Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 138,066,718 |
K556R |
probably damaging |
Het |
4933406P04Rik |
A |
T |
10: 20,311,147 |
|
probably benign |
Het |
A530099J19Rik |
T |
C |
13: 19,729,679 |
|
noncoding transcript |
Het |
Acmsd |
C |
A |
1: 127,759,756 |
Y258* |
probably null |
Het |
Adgrf5 |
A |
T |
17: 43,451,082 |
I1223F |
probably damaging |
Het |
Afp |
C |
T |
5: 90,490,796 |
P6S |
probably benign |
Het |
Agap2 |
C |
A |
10: 127,091,671 |
H1120Q |
probably damaging |
Het |
Angpt1 |
A |
G |
15: 42,512,404 |
V152A |
probably damaging |
Het |
Ankrd1 |
A |
T |
19: 36,119,359 |
F23I |
probably damaging |
Het |
Armc12 |
T |
C |
17: 28,538,895 |
S334P |
possibly damaging |
Het |
Arnt2 |
C |
A |
7: 84,275,375 |
D415Y |
probably damaging |
Het |
Cacna1s |
G |
T |
1: 136,076,854 |
V131L |
probably benign |
Het |
Cacna2d2 |
T |
C |
9: 107,527,433 |
V1141A |
possibly damaging |
Het |
Cfap61 |
T |
C |
2: 146,042,622 |
L580P |
probably damaging |
Het |
Chga |
A |
T |
12: 102,555,905 |
S23C |
probably damaging |
Het |
Chrna5 |
A |
G |
9: 55,004,875 |
T320A |
probably damaging |
Het |
Col17a1 |
G |
T |
19: 47,650,862 |
N1081K |
possibly damaging |
Het |
Cox7b2 |
A |
T |
5: 71,443,063 |
C51S |
possibly damaging |
Het |
Cwc22 |
A |
T |
2: 77,929,453 |
D83E |
possibly damaging |
Het |
D130043K22Rik |
A |
C |
13: 24,883,894 |
D871A |
probably damaging |
Het |
Dab2 |
A |
T |
15: 6,435,467 |
M361L |
probably benign |
Het |
Dnah11 |
A |
C |
12: 117,916,788 |
Y3866D |
probably damaging |
Het |
Dnmbp |
A |
G |
19: 43,901,720 |
I536T |
probably benign |
Het |
Ehmt1 |
A |
T |
2: 24,884,290 |
S43R |
probably damaging |
Het |
Ercc5 |
T |
C |
1: 44,173,380 |
L666P |
probably benign |
Het |
F5 |
A |
G |
1: 164,182,834 |
H378R |
probably damaging |
Het |
Fam84a |
T |
C |
12: 14,150,225 |
Y167C |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,283,892 |
N1998K |
probably damaging |
Het |
Fbxo28 |
T |
C |
1: 182,341,534 |
D13G |
unknown |
Het |
Gm4758 |
T |
A |
16: 36,312,533 |
D57E |
probably damaging |
Het |
Gm5624 |
T |
A |
14: 44,561,845 |
N41I |
probably damaging |
Het |
Gm6768 |
A |
T |
12: 119,261,771 |
|
noncoding transcript |
Het |
Gm8104 |
A |
G |
14: 43,101,571 |
I73V |
possibly damaging |
Het |
Gpr68 |
G |
A |
12: 100,878,908 |
P126S |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,582,685 |
T156S |
possibly damaging |
Het |
Hacl1 |
T |
A |
14: 31,614,264 |
Y429F |
probably damaging |
Het |
Haus3 |
A |
C |
5: 34,163,572 |
L510R |
probably damaging |
Het |
Helq |
C |
T |
5: 100,774,124 |
G738D |
probably benign |
Het |
Hsd3b2 |
G |
C |
3: 98,712,237 |
P131A |
probably damaging |
Het |
Il22ra1 |
G |
T |
4: 135,748,160 |
C247F |
probably benign |
Het |
Ivl |
T |
C |
3: 92,572,584 |
E58G |
unknown |
Het |
Kcnk9 |
G |
T |
15: 72,546,099 |
Q61K |
probably benign |
Het |
Kremen1 |
CGGG |
CGGGGGG |
11: 5,201,791 |
|
probably benign |
Het |
Loxhd1 |
G |
T |
18: 77,402,502 |
A1314S |
probably damaging |
Het |
Lrba |
A |
G |
3: 86,351,868 |
I1397V |
probably benign |
Het |
Lrig3 |
T |
A |
10: 125,997,051 |
|
