Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931414P19Rik |
G |
A |
14: 54,828,857 (GRCm39) |
R215* |
probably null |
Het |
Brinp2 |
C |
A |
1: 158,074,416 (GRCm39) |
L568F |
probably damaging |
Het |
Brip1 |
T |
C |
11: 86,043,616 (GRCm39) |
Y316C |
probably damaging |
Het |
Cdk5rap2 |
ATGTG |
ATG |
4: 70,208,214 (GRCm39) |
|
probably null |
Het |
Cfap69 |
G |
T |
5: 5,634,645 (GRCm39) |
|
probably benign |
Het |
Chrnb4 |
T |
C |
9: 54,951,182 (GRCm39) |
E27G |
probably damaging |
Het |
Crygs |
A |
G |
16: 22,625,262 (GRCm39) |
Y60H |
probably damaging |
Het |
Dpp10 |
T |
A |
1: 123,281,216 (GRCm39) |
Q611L |
probably damaging |
Het |
Entpd1 |
T |
C |
19: 40,725,264 (GRCm39) |
L450P |
probably damaging |
Het |
Eogt |
G |
A |
6: 97,097,151 (GRCm39) |
S317L |
probably damaging |
Het |
Exosc10 |
T |
A |
4: 148,657,376 (GRCm39) |
S584T |
probably benign |
Het |
Fam184a |
C |
T |
10: 53,575,157 (GRCm39) |
V151I |
probably damaging |
Het |
Fbxo43 |
A |
G |
15: 36,152,258 (GRCm39) |
V517A |
probably damaging |
Het |
Flii |
T |
C |
11: 60,610,698 (GRCm39) |
T533A |
possibly damaging |
Het |
Frmpd1 |
T |
G |
4: 45,284,093 (GRCm39) |
H971Q |
probably benign |
Het |
Gata3 |
A |
T |
2: 9,867,954 (GRCm39) |
N333K |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,815,513 (GRCm39) |
S1525P |
probably damaging |
Het |
Ibtk |
A |
G |
9: 85,600,479 (GRCm39) |
I816T |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Krt34 |
T |
C |
11: 99,931,791 (GRCm39) |
T143A |
probably benign |
Het |
Lipn |
G |
T |
19: 34,046,828 (GRCm39) |
M43I |
probably benign |
Het |
Lrp1b |
A |
G |
2: 41,335,206 (GRCm39) |
C779R |
probably damaging |
Het |
Mios |
G |
A |
6: 8,233,189 (GRCm39) |
R779Q |
probably damaging |
Het |
Mme |
A |
T |
3: 63,269,480 (GRCm39) |
|
probably benign |
Het |
Ncstn |
A |
G |
1: 171,897,640 (GRCm39) |
S418P |
probably benign |
Het |
Oprk1 |
T |
A |
1: 5,672,884 (GRCm39) |
C340* |
probably null |
Het |
Or10d1c |
T |
A |
9: 38,894,166 (GRCm39) |
Y58F |
probably damaging |
Het |
Or4c29 |
T |
C |
2: 88,739,952 (GRCm39) |
T262A |
possibly damaging |
Het |
Or4k39 |
T |
C |
2: 111,238,967 (GRCm39) |
V69A |
possibly damaging |
Het |
Or6c210 |
C |
T |
10: 129,496,143 (GRCm39) |
P156L |
probably benign |
Het |
Or6z7 |
G |
A |
7: 6,484,131 (GRCm39) |
A8V |
probably benign |
Het |
Pald1 |
T |
A |
10: 61,183,266 (GRCm39) |
N323Y |
probably damaging |
Het |
Pcdhac1 |
C |
A |
18: 37,224,945 (GRCm39) |
A586E |
probably damaging |
Het |
Pcnx2 |
C |
T |
8: 126,614,897 (GRCm39) |
A185T |
probably benign |
Het |
Pik3r1 |
G |
A |
13: 101,821,465 (GRCm39) |
H430Y |
probably benign |
Het |
Polr3b |
G |
A |
10: 84,556,382 (GRCm39) |
|
probably null |
Het |
Prl8a6 |
A |
T |
13: 27,617,015 (GRCm39) |
L225* |
probably null |
Het |
Psme4 |
T |
C |
11: 30,806,068 (GRCm39) |
S89P |
probably damaging |
Het |
Pygl |
G |
A |
12: 70,248,113 (GRCm39) |
T250I |
probably damaging |
Het |
Rgs13 |
T |
A |
1: 144,016,528 (GRCm39) |
K72* |
probably null |
Het |
Ryr2 |
T |
A |
13: 11,603,045 (GRCm39) |
I4514F |
probably damaging |
Het |
Septin3 |
A |
T |
15: 82,170,002 (GRCm39) |
D32V |
probably damaging |
Het |
Sfrp2 |
C |
T |
3: 83,674,335 (GRCm39) |
P163S |
