Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
C |
11: 109,971,814 |
K375R |
possibly damaging |
Het |
Adrb2 |
T |
C |
18: 62,178,800 |
N318S |
probably damaging |
Het |
Akap5 |
A |
C |
12: 76,329,262 |
E489D |
possibly damaging |
Het |
Aldh7a1 |
T |
A |
18: 56,532,061 |
I385F |
probably damaging |
Het |
Astn1 |
T |
A |
1: 158,579,576 |
|
probably benign |
Het |
Atp7b |
T |
A |
8: 21,997,358 |
T1314S |
probably damaging |
Het |
Bhmt2 |
C |
A |
13: 93,662,339 |
G325C |
probably damaging |
Het |
Brpf1 |
T |
A |
6: 113,319,089 |
V781E |
probably benign |
Het |
Cacna1c |
T |
A |
6: 118,598,759 |
Y1860F |
probably benign |
Het |
Ccdc7a |
T |
C |
8: 129,061,681 |
T56A |
probably damaging |
Het |
Cep78 |
A |
G |
19: 15,959,663 |
S560P |
probably damaging |
Het |
Cnot1 |
G |
A |
8: 95,743,213 |
T1343I |
probably benign |
Het |
Coq10b |
T |
C |
1: 55,064,257 |
S65P |
probably damaging |
Het |
Creld1 |
T |
A |
6: 113,489,784 |
C243S |
probably damaging |
Het |
Cst12 |
A |
T |
2: 148,793,252 |
I121F |
possibly damaging |
Het |
Cyp26a1 |
A |
C |
19: 37,698,860 |
E165A |
probably benign |
Het |
Cyp2d12 |
T |
G |
15: 82,558,136 |
M273R |
probably damaging |
Het |
Dnajb7 |
T |
A |
15: 81,407,456 |
S227C |
probably damaging |
Het |
Evc |
T |
A |
5: 37,319,035 |
Q390L |
probably damaging |
Het |
F830016B08Rik |
T |
A |
18: 60,300,898 |
L351* |
probably null |
Het |
Fga |
T |
C |
3: 83,031,838 |
S507P |
probably benign |
Het |
Gba |
A |
T |
3: 89,206,148 |
Y239F |
probably damaging |
Het |
Golga2 |
C |
A |
2: 32,305,984 |
Y843* |
probably null |
Het |
Gria4 |
C |
A |
9: 4,793,865 |
L64F |
probably damaging |
Het |
Hectd3 |
A |
G |
4: 117,002,994 |
Y803C |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,669,421 |
K2812E |
probably damaging |
Het |
Il17b |
T |
G |
18: 61,690,245 |
V50G |
probably damaging |
Het |
Itga2b |
A |
T |
11: 102,466,325 |
L243* |
probably null |
Het |
Kank4 |
C |
A |
4: 98,779,029 |
V394L |
possibly damaging |
Het |
Kat14 |
T |
A |
2: 144,373,791 |
D65E |
probably benign |
Het |
Kcnh3 |
T |
C |
15: 99,238,209 |
Y696H |
probably damaging |
Het |
Kctd19 |
C |
A |
8: 105,395,376 |
D180Y |
probably damaging |
Het |
Klra8 |
A |
C |
6: 130,115,640 |
S233A |
probably benign |
Het |
Masp2 |
A |
T |
4: 148,612,106 |
T387S |
possibly damaging |
Het |
Midn |
C |
A |
10: 80,154,123 |
T275N |
probably damaging |
Het |
Mis18bp1 |
A |
G |
12: 65,133,813 |
F965L |
probably benign |
Het |
Myo3a |
G |
T |
2: 22,282,634 |
V186L |
probably damaging |
Het |
Ncoa2 |
T |
A |
1: 13,165,057 |
N884I |
probably benign |
Het |
Olfr1082 |
T |
A |
2: 86,594,604 |
T75S |
probably damaging |
Het |
Olfr272 |
A |
T |
4: 52,911,502 |
C97* |
probably null |
Het |
Olfr963 |
T |
C |
9: 39,669,720 |
I221T |
probably damaging |
Het |
Osr2 |
T |
C |
15: 35,300,667 |
V123A |
probably benign |
Het |
P4ha2 |
A |
G |
11: 54,117,645 |
H226R |
probably benign |
Het |
Pcdhb16 |
T |
A |
18: 37,478,098 |
V37E |
probably benign |
Het |
Pcdhb18 |
T |
A |
18: 37,489,620 |
M1K |
probably null |
Het |
Pcsk1 |
T |
A |
13: 75,098,047 |
Y181* |
probably null |
Het |
Pros1 |
G |
T |
16: 62,885,512 |
C63F |
probably damaging |
Het |
Ranbp3l |
T |
A |
15: 9,065,001 |
C353* |
probably null |
Het |
Rev3l |
T |
C |
10: 39,838,443 |
Y2388H |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,110,324 |
|
probably benign |
Het |
Rpl12-ps1 |
G |
T |
1: 36,958,377 |
|
noncoding transcript |
Het |
Rttn |
T |
C |
18: 89,113,350 |
V1951A |
probably benign |
Het |
Scn9a |
G |
A |
2: 66,505,027 |
|
probably benign |
Het |
Sdk1 |
T |
C |
5: 142,127,836 |
F1546S |
probably damaging |
Het |
Sh3glb2 |
C |
T |
2: 30,354,975 |
R71Q |
probably damaging |
Het |
Slc30a6 |
T |
C |
17: 74,408,847 |
F101L |
probably benign |
Het |
Snrpd1 |
T |
C |
18: 10,626,913 |
I60T |
probably damaging |
Het |
Sox10 |
T |
A |
15: 79,159,178 |
E218D |
probably benign |
Het |
Tekt3 |
C |
A |
11: 63,070,490 |
H162N |
probably damaging |
Het |
Tnfsf13 |
T |
C |
11: 69,684,738 |
S246G |
possibly damaging |
Het |
Trim10 |
T |
A |
17: 36,872,454 |
I214N |
probably damaging |
Het |
Trp63 |
C |
A |
16: 25,889,253 |
D566E |
probably damaging |
Het |
Uck2 |
T |
C |
1: 167,234,724 |
D156G |
probably damaging |
Het |
Zfp386 |
T |
A |
12: 116,059,605 |
S314R |
possibly damaging |
Het |
Zfp467 |
C |
T |
6: 48,438,236 |
R494H |
probably damaging |
Het |
Zfyve26 |
T |
C |
12: 79,252,151 |
E445G |
probably damaging |
Het |
|