Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
T |
C |
4: 40,177,783 (GRCm39) |
L268P |
probably damaging |
Het |
Adam22 |
A |
T |
5: 8,380,048 (GRCm39) |
H83Q |
probably damaging |
Het |
Anln |
T |
C |
9: 22,264,122 (GRCm39) |
D886G |
probably benign |
Het |
Arhgef11 |
T |
A |
3: 87,596,159 (GRCm39) |
|
probably null |
Het |
Ark2c |
T |
A |
18: 77,571,950 (GRCm39) |
Q91L |
probably damaging |
Het |
Arl8b |
A |
T |
6: 108,792,287 (GRCm39) |
D116V |
possibly damaging |
Het |
BC051665 |
C |
T |
13: 60,931,859 (GRCm39) |
G180D |
probably damaging |
Het |
Bloc1s2 |
A |
G |
19: 44,131,589 (GRCm39) |
|
probably benign |
Het |
Cd101 |
T |
C |
3: 100,915,408 (GRCm39) |
K720E |
possibly damaging |
Het |
Cdh23 |
C |
A |
10: 60,222,725 (GRCm39) |
A1236S |
probably damaging |
Het |
Chd1 |
G |
A |
17: 15,954,604 (GRCm39) |
A491T |
probably damaging |
Het |
Chdh |
T |
C |
14: 29,754,815 (GRCm39) |
V275A |
possibly damaging |
Het |
Cmtm2b |
A |
T |
8: 105,057,047 (GRCm39) |
I136F |
probably damaging |
Het |
Cps1 |
T |
C |
1: 67,204,551 (GRCm39) |
V457A |
probably damaging |
Het |
Cwf19l1 |
A |
G |
19: 44,103,129 (GRCm39) |
V362A |
probably benign |
Het |
Cyp4f17 |
T |
C |
17: 32,743,797 (GRCm39) |
|
probably benign |
Het |
Cyp4f18 |
C |
A |
8: 72,749,861 (GRCm39) |
V263L |
probably benign |
Het |
Dclre1a |
A |
G |
19: 56,529,922 (GRCm39) |
|
probably benign |
Het |
Dpp6 |
T |
C |
5: 27,866,640 (GRCm39) |
I446T |
probably benign |
Het |
F11r |
T |
C |
1: 171,288,156 (GRCm39) |
W61R |
probably damaging |
Het |
Fam120b |
C |
T |
17: 15,646,550 (GRCm39) |
|
probably benign |
Het |
Fastkd2 |
T |
C |
1: 63,791,499 (GRCm39) |
V669A |
possibly damaging |
Het |
Foxg1 |
T |
C |
12: 49,431,314 (GRCm39) |
|
probably benign |
Het |
Foxo3 |
A |
G |
10: 42,073,477 (GRCm39) |
Y347H |
probably damaging |
Het |
G3bp1 |
T |
C |
11: 55,389,452 (GRCm39) |
F383L |
probably damaging |
Het |
Gbp7 |
C |
A |
3: 142,252,078 (GRCm39) |
|
probably benign |
Het |
Glipr1 |
T |
C |
10: 111,832,754 (GRCm39) |
|
probably benign |
Het |
Gm11555 |
A |
G |
11: 99,540,986 (GRCm39) |
S8P |
unknown |
Het |
H6pd |
G |
A |
4: 150,067,393 (GRCm39) |
|
probably benign |
Het |
Haus8 |
C |
A |
8: 71,709,181 (GRCm39) |
G76W |
probably damaging |
Het |
Haus8 |
C |
T |
8: 71,709,182 (GRCm39) |
M75I |
probably benign |
Het |
Kcnj13 |
C |
A |
1: 87,314,752 (GRCm39) |
V157L |
probably damaging |
Het |
Kcnt2 |
T |
A |
1: 140,437,218 (GRCm39) |
C550* |
probably null |
Het |
Kdm5d |
A |
G |
Y: 927,107 (GRCm39) |
N615S |
probably damaging |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Ncapd2 |
G |
A |
6: 125,160,990 (GRCm39) |
R292* |
probably null |
Het |
Ngef |
T |
A |
1: 87,406,848 (GRCm39) |
N640I |
probably damaging |
Het |
Nhlrc3 |
T |
C |
3: 53,359,858 (GRCm39) |
Y335C |
probably damaging |
Het |
Nipbl |
A |
T |
15: 8,368,354 (GRCm39) |
|
probably benign |
Het |
Nop2 |
A |
G |
6: 125,117,636 (GRCm39) |
K434R |
probably null |
Het |
Nr4a3 |
T |
C |
4: 48,056,525 (GRCm39) |
|
probably benign |
Het |
Or8b35 |
A |
G |
9: 37,903,998 (GRCm39) |
N70S |
possibly damaging |
Het |
Piezo2 |
A |
C |
18: 63,162,132 (GRCm39) |
I2233R |
probably damaging |
Het |
Prag1 |
A |
T |
8: 36,613,787 (GRCm39) |
E1113V |
probably damaging |
Het |
Prpsap2 |
A |
G |
11: 61,631,826 (GRCm39) |
I177T |
possibly damaging |
Het |
Psmd1 |
T |
A |
1: 86,022,012 (GRCm39) |
N611K |
probably damaging |
Het |
Ptpn7 |
C |
T |
1: 135,065,096 (GRCm39) |
T168I |
probably damaging |
Het |
Pus1 |
A |
T |
5: 110,927,596 (GRCm39) |
V53E |
probably damaging |
Het |
Rgs22 |
A |
G |
15: 36,093,028 (GRCm39) |
M415T |
probably damaging |
Het |
Rnf17 |
C |
T |
14: 56,751,632 (GRCm39) |
T1490M |
