Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
C |
T |
15: 64,704,705 |
V1003I |
possibly damaging |
Het |
Adgra3 |
T |
A |
5: 49,961,389 |
Y939F |
probably benign |
Het |
Adra2b |
T |
C |
2: 127,363,584 |
V2A |
probably benign |
Het |
Aga |
T |
A |
8: 53,521,129 |
Y296N |
possibly damaging |
Het |
Apc |
A |
G |
18: 34,268,317 |
Q52R |
probably damaging |
Het |
Arfgef1 |
A |
T |
1: 10,199,837 |
S362R |
probably benign |
Het |
Arhgef7 |
C |
T |
8: 11,758,451 |
|
probably benign |
Het |
Bmp5 |
A |
T |
9: 75,898,553 |
M446L |
probably damaging |
Het |
Carmil3 |
C |
T |
14: 55,496,077 |
T350I |
probably damaging |
Het |
Cd44 |
T |
A |
2: 102,853,018 |
T224S |
probably damaging |
Het |
Cep112 |
A |
T |
11: 108,752,434 |
I7F |
possibly damaging |
Het |
Chrna2 |
G |
A |
14: 66,142,232 |
A7T |
probably benign |
Het |
Cldn16 |
G |
A |
16: 26,482,520 |
V193I |
probably benign |
Het |
Clec4a3 |
G |
A |
6: 122,966,520 |
E100K |
possibly damaging |
Het |
Cntln |
C |
T |
4: 85,067,873 |
T1026I |
possibly damaging |
Het |
Cyp4v3 |
T |
A |
8: 45,308,527 |
I420F |
probably benign |
Het |
Dcbld2 |
G |
A |
16: 58,450,762 |
A301T |
|
Het |
Dnah1 |
A |
T |
14: 31,285,993 |
D2152E |
probably benign |
Het |
Dpy19l4 |
A |
G |
4: 11,290,195 |
V179A |
probably benign |
Het |
Dusp4 |
T |
A |
8: 34,817,308 |
I259N |
probably damaging |
Het |
Enpp1 |
T |
A |
10: 24,669,028 |
I318F |
probably benign |
Het |
Entpd6 |
T |
C |
2: 150,753,085 |
V15A |
possibly damaging |
Het |
Epb41l1 |
C |
G |
2: 156,522,003 |
Q811E |
probably benign |
Het |
Epb41l5 |
T |
C |
1: 119,642,562 |
H32R |
probably damaging |
Het |
Fam135b |
C |
T |
15: 71,462,214 |
V1044I |
possibly damaging |
Het |
Fbxw28 |
T |
A |
9: 109,338,789 |
|
probably null |
Het |
Flnb |
T |
G |
14: 7,892,874 |
V648G |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,904,688 |
Y1030* |
probably null |
Het |
Fndc3a |
T |
C |
14: 72,556,970 |
T787A |
probably benign |
Het |
Gli2 |
T |
A |
1: 118,855,457 |
H106L |
probably damaging |
Het |
Gm10283 |
T |
A |
8: 60,501,356 |
|
probably null |
Het |
Gm3336 |
C |
T |
8: 70,721,896 |
R67* |
probably null |
Het |
Gsr |
T |
G |
8: 33,693,908 |
I399M |
possibly damaging |
Het |
Gtf2ird2 |
T |
A |
5: 134,216,754 |
M618K |
probably damaging |
Het |
Gtf3c3 |
T |
A |
1: 54,423,563 |
D347V |
probably benign |
Het |
H2afy2 |
A |
T |
10: 61,757,831 |
I22N |
probably damaging |
Het |
Hspa12a |
T |
C |
19: 58,799,626 |
Y588C |
probably damaging |
Het |
Il20ra |
A |
G |
10: 19,759,412 |
E467G |
possibly damaging |
Het |
Inf2 |
A |
G |
12: 112,610,564 |
I991V |
unknown |
Het |
Irx6 |
T |
C |
8: 92,678,412 |
C303R |
probably damaging |
Het |
Kcnmb4 |
T |
A |
10: 116,473,476 |
K16* |
probably null |
Het |
Kirrel3 |
T |
C |
9: 34,944,442 |
L86P |
probably damaging |
Het |
Lipo5 |
A |
C |
19: 33,473,130 |
F21V |
|
Het |
Lrmp |
A |
T |
6: 145,171,664 |
M376L |
