Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
G |
T |
5: 121,639,250 (GRCm39) |
D598E |
probably benign |
Het |
Ascc3 |
A |
G |
10: 50,718,273 (GRCm39) |
K1989E |
probably benign |
Het |
Asic5 |
A |
T |
3: 81,916,773 (GRCm39) |
T288S |
possibly damaging |
Het |
Chd1 |
A |
G |
17: 15,945,692 (GRCm39) |
N72S |
probably benign |
Het |
Ciita |
T |
A |
16: 10,329,609 (GRCm39) |
V628E |
probably benign |
Het |
Cyp2c50 |
A |
G |
19: 40,079,046 (GRCm39) |
T130A |
probably benign |
Het |
Dapk1 |
T |
A |
13: 60,908,975 (GRCm39) |
V1196E |
probably damaging |
Het |
Dis3l2 |
T |
A |
1: 86,673,216 (GRCm39) |
I69N |
probably damaging |
Het |
Fcgbp |
A |
T |
7: 27,813,404 (GRCm39) |
Q2313L |
possibly damaging |
Het |
Gm2888 |
A |
G |
14: 3,037,722 (GRCm38) |
H238R |
possibly damaging |
Het |
Gm5622 |
A |
G |
14: 51,895,200 (GRCm39) |
K120E |
probably damaging |
Het |
Gpr155 |
A |
T |
2: 73,179,989 (GRCm39) |
I157N |
probably damaging |
Het |
Hltf |
T |
C |
3: 20,126,558 (GRCm39) |
V245A |
probably damaging |
Het |
Kmt2e |
G |
A |
5: 23,668,024 (GRCm39) |
V28I |
probably damaging |
Het |
Lsm3 |
GATATATA |
GATATATATA |
6: 91,496,617 (GRCm39) |
|
probably null |
Het |
Nprl3 |
C |
T |
11: 32,184,812 (GRCm39) |
R399Q |
probably benign |
Het |
Or6c6c |
C |
T |
10: 129,540,932 (GRCm39) |
R62C |
probably benign |
Het |
Ptgs2 |
T |
C |
1: 149,979,738 (GRCm39) |
V281A |
possibly damaging |
Het |
Speer4f2 |
A |
G |
5: 17,579,420 (GRCm39) |
E73G |
probably damaging |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Trav13n-3 |
A |
G |
14: 53,574,618 (GRCm39) |
T14A |
probably benign |
Het |
Trav9d-4 |
A |
T |
14: 53,221,198 (GRCm39) |
Q63L |
probably benign |
Het |
Vmn2r75 |
T |
A |
7: 85,813,453 (GRCm39) |
N450Y |
probably benign |
Het |
Vmn2r97 |
G |
A |
17: 19,150,566 (GRCm39) |
W471* |
probably null |
Het |
Zfp27 |
G |
A |
7: 29,595,818 (GRCm39) |
T49I |
possibly damaging |
Het |
Zpld2 |
A |
G |
4: 133,929,367 (GRCm39) |
S313P |
probably damaging |
Het |
|
Other mutations in Exph5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Exph5
|
APN |
9 |
53,288,006 (GRCm39) |
nonsense |
probably null |
|
IGL01387:Exph5
|
APN |
9 |
53,285,265 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01985:Exph5
|
APN |
9 |
53,287,869 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02122:Exph5
|
APN |
9 |
53,284,974 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02156:Exph5
|
APN |
9 |
53,286,941 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02192:Exph5
|
APN |
9 |
53,287,625 (GRCm39) |
nonsense |
probably null |
|
IGL02491:Exph5
|
APN |
9 |
53,286,343 (GRCm39) |
missense |
possibly damaging |
0.89 |
PIT4802001:Exph5
|
UTSW |
9 |
53,286,278 (GRCm39) |
missense |
probably damaging |
0.96 |
R0002:Exph5
|
UTSW |
9 |
53,285,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R0026:Exph5
|
UTSW |
9 |
53,287,779 (GRCm39) |
missense |
probably benign |
0.38 |
R0086:Exph5
|
UTSW |
9 |
53,249,230 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0152:Exph5
|
UTSW |
9 |
53,264,504 (GRCm39) |
critical splice donor site |
probably null |
|
R0369:Exph5
|
UTSW |
9 |
53,284,602 (GRCm39) |
missense |
probably benign |
0.35 |
R0409:Exph5
|
UTSW |
9 |
53,285,643 (GRCm39) |
missense |
probably benign |
0.00 |
R0517:Exph5
|
UTSW |
9 |
53,284,062 (GRCm39) |
missense |
probably benign |
0.02 |
R0658:Exph5
|
UTSW |
9 |
53,288,775 (GRCm39) |
missense |
unknown |
|
R1606:Exph5
|
UTSW |
9 |
53,285,595 (GRCm39) |
missense |
probably benign |
0.37 |
R1739:Exph5
|
UTSW |
9 |
53,286,888 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1769:Exph5
|
UTSW |
9 |
53,285,109 (GRCm39) |
missense |
probably benign |
0.35 |
R1828:Exph5
|
UTSW |
9 |
53,287,941 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1862:Exph5
