Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
G |
17: 46,635,277 (GRCm39) |
L242P |
probably damaging |
Het |
Adam22 |
T |
C |
5: 8,217,379 (GRCm39) |
I139V |
probably benign |
Het |
Ahr |
G |
T |
12: 35,553,751 (GRCm39) |
Y789* |
probably null |
Het |
Ankrd27 |
C |
A |
7: 35,306,523 (GRCm39) |
|
probably null |
Het |
Ano1 |
T |
C |
7: 144,149,176 (GRCm39) |
|
probably null |
Het |
Ap4e1 |
T |
A |
2: 126,905,317 (GRCm39) |
M996K |
probably benign |
Het |
Bglap |
T |
C |
3: 88,291,312 (GRCm39) |
K42E |
probably benign |
Het |
Ccdc30 |
A |
T |
4: 119,216,779 (GRCm39) |
S220R |
probably damaging |
Het |
Clic5 |
A |
G |
17: 44,548,105 (GRCm39) |
N50S |
probably benign |
Het |
Cyp20a1 |
T |
G |
1: 60,405,840 (GRCm39) |
D211E |
probably damaging |
Het |
Dctn1 |
G |
A |
6: 83,168,266 (GRCm39) |
V408I |
possibly damaging |
Het |
Exoc6 |
T |
C |
19: 37,588,020 (GRCm39) |
I551T |
probably benign |
Het |
Fat4 |
C |
T |
3: 38,946,168 (GRCm39) |
T1687M |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,063,513 (GRCm39) |
C4490S |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,815,336 (GRCm39) |
I1351N |
probably damaging |
Het |
Igkv2-116 |
T |
C |
6: 68,129,327 (GRCm39) |
|
noncoding transcript |
Het |
Iws1 |
T |
G |
18: 32,221,301 (GRCm39) |
|
probably benign |
Het |
Mlh1 |
A |
T |
9: 111,097,311 (GRCm39) |
I61N |
probably damaging |
Het |
Mtmr7 |
C |
T |
8: 41,061,972 (GRCm39) |
V38M |
probably damaging |
Het |
Myh7 |
G |
T |
14: 55,212,818 (GRCm39) |
A1409D |
probably damaging |
Het |
Myt1 |
A |
T |
2: 181,439,638 (GRCm39) |
I387F |
probably damaging |
Het |
Nars2 |
A |
G |
7: 96,689,220 (GRCm39) |
N381D |
possibly damaging |
Het |
Nsd3 |
T |
C |
8: 26,165,765 (GRCm39) |
|
probably benign |
Het |
Nup107 |
A |
G |
10: 117,617,933 (GRCm39) |
S162P |
probably damaging |
Het |
Oog2 |
T |
C |
4: 143,920,576 (GRCm39) |
F3S |
probably benign |
Het |
Or8b1b |
A |
G |
9: 38,375,517 (GRCm39) |
Y60C |
probably damaging |
Het |
Oxgr1 |
T |
C |
14: 120,260,022 (GRCm39) |
M62V |
possibly damaging |
Het |
Pcgf1 |
A |
G |
6: 83,056,121 (GRCm39) |
Y75C |
probably damaging |
Het |
Ppp3cc |
C |
A |
14: 70,462,477 (GRCm39) |
E396* |
probably null |
Het |
Ptx4 |
T |
A |
17: 25,343,649 (GRCm39) |
C300S |
probably damaging |
Het |
Rassf4 |
C |
T |
6: 116,618,708 (GRCm39) |
V192I |
probably damaging |
Het |
Rundc3b |
T |
C |
5: 8,598,261 (GRCm39) |
T203A |
possibly damaging |
Het |
Serpinb3c |
T |
C |
1: 107,199,603 (GRCm39) |
D306G |
probably benign |
Het |
Sipa1l2 |
T |
C |
8: 126,218,398 (GRCm39) |
E313G |
possibly damaging |
Het |
Snx5 |
G |
A |
2: 144,095,674 (GRCm39) |
A329V |
probably damaging |
Het |
Stx1b |
T |
C |
7: 127,407,056 (GRCm39) |
D213G |
probably damaging |
Het |
Tpd52l2 |
G |
A |
2: 181,156,879 (GRCm39) |
V172I |
probably benign |
Het |
Trim50 |
A |
T |
5: 135,392,807 (GRCm39) |
I241F |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,580,760 (GRCm39) |
H23378Y |
probably benign |
Het |
Vmn1r193 |
T |
A |
13: 22,403,939 (GRCm39) |
M18L |
probably benign |
Het |
Vmn1r226 |
A |
G |
17: 20,908,446 (GRCm39) |
N226S |
probably benign |
Het |
Vmn2r14 |
T |
A |
5: 109,367,702 (GRCm39) |
Q430L |
probably null |
Het |
Xirp2 |
T |
A |
2: 67,345,538 (GRCm39) |
V2593D |
probably damaging |
Het |
Zfp169 |
A |
T |
13: 48,643,400 (GRCm39) |
F576I |
possibly damaging |
Het |
Zfp667 |
T |
C |
7: 6,292,438 (GRCm39) |
|
probably null |
Het |
Zzef1 |
A |
G |
11: 72,777,601 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Csnk2a1-ps3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R5578:Csnk2a1-ps3
|
UTSW |
1 |
156,352,800 (GRCm39) |
missense |
probably benign |
|
R6058:Csnk2a1-ps3
|
UTSW |
1 |
156,352,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R6249:Csnk2a1-ps3
|
UTSW |
1 |
156,352,800 (GRCm39) |
missense |
probably benign |
|
R6965:Csnk2a1-ps3
|
UTSW |
1 |
156,352,119 (GRCm39) |
nonsense |
probably null |
|
R7514:Csnk2a1-ps3
|
UTSW |
1 |
156,352,324 (GRCm39) |
missense |
probably benign |
0.05 |
R7761:Csnk2a1-ps3
|
UTSW |
1 |
156,352,707 (GRCm39) |
nonsense |
probably null |
|
R7765:Csnk2a1-ps3
|
UTSW |
1 |
156,352,354 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7782:Csnk2a1-ps3
|
UTSW |
1 |
156,352,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7889:Csnk2a1-ps3
|
UTSW |
1 |
156,352,965 (GRCm39) |
missense |
probably benign |
|
R7922:Csnk2a1-ps3
|
UTSW |
1 |
156,352,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Csnk2a1-ps3
|
UTSW |
1 |
156,352,873 (GRCm39) |
missense |
probably benign |
0.00 |
R9095:Csnk2a1-ps3
|
UTSW |
1 |
156,352,213 (GRCm39) |
missense |
probably benign |
0.00 |
|