Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acr |
A |
G |
15: 89,458,197 (GRCm39) |
N293D |
probably benign |
Het |
Ankrd49 |
A |
G |
9: 14,692,645 (GRCm39) |
L173P |
probably damaging |
Het |
Ccdc152 |
A |
G |
15: 3,323,329 (GRCm39) |
|
probably benign |
Het |
Dnajc10 |
A |
T |
2: 80,151,631 (GRCm39) |
R137S |
probably benign |
Het |
Htra2 |
A |
G |
6: 83,031,304 (GRCm39) |
L35P |
probably damaging |
Het |
Il23r |
A |
T |
6: 67,403,626 (GRCm39) |
M425K |
probably benign |
Het |
Nfkb2 |
G |
T |
19: 46,296,455 (GRCm39) |
R241L |
probably damaging |
Het |
Nup205 |
A |
G |
6: 35,176,894 (GRCm39) |
D630G |
probably benign |
Het |
Or1j15 |
T |
A |
2: 36,458,754 (GRCm39) |
L48H |
probably damaging |
Het |
Peli2 |
T |
C |
14: 48,493,914 (GRCm39) |
Y379H |
probably damaging |
Het |
Plekhg6 |
G |
T |
6: 125,349,587 (GRCm39) |
|
probably benign |
Het |
Samd14 |
G |
T |
11: 94,914,081 (GRCm39) |
|
probably benign |
Het |
Setd7 |
A |
T |
3: 51,428,730 (GRCm39) |
*367R |
probably null |
Het |
Slc26a8 |
A |
G |
17: 28,873,922 (GRCm39) |
V355A |
probably benign |
Het |
Slc46a2 |
T |
A |
4: 59,911,926 (GRCm39) |
K429* |
probably null |
Het |
Styxl2 |
T |
G |
1: 165,928,073 (GRCm39) |
D513A |
probably damaging |
Het |
Tspan32 |
T |
C |
7: 142,568,691 (GRCm39) |
|
probably benign |
Het |
Unc80 |
T |
C |
1: 66,661,645 (GRCm39) |
V1690A |
probably benign |
Het |
Ush2a |
C |
A |
1: 188,643,819 (GRCm39) |
Q4394K |
probably benign |
Het |
Zfp277 |
C |
A |
12: 40,428,825 (GRCm39) |
G174V |
probably benign |
Het |
|
Other mutations in Cdh3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01103:Cdh3
|
APN |
8 |
107,281,937 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01431:Cdh3
|
APN |
8 |
107,274,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01794:Cdh3
|
APN |
8 |
107,263,758 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02100:Cdh3
|
APN |
8 |
107,270,322 (GRCm39) |
missense |
probably benign |
|
IGL02272:Cdh3
|
APN |
8 |
107,274,468 (GRCm39) |
splice site |
probably null |
|
IGL02292:Cdh3
|
APN |
8 |
107,271,833 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02553:Cdh3
|
APN |
8 |
107,270,880 (GRCm39) |
nonsense |
probably null |
|
IGL03245:Cdh3
|
APN |
8 |
107,279,631 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03376:Cdh3
|
APN |
8 |
107,268,036 (GRCm39) |
missense |
probably benign |
0.01 |
Arctus
|
UTSW |
8 |
107,266,488 (GRCm39) |
missense |
probably damaging |
1.00 |
Bebe
|
UTSW |
8 |
107,271,860 (GRCm39) |
critical splice donor site |
probably null |
|
Byte
|
UTSW |
8 |
107,237,973 (GRCm39) |
missense |
probably benign |
|
puffin
|
UTSW |
8 |
107,270,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R7512_Cdh3_158
|
UTSW |
8 |
107,265,640 (GRCm39) |
nonsense |
probably null |
|
PIT4486001:Cdh3
|
UTSW |
8 |
107,268,122 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0143:Cdh3
|
UTSW |
8 |
107,237,857 (GRCm39) |
missense |
probably benign |
0.35 |
R0388:Cdh3
|
UTSW |
8 |
107,265,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R0462:Cdh3
|
UTSW |
8 |
107,282,012 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0526:Cdh3
|
UTSW |
8 |
107,282,078 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0788:Cdh3
|
UTSW |
8 |
107,268,047 (GRCm39) |
missense |
probably benign |
0.05 |
R1495:Cdh3
|
UTSW |
8 |
107,265,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R1653:Cdh3
|
UTSW |
8 |
107,265,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R1806:Cdh3
|
UTSW |
8 |
107,263,547 (GRCm39) |
missense |
probably benign |
0.02 |
R2124:Cdh3
|
UTSW |
8 |
107,279,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2302:Cdh3
|
UTSW |
8 |
107,271,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R2326:Cdh3
|
UTSW |
8 |
107,237,940 (GRCm39) |
missense |
probably benign |
|
R2508:Cdh3
|
UTSW |
8 |
107,279,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3625:Cdh3
|
UTSW |
8 |
107,270,310 (GRCm39) |
missense |
probably damaging |
0.98 |
R3767:Cdh3
|
UTSW |
8 |
107,263,606 (GRCm39) |
splice site |
probably null |
|
R4679:Cdh3
|
UTSW |
8 |
107,266,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Cdh3
|
UTSW |
8 |
107,270,520 (GRCm39) |
missense |
probably benign |
|
R4778:Cdh3
|
UTSW |
8 |
107,270,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R4928:Cdh3
|
UTSW |
8 |
107,263,242 (GRCm39) |
missense |
probably benign |
0.15 |
R5069:Cdh3
|
UTSW |
8 |
107,263,458 (GRCm39) |
missense |
probably benign |
0.19 |
R5101:Cdh3
|
UTSW |
8 |
107,268,024 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5204:Cdh3
|
UTSW |
8 |
107,270,871 (GRCm39) |
missense |
probably benign |
0.29 |
R5309:Cdh3
|
UTSW |
8 |
107,265,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R5343:Cdh3
|
UTSW |
8 |
107,279,568 (GRCm39) |
missense |
probably benign |
|
R5408:Cdh3
|
UTSW |
8 |
107,263,269 (GRCm39) |
missense |
probably damaging |
0.98 |
R6253:Cdh3
|
UTSW |
8 |
107,263,695 (GRCm39) |
splice site |
probably null |
|
R6637:Cdh3
|
UTSW |
8 |
107,237,973 (GRCm39) |
missense |
probably benign |
|
R6639:Cdh3
|
UTSW |
8 |
107,237,973 (GRCm39) |
missense |
probably benign |
|
R7142:Cdh3
|
UTSW |
8 |
107,271,860 (GRCm39) |
critical splice donor site |
probably null |
|
R7371:Cdh3
|
UTSW |
8 |
107,279,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7397:Cdh3
|
UTSW |
8 |
107,263,241 (GRCm39) |
nonsense |
probably null |
|
R7458:Cdh3
|
UTSW |
8 |
107,263,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Cdh3
|
UTSW |
8 |
107,265,640 (GRCm39) |
nonsense |
probably null |
|
R7522:Cdh3
|
UTSW |
8 |
107,268,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7586:Cdh3
|
UTSW |
8 |
107,237,975 (GRCm39) |
critical splice donor site |
probably null |
|
R9467:Cdh3
|
UTSW |
8 |
107,266,425 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9680:Cdh3
|
UTSW |
8 |
107,274,396 (GRCm39) |
missense |
probably benign |
|
|