|
UTSW |
9 |
53,287,548 (GRCm39) |
missense |
probably benign |
|
R1993:Exph5
|
UTSW |
9 |
53,284,935 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2012:Exph5
|
UTSW |
9 |
53,278,466 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2044:Exph5
|
UTSW |
9 |
53,283,979 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2402:Exph5
|
UTSW |
9 |
53,286,225 (GRCm39) |
nonsense |
probably null |
|
R3817:Exph5
|
UTSW |
9 |
53,286,794 (GRCm39) |
nonsense |
probably null |
|
R4771:Exph5
|
UTSW |
9 |
53,284,965 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4869:Exph5
|
UTSW |
9 |
53,287,539 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4926:Exph5
|
UTSW |
9 |
53,287,925 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4996:Exph5
|
UTSW |
9 |
53,286,910 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5254:Exph5
|
UTSW |
9 |
53,249,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R5522:Exph5
|
UTSW |
9 |
53,285,613 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5947:Exph5
|
UTSW |
9 |
53,286,522 (GRCm39) |
missense |
probably benign |
0.04 |
R5961:Exph5
|
UTSW |
9 |
53,288,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R6093:Exph5
|
UTSW |
9 |
53,283,917 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6144:Exph5
|
UTSW |
9 |
53,284,328 (GRCm39) |
missense |
probably benign |
0.21 |
R6254:Exph5
|
UTSW |
9 |
53,284,010 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6279:Exph5
|
UTSW |
9 |
53,285,246 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6300:Exph5
|
UTSW |
9 |
53,285,246 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6485:Exph5
|
UTSW |
9 |
53,287,991 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6792:Exph5
|
UTSW |
9 |
53,286,617 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7026:Exph5
|
UTSW |
9 |
53,251,728 (GRCm39) |
missense |
probably benign |
0.27 |
R7340:Exph5
|
UTSW |
9 |
53,288,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R7347:Exph5
|
UTSW |
9 |
53,287,196 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7352:Exph5
|
UTSW |
9 |
53,287,022 (GRCm39) |
missense |
probably benign |
0.00 |
R7520:Exph5
|
UTSW |
9 |
53,278,514 (GRCm39) |
critical splice donor site |
probably null |
|
R7521:Exph5
|
UTSW |
9 |
53,285,377 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7560:Exph5
|
UTSW |
9 |
53,287,073 (GRCm39) |
missense |
probably benign |
0.41 |
R7581:Exph5
|
UTSW |
9 |
53,283,857 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7726:Exph5
|
UTSW |
9 |
53,284,475 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7976:Exph5
|
UTSW |
9 |
53,287,935 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8017:Exph5
|
UTSW |
9 |
53,284,752 (GRCm39) |
missense |
probably benign |
|
R8019:Exph5
|
UTSW |
9 |
53,284,752 (GRCm39) |
missense |
probably benign |
|
R8302:Exph5
|
UTSW |
9 |
53,287,776 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8420:Exph5
|
UTSW |
9 |
53,287,148 (GRCm39) |
nonsense |
probably null |
|
R8551:Exph5
|
UTSW |
9 |
53,285,351 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8708:Exph5
|
UTSW |
9 |
53,287,096 (GRCm39) |
missense |
probably benign |
|
R8889:Exph5
|
UTSW |
9 |
53,287,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R9048:Exph5
|
UTSW |
9 |
53,284,935 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9255:Exph5
|
UTSW |
9 |
53,284,609 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9727:Exph5
|
UTSW |
9 |
53,287,702 (GRCm39) |
missense |
probably damaging |
0.96 |
X0028:Exph5
|
UTSW |
9 |
53,287,563 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Exph5
|
UTSW |
9 |
53,288,719 (GRCm39) |
missense |
probably benign |
|
Z1177:Exph5
|
UTSW |
9 |
53,285,513 (GRCm39) |
missense |
probably benign |
0.44 |
|