Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra3 |
A |
G |
5: 50,159,272 (GRCm39) |
V326A |
probably damaging |
Het |
AI429214 |
C |
T |
8: 37,461,071 (GRCm39) |
S73L |
probably benign |
Het |
Atp13a4 |
G |
T |
16: 29,232,567 (GRCm39) |
T923K |
probably damaging |
Het |
Ccdc150 |
A |
G |
1: 54,395,932 (GRCm39) |
D805G |
probably benign |
Het |
Ccdc185 |
T |
G |
1: 182,576,313 (GRCm39) |
Q125H |
possibly damaging |
Het |
Ccdc88a |
T |
A |
11: 29,436,006 (GRCm39) |
C10S |
probably damaging |
Het |
Cpsf1 |
G |
T |
15: 76,485,981 (GRCm39) |
Y396* |
probably null |
Het |
Dnpep |
A |
G |
1: 75,293,270 (GRCm39) |
V33A |
probably damaging |
Het |
Fbn1 |
G |
A |
2: 125,254,585 (GRCm39) |
A226V |
possibly damaging |
Het |
Frmd4a |
A |
T |
2: 4,157,839 (GRCm39) |
|
probably benign |
Het |
Gipr |
A |
G |
7: 18,893,719 (GRCm39) |
V318A |
possibly damaging |
Het |
Gsdmc4 |
A |
G |
15: 63,763,895 (GRCm39) |
S401P |
probably benign |
Het |
H2-M10.6 |
T |
A |
17: 37,124,893 (GRCm39) |
V270E |
probably damaging |
Het |
Klhl7 |
G |
T |
5: 24,343,319 (GRCm39) |
V212L |
probably damaging |
Het |
Krt10 |
C |
A |
11: 99,278,087 (GRCm39) |
R322L |
probably damaging |
Het |
Lrrn4 |
A |
G |
2: 132,721,781 (GRCm39) |
L12P |
unknown |
Het |
Mast2 |
C |
G |
4: 116,168,107 (GRCm39) |
E881Q |
possibly damaging |
Het |
Nod1 |
G |
T |
6: 54,921,902 (GRCm39) |
R139S |
probably benign |
Het |
Notch3 |
C |
T |
17: 32,369,676 (GRCm39) |
V772M |
possibly damaging |
Het |
Nrxn1 |
G |
A |
17: 90,515,795 (GRCm39) |
T19M |
probably damaging |
Het |
Or10g1 |
T |
A |
14: 52,647,818 (GRCm39) |
R170S |
possibly damaging |
Het |
Or4c1 |
A |
G |
2: 89,133,717 (GRCm39) |
F73S |
probably benign |
Het |
Or4c115 |
T |
C |
2: 88,927,668 (GRCm39) |
N201S |
possibly damaging |
Het |
Or5b101 |
G |
C |
19: 13,005,411 (GRCm39) |
A94G |
probably benign |
Het |
Or5w8 |
T |
A |
2: 87,688,005 (GRCm39) |
L162* |
probably null |
Het |
Or8c9 |
T |
A |
9: 38,241,640 (GRCm39) |
S252R |
possibly damaging |
Het |
Pcdhb6 |
A |
G |
18: 37,468,945 (GRCm39) |
E622G |
probably damaging |
Het |
Pitrm1 |
G |
A |
13: 6,628,517 (GRCm39) |
A937T |
possibly damaging |
Het |
Plxnb1 |
G |
A |
9: 108,935,681 (GRCm39) |
|
probably null |
Het |
Ripk3 |
T |
G |
14: 56,025,698 (GRCm39) |
N54T |
probably damaging |
Het |
Rpn2 |
C |
A |
2: 157,132,572 (GRCm39) |
A108E |
possibly damaging |
Het |
Scaf11 |
A |
G |
15: 96,312,745 (GRCm39) |
V1432A |
probably damaging |
Het |
Sec14l5 |
C |
T |
16: 4,983,518 (GRCm39) |
|
probably null |
Het |
Serpina3n |
A |
G |
12: 104,377,536 (GRCm39) |
E263G |
possibly damaging |
Het |
Six4 |
A |
G |
12: 73,159,657 (GRCm39) |
F101S |
probably damaging |
Het |
Slc12a1 |
A |
G |
2: 124,996,071 (GRCm39) |
T75A |
probably benign |
Het |
Slc26a9 |
T |
C |
1: 131,691,682 (GRCm39) |
S642P |
probably benign |
Het |
Smu1 |
T |
C |
4: 40,752,008 (GRCm39) |
T183A |
probably benign |
Het |
Sptb |
T |
G |
12: 76,657,589 (GRCm39) |
K1311Q |
possibly damaging |
Het |
Tal2 |
A |
G |
4: 53,785,843 (GRCm39) |
N8S |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,544,367 (GRCm39) |
T2128A |
probably damaging |
Het |
Tmem67 |
A |
T |
4: 12,073,952 (GRCm39) |
M288K |
probably benign |
Het |
Ubr1 |
A |
C |
2: 120,793,929 (GRCm39) |
I85S |
probably benign |
Het |
Vmn2r90 |
G |
T |
17: 17,953,638 (GRCm39) |
V601L |
probably benign |
Het |
Zfhx4 |
C |
T |
3: 5,468,418 (GRCm39) |
P2859S |
probably benign |
Het |
|
Other mutations in Nudcd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Nudcd1
|
APN |
15 |
44,284,222 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01956:Nudcd1
|
APN |
15 |
44,263,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Nudcd1
|
APN |
15 |
44,269,357 (GRCm39) |
missense |
probably benign |
0.41 |
R0333:Nudcd1
|
UTSW |
15 |
44,264,683 (GRCm39) |
missense |
probably benign |
|
R0960:Nudcd1
|
UTSW |
15 |
44,291,047 (GRCm39) |
unclassified |
probably benign |
|
R3410:Nudcd1
|
UTSW |
15 |
44,284,207 (GRCm39) |
missense |
probably benign |
0.17 |
R4771:Nudcd1
|
UTSW |
15 |
44,268,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R4970:Nudcd1
|
UTSW |
15 |
44,240,039 (GRCm39) |
nonsense |
probably null |
|
R5112:Nudcd1
|
UTSW |
15 |
44,240,039 (GRCm39) |
nonsense |
probably null |
|
R5789:Nudcd1
|
UTSW |
15 |
44,251,879 (GRCm39) |
nonsense |
probably null |
|
R6353:Nudcd1
|
UTSW |
15 |
44,284,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Nudcd1
|
UTSW |
15 |
44,269,226 (GRCm39) |
missense |
probably benign |
0.00 |
R7483:Nudcd1
|
UTSW |
15 |
44,269,253 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7742:Nudcd1
|
UTSW |
15 |
44,268,754 (GRCm39) |
missense |
probably benign |
0.06 |
R8949:Nudcd1
|
UTSW |
15 |
44,251,971 (GRCm39) |
missense |
probably benign |
0.00 |
R9066:Nudcd1
|
UTSW |
15 |
44,243,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Nudcd1
|
UTSW |
15 |
44,263,473 (GRCm39) |
missense |
probably benign |
0.00 |
R9438:Nudcd1
|
UTSW |
15 |
44,269,321 (GRCm39) |
missense |
probably benign |
0.15 |
Z1177:Nudcd1
|
UTSW |
15 |
44,268,828 (GRCm39) |
missense |
probably benign |
0.01 |
|