Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530084C06Rik |
G |
T |
13: 31,742,978 (GRCm39) |
R92S |
unknown |
Het |
Adam1b |
A |
G |
5: 121,639,981 (GRCm39) |
C355R |
probably damaging |
Het |
Adamtsl3 |
T |
C |
7: 82,223,117 (GRCm39) |
L966P |
probably damaging |
Het |
Aldh18a1 |
A |
G |
19: 40,553,291 (GRCm39) |
C486R |
probably damaging |
Het |
Arhgap28 |
A |
G |
17: 68,178,961 (GRCm39) |
L350P |
probably damaging |
Het |
Art3 |
A |
G |
5: 92,551,514 (GRCm39) |
Q291R |
probably benign |
Het |
Asb15 |
A |
G |
6: 24,559,029 (GRCm39) |
|
probably null |
Het |
Bmp8b |
T |
C |
4: 122,999,448 (GRCm39) |
I102T |
possibly damaging |
Het |
Bsn |
T |
C |
9: 107,992,014 (GRCm39) |
D1246G |
probably benign |
Het |
Cass4 |
G |
A |
2: 172,268,718 (GRCm39) |
G267S |
probably benign |
Het |
Cass4 |
G |
T |
2: 172,268,719 (GRCm39) |
G267V |
probably benign |
Het |
Ccr7 |
T |
C |
11: 99,036,727 (GRCm39) |
Y65C |
probably damaging |
Het |
Clstn2 |
A |
C |
9: 97,464,597 (GRCm39) |
I186S |
probably benign |
Het |
Cyp2r1 |
A |
G |
7: 114,153,879 (GRCm39) |
I105T |
possibly damaging |
Het |
Efr3a |
T |
A |
15: 65,687,262 (GRCm39) |
|
probably null |
Het |
Erg |
A |
C |
16: 95,170,179 (GRCm39) |
|
probably null |
Het |
Eya4 |
A |
T |
10: 22,987,557 (GRCm39) |
V524E |
probably damaging |
Het |
Farp1 |
C |
A |
14: 121,472,589 (GRCm39) |
N241K |
possibly damaging |
Het |
Fat1 |
A |
T |
8: 45,442,031 (GRCm39) |
Y1111F |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,185,947 (GRCm39) |
E1607G |
probably damaging |
Het |
Fbn2 |
A |
T |
18: 58,153,536 (GRCm39) |
C2575* |
probably null |
Het |
Fsip2 |
A |
T |
2: 82,824,337 (GRCm39) |
D6690V |
probably damaging |
Het |
Fzd4 |
T |
C |
7: 89,056,346 (GRCm39) |
V131A |
possibly damaging |
Het |
Gfral |
T |
A |
9: 76,106,257 (GRCm39) |
N110I |
probably benign |
Het |
Glce |
T |
C |
9: 61,968,275 (GRCm39) |
D292G |
probably damaging |
Het |
Gm19410 |
T |
A |
8: 36,266,500 (GRCm39) |
I1051K |
probably benign |
Het |
Gm5773 |
A |
T |
3: 93,680,323 (GRCm39) |
|
probably benign |
Het |
Hcn3 |
A |
T |
3: 89,057,307 (GRCm39) |
H430Q |
probably null |
Het |
Hspa8 |
T |
A |
9: 40,714,255 (GRCm39) |
|
probably null |
Het |
Ifna7 |
A |
T |
4: 88,734,664 (GRCm39) |
D67V |
possibly damaging |
Het |
Kif5c |
T |
A |
2: 49,591,105 (GRCm39) |
M319K |
probably benign |
Het |
Klk7 |
G |
T |
7: 43,462,197 (GRCm39) |
|
probably null |
Het |
Kmt2c |
T |
C |
5: 25,619,968 (GRCm39) |
K102E |
possibly damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
C |
T |
2: 40,765,134 (GRCm39) |
M2897I |
|
Het |
Lysmd2 |
T |
C |
9: 75,544,519 (GRCm39) |
S211P |
probably damaging |
Het |
Magi1 |
T |
G |
6: 93,685,095 (GRCm39) |
E761A |
probably benign |
Het |
Mbd5 |
T |
A |
2: 49,141,355 (GRCm39) |
I106N |
probably damaging |
Het |
Mdc1 |
G |
A |
17: 36,159,749 (GRCm39) |
A669T |
probably null |
Het |
Mmp1b |
A |
G |
9: 7,384,753 (GRCm39) |
I265T |
probably benign |
Het |
Mmp2 |
T |
A |
8: 93,563,594 (GRCm39) |
L356Q |
probably null |
Het |
Mroh8 |
A |
G |
