Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
TTCCTCCTCCTCCTCCTCCTCC |
TTCCTCCTCCTCCTCCTCC |
3: 137,771,595 (GRCm39) |
|
probably benign |
Het |
Adra1d |
C |
A |
2: 131,388,134 (GRCm39) |
V474F |
probably benign |
Het |
Alg8 |
A |
T |
7: 97,032,891 (GRCm39) |
|
probably null |
Het |
Ash1l |
A |
G |
3: 88,974,529 (GRCm39) |
D2618G |
possibly damaging |
Het |
Atp6v1c2 |
C |
A |
12: 17,344,676 (GRCm39) |
|
probably null |
Het |
Cacna1d |
A |
G |
14: 29,845,453 (GRCm39) |
V572A |
probably benign |
Het |
Camta1 |
A |
G |
4: 151,228,187 (GRCm39) |
W882R |
probably damaging |
Het |
Cd72 |
A |
G |
4: 43,453,163 (GRCm39) |
V91A |
probably benign |
Het |
Cdx2 |
G |
T |
5: 147,240,097 (GRCm39) |
T193K |
probably damaging |
Het |
Cfap70 |
A |
C |
14: 20,498,673 (GRCm39) |
S5A |
probably benign |
Het |
Chmp7 |
A |
G |
14: 69,958,446 (GRCm39) |
V241A |
probably damaging |
Het |
D3Ertd751e |
A |
G |
3: 41,708,313 (GRCm39) |
Y150C |
probably damaging |
Het |
Depdc5 |
T |
C |
5: 33,100,584 (GRCm39) |
S832P |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,370,738 (GRCm39) |
S4673G |
probably benign |
Het |
Dock4 |
G |
T |
12: 40,787,539 (GRCm39) |
S818I |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,041,461 (GRCm39) |
Q156* |
probably null |
Het |
Elp1 |
C |
A |
4: 56,784,596 (GRCm39) |
V466L |
probably benign |
Het |
Espnl |
T |
C |
1: 91,250,009 (GRCm39) |
V52A |
probably damaging |
Het |
Flcn |
T |
C |
11: 59,691,902 (GRCm39) |
N249S |
probably benign |
Het |
Gemin6 |
C |
A |
17: 80,533,139 (GRCm39) |
A24D |
probably damaging |
Het |
Gm5773 |
A |
G |
3: 93,681,339 (GRCm39) |
H337R |
probably benign |
Het |
Hal |
T |
C |
10: 93,339,344 (GRCm39) |
S478P |
possibly damaging |
Het |
Hectd1 |
T |
A |
12: 51,816,101 (GRCm39) |
M1324L |
possibly damaging |
Het |
Hyal5 |
T |
A |
6: 24,876,343 (GRCm39) |
L72Q |
probably damaging |
Het |
Ift140 |
C |
A |
17: 25,264,497 (GRCm39) |
C557* |
probably null |
Het |
Kbtbd3 |
G |
T |
9: 4,330,144 (GRCm39) |
V173L |
possibly damaging |
Het |
Kif14 |
A |
G |
1: 136,455,131 (GRCm39) |
E1551G |
probably damaging |
Het |
Krt17 |
G |
A |
11: 100,151,704 (GRCm39) |
R30* |
probably null |
Het |
Lamb3 |
A |
T |
1: 193,003,361 (GRCm39) |
D100V |
probably damaging |
Het |
Map2 |
A |
G |
1: 66,455,265 (GRCm39) |
D1385G |
probably damaging |
Het |
Mettl25 |
C |
T |
10: 105,662,386 (GRCm39) |
V195I |
probably damaging |
Het |
Myh8 |
A |
G |
11: 67,192,518 (GRCm39) |
T1466A |
probably benign |
Het |
Myo3b |
T |
A |
2: 69,935,769 (GRCm39) |
C61S |
probably benign |
Het |
Nacc2 |
T |
G |
2: 25,952,273 (GRCm39) |
N361T |
probably damaging |
Het |
Nf1 |
A |
T |
11: 79,309,400 (GRCm39) |
K438M |
possibly damaging |
Het |
Nipal4 |
A |
G |
11: 46,041,268 (GRCm39) |
V309A |
possibly damaging |
Het |
Nomo1 |
T |
C |
7: 45,729,018 (GRCm39) |
|
probably null |
Het |
Nubp2 |
T |
C |
17: 25,103,445 (GRCm39) |
E144G |
probably damaging |
Het |
Nwd2 |
A |
T |
5: 63,957,467 (GRCm39) |
I266F |
probably benign |
Het |
Or12e7 |
T |
C |
2: 87,288,381 (GRCm39) |
F291L |
probably benign |
Het |
Or2ag1b |
A |
G |
7: 106,288,462 (GRCm39) |
Y159H |
probably benign |
Het |
Or52s1 |
G |
A |
7: 102,861,933 (GRCm39) |
V289M |
possibly damaging |
Het |
