Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atat1 |
T |
A |
17: 36,219,456 (GRCm39) |
Q136L |
probably damaging |
Het |
Atm |
A |
G |
9: 53,399,887 (GRCm39) |
L1531P |
probably damaging |
Het |
Brca2 |
G |
A |
5: 150,480,354 (GRCm39) |
R2708H |
probably damaging |
Het |
Cand1 |
G |
A |
10: 119,053,915 (GRCm39) |
A141V |
possibly damaging |
Het |
Ces4a |
G |
A |
8: 105,864,806 (GRCm39) |
|
probably null |
Het |
Colec10 |
T |
A |
15: 54,323,203 (GRCm39) |
M142K |
possibly damaging |
Het |
Crtc1 |
G |
T |
8: 70,858,839 (GRCm39) |
D90E |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,142,319 (GRCm39) |
E1528G |
possibly damaging |
Het |
Csnk2a2 |
A |
G |
8: 96,184,097 (GRCm39) |
V154A |
possibly damaging |
Het |
Daglb |
T |
C |
5: 143,480,358 (GRCm39) |
I454T |
probably benign |
Het |
Dtna |
C |
A |
18: 23,755,113 (GRCm39) |
N478K |
possibly damaging |
Het |
E330034G19Rik |
A |
T |
14: 24,343,448 (GRCm39) |
|
probably benign |
Het |
Ecpas |
G |
T |
4: 58,826,453 (GRCm39) |
S1038Y |
possibly damaging |
Het |
Eefsec |
A |
T |
6: 88,332,611 (GRCm39) |
S200T |
probably benign |
Het |
Enthd1 |
T |
A |
15: 80,336,916 (GRCm39) |
D506V |
probably damaging |
Het |
Erbb2 |
A |
G |
11: 98,324,075 (GRCm39) |
Y736C |
probably damaging |
Het |
Gabrg1 |
A |
G |
5: 70,938,056 (GRCm39) |
C183R |
probably damaging |
Het |
Ginm1 |
T |
A |
10: 7,651,097 (GRCm39) |
H103L |
probably benign |
Het |
Golgb1 |
C |
A |
16: 36,735,033 (GRCm39) |
Q1427K |
possibly damaging |
Het |
Grb14 |
G |
T |
2: 64,852,964 (GRCm39) |
Q9K |
possibly damaging |
Het |
Hbp1 |
A |
T |
12: 31,987,246 (GRCm39) |
M192K |
probably damaging |
Het |
Herpud2 |
A |
T |
9: 25,020,284 (GRCm39) |
D357E |
probably damaging |
Het |
Idi1 |
A |
G |
13: 8,937,541 (GRCm39) |
S111G |
probably damaging |
Het |
Lrrc32 |
T |
C |
7: 98,147,748 (GRCm39) |
V176A |
probably benign |
Het |
Matn1 |
T |
A |
4: 130,679,277 (GRCm39) |
D310E |
probably benign |
Het |
Mbtps1 |
A |
T |
8: 120,257,830 (GRCm39) |
L469Q |
possibly damaging |
Het |
Muc4 |
A |
G |
16: 32,579,682 (GRCm39) |
D2417G |
unknown |
Het |
Myo7b |
T |
C |
18: 32,101,043 (GRCm39) |
T1551A |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,075,293 (GRCm39) |
M224T |
probably benign |
Het |
Ola1 |
A |
T |
2: 73,029,842 (GRCm39) |
D92E |
probably damaging |
Het |
Or1e28-ps1 |
A |
C |
11: 73,615,386 (GRCm39) |
C155G |
unknown |
Het |
Or4l1 |
A |
T |
14: 50,166,119 (GRCm39) |
M294K |
probably damaging |
Het |
Or5ar1 |
T |
G |
2: 85,671,458 (GRCm39) |
I226L |
probably benign |
Het |
Or8b48 |
T |
A |
9: 38,450,440 (GRCm39) |
M83K |
probably damaging |
Het |
Otud4 |
T |
C |
8: 80,400,525 (GRCm39) |
Y1080H |
probably damaging |
Het |
Plce1 |
G |
A |
19: 38,513,195 (GRCm39) |
A165T |
probably benign |
Het |
Prelid2 |
T |
C |
18: 42,045,530 (GRCm39) |
I127V |
probably benign |
Het |
Rab35 |
A |
G |
5: 115,778,147 (GRCm39) |
I38V |
probably damaging |
Het |
Rab3d |
T |
C |
9: 21,821,815 (GRCm39) |
T209A |
probably benign |
Het |
Rapgef1 |
A |
G |
2: 29,590,744 (GRCm39) |
E321G |
probably damaging |
Het |
Rem1 |
T |
C |
2: 152,470,017 (GRCm39) |
M1T |
probably null |
Het |
Rgsl1 |
T |
C |
1: 153,675,618 (GRCm39) |
K181R |
possibly damaging |
Het |