2: 157,111,492 (GRCm39) |
L154P |
probably benign |
Het |
Muc13 |
T |
C |
16: 33,619,806 (GRCm39) |
S185P |
unknown |
Het |
Nuak1 |
T |
A |
10: 84,210,403 (GRCm39) |
I562F |
probably benign |
Het |
Obscn |
C |
A |
11: 58,933,664 (GRCm39) |
|
probably null |
Het |
Or51t4 |
T |
C |
7: 102,597,798 (GRCm39) |
I42T |
possibly damaging |
Het |
Or5w14 |
A |
T |
2: 87,542,115 (GRCm39) |
M45K |
probably damaging |
Het |
Or9k7 |
T |
C |
10: 130,046,853 (GRCm39) |
M49V |
probably benign |
Het |
Pex3 |
T |
C |
10: 13,418,414 (GRCm39) |
M81V |
probably benign |
Het |
Pex5l |
T |
A |
3: 33,136,184 (GRCm39) |
I12F |
probably benign |
Het |
Phf3 |
G |
T |
1: 30,870,556 (GRCm39) |
T164N |
probably benign |
Het |
Phpt1 |
G |
T |
2: 25,464,844 (GRCm39) |
A3E |
probably benign |
Het |
Pja2 |
A |
T |
17: 64,616,410 (GRCm39) |
L162M |
probably damaging |
Het |
Pkdrej |
T |
A |
15: 85,703,994 (GRCm39) |
K647N |
probably damaging |
Het |
Ppp2r1a |
T |
C |
17: 21,182,944 (GRCm39) |
S543P |
possibly damaging |
Het |
Prdm13 |
C |
A |
4: 21,679,072 (GRCm39) |
D473Y |
probably damaging |
Het |
Prl6a1 |
A |
T |
13: 27,502,954 (GRCm39) |
E183D |
probably damaging |
Het |
Psmd3 |
C |
T |
11: 98,581,787 (GRCm39) |
T304M |
probably benign |
Het |
Ptpn5 |
C |
T |
7: 46,735,874 (GRCm39) |
|
probably null |
Het |
Rassf6 |
T |
G |
5: 90,754,661 (GRCm39) |
I206L |
probably damaging |
Het |
Rif1 |
A |
G |
2: 51,968,519 (GRCm39) |
H234R |
possibly damaging |
Het |
Rint1 |
T |
C |
5: 24,020,702 (GRCm39) |
V575A |
probably benign |
Het |
Ros1 |
G |
A |
10: 52,021,930 (GRCm39) |
T639I |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,752,871 (GRCm39) |
F1817L |
probably benign |
Het |
Ska1 |
T |
C |
18: 74,333,088 (GRCm39) |
D110G |
probably benign |
Het |
Slc25a41 |
G |
A |
17: 57,340,791 (GRCm39) |
T227I |
probably damaging |
Het |
Slc6a15 |
T |
C |
10: 103,224,998 (GRCm39) |
S29P |
probably benign |
Het |
Slc8a3 |
A |
T |
12: 81,361,544 (GRCm39) |
I425K |
probably benign |
Het |
Sox8 |
T |
A |
17: 25,786,935 (GRCm39) |
Q256L |
probably damaging |
Het |
Tars3 |
T |
C |
7: 65,297,341 (GRCm39) |
V152A |
probably damaging |
Het |
Tbx10 |
A |
T |
19: 4,046,651 (GRCm39) |
T44S |
probably benign |
Het |
Terb1 |
T |
A |
8: 105,224,716 (GRCm39) |
I52F |
possibly damaging |
Het |
Tes |
AGCCGGCC |
AGCC |
6: 17,099,740 (GRCm39) |
|
probably null |
Het |
Tgm1 |
A |
G |
14: 55,943,360 (GRCm39) |
V527A |
probably benign |
Het |
Tmed10 |
G |
T |
12: 85,391,036 (GRCm39) |
Y167* |
probably null |
Het |
Tmem165 |
T |
G |
5: 76,356,415 (GRCm39) |
S318R |
possibly damaging |
Het |
Trim9 |
G |
T |
12: 70,393,715 (GRCm39) |
S76R |
probably damaging |
Het |
Tti1 |
A |
G |
2: 157,849,088 (GRCm39) |
V717A |
probably damaging |
Het |
Vmn2r86 |
T |
A |
10: 130,282,697 (GRCm39) |
I640F |
probably damaging |
Het |
Vwf |
A |
G |
6: 125,603,230 (GRCm39) |
N860S |
|
Het |
Xirp2 |
A |
G |
2: 67,339,241 (GRCm39) |
K494R |
possibly damaging |
Het |
Zkscan4 |
G |
A |
13: 21,668,419 (GRCm39) |
S319N |
probably damaging |
Het |
|