Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp3 |
T |
A |
9: 104,204,116 (GRCm39) |
E59D |
probably damaging |
Het |
Akap7 |
T |
A |
10: 25,155,640 (GRCm39) |
|
probably benign |
Het |
Anpep |
C |
A |
7: 79,476,618 (GRCm39) |
|
probably null |
Het |
Aste1 |
T |
A |
9: 105,274,886 (GRCm39) |
Y314* |
probably null |
Het |
Cd4 |
A |
T |
6: 124,847,402 (GRCm39) |
I254N |
probably damaging |
Het |
Crot |
G |
T |
5: 9,019,994 (GRCm39) |
H449Q |
probably damaging |
Het |
Dact2 |
A |
T |
17: 14,418,214 (GRCm39) |
W164R |
possibly damaging |
Het |
Dapk3 |
C |
A |
10: 81,026,152 (GRCm39) |
|
probably null |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Fbrsl1 |
G |
A |
5: 110,527,272 (GRCm39) |
|
probably benign |
Het |
Flg |
T |
C |
3: 93,184,922 (GRCm39) |
F15L |
probably damaging |
Het |
Fscn2 |
A |
G |
11: 120,252,686 (GRCm39) |
D51G |
probably damaging |
Het |
H2-Ob |
G |
T |
17: 34,460,102 (GRCm39) |
G71V |
probably damaging |
Het |
Hmgcs1 |
T |
C |
13: 120,161,520 (GRCm39) |
V104A |
possibly damaging |
Het |
Hs3st4 |
G |
T |
7: 123,996,518 (GRCm39) |
D395Y |
probably damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Ldlrad3 |
G |
A |
2: 101,900,329 (GRCm39) |
R58C |
probably damaging |
Het |
Lpin1 |
A |
G |
12: 16,626,983 (GRCm39) |
S188P |
probably damaging |
Het |
Mamdc2 |
G |
T |
19: 23,336,516 (GRCm39) |
T331K |
possibly damaging |
Het |
Matr3 |
G |
A |
18: 35,715,135 (GRCm39) |
S195N |
probably damaging |
Het |
Nktr |
T |
C |
9: 121,577,176 (GRCm39) |
Y390H |
possibly damaging |
Het |
Notch3 |
C |
T |
17: 32,376,864 (GRCm39) |
|
probably null |
Het |
Olfm3 |
T |
C |
3: 114,698,202 (GRCm39) |
|
probably null |
Het |
Or10ak11 |
A |
G |
4: 118,686,767 (GRCm39) |
V290A |
probably damaging |
Het |
Or2a20 |
T |
C |
6: 43,194,594 (GRCm39) |
L249P |
probably damaging |
Het |
Or5h25 |
C |
T |
16: 58,930,436 (GRCm39) |
C179Y |
possibly damaging |
Het |
Or7e173 |
T |
A |
9: 19,938,551 (GRCm39) |
I228F |
probably damaging |
Het |
Or7g17 |
T |
A |
9: 18,768,632 (GRCm39) |
M237K |
probably benign |
Het |
Pask |
A |
G |
1: 93,249,819 (GRCm39) |
V527A |
probably benign |
Het |
Pcdha6 |
A |
T |
18: 37,102,016 (GRCm39) |
N403I |
probably damaging |
Het |
Peg3 |
T |
C |
7: 6,710,848 (GRCm39) |
E1458G |
probably damaging |
Het |
Pip4k2b |
G |
A |
11: 97,610,569 (GRCm39) |
T386M |
probably damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,892,004 (GRCm39) |
M272V |
probably benign |
Het |
Plcb4 |
A |
G |
2: 135,844,571 (GRCm39) |
E163G |
probably damaging |
Het |
Plk5 |
C |
A |
10: 80,194,723 (GRCm39) |
R149S |
possibly damaging |
Het |
Pou4f3 |
A |
T |
18: 42,528,933 (GRCm39) |
Y292F |
probably damaging |
Het |
Rasgef1c |
A |
G |
11: 49,860,332 (GRCm39) |
K272E |
probably damaging |
Het |
Rbl2 |
C |
T |
8: 91,841,759 (GRCm39) |
T942M |
probably benign |
Het |
Sipa1l3 |
G |
A |
7: 29,048,000 (GRCm39) |
S247F |
probably damaging |
Het |
Smarca4 |