probably benign |
Het |
Lrrc31 |
T |
A |
3: 30,679,118 |
R482S |
probably benign |
Het |
Lrrc3b |
C |
T |
14: 15,358,159 |
C149Y |
probably damaging |
Het |
Lrrk1 |
A |
G |
7: 66,269,825 |
M446T |
probably benign |
Het |
Mettl14 |
C |
T |
3: 123,374,044 |
D222N |
probably benign |
Het |
Mfsd4b3 |
G |
A |
10: 39,948,076 |
H63Y |
probably benign |
Het |
Myo16 |
T |
C |
8: 10,376,175 |
W311R |
probably damaging |
Het |
Nccrp1 |
A |
T |
7: 28,546,203 |
N151K |
probably benign |
Het |
Obsl1 |
T |
C |
1: 75,503,849 |
D377G |
probably damaging |
Het |
Olfr1356 |
G |
T |
10: 78,847,742 |
P58T |
probably damaging |
Het |
Olfr1447 |
T |
A |
19: 12,901,214 |
T189S |
probably benign |
Het |
Olfr371 |
T |
A |
8: 85,231,284 |
I263N |
probably benign |
Het |
Olfr508 |
T |
A |
7: 108,630,299 |
C102* |
probably null |
Het |
Pigb |
T |
C |
9: 73,038,701 |
N63S |
probably damaging |
Het |
Plch2 |
T |
C |
4: 154,992,566 |
E577G |
probably benign |
Het |
Prkab2 |
T |
C |
3: 97,666,627 |
V194A |
probably benign |
Het |
Psd3 |
T |
C |
8: 67,963,809 |
I479V |
probably benign |
Het |
Ralgapb |
C |
A |
2: 158,437,344 |
P117T |
probably benign |
Het |
Ralgapb |
C |
G |
2: 158,495,469 |
T1116R |
probably damaging |
Het |
Rpap2 |
T |
A |
5: 107,620,495 |
S400T |
possibly damaging |
Het |
Rpgrip1l |
C |
A |
8: 91,280,828 |
W378L |
possibly damaging |
Het |
Rps20 |
T |
A |
4: 3,834,617 |
M82L |
probably benign |
Het |
Rps5 |
T |
C |
7: 12,925,513 |
M77T |
possibly damaging |
Het |
Scaf11 |
A |
G |
15: 96,420,490 |
S398P |
probably damaging |
Het |
Sdf2 |
T |
A |
11: 78,254,937 |
D153E |
probably benign |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,819,695 |
|
probably benign |
Het |
Slc12a9 |
T |
C |
5: 137,331,008 |
N128S |
probably damaging |
Het |
Slc25a32 |
C |
A |
15: 39,097,551 |
G246C |
probably damaging |
Het |
Slc38a4 |
C |
T |
15: 97,016,781 |
A64T |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,698,380 |
V1254A |
probably damaging |
Het |
Slx4 |
T |
C |
16: 3,990,247 |
K481R |
probably benign |
Het |
Tcea1 |
A |
G |
1: 4,889,509 |
T136A |
probably benign |
Het |
Thra |
A |
G |
11: 98,753,623 |
D13G |
possibly damaging |
Het |
Tmed9 |
G |
A |
13: 55,596,962 |
S227N |
probably benign |
Het |
Trim80 |
C |
A |
11: 115,440,712 |
T20K |
probably benign |
Het |
Trmt61a |
G |
T |
12: 111,682,822 |
V276L |
probably benign |
Het |
Trpc4ap |
T |
C |
2: 155,666,251 |
D160G |
possibly damaging |
Het |
Ubr5 |
C |
T |
15: 38,029,581 |
E467K |
|
Het |
Vars2 |
C |
A |
17: 35,661,649 |
G26W |
probably damaging |
Het |
Vmn1r226 |
G |
T |
17: 20,688,025 |
R173L |
possibly damaging |
Het |
Vmn1r29 |
G |
T |
6: 58,307,299 |
M1I |
probably null |
Het |
Vmn2r3 |
G |
T |
3: 64,261,382 |
P578Q |
possibly damaging |
Het |
Vmn2r57 |
A |
T |
7: 41,400,147 |
I726N |
possibly damaging |
Het |
Zfp39 |
A |
T |
11: 58,890,120 |
Y605* |
probably null |
Het |
|