Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,240,732 (GRCm39) |
E865G |
probably benign |
Het |
Actrt2 |
A |
C |
4: 154,751,880 (GRCm39) |
D85E |
probably benign |
Het |
Ankrd55 |
A |
G |
13: 112,472,787 (GRCm39) |
E153G |
probably damaging |
Het |
Arfgef3 |
T |
A |
10: 18,501,139 (GRCm39) |
H1037L |
probably benign |
Het |
Camk2a |
A |
G |
18: 61,076,277 (GRCm39) |
Y85C |
unknown |
Het |
Caprin1 |
A |
T |
2: 103,609,819 (GRCm39) |
V153E |
possibly damaging |
Het |
Caskin2 |
G |
A |
11: 115,692,722 (GRCm39) |
P688S |
probably benign |
Het |
Catsper2 |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
2: 121,228,053 (GRCm39) |
|
probably benign |
Het |
Cdh9 |
G |
A |
15: 16,778,341 (GRCm39) |
R52H |
probably damaging |
Het |
Cdk5rap2 |
A |
G |
4: 70,255,666 (GRCm39) |
L406S |
probably damaging |
Het |
Cep350 |
A |
G |
1: 155,786,499 (GRCm39) |
M1449T |
probably damaging |
Het |
Chst8 |
T |
A |
7: 34,375,361 (GRCm39) |
K159N |
probably damaging |
Het |
Dcdc2a |
A |
G |
13: 25,286,374 (GRCm39) |
H136R |
probably benign |
Het |
Dip2a |
C |
T |
10: 76,108,366 (GRCm39) |
|
probably null |
Het |
Dock2 |
G |
A |
11: 34,605,340 (GRCm39) |
R260* |
probably null |
Het |
Dscam |
A |
G |
16: 96,622,008 (GRCm39) |
V481A |
probably damaging |
Het |
E130308A19Rik |
A |
G |
4: 59,690,502 (GRCm39) |
D112G |
probably damaging |
Het |
Ezh2 |
T |
C |
6: 47,510,708 (GRCm39) |
K634E |
probably damaging |
Het |
Fcgr2b |
A |
G |
1: 170,793,269 (GRCm39) |
|
probably null |
Het |
Fgfrl1 |
T |
C |
5: 108,851,365 (GRCm39) |
V94A |
possibly damaging |
Het |
Gpr156 |
C |
A |
16: 37,768,103 (GRCm39) |
N6K |
probably damaging |
Het |
Gsdmc2 |
A |
T |
15: 63,705,183 (GRCm39) |
F177I |
probably benign |
Het |
Igkv4-54 |
T |
A |
6: 69,608,842 (GRCm39) |
S26C |
probably damaging |
Het |
Iglc3 |
T |
C |
16: 18,884,191 (GRCm39) |
H80R |
|
Het |
Immp1l |
G |
A |
2: 105,767,401 (GRCm39) |
G87S |
probably damaging |
Het |
Itgav |
A |
T |
2: 83,555,179 (GRCm39) |
D34V |
probably damaging |
Het |
Lrp1b |
G |
A |
2: 41,159,224 (GRCm39) |
T1686I |
|
Het |
Ltn1 |
T |
C |
16: 87,206,275 (GRCm39) |
D935G |
probably benign |
Het |
Map3k8 |
T |
C |
18: 4,334,036 (GRCm39) |
D352G |
probably damaging |
Het |
Map3k9 |
T |
C |
12: 81,772,604 (GRCm39) |
K610E |
possibly damaging |
Het |
Marchf4 |
G |
T |
1: 72,491,637 (GRCm39) |
Y211* |
probably null |
Het |
Marf1 |
A |
T |
16: 13,944,957 (GRCm39) |
L1304Q |
probably damaging |
Het |
Matcap1 |
A |
T |
8: 106,011,331 (GRCm39) |
Y268N |
probably benign |
Het |
Mecom |
A |
G |
3: 30,194,505 (GRCm39) |
V5A |
unknown |
Het |
Mep1a |
A |
T |
17: 43,785,995 (GRCm39) |
V711D |
possibly damaging |
Het |
Naca |
T |
A |
10: 127,878,467 (GRCm39) |
D1166E |
unknown |
Het |
Neb |
G |
T |
2: 52,148,753 (GRCm39) |
P2598Q |
probably damaging |
Het |
Notch4 |
A |
T |
17: 34,791,491 (GRCm39) |
E546V |
probably damaging |
Het |
Nudt18 |
A |
G |
14: 70,815,422 (GRCm39) |
T12A |
unknown |
Het |
Nvl |
A |
C |
1: 180,939,851 (GRCm39) |
|
probably null |
Het |
Obscn |
G |
T |
11: 58,994,144 (GRCm39) |
C1579* |
probably null |
Het |
Or4b13 |
G |
A |
2: 90,083,165 (GRCm39) |
P56S |
probably damaging |
Het |
Or51e2 |
T |
C |
7: 102,391,551 (GRCm39) |
I220V |
probably damaging |
Het |
Or6c5b |
T |
C |
10: 129,246,051 (GRCm39) |
V272A |
probably damaging |
Het |
Or7g33 |
A |
T |
9: 19,448,629 (GRCm39) |
I199K |
probably benign |
Het |
Or8g19 |
T |
A |
9: 39,056,153 (GRCm39) |
Y252* |
probably null |
Het |
Oxa1l |
A |
T |
14: 54,598,312 (GRCm39) |
M1L |
probably benign |
Het |
Paqr9 |
A |
G |
9: 95,442,246 (GRCm39) |
T79A |
possibly damaging |
Het |
Plec |
A |
T |
15: 76,061,543 (GRCm39) |