T |
C |
9: 21,572,059 (GRCm39) |
L777P |
probably damaging |
Het |
Smpd1 |
T |
C |
7: 105,206,185 (GRCm39) |
Y438H |
probably damaging |
Het |
Sorl1 |
T |
C |
9: 41,887,673 (GRCm39) |
K2052R |
probably benign |
Het |
Spata31d1c |
C |
A |
13: 65,182,944 (GRCm39) |
P162Q |
probably damaging |
Het |
Spmip9 |
A |
G |
6: 70,892,688 (GRCm39) |
S20P |
possibly damaging |
Het |
Ston1 |
A |
T |
17: 88,944,002 (GRCm39) |
E469D |
probably benign |
Het |
Syde2 |
AGTTC |
AGTTCGTTC |
3: 145,707,164 (GRCm39) |
|
probably null |
Het |
Syde2 |
CAGTT |
CAGTTAGTT |
3: 145,707,163 (GRCm39) |
|
probably null |
Het |
Taar5 |
T |
A |
10: 23,846,836 (GRCm39) |
L78Q |
probably damaging |
Het |
Tas2r114 |
A |
T |
6: 131,666,251 (GRCm39) |
L259* |
probably null |
Het |
Topaz1 |
T |
A |
9: 122,577,883 (GRCm39) |
H264Q |
probably benign |
Het |
Vcl |
G |
T |
14: 21,059,027 (GRCm39) |
V548L |
possibly damaging |
Het |
Vmn2r57 |
C |
A |
7: 41,075,974 (GRCm39) |
|
probably null |
Het |
Vmn2r92 |
A |
G |
17: 18,405,439 (GRCm39) |
*861W |
probably null |
Het |
Ylpm1 |
T |
G |
12: 85,076,095 (GRCm39) |
V940G |
probably damaging |
Het |
Zfp236 |
A |
G |
18: 82,627,556 (GRCm39) |
S1500P |
probably damaging |
Het |
Zfp384 |
G |
T |
6: 125,000,642 (GRCm39) |
|
probably benign |
Het |
Zfp786 |
T |
C |
6: 47,796,953 (GRCm39) |
M662V |
probably benign |
Het |
|
Other mutations in Ccdc183 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00858:Ccdc183
|
APN |
2 |
25,499,783 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02177:Ccdc183
|
APN |
2 |
25,502,095 (GRCm39) |
missense |
probably benign |
0.03 |
R1354:Ccdc183
|
UTSW |
2 |
25,502,151 (GRCm39) |
missense |
probably benign |
0.33 |
R1547:Ccdc183
|
UTSW |
2 |
25,499,362 (GRCm39) |
missense |
probably benign |
0.05 |
R5579:Ccdc183
|
UTSW |
2 |
25,505,434 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6188:Ccdc183
|
UTSW |
2 |
25,499,764 (GRCm39) |
missense |
probably benign |
0.28 |
R6224:Ccdc183
|
UTSW |
2 |
25,500,594 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6372:Ccdc183
|
UTSW |
2 |
25,506,176 (GRCm39) |
missense |
probably benign |
0.21 |
R6994:Ccdc183
|
UTSW |
2 |
25,507,057 (GRCm39) |
missense |
probably benign |
0.00 |
R7041:Ccdc183
|
UTSW |
2 |
25,503,682 (GRCm39) |
missense |
probably benign |
0.00 |
R7132:Ccdc183
|
UTSW |
2 |
25,506,542 (GRCm39) |
critical splice donor site |
probably null |
|
R7177:Ccdc183
|
UTSW |
2 |
25,506,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R7432:Ccdc183
|
UTSW |
2 |
25,499,469 (GRCm39) |
missense |
probably benign |
|
R7561:Ccdc183
|
UTSW |
2 |
25,501,529 (GRCm39) |
missense |
probably benign |
0.00 |
R8283:Ccdc183
|
UTSW |
2 |
25,502,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R8781:Ccdc183
|
UTSW |
2 |
25,502,208 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9623:Ccdc183
|
UTSW |
2 |
25,499,520 (GRCm39) |
missense |
probably benign |
0.01 |
|