Orc1 |
T |
C |
4: 108,452,843 (GRCm39) |
|
probably null |
Het |
Otogl |
T |
A |
10: 107,642,557 (GRCm39) |
N1291I |
probably damaging |
Het |
Pah |
C |
T |
10: 87,403,143 (GRCm39) |
P173S |
possibly damaging |
Het |
Pga5 |
A |
G |
19: 10,646,817 (GRCm39) |
Y305H |
probably damaging |
Het |
Plekha4 |
A |
G |
7: 45,181,782 (GRCm39) |
H62R |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,945,754 (GRCm39) |
D906E |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,256,927 (GRCm39) |
E98G |
possibly damaging |
Het |
Ptk2 |
A |
T |
15: 73,215,132 (GRCm39) |
|
probably null |
Het |
Raet1e |
C |
A |
10: 22,056,761 (GRCm39) |
H112Q |
possibly damaging |
Het |
Scai |
T |
A |
2: 38,965,054 (GRCm39) |
I597F |
probably benign |
Het |
Sirpd |
A |
G |
3: 15,361,661 (GRCm39) |
L163P |
probably damaging |
Het |
Slc35c2 |
C |
T |
2: 165,122,757 (GRCm39) |
G176S |
probably damaging |
Het |
Slc35f4 |
A |
T |
14: 49,541,713 (GRCm39) |
I347N |
possibly damaging |
Het |
Slc52a3 |
T |
C |
2: 151,850,076 (GRCm39) |
*461Q |
probably null |
Het |
Slc6a1 |
G |
A |
6: 114,279,761 (GRCm39) |
V142I |
probably benign |
Het |
Tbc1d31 |
C |
A |
15: 57,804,149 (GRCm39) |
T388N |
probably benign |
Het |
Tmem63c |
T |
C |
12: 87,122,413 (GRCm39) |
W404R |
probably damaging |
Het |
Tmem79 |
A |
G |
3: 88,240,628 (GRCm39) |
S107P |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,850,987 (GRCm39) |
E741K |
probably damaging |
Het |
Trpm5 |
G |
T |
7: 142,636,695 (GRCm39) |
T414N |
probably damaging |
Het |
Tsnaxip1 |
T |
A |
8: 106,571,120 (GRCm39) |
I660N |
possibly damaging |
Het |
Ube2q2 |
T |
C |
9: 55,070,291 (GRCm39) |
S78P |
probably damaging |
Het |
Vac14 |
A |
T |
8: 111,362,007 (GRCm39) |
|
probably null |
Het |
Vps51 |
G |
T |
19: 6,121,467 (GRCm39) |
S185* |
probably null |
Het |
Zfp11 |
C |
T |
5: 129,735,302 (GRCm39) |
G53E |
possibly damaging |
Het |
Zfp532 |
A |
T |
18: 65,816,056 (GRCm39) |
I810F |
possibly damaging |
Het |
Zfp599 |
C |
T |
9: 22,161,055 (GRCm39) |
C370Y |
probably damaging |
Het |
|
Other mutations in Cdh12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01351:Cdh12
|
APN |
15 |
21,237,989 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01414:Cdh12
|
APN |
15 |
21,492,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Cdh12
|
APN |
15 |
21,480,425 (GRCm39) |
nonsense |
probably null |
|
IGL02894:Cdh12
|
APN |
15 |
21,586,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Cdh12
|
APN |
15 |
21,480,416 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03271:Cdh12
|
APN |
15 |
21,586,539 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03402:Cdh12
|
APN |
15 |
21,583,826 (GRCm39) |
missense |
probably benign |
0.08 |
R0042:Cdh12
|
UTSW |
15 |
21,537,763 (GRCm39) |
splice site |
probably benign |
|
R0126:Cdh12
|
UTSW |
15 |
21,584,031 (GRCm39) |
missense |
probably benign |
|
R0239:Cdh12
|
UTSW |
15 |
21,586,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R0335:Cdh12
|
UTSW |
15 |
21,578,635 (GRCm39) |
critical splice donor site |
probably null |
|
R0421:Cdh12
|
UTSW |
15 |
21,480,310 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0918:Cdh12
|
UTSW |
15 |
21,492,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R0972:Cdh12
