Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
C |
A |
15: 102,248,457 (GRCm39) |
R286L |
probably null |
Het |
Actrt2 |
A |
G |
4: 154,751,836 (GRCm39) |
V100A |
probably damaging |
Het |
Adra1b |
A |
G |
11: 43,666,833 (GRCm39) |
L468P |
possibly damaging |
Het |
Ankhd1 |
A |
G |
18: 36,776,022 (GRCm39) |
E1457G |
probably benign |
Het |
Aspm |
A |
T |
1: 139,398,255 (GRCm39) |
M974L |
possibly damaging |
Het |
Atp8a2 |
T |
A |
14: 60,245,857 (GRCm39) |
I612F |
probably benign |
Het |
Cabin1 |
A |
G |
10: 75,582,564 (GRCm39) |
L284P |
probably damaging |
Het |
Cand2 |
T |
A |
6: 115,776,930 (GRCm39) |
M1106K |
probably benign |
Het |
Ccbe1 |
A |
T |
18: 66,194,459 (GRCm39) |
F376I |
possibly damaging |
Het |
Celsr3 |
A |
G |
9: 108,704,549 (GRCm39) |
D344G |
probably damaging |
Het |
Chaf1b |
A |
G |
16: 93,688,393 (GRCm39) |
K163E |
probably damaging |
Het |
Clec2d |
C |
A |
6: 129,161,107 (GRCm39) |
T68K |
probably benign |
Het |
Cwc27 |
T |
C |
13: 104,947,809 (GRCm39) |
T19A |
probably damaging |
Het |
Dnah7c |
A |
T |
1: 46,668,050 (GRCm39) |
Y1519F |
possibly damaging |
Het |
E130308A19Rik |
A |
T |
4: 59,752,288 (GRCm39) |
K467M |
probably damaging |
Het |
Garnl3 |
T |
C |
2: 32,944,208 (GRCm39) |
Y117C |
probably damaging |
Het |
Gas2l3 |
T |
C |
10: 89,249,231 (GRCm39) |
Y629C |
probably benign |
Het |
Lama1 |
A |
G |
17: 68,053,868 (GRCm39) |
N470D |
unknown |
Het |
Lmtk2 |
T |
A |
5: 144,110,615 (GRCm39) |
I445N |
probably damaging |
Het |
Lrba |
A |
G |
3: 86,261,570 (GRCm39) |
D1508G |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,416,021 (GRCm39) |
H2989R |
probably benign |
Het |
Niban2 |
T |
C |
2: 32,801,460 (GRCm39) |
|
probably null |
Het |
Nln |
A |
T |
13: 104,172,163 (GRCm39) |
W638R |
probably damaging |
Het |
Nup133 |
T |
C |
8: 124,671,017 (GRCm39) |
I127V |
possibly damaging |
Het |
Nup155 |
C |
T |
15: 8,165,379 (GRCm39) |
R672* |
probably null |
Het |
Prkcb |
A |
G |
7: 122,193,887 (GRCm39) |
Y532C |
probably damaging |
Het |
Ptpro |
A |
G |
6: 137,395,279 (GRCm39) |
|
probably null |
Het |
Rab11fip5 |
A |
G |
6: 85,319,152 (GRCm39) |
L579S |
probably benign |
Het |
Rtca |
A |
G |
3: 116,301,398 (GRCm39) |
|
probably null |
Het |
Sdccag8 |
A |
G |
1: 176,682,193 (GRCm39) |
|
probably null |
Het |
Svil |
G |
T |
18: 5,056,437 (GRCm39) |
D524Y |
probably damaging |
Het |
Unc80 |
A |
G |
1: 66,560,636 (GRCm39) |
N788S |
probably benign |
Het |
Wdfy4 |
G |
T |
14: 32,764,469 (GRCm39) |
R2140S |
probably damaging |
Het |
Zfp518a |
A |
G |
19: 40,902,192 (GRCm39) |
K707R |
probably damaging |
Het |
|
Other mutations in Ceacam14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Ceacam14
|
APN |
7 |
17,548,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R0452:Ceacam14
|
UTSW |
7 |
17,549,248 (GRCm39) |
missense |
probably benign |
|
R1613:Ceacam14
|
UTSW |
7 |
17,547,973 (GRCm39) |
splice site |
probably benign |
|
R1990:Ceacam14
|
UTSW |
7 |
17,549,290 (GRCm39) |
nonsense |
probably null |
|
R2153:Ceacam14
|
UTSW |
7 |
17,548,153 (GRCm39) |
missense |
probably benign |
0.00 |
R3887:Ceacam14
|
UTSW |
7 |
17,548,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Ceacam14
|
UTSW |
7 |
17,547,975 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5323:Ceacam14
|
UTSW |
7 |
17,549,402 (GRCm39) |
makesense |
probably null |
|
R5454:Ceacam14
|
UTSW |
7 |
17,548,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Ceacam14
|
UTSW |
7 |
17,548,267 (GRCm39) |
missense |
probably damaging |
0.97 |
R6318:Ceacam14
|
UTSW |
7 |
17,548,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R7607:Ceacam14
|
UTSW |
7 |
17,548,246 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7789:Ceacam14
|
UTSW |
7 |
17,548,096 (GRCm39) |
missense |
probably damaging |
0.99 |
R8946:Ceacam14
|
UTSW |
7 |
17,547,999 (GRCm39) |
missense |
probably benign |
0.01 |
R9781:Ceacam14
|
UTSW |
7 |
17,549,082 (GRCm39) |
missense |
possibly damaging |
0.60 |
|