probably null |
Het |
Lrrc36 |
A |
G |
8: 105,449,765 |
D378G |
probably damaging |
Het |
Lrrc49 |
G |
A |
9: 60,598,191 |
T527I |
probably damaging |
Het |
Map4k4 |
C |
A |
1: 40,023,460 |
T1195K |
probably damaging |
Het |
Mrps33 |
G |
A |
6: 39,802,495 |
R89C |
probably damaging |
Het |
Mtor |
T |
C |
4: 148,462,892 |
V444A |
probably benign |
Het |
Myh2 |
A |
G |
11: 67,188,938 |
E1046G |
probably damaging |
Het |
Myo15b |
G |
T |
11: 115,880,509 |
|
probably null |
Het |
Myo5c |
T |
C |
9: 75,246,164 |
Y111H |
probably damaging |
Het |
Ndufv2 |
G |
C |
17: 66,083,486 |
T163R |
probably damaging |
Het |
Nf1 |
A |
G |
11: 79,553,968 |
N373S |
possibly damaging |
Het |
Nwd2 |
A |
G |
5: 63,805,574 |
M834V |
probably benign |
Het |
Ogfod2 |
T |
C |
5: 124,114,956 |
V343A |
probably damaging |
Het |
Olfr1220 |
T |
A |
2: 89,097,706 |
T74S |
probably benign |
Het |
Olfr401 |
A |
T |
11: 74,121,408 |
T40S |
probably benign |
Het |
Olfr597 |
T |
A |
7: 103,320,414 |
M1K |
probably null |
Het |
Olfr610 |
T |
C |
7: 103,506,041 |
I302V |
possibly damaging |
Het |
Olfr736 |
C |
A |
14: 50,393,329 |
S191* |
probably null |
Het |
Olfr744 |
C |
T |
14: 50,618,686 |
L155F |
probably benign |
Het |
Olfr954 |
A |
T |
9: 39,462,114 |
I228F |
probably damaging |
Het |
Parp1 |
T |
A |
1: 180,600,526 |
|
probably null |
Het |
Ppp3ca |
A |
T |
3: 136,935,031 |
I448F |
probably damaging |
Het |
Prss44 |
T |
C |
9: 110,817,204 |
V333A |
probably damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 |
R441* |
probably null |
Het |
Rars |
A |
C |
11: 35,825,995 |
D231E |
probably benign |
Het |
Rfc1 |
T |
C |
5: 65,264,379 |
Y1059C |
probably damaging |
Het |
Rilpl1 |
T |
A |
5: 124,514,656 |
I2F |
probably damaging |
Het |
Sarm1 |
G |
T |
11: 78,490,994 |
A221E |
possibly damaging |
Het |
Serpina3f |
A |
G |
12: 104,217,406 |
T176A |
probably damaging |
Het |
Slc22a20 |
T |
C |
19: 5,985,667 |
E131G |
probably benign |
Het |
Slc26a11 |
T |
C |
11: 119,373,153 |
V343A |
probably damaging |
Het |
Slc2a4 |
A |
G |
11: 69,946,307 |
I9T |
probably benign |
Het |
Slc39a6 |
G |
T |
18: 24,585,202 |
D599E |
probably damaging |
Het |
Slc5a6 |
G |
T |
5: 31,040,676 |
S285* |
probably null |
Het |
Spata9 |
A |
G |
13: 75,977,641 |
H81R |
probably benign |
Het |
St7l |
A |
G |
3: 104,919,496 |
E436G |
probably damaging |
Het |
Tecrl |
A |
G |
5: 83,279,230 |
I357T |
probably damaging |
Het |
Thop1 |
C |
T |
10: 81,073,209 |
R25C |
probably damaging |
Het |
Tmprss12 |
A |
G |
15: 100,292,547 |
E266G |
probably benign |
Het |
Tpgs1 |
T |
A |
10: 79,675,510 |
V162D |
possibly damaging |
Het |
Trpa1 |
C |
T |
1: 14,874,424 |
R1032Q |
probably benign |
Het |
Tspan12 |
A |
G |
6: 21,795,700 |
Y164H |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,407,963 |
Y869H |
probably damaging |
Het |
Vmn1r21 |
A |
G |
6: 57,843,814 |
I215T |
probably benign |
Het |
Zan |
A |
T |
5: 137,386,451 |
S5104T |
unknown |
Het |
Zfp318 |
T |
C |
17: 46,412,054 |
V1661A |
probably benign |
Het |
Zfp365 |
C |
T |
10: 67,888,942 |
R372K |
probably damaging |
Het |
|