Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acod1 |
T |
C |
14: 103,292,882 (GRCm39) |
S469P |
possibly damaging |
Het |
Adgrf5 |
A |
T |
17: 43,757,927 (GRCm39) |
N787I |
possibly damaging |
Het |
Ank2 |
T |
C |
3: 126,723,493 (GRCm39) |
T945A |
probably benign |
Het |
Aox4 |
T |
A |
1: 58,293,093 (GRCm39) |
I863N |
probably damaging |
Het |
Ap3d1 |
A |
G |
10: 80,548,019 (GRCm39) |
I891T |
probably benign |
Het |
Apex1 |
A |
G |
14: 51,163,714 (GRCm39) |
T109A |
probably benign |
Het |
Arhgef1 |
G |
A |
7: 24,618,697 (GRCm39) |
G107S |
probably damaging |
Het |
Atxn7l1 |
A |
G |
12: 33,417,599 (GRCm39) |
T587A |
probably damaging |
Het |
Atxn7l3 |
T |
C |
11: 102,184,729 (GRCm39) |
D128G |
probably damaging |
Het |
Cacna1h |
T |
C |
17: 25,611,427 (GRCm39) |
Y457C |
probably damaging |
Het |
Ccdc60 |
A |
C |
5: 116,310,514 (GRCm39) |
C183G |
probably damaging |
Het |
Cep131 |
G |
A |
11: 119,958,011 (GRCm39) |
R772* |
probably null |
Het |
Cnst |
C |
T |
1: 179,407,279 (GRCm39) |
P109S |
probably benign |
Het |
Crtc2 |
G |
T |
3: 90,169,877 (GRCm39) |
L509F |
probably damaging |
Het |
Ctsr |
A |
T |
13: 61,309,750 (GRCm39) |
I153N |
possibly damaging |
Het |
Dffa |
A |
T |
4: 149,188,708 (GRCm39) |
M1L |
possibly damaging |
Het |
Dnajc16 |
G |
A |
4: 141,490,964 (GRCm39) |
R729* |
probably null |
Het |
Eef2k |
T |
A |
7: 120,498,594 (GRCm39) |
C91* |
probably null |
Het |
Eml5 |
T |
C |
12: 98,782,283 (GRCm39) |
D1336G |
probably damaging |
Het |
F12 |
G |
A |
13: 55,569,035 (GRCm39) |
|
probably null |
Het |
Fam43b |
G |
C |
4: 138,122,409 (GRCm39) |
R304G |
probably benign |
Het |
Fbxo40 |
A |
T |
16: 36,789,445 (GRCm39) |
L555Q |
probably damaging |
Het |
Frmpd1 |
T |
C |
4: 45,283,698 (GRCm39) |
S840P |
probably damaging |
Het |
Gadd45a |
C |
T |
6: 67,013,989 (GRCm39) |
|
probably null |
Het |
Galnt7 |
T |
C |
8: 57,985,658 (GRCm39) |
|
probably benign |
Het |
Gm5592 |
G |
A |
7: 40,807,259 (GRCm39) |
|
probably benign |
Het |
Gpr171 |
T |
C |
3: 59,005,506 (GRCm39) |
T90A |
probably damaging |
Het |
Gpr82 |
A |
T |
X: 13,531,577 (GRCm39) |
T42S |
probably benign |
Het |
Hk2 |
T |
C |
6: 82,713,657 (GRCm39) |
E447G |
possibly damaging |
Het |
Hspa4l |
C |
A |
3: 40,739,821 (GRCm39) |
H698Q |
probably benign |
Het |
Idi1 |
G |
T |
13: 8,935,968 (GRCm39) |
A25S |
probably benign |
Het |
Kdm4a |
C |
T |
4: 118,010,428 (GRCm39) |
R605H |
probably damaging |
Het |
Nhlrc2 |
T |
C |
19: 56,576,703 (GRCm39) |
|
probably null |
Het |
Nt5c2 |
A |
G |
19: 46,884,957 (GRCm39) |
V252A |
probably damaging |
Het |
Or52ae7 |
T |
A |
7: 103,119,867 (GRCm39) |
V207E |
probably damaging |
Het |
Pbp2 |
A |
G |
6: 135,287,143 (GRCm39) |
L68P |
probably benign |
Het |
Pcnx3 |
G |
T |
19: 5,728,995 (GRCm39) |
T547K |
probably benign |
Het |
Ppp1r12a |
T |
C |
10: 108,089,362 (GRCm39) |
|
probably benign |
Het |
Prmt9 |
G |
A |
8: 78,294,894 (GRCm39) |
V413I |