|
UTSW |
15 |
21,237,850 (GRCm39) |
missense |
probably benign |
0.27 |
R1014:Cdh12
|
UTSW |
15 |
21,492,706 (GRCm39) |
missense |
probably damaging |
0.97 |
R1304:Cdh12
|
UTSW |
15 |
21,584,023 (GRCm39) |
missense |
probably benign |
0.10 |
R1677:Cdh12
|
UTSW |
15 |
21,520,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R1735:Cdh12
|
UTSW |
15 |
21,520,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1916:Cdh12
|
UTSW |
15 |
21,520,336 (GRCm39) |
splice site |
probably null |
|
R1950:Cdh12
|
UTSW |
15 |
21,237,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R2059:Cdh12
|
UTSW |
15 |
21,583,826 (GRCm39) |
missense |
probably benign |
0.08 |
R2157:Cdh12
|
UTSW |
15 |
21,583,873 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2404:Cdh12
|
UTSW |
15 |
21,537,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3625:Cdh12
|
UTSW |
15 |
21,358,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R3703:Cdh12
|
UTSW |
15 |
21,583,912 (GRCm39) |
missense |
probably damaging |
0.97 |
R3704:Cdh12
|
UTSW |
15 |
21,583,912 (GRCm39) |
missense |
probably damaging |
0.97 |
R3743:Cdh12
|
UTSW |
15 |
21,537,745 (GRCm39) |
missense |
probably damaging |
0.98 |
R3771:Cdh12
|
UTSW |
15 |
21,578,640 (GRCm39) |
splice site |
probably benign |
|
R3780:Cdh12
|
UTSW |
15 |
21,586,063 (GRCm39) |
splice site |
probably null |
|
R4750:Cdh12
|
UTSW |
15 |
21,583,894 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5373:Cdh12
|
UTSW |
15 |
21,583,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5374:Cdh12
|
UTSW |
15 |
21,583,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5443:Cdh12
|
UTSW |
15 |
21,237,935 (GRCm39) |
missense |
probably benign |
0.01 |
R5548:Cdh12
|
UTSW |
15 |
21,492,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R5746:Cdh12
|
UTSW |
15 |
21,358,810 (GRCm39) |
missense |
probably null |
1.00 |
R5960:Cdh12
|
UTSW |
15 |
21,492,562 (GRCm39) |
splice site |
probably null |
|
R6248:Cdh12
|
UTSW |
15 |
21,237,800 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6379:Cdh12
|
UTSW |
15 |
21,492,743 (GRCm39) |
missense |
probably benign |
0.02 |
R6419:Cdh12
|
UTSW |
15 |
21,520,483 (GRCm39) |
missense |
probably damaging |
0.99 |
R6561:Cdh12
|
UTSW |
15 |
21,492,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Cdh12
|
UTSW |
15 |
21,583,872 (GRCm39) |
missense |
probably benign |
0.01 |
R7025:Cdh12
|
UTSW |
15 |
21,358,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7070:Cdh12
|
UTSW |
15 |
21,583,915 (GRCm39) |
missense |
probably benign |
0.38 |
R7508:Cdh12
|
UTSW |
15 |
21,583,851 (GRCm39) |
missense |
probably benign |
|
R8126:Cdh12
|
UTSW |
15 |
21,558,393 (GRCm39) |
missense |
probably benign |
0.02 |
R8307:Cdh12
|
UTSW |
15 |
21,358,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Cdh12
|
UTSW |
15 |
21,358,949 (GRCm39) |
missense |
probably benign |
|
R8969:Cdh12
|
UTSW |
15 |
21,492,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Cdh12
|
UTSW |
15 |
21,237,825 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9272:Cdh12
|
UTSW |
15 |
21,492,801 (GRCm39) |
splice site |
probably benign |
|
X0065:Cdh12
|
UTSW |
15 |
21,358,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|