Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
A |
17: 24,537,159 (GRCm39) |
I475L |
probably benign |
Het |
Abcc2 |
C |
T |
19: 43,807,797 (GRCm39) |
R813W |
probably damaging |
Het |
Adam34 |
T |
C |
8: 44,105,067 (GRCm39) |
T193A |
probably benign |
Het |
Adgb |
T |
C |
10: 10,254,531 (GRCm39) |
D1118G |
probably damaging |
Het |
Adprh |
A |
C |
16: 38,267,746 (GRCm39) |
S180A |
probably benign |
Het |
Atad5 |
A |
T |
11: 79,985,003 (GRCm39) |
D30V |
probably damaging |
Het |
Best3 |
G |
A |
10: 116,843,532 (GRCm39) |
D303N |
probably damaging |
Het |
Bmp2k |
G |
C |
5: 97,235,595 (GRCm39) |
|
probably benign |
Het |
Btc |
A |
T |
5: 91,514,004 (GRCm39) |
V86E |
probably damaging |
Het |
Cacna2d4 |
G |
T |
6: 119,258,659 (GRCm39) |
A582S |
probably benign |
Het |
Carm1 |
A |
G |
9: 21,486,598 (GRCm39) |
|
probably benign |
Het |
Catsperg1 |
A |
T |
7: 28,906,040 (GRCm39) |
S180T |
probably damaging |
Het |
Ccdc185 |
A |
T |
1: 182,575,047 (GRCm39) |
H547Q |
probably benign |
Het |
Ccl6 |
A |
G |
11: 83,479,658 (GRCm39) |
I115T |
possibly damaging |
Het |
Cd44 |
C |
T |
2: 102,654,648 (GRCm39) |
V470M |
probably damaging |
Het |
Cdc25a |
T |
C |
9: 109,718,861 (GRCm39) |
V354A |
probably damaging |
Het |
Cdhr2 |
C |
A |
13: 54,881,832 (GRCm39) |
Q1122K |
probably benign |
Het |
Cep290 |
A |
G |
10: 100,387,692 (GRCm39) |
K1958E |
probably damaging |
Het |
Cfap53 |
C |
T |
18: 74,492,811 (GRCm39) |
P512S |
possibly damaging |
Het |
Chrdl2 |
A |
T |
7: 99,659,200 (GRCm39) |
|
probably benign |
Het |
Cibar1 |
A |
G |
4: 12,171,919 (GRCm39) |
|
probably benign |
Het |
Cracd |
A |
C |
5: 76,989,581 (GRCm39) |
|
probably benign |
Het |
Dhx29 |
A |
G |
13: 113,101,002 (GRCm39) |
K1182E |
probably benign |
Het |
Dnah11 |
G |
T |
12: 117,878,371 (GRCm39) |
|
probably null |
Het |
Dnmt3a |
A |
G |
12: 3,916,096 (GRCm39) |
S94G |
possibly damaging |
Het |
Ecpas |
A |
T |
4: 58,849,948 (GRCm39) |
M425K |
possibly damaging |
Het |
Egfem1 |
T |
C |
3: 29,637,077 (GRCm39) |
V42A |
possibly damaging |
Het |
Eif3e |
T |
A |
15: 43,138,728 (GRCm39) |
|
probably null |
Het |
Exosc9 |
T |
A |
3: 36,609,774 (GRCm39) |
|
probably benign |
Het |
Fbxw18 |
T |
A |
9: 109,529,149 (GRCm39) |
T135S |
probably damaging |
Het |
Fbxw21 |
T |
C |
9: 108,972,893 (GRCm39) |
E347G |
possibly damaging |
Het |
Gcm2 |
A |
G |
13: 41,256,874 (GRCm39) |
Y292H |
probably benign |
Het |
Gltpd2 |
C |
A |
11: 70,410,179 (GRCm39) |
Q46K |
probably benign |
Het |
Gm6741 |
A |
G |
17: 91,544,528 (GRCm39) |
Y97C |
probably damaging |
Het |
Golgb1 |
T |
C |
16: 36,732,349 (GRCm39) |
L532S |
probably damaging |
Het |
Hdac3 |
C |
T |
18: 38,074,394 (GRCm39) |
|
probably benign |
Het |
Helz2 |
A |
T |
2: 180,872,177 (GRCm39) |
F2554L |
possibly damaging |
Het |
Hmbox1 |
T |
A |
14: 65,061,122 (GRCm39) |
H384L |
possibly damaging |
Het |
Hmcn1 |
G |
T |
1: 150,474,648 (GRCm39) |
D4746E |
possibly damaging |
Het |
Il17rb |
C |
A |
14: 29,726,232 (GRCm39) |
|
probably null |
Het |
Irak2 |
A |
T |
6: 113,653,587 (GRCm39) |
I252F |
probably damaging |
Het |
Khnyn |
C |
T |
14: 56,123,344 (GRCm39) |
R33C |
probably damaging |
Het |
Ksr1 |
G |
A |
11: 78,950,545 (GRCm39) |
P20L |
probably damaging |
Het |
Lamc3 |
T |
C |
2: 31,811,721 (GRCm39) |
Y903H |
probably benign |
Het |
Miga2 |
T |
C |
2: 30,258,875 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
A |
C |
1: 88,169,340 (GRCm39) |
I672L |
probably benign |
Het |
Ncoa4 |
T |
C |
14: 31,888,678 (GRCm39) |
|
probably null |
Het |
Nphp3 |
T |
C |
9: 103,912,996 (GRCm39) |
Y925H |
probably benign |
Het |
Nr2c1 |
T |
G |
10: 94,024,055 (GRCm39) |
L420R |
probably damaging |
Het |
Onecut1 |
A |
G |
9: 74,770,066 (GRCm39) |
N163S |
probably benign |
Het |
Or5ac21 |
