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 |
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 |
Nudcd1 |
T |
C |
15: 44,284,207 (GRCm39) |
M60V |
probably benign |
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 Ccdc185 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Ccdc185
|
APN |
1 |
182,574,988 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01121:Ccdc185
|
APN |
1 |
182,576,222 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01143:Ccdc185
|
APN |
1 |
182,575,417 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01721:Ccdc185
|
APN |
1 |
182,576,543 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01941:Ccdc185
|
APN |
1 |
182,575,769 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01945:Ccdc185
|
APN |
1 |
182,576,441 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03333:Ccdc185
|
APN |
1 |
182,576,398 (GRCm39) |
missense |
probably damaging |
1.00 |
Ratas
|
UTSW |
1 |
182,576,582 (GRCm39) |
missense |
possibly damaging |
0.73 |
Ratones
|
UTSW |
1 |
182,575,085 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0486:Ccdc185
|
UTSW |
1 |
182,575,424 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0653:Ccdc185
|
UTSW |
1 |
182,575,129 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1263:Ccdc185
|
UTSW |
1 |
182,574,918 (GRCm39) |
nonsense |
probably null |
|
R1450:Ccdc185
|
UTSW |
1 |
182,575,129 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1464:Ccdc185
|
UTSW |
1 |
182,576,263 (GRCm39) |
missense |
probably benign |
|
R1464:Ccdc185
|
UTSW |
1 |
182,576,263 (GRCm39) |
missense |
probably benign |
|
R2146:Ccdc185
|
UTSW |
1 |
182,575,085 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3410:Ccdc185
|
UTSW |
1 |
182,576,313 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3765:Ccdc185
|
UTSW |
1 |
182,575,117 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4012:Ccdc185
|
UTSW |
1 |
182,576,453 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4953:Ccdc185
|
UTSW |
1 |
182,576,582 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5096:Ccdc185
|
UTSW |
1 |
182,576,354 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5166:Ccdc185
|
UTSW |
1 |
182,576,564 (GRCm39) |
nonsense |
probably null |
|
R5300:Ccdc185
|
UTSW |
1 |
182,575,645 (GRCm39) |
missense |
probably benign |
0.00 |
R5504:Ccdc185
|
UTSW |
1 |
182,575,192 (GRCm39) |
missense |
probably damaging |
0.97 |
R5863:Ccdc185
|
UTSW |
1 |
182,576,122 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5928:Ccdc185
|
UTSW |
1 |
182,575,047 (GRCm39) |
missense |
probably benign |
0.00 |
R7127:Ccdc185
|
UTSW |
1 |
182,576,421 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8125:Ccdc185
|
UTSW |
1 |
182,574,835 (GRCm39) |
missense |
probably benign |
0.10 |
R8197:Ccdc185
|
UTSW |
1 |
182,576,324 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9248:Ccdc185
|
UTSW |
1 |
182,576,221 (GRCm39) |
missense |
probably benign |
0.33 |
Z1177:Ccdc185
|
UTSW |
1 |
182,576,079 (GRCm39) |
missense |
possibly damaging |
0.72 |
|