Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asph |
C |
T |
4: 9,542,275 (GRCm39) |
D305N |
probably damaging |
Het |
Atp13a3 |
T |
C |
16: 30,170,205 (GRCm39) |
K327R |
probably damaging |
Het |
Cacna1s |
T |
C |
1: 136,026,264 (GRCm39) |
|
probably benign |
Het |
Ccnk |
T |
C |
12: 108,161,834 (GRCm39) |
|
probably benign |
Het |
Cep55 |
T |
C |
19: 38,048,622 (GRCm39) |
S93P |
possibly damaging |
Het |
Cfh |
A |
G |
1: 140,085,081 (GRCm39) |
|
probably benign |
Het |
Clptm1l |
A |
G |
13: 73,754,462 (GRCm39) |
T129A |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 116,220,206 (GRCm39) |
E672G |
probably benign |
Het |
Cpped1 |
C |
A |
16: 11,646,314 (GRCm39) |
W170L |
probably damaging |
Het |
Crygb |
T |
C |
1: 65,121,100 (GRCm39) |
I76V |
probably benign |
Het |
Cyp3a25 |
A |
G |
5: 145,931,746 (GRCm39) |
S121P |
probably damaging |
Het |
Cyp4b1 |
T |
C |
4: 115,484,024 (GRCm39) |
D395G |
probably damaging |
Het |
Dll4 |
T |
C |
2: 119,163,170 (GRCm39) |
V597A |
probably damaging |
Het |
Dock7 |
T |
C |
4: 98,833,528 (GRCm39) |
D1891G |
probably damaging |
Het |
Dsel |
T |
C |
1: 111,787,682 (GRCm39) |
D951G |
possibly damaging |
Het |
Dync2h1 |
C |
A |
9: 7,015,497 (GRCm39) |
V3603F |
possibly damaging |
Het |
Fam167b |
C |
A |
4: 129,472,078 (GRCm39) |
A31S |
probably damaging |
Het |
Fgfrl1 |
T |
A |
5: 108,852,539 (GRCm39) |
I25N |
probably damaging |
Het |
Gzf1 |
C |
T |
2: 148,526,569 (GRCm39) |
R347* |
probably null |
Het |
Heatr5b |
T |
A |
17: 79,103,825 (GRCm39) |
I1117F |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,907,767 (GRCm39) |
V456A |
possibly damaging |
Het |
Macc1 |
C |
A |
12: 119,411,251 (GRCm39) |
S673* |
probably null |
Het |
Mpp4 |
T |
C |
1: 59,160,581 (GRCm39) |
E574G |
probably damaging |
Het |
Muc20 |
C |
T |
16: 32,613,858 (GRCm39) |
M506I |
probably benign |
Het |
Ncbp1 |
A |
G |
4: 46,152,056 (GRCm39) |
T218A |
probably benign |
Het |
Nfxl1 |
A |
T |
5: 72,716,473 (GRCm39) |
V46E |
probably benign |
Het |
Nfyc |
G |
T |
4: 120,625,931 (GRCm39) |
|
probably benign |
Het |
Niban1 |
A |
G |
1: 151,581,766 (GRCm39) |
E454G |
probably benign |
Het |
Or51f5 |
T |
A |
7: 102,423,739 (GRCm39) |
S3T |
probably benign |
Het |
Or8g55 |
A |
T |
9: 39,784,643 (GRCm39) |
Q24L |
probably damaging |
Het |
Osbpl8 |
T |
C |
10: 111,122,101 (GRCm39) |
F681S |
possibly damaging |
Het |
Pcm1 |
G |
C |
8: 41,740,848 (GRCm39) |
E1031D |
probably damaging |
Het |
Pdcd11 |
A |
G |
19: 47,115,730 (GRCm39) |
E1486G |
probably benign |
Het |
Pex12 |
G |
T |
11: 83,188,860 (GRCm39) |
A45E |
probably damaging |
Het |
Pheta1 |
T |
A |
5: 121,991,314 (GRCm39) |
H225Q |
probably benign |
Het |
Pigm |
A |
G |
1: 172,204,384 (GRCm39) |
D40G |
probably damaging |
Het |
Pkp1 |
G |
T |
1: 135,808,478 (GRCm39) |
N496K |
probably benign |
Het |
Psmc4 |
T |
C |
7: 27,748,287 (GRCm39) |
I54V |
probably benign |
Het |
Rbm33 |
T |
C |
5: 28,599,481 (GRCm39) |
V951A |
unknown |
Het |
Selenbp2 |
G |
T |
3: 94,604,809 (GRCm39) |
|
probably benign |
Het |
Slc3a1 |
G |
A |
17: 85,368,263 (GRCm39) |
W510* |
probably null |
Het |
Stx12 |
A |
C |
4: 132,584,701 (GRCm39) |
|
probably benign |
Het |
Tas2r125 |
G |
T |
6: 132,887,085 (GRCm39) |
D158Y |
probably benign |
Het |
Tchp |
C |
A |
5: 114,857,682 (GRCm39) |
Q392K |
probably benign |
Het |
Tmed11 |
T |
A |
5: 108,926,855 (GRCm39) |
D139V |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,578,654 (GRCm39) |
V24080M |
probably damaging |
Het |
Ush2a |
G |
A |
1: 188,683,722 (GRCm39) |
G4967D |
probably damaging |
Het |
Vezf1 |
T |
C |
11: 87,964,156 (GRCm39) |
S103P |
probably benign |
Het |
Xpnpep3 |
T |
C |
15: 81,315,043 (GRCm39) |
S248P |
probably damaging |
Het |
Yipf2 |
G |
C |
9: 21,503,519 (GRCm39) |
|
probably null |
Het |
Zfp110 |
A |
T |
7: 12,570,290 (GRCm39) |
Q39L |
possibly damaging |
Het |
Zfp287 |
A |
T |
11: 62,605,039 (GRCm39) |
C623S |
probably damaging |
Het |
|
Other mutations in Cfap300 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Cfap300
|
APN |
9 |
8,022,433 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00481:Cfap300
|
APN |
9 |
8,042,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Cfap300
|
UTSW |
9 |
8,027,184 (GRCm39) |
missense |
probably benign |
0.40 |
R1455:Cfap300
|
UTSW |
9 |
8,022,457 (GRCm39) |
missense |
probably benign |
0.03 |
R1735:Cfap300
|
UTSW |
9 |
8,027,266 (GRCm39) |
missense |
probably benign |
0.01 |
R2140:Cfap300
|
UTSW |
9 |
8,022,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R2966:Cfap300
|
UTSW |
9 |
8,027,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4165:Cfap300
|
UTSW |
9 |
8,026,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Cfap300
|
UTSW |
9 |
8,026,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:Cfap300
|
UTSW |
9 |
8,027,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Cfap300
|
UTSW |
9 |
8,022,494 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7797:Cfap300
|
UTSW |
9 |
8,027,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7979:Cfap300
|
UTSW |
9 |
8,027,111 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8061:Cfap300
|
UTSW |
9 |
8,042,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|