G |
A |
16: 59,123,521 (GRCm39) |
E2K |
probably damaging |
Het |
Or5d47 |
T |
A |
2: 87,804,380 (GRCm39) |
S210C |
probably benign |
Het |
Or7e166 |
A |
T |
9: 19,625,049 (GRCm39) |
T309S |
probably benign |
Het |
Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
Per2 |
C |
T |
1: 91,372,373 (GRCm39) |
V234I |
probably damaging |
Het |
Pign |
A |
G |
1: 105,485,792 (GRCm39) |
V735A |
possibly damaging |
Het |
Plekha7 |
T |
C |
7: 115,727,809 (GRCm39) |
K85R |
probably benign |
Het |
Pnma2 |
C |
T |
14: 67,154,323 (GRCm39) |
T249I |
probably benign |
Het |
Polr2b |
A |
G |
5: 77,493,189 (GRCm39) |
D1057G |
probably damaging |
Het |
Polrmt |
A |
T |
10: 79,576,186 (GRCm39) |
L519H |
probably damaging |
Het |
Ptar1 |
T |
C |
19: 23,695,277 (GRCm39) |
I248T |
probably benign |
Het |
Ptprh |
A |
C |
7: 4,576,507 (GRCm39) |
L251R |
probably damaging |
Het |
Purg |
T |
C |
8: 33,876,980 (GRCm39) |
M206T |
probably benign |
Het |
Pwp2 |
A |
T |
10: 78,018,290 (GRCm39) |
F134I |
probably damaging |
Het |
Riok3 |
T |
A |
18: 12,286,075 (GRCm39) |
H434Q |
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,216,220 (GRCm39) |
I187V |
probably damaging |
Het |
Tbc1d2b |
T |
C |
9: 90,101,197 (GRCm39) |
I598V |
probably benign |
Het |
Tdg |
T |
A |
10: 82,477,204 (GRCm39) |
V85E |
probably benign |
Het |
Tfb1m |
C |
T |
17: 3,593,422 (GRCm39) |
V166I |
probably benign |
Het |
Tmem163 |
A |
T |
1: 127,419,383 (GRCm39) |
M274K |
probably damaging |
Het |
Tpr |
T |
C |
1: 150,303,878 (GRCm39) |
I1343T |
probably benign |
Het |
Ttn |
T |
A |
2: 76,719,794 (GRCm39) |
|
probably benign |
Het |
Tut7 |
G |
A |
13: 59,969,880 (GRCm39) |
A5V |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,386,040 (GRCm39) |
T2156A |
probably damaging |
Het |
Vmn1r215 |
A |
T |
13: 23,260,487 (GRCm39) |
T176S |
possibly damaging |
Het |
Vps52 |
C |
T |
17: 34,180,100 (GRCm39) |
P268L |
possibly damaging |
Het |
Xbp1 |
G |
A |
11: 5,473,514 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
T |
A |
18: 44,966,272 (GRCm39) |
F169L |
probably benign |
Het |
Zfyve16 |
T |
C |
13: 92,658,625 (GRCm39) |
R429G |
probably benign |
Het |
Zzef1 |
A |
G |
11: 72,803,678 (GRCm39) |
E2504G |
probably damaging |
Het |
|
Other mutations in Clec7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01339:Clec7a
|
APN |
6 |
129,442,449 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01383:Clec7a
|
APN |
6 |
129,449,603 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Clec7a
|
APN |
6 |
129,449,640 (GRCm39) |
nonsense |
probably null |
|
IGL01886:Clec7a
|
APN |
6 |
129,440,140 (GRCm39) |
splice site |
probably benign |
|
IGL01983:Clec7a
|
APN |
6 |
129,442,539 (GRCm39) |
splice site |
probably benign |
|
IGL02948:Clec7a
|
APN |
6 |
129,442,441 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1210:Clec7a
|
UTSW |
6 |
129,442,488 (GRCm39) |
missense |
probably damaging |
0.96 |
R1469:Clec7a
|
UTSW |
6 |
129,449,535 (GRCm39) |
splice site |
probably benign |
|
R2126:Clec7a
|
UTSW |
6 |
129,447,918 (GRCm39) |
missense |
probably benign |
0.02 |
R2246:Clec7a
|
UTSW |
6 |
129,444,532 (GRCm39) |
missense |
probably benign |
0.27 |
R2887:Clec7a
|
UTSW |
6 |
129,447,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R3901:Clec7a
|
UTSW |
6 |
129,445,877 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7218:Clec7a
|
UTSW |
6 |
129,445,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Clec7a
|
UTSW |
6 |
129,442,518 (GRCm39) |
missense |
probably benign |
0.37 |
R9066:Clec7a
|
UTSW |
6 |
129,444,491 (GRCm39) |
missense |
probably benign |
|
R9425:Clec7a
|
UTSW |
6 |
129,442,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R9474:Clec7a
|
UTSW |
6 |
129,440,126 (GRCm39) |
nonsense |
probably null |
|
|