V2798E |
probably damaging |
Het |
Potefam3f |
A |
G |
8: 20,479,022 (GRCm39) |
N10S |
|
Het |
Ptpn4 |
A |
T |
1: 119,617,764 (GRCm39) |
*557R |
probably null |
Het |
Ptprt |
T |
C |
2: 161,375,443 (GRCm39) |
E1379G |
probably benign |
Het |
Rad18 |
G |
T |
6: 112,642,286 (GRCm39) |
T327K |
possibly damaging |
Het |
Rps2 |
T |
A |
17: 24,939,554 (GRCm39) |
I75N |
possibly damaging |
Het |
Scgb2b2 |
A |
T |
7: 31,003,021 (GRCm39) |
R39W |
probably damaging |
Het |
Sh3d21 |
A |
G |
4: 126,045,908 (GRCm39) |
F307S |
probably benign |
Het |
Snap91 |
A |
G |
9: 86,674,669 (GRCm39) |
V507A |
unknown |
Het |
Srgap1 |
T |
A |
10: 121,705,695 (GRCm39) |
Y243F |
probably damaging |
Het |
Stim1 |
T |
A |
7: 102,070,739 (GRCm39) |
|
probably null |
Het |
Top2b |
T |
C |
14: 16,416,962 (GRCm38) |
V1161A |
probably benign |
Het |
Tpcn1 |
T |
C |
5: 120,723,315 (GRCm39) |
D16G |
possibly damaging |
Het |
Trank1 |
A |
T |
9: 111,196,580 (GRCm39) |
I1535F |
probably damaging |
Het |
Txnrd2 |
T |
C |
16: 18,274,822 (GRCm39) |
F278L |
probably damaging |
Het |
Ufl1 |
A |
T |
4: 25,254,637 (GRCm39) |
D579E |
probably damaging |
Het |
Vps45 |
T |
C |
3: 95,948,717 (GRCm39) |
N346S |
probably benign |
Het |
Vps51 |
T |
A |
19: 6,127,419 (GRCm39) |
|
probably benign |
Het |
Zfp536 |
T |
C |
7: 37,268,631 (GRCm39) |
N262D |
probably benign |
Het |
Zmynd10 |
A |
G |
9: 107,425,976 (GRCm39) |
I103M |
possibly damaging |
Het |
Zswim1 |
C |
T |
2: 164,667,719 (GRCm39) |
H324Y |
possibly damaging |
Het |
Zxdc |
T |
C |
6: 90,361,155 (GRCm39) |
W507R |
unknown |
Het |
|
Other mutations in Ccdc116 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01082:Ccdc116
|
APN |
16 |
16,959,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01905:Ccdc116
|
APN |
16 |
16,960,425 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02751:Ccdc116
|
APN |
16 |
16,959,836 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03183:Ccdc116
|
APN |
16 |
16,960,718 (GRCm39) |
missense |
probably benign |
0.07 |
R0009:Ccdc116
|
UTSW |
16 |
16,961,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Ccdc116
|
UTSW |
16 |
16,961,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0122:Ccdc116
|
UTSW |
16 |
16,960,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Ccdc116
|
UTSW |
16 |
16,959,476 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1664:Ccdc116
|
UTSW |
16 |
16,960,492 (GRCm39) |
missense |
probably benign |
0.02 |
R1718:Ccdc116
|
UTSW |
16 |
16,959,772 (GRCm39) |
missense |
probably benign |
|
R2921:Ccdc116
|
UTSW |
16 |
16,960,307 (GRCm39) |
missense |
probably benign |
0.02 |
R2922:Ccdc116
|
UTSW |
16 |
16,960,307 (GRCm39) |
missense |
probably benign |
0.02 |
R2923:Ccdc116
|
UTSW |
16 |
16,960,307 (GRCm39) |
missense |
probably benign |
0.02 |
R4119:Ccdc116
|
UTSW |
16 |
16,960,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4223:Ccdc116
|
UTSW |
16 |
16,964,809 (GRCm39) |
unclassified |
probably benign |
|
R5000:Ccdc116
|
UTSW |
16 |
16,959,657 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5293:Ccdc116
|
UTSW |
16 |
16,959,651 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5435:Ccdc116
|
UTSW |
16 |
16,960,626 (GRCm39) |
missense |
probably benign |
0.38 |
R6694:Ccdc116
|
UTSW |
16 |
16,960,655 (GRCm39) |
missense |
probably benign |
0.44 |
R7215:Ccdc116
|
UTSW |
16 |
16,957,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Ccdc116
|
UTSW |
16 |
16,957,455 (GRCm39) |
missense |
probably benign |
0.00 |
R9591:Ccdc116
|
UTSW |
16 |
16,960,598 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Ccdc116
|
UTSW |
16 |
16,965,035 (GRCm39) |
unclassified |
probably benign |
|
|