probably benign |
Het |
Rnf20 |
C |
A |
4: 49,645,907 (GRCm39) |
L332I |
possibly damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Spam1 |
A |
T |
6: 24,796,394 (GRCm39) |
Q115L |
probably damaging |
Het |
Syce1l |
A |
T |
8: 114,381,395 (GRCm39) |
|
probably null |
Het |
Synj1 |
T |
C |
16: 90,735,151 (GRCm39) |
|
probably benign |
Het |
Tas2r126 |
A |
T |
6: 42,412,225 (GRCm39) |
I253F |
probably benign |
Het |
Tecpr2 |
G |
A |
12: 110,862,803 (GRCm39) |
V72I |
probably benign |
Het |
Tfap2a |
G |
T |
13: 40,882,170 (GRCm39) |
P45Q |
probably damaging |
Het |
Trip12 |
C |
A |
1: 84,738,805 (GRCm39) |
G714* |
probably null |
Het |
Wdr31 |
A |
G |
4: 62,372,130 (GRCm39) |
S330P |
probably damaging |
Het |
Wdr64 |
T |
C |
1: 175,622,769 (GRCm39) |
|
probably benign |
Het |
Yes1 |
T |
A |
5: 32,812,926 (GRCm39) |
Y343* |
probably null |
Het |
|
Other mutations in Ccdc185 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Ccdc185
|
APN |
1 |
182,574,988 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01121:Ccdc185
|
APN |
1 |
182,576,222 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01143:Ccdc185
|
APN |
1 |
182,575,417 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01721:Ccdc185
|
APN |
1 |
182,576,543 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01941:Ccdc185
|
APN |
1 |
182,575,769 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01945:Ccdc185
|
APN |
1 |
182,576,441 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03333:Ccdc185
|
APN |
1 |
182,576,398 (GRCm39) |
missense |
probably damaging |
1.00 |
Ratas
|
UTSW |
1 |
182,576,582 (GRCm39) |
missense |
possibly damaging |
0.73 |
Ratones
|
UTSW |
1 |
182,575,085 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0653:Ccdc185
|
UTSW |
1 |
182,575,129 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1263:Ccdc185
|
UTSW |
1 |
182,574,918 (GRCm39) |
nonsense |
probably null |
|
R1450:Ccdc185
|
UTSW |
1 |
182,575,129 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1464:Ccdc185
|
UTSW |
1 |
182,576,263 (GRCm39) |
missense |
probably benign |
|
R1464:Ccdc185
|
UTSW |
1 |
182,576,263 (GRCm39) |
missense |
probably benign |
|
R2146:Ccdc185
|
UTSW |
1 |
182,575,085 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3409:Ccdc185
|
UTSW |
1 |
182,576,313 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3410:Ccdc185
|
UTSW |
1 |
182,576,313 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3765:Ccdc185
|
UTSW |
1 |
182,575,117 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4012:Ccdc185
|
UTSW |
1 |
182,576,453 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4953:Ccdc185
|
UTSW |
1 |
182,576,582 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5096:Ccdc185
|
UTSW |
1 |
182,576,354 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5166:Ccdc185
|
UTSW |
1 |
182,576,564 (GRCm39) |
nonsense |
probably null |
|
R5300:Ccdc185
|
UTSW |
1 |
182,575,645 (GRCm39) |
missense |
probably benign |
0.00 |
R5504:Ccdc185
|
UTSW |
1 |
182,575,192 (GRCm39) |
missense |
probably damaging |
0.97 |
R5863:Ccdc185
|
UTSW |
1 |
182,576,122 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5928:Ccdc185
|
UTSW |
1 |
182,575,047 (GRCm39) |
missense |
probably benign |
0.00 |
R7127:Ccdc185
|
UTSW |
1 |
182,576,421 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8125:Ccdc185
|
UTSW |
1 |
182,574,835 (GRCm39) |
missense |
probably benign |
0.10 |
R8197:Ccdc185
|
UTSW |
1 |
182,576,324 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9248:Ccdc185
|
UTSW |
1 |
182,576,221 (GRCm39) |
missense |
probably benign |
0.33 |
Z1177:Ccdc185
|
UTSW |
1 |
182,576,079 (GRCm39) |
missense |
possibly damaging |
0.72 |
|