39) |
R107Q |
probably damaging |
Het |
Syce1 |
C |
T |
7: 140,357,593 (GRCm39) |
R324H |
possibly damaging |
Het |
Tnk1 |
G |
T |
11: 69,743,119 (GRCm39) |
|
probably benign |
Het |
Trim46 |
A |
G |
3: 89,150,968 (GRCm39) |
F198L |
probably damaging |
Het |
Trip4 |
A |
T |
9: 65,788,233 (GRCm39) |
W71R |
probably damaging |
Het |
Ubox5 |
A |
C |
2: 130,439,213 (GRCm39) |
|
probably benign |
Het |
Ust |
G |
A |
10: 8,183,202 (GRCm39) |
T167M |
probably damaging |
Het |
Zbtb2 |
T |
C |
10: 4,318,697 (GRCm39) |
Q443R |
probably benign |
Het |
Zfp407 |
A |
G |
18: 84,361,196 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Areg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01391:Areg
|
APN |
5 |
91,288,954 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01929:Areg
|
APN |
5 |
91,292,312 (GRCm39) |
missense |
probably benign |
|
IGL01971:Areg
|
APN |
5 |
91,288,870 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02250:Areg
|
APN |
5 |
91,288,967 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1674:Areg
|
UTSW |
5 |
91,291,485 (GRCm39) |
missense |
probably damaging |
0.96 |
R1699:Areg
|
UTSW |
5 |
91,291,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R4239:Areg
|
UTSW |
5 |
91,291,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R4240:Areg
|
UTSW |
5 |
91,291,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Areg
|
UTSW |
5 |
91,291,363 (GRCm39) |
missense |
probably benign |
0.34 |
R4738:Areg
|
UTSW |
5 |
91,294,583 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5040:Areg
|
UTSW |
5 |
91,292,198 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5305:Areg
|
UTSW |
5 |
91,292,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R5987:Areg
|
UTSW |
5 |
91,294,577 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6075:Areg
|
UTSW |
5 |
91,291,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R7210:Areg
|
UTSW |
5 |
91,288,764 (GRCm39) |
nonsense |
probably null |
|
R8165:Areg
|
UTSW |
5 |
91,291,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R9054:Areg
|
UTSW |
5 |
91,292,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Areg
|
UTSW |
5 |
91,294,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|