Scel |
C |
A |
14: 103,822,572 (GRCm39) |
N395K |
possibly damaging |
Het |
Septin9 |
A |
G |
11: 117,181,626 (GRCm39) |
E142G |
possibly damaging |
Het |
Shcbp1 |
A |
C |
8: 4,814,905 (GRCm39) |
M191R |
probably benign |
Het |
Slc22a19 |
T |
C |
19: 7,651,647 (GRCm39) |
N520S |
probably damaging |
Het |
Slc28a1 |
C |
T |
7: 80,765,311 (GRCm39) |
R9* |
probably null |
Het |
Slc2a7 |
T |
C |
4: 150,252,884 (GRCm39) |
V508A |
probably benign |
Het |
Slc8a3 |
G |
A |
12: 81,361,124 (GRCm39) |
P565L |
probably damaging |
Het |
Svil |
T |
G |
18: 5,106,724 (GRCm39) |
V1855G |
probably damaging |
Het |
Tenm3 |
T |
G |
8: 48,796,441 (GRCm39) |
I455L |
possibly damaging |
Het |
Tmem267 |
T |
C |
13: 120,070,767 (GRCm39) |
S141P |
probably damaging |
Het |
Tnn |
T |
A |
1: 159,925,848 (GRCm39) |
D1383V |
probably damaging |
Het |
Usp9y |
G |
T |
Y: 1,454,199 (GRCm39) |
Q23K |
probably benign |
Het |
Vmn1r46 |
T |
C |
6: 89,953,241 (GRCm39) |
I30T |
possibly damaging |
Het |
Zfp382 |
T |
C |
7: 29,833,015 (GRCm39) |
L222P |
probably damaging |
Het |
Zfp950 |
T |
A |
19: 61,108,863 (GRCm39) |
K73N |
possibly damaging |
Het |
|
Other mutations in Cdcp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01149:Cdcp2
|
APN |
4 |
106,964,308 (GRCm39) |
missense |
probably benign |
|
IGL02041:Cdcp2
|
APN |
4 |
106,964,386 (GRCm39) |
intron |
probably benign |
|
IGL03396:Cdcp2
|
APN |
4 |
106,964,369 (GRCm39) |
nonsense |
probably null |
|
R0128:Cdcp2
|
UTSW |
4 |
106,963,904 (GRCm39) |
splice site |
probably benign |
|
R0130:Cdcp2
|
UTSW |
4 |
106,963,904 (GRCm39) |
splice site |
probably benign |
|
R0519:Cdcp2
|
UTSW |
4 |
106,964,389 (GRCm39) |
intron |
probably benign |
|
R0543:Cdcp2
|
UTSW |
4 |
106,954,873 (GRCm39) |
splice site |
probably null |
|
R1376:Cdcp2
|
UTSW |
4 |
106,959,956 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1376:Cdcp2
|
UTSW |
4 |
106,959,956 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1606:Cdcp2
|
UTSW |
4 |
106,959,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Cdcp2
|
UTSW |
4 |
106,964,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R1887:Cdcp2
|
UTSW |
4 |
106,959,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R2944:Cdcp2
|
UTSW |
4 |
106,959,755 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4620:Cdcp2
|
UTSW |
4 |
106,963,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R4816:Cdcp2
|
UTSW |
4 |
106,963,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5298:Cdcp2
|
UTSW |
4 |
106,964,182 (GRCm39) |
missense |
probably benign |
0.01 |
R5646:Cdcp2
|
UTSW |
4 |
106,962,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Cdcp2
|
UTSW |
4 |
106,962,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Cdcp2
|
UTSW |
4 |
106,964,283 (GRCm39) |
missense |
probably benign |
|
R8114:Cdcp2
|
UTSW |
4 |
106,962,555 (GRCm39) |
missense |
probably damaging |
0.99 |
R8472:Cdcp2
|
UTSW |
4 |
106,959,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Cdcp2
|
UTSW |
4 |
106,964,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9726:Cdcp2
|
UTSW |
4 |
106,959,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Cdcp2
|
UTSW |
4 |
106,964,262 (GRCm39) |
missense |
possibly damaging |
0.63 |
|