probably benign |
Het |
Pudp |
T |
C |
18: 50,701,124 (GRCm39) |
N203S |
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,371,765 (GRCm39) |
|
probably benign |
Het |
Sall3 |
G |
A |
18: 81,015,717 (GRCm39) |
T737M |
probably damaging |
Het |
Scn2b |
A |
G |
9: 45,036,759 (GRCm39) |
N89S |
possibly damaging |
Het |
Sgsm1 |
A |
G |
5: 113,411,125 (GRCm39) |
V580A |
probably benign |
Het |
Slc13a4 |
C |
A |
6: 35,248,539 (GRCm39) |
|
probably null |
Het |
Slc4a4 |
A |
C |
5: 89,380,698 (GRCm39) |
S1015R |
probably benign |
Het |
Slc8a1 |
T |
C |
17: 81,955,803 (GRCm39) |
T412A |
probably benign |
Het |
Spag17 |
A |
T |
3: 100,014,075 (GRCm39) |
D2116V |
probably damaging |
Het |
Trim55 |
T |
C |
3: 19,727,120 (GRCm39) |
F396L |
probably benign |
Het |
Usp54 |
C |
A |
14: 20,638,488 (GRCm39) |
M197I |
probably damaging |
Het |
Vmn1r189 |
A |
T |
13: 22,286,439 (GRCm39) |
F133I |
possibly damaging |
Het |
Zfp735 |
T |
C |
11: 73,602,282 (GRCm39) |
S409P |
probably benign |
Het |
|
Other mutations in H2-M10.6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01018:H2-M10.6
|
APN |
17 |
37,123,112 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01590:H2-M10.6
|
APN |
17 |
37,123,641 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03200:H2-M10.6
|
APN |
17 |
37,124,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03278:H2-M10.6
|
APN |
17 |
37,124,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R0018:H2-M10.6
|
UTSW |
17 |
37,124,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:H2-M10.6
|
UTSW |
17 |
37,123,133 (GRCm39) |
missense |
probably damaging |
0.99 |
R0194:H2-M10.6
|
UTSW |
17 |
37,124,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:H2-M10.6
|
UTSW |
17 |
37,124,052 (GRCm39) |
missense |
probably benign |
|
R1757:H2-M10.6
|
UTSW |
17 |
37,124,043 (GRCm39) |
missense |
probably benign |
0.00 |
R1773:H2-M10.6
|
UTSW |
17 |
37,123,076 (GRCm39) |
missense |
probably benign |
0.00 |
R2029:H2-M10.6
|
UTSW |
17 |
37,124,799 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3409:H2-M10.6
|
UTSW |
17 |
37,124,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R4373:H2-M10.6
|
UTSW |
17 |
37,123,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:H2-M10.6
|
UTSW |
17 |
37,123,425 (GRCm39) |
missense |
probably benign |
0.04 |
R5684:H2-M10.6
|
UTSW |
17 |
37,124,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:H2-M10.6
|
UTSW |
17 |
37,123,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6180:H2-M10.6
|
UTSW |
17 |
37,125,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:H2-M10.6
|
UTSW |
17 |
37,124,836 (GRCm39) |
missense |
probably damaging |
0.96 |
R8245:H2-M10.6
|
UTSW |
17 |
37,124,155 (GRCm39) |
critical splice donor site |
probably null |
|
R9687:H2-M10.6
|
UTSW |
17 |
37,125,147 (GRCm39) |
missense |
probably benign |
0.01 |
R9705:H2-M10.6
|
UTSW |
17 |
37,123,642 (GRCm39) |
missense |
probably benign |
0.09 |
|