possibly damaging |
Het |
Spata31 |
A |
G |
13: 65,068,745 (GRCm39) |
T298A |
probably benign |
Het |
Stxbp2 |
T |
C |
8: 3,683,369 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
T |
10: 5,002,345 (GRCm39) |
M282K |
possibly damaging |
Het |
Timd2 |
T |
C |
11: 46,561,847 (GRCm39) |
|
probably null |
Het |
Tlr11 |
G |
A |
14: 50,600,611 (GRCm39) |
V866I |
probably benign |
Het |
Trappc10 |
T |
C |
10: 78,056,020 (GRCm39) |
|
probably null |
Het |
Zfp512b |
AG |
AGG |
2: 181,230,556 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Clec14a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01933:Clec14a
|
APN |
12 |
58,315,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02109:Clec14a
|
APN |
12 |
58,314,934 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02121:Clec14a
|
APN |
12 |
58,315,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Clec14a
|
APN |
12 |
58,315,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02818:Clec14a
|
APN |
12 |
58,314,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Clec14a
|
UTSW |
12 |
58,315,580 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0382:Clec14a
|
UTSW |
12 |
58,315,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R0419:Clec14a
|
UTSW |
12 |
58,314,451 (GRCm39) |
missense |
probably damaging |
0.97 |
R2972:Clec14a
|
UTSW |
12 |
58,314,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R3796:Clec14a
|
UTSW |
12 |
58,314,695 (GRCm39) |
missense |
probably benign |
0.34 |
R3797:Clec14a
|
UTSW |
12 |
58,314,695 (GRCm39) |
missense |
probably benign |
0.34 |
R4602:Clec14a
|
UTSW |
12 |
58,314,767 (GRCm39) |
missense |
probably benign |
0.03 |
R4708:Clec14a
|
UTSW |
12 |
58,314,489 (GRCm39) |
missense |
probably benign |
0.00 |
R4994:Clec14a
|
UTSW |
12 |
58,315,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R5193:Clec14a
|
UTSW |
12 |
58,315,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Clec14a
|
UTSW |
12 |
58,315,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Clec14a
|
UTSW |
12 |
58,314,612 (GRCm39) |
missense |
probably benign |
0.05 |
R6318:Clec14a
|
UTSW |
12 |
58,315,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R6388:Clec14a
|
UTSW |
12 |
58,314,243 (GRCm39) |
makesense |
probably null |
|
R6828:Clec14a
|
UTSW |
12 |
58,315,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Clec14a
|
UTSW |
12 |
58,315,580 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7418:Clec14a
|
UTSW |
12 |
58,315,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R7635:Clec14a
|
UTSW |
12 |
58,315,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Clec14a
|
UTSW |
12 |
58,314,543 (GRCm39) |
missense |
probably benign |
0.05 |
R7908:Clec14a
|
UTSW |
12 |
58,314,465 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8844:Clec14a
|
UTSW |
12 |
58,315,599 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9294:Clec14a
|
UTSW |
12 |
58,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R9477:Clec14a
|
UTSW |
12 |
58,314,620 (GRCm39) |
missense |
probably benign |
0.01 |
R9711:Clec14a
|
UTSW |
12 |
58,314,432 (GRCm39) |
missense |
probably damaging |
0.97 |
X0024:Clec14a
|
UTSW |
12 |
58,315,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|