Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019D03Rik |
T |
A |
1: 52,964,662 (GRCm39) |
H22L |
possibly damaging |
Het |
Abca2 |
C |
A |
2: 25,326,895 (GRCm39) |
Y590* |
probably null |
Het |
Acot1 |
G |
T |
12: 84,061,353 (GRCm39) |
E220* |
probably null |
Het |
Acsl5 |
T |
G |
19: 55,271,744 (GRCm39) |
I292S |
probably benign |
Het |
Acvr1b |
C |
T |
15: 101,092,710 (GRCm39) |
H118Y |
probably benign |
Het |
Aggf1 |
A |
G |
13: 95,507,450 (GRCm39) |
C112R |
probably benign |
Het |
Ap2a2 |
T |
A |
7: 141,178,689 (GRCm39) |
N105K |
probably benign |
Het |
Aste1 |
G |
A |
9: 105,273,880 (GRCm39) |
C40Y |
probably benign |
Het |
Carmil1 |
T |
C |
13: 24,323,357 (GRCm39) |
T232A |
probably benign |
Het |
Ccser2 |
A |
G |
14: 36,631,090 (GRCm39) |
F649L |
probably benign |
Het |
Cdcp3 |
T |
C |
7: 130,836,815 (GRCm39) |
V419A |
possibly damaging |
Het |
Cenpf |
G |
A |
1: 189,388,978 (GRCm39) |
T1618I |
probably damaging |
Het |
Ces5a |
G |
A |
8: 94,262,308 (GRCm39) |
Q10* |
probably null |
Het |
Cfap20dc |
A |
G |
14: 8,659,452 (GRCm38) |
F48L |
probably damaging |
Het |
Cfh |
A |
T |
1: 140,040,320 (GRCm39) |
L592Q |
possibly damaging |
Het |
Chchd6 |
T |
C |
6: 89,396,763 (GRCm39) |
H216R |
probably damaging |
Het |
Chrm5 |
A |
T |
2: 112,311,040 (GRCm39) |
H25Q |
probably damaging |
Het |
Clasp2 |
C |
T |
9: 113,737,866 (GRCm39) |
T1080I |
probably benign |
Het |
Clic6 |
G |
T |
16: 92,295,588 (GRCm39) |
G83C |
probably damaging |
Het |
Coro1c |
A |
T |
5: 113,988,781 (GRCm39) |
S187R |
probably damaging |
Het |
Cyp2a4 |
A |
G |
7: 26,008,004 (GRCm39) |
D137G |
probably benign |
Het |
Ddhd1 |
G |
T |
14: 45,894,679 (GRCm39) |
Q264K |
possibly damaging |
Het |
Dhdds |
A |
T |
4: 133,707,497 (GRCm39) |
Y235N |
probably damaging |
Het |
Ephb1 |
T |
C |
9: 101,918,486 (GRCm39) |
E341G |
probably damaging |
Het |
Fam53b |
T |
C |
7: 132,361,740 (GRCm39) |
D96G |
probably benign |
Het |
Fcgbpl1 |
A |
G |
7: 27,836,891 (GRCm39) |
D270G |
probably benign |
Het |
Fermt1 |
G |
T |
2: 132,781,388 (GRCm39) |
R67S |
probably benign |
Het |
Fmnl2 |
C |
A |
2: 52,998,312 (GRCm39) |
P559H |
unknown |
Het |
Foxo3 |
C |
T |
10: 42,073,021 (GRCm39) |
V499M |
probably damaging |
Het |
Frmpd2 |
T |
A |
14: 33,227,404 (GRCm39) |
F261I |
probably benign |
Het |
Garem2 |
T |
A |
5: 30,321,750 (GRCm39) |
L703Q |
possibly damaging |
Het |
Ggct |
T |
A |
6: 54,962,872 (GRCm39) |
I180F |
possibly damaging |
Het |
Gigyf2 |
T |
A |
1: 87,331,446 (GRCm39) |
I198K |
unknown |
Het |
Gucy2d |
T |
C |
7: 98,107,942 (GRCm39) |
F700L |
probably benign |
Het |
Gucy2g |
T |
A |
19: 55,198,816 (GRCm39) |
I776F |
probably damaging |
Het |
H2ac8 |
T |
C |
13: 23,755,045 (GRCm39) |
I80V |
probably benign |
Het |
Has1 |
T |
C |
17: 18,063,971 (GRCm39) |
Y556C |
probably damaging |
Het |
Hecw1 |
T |
C |
13: 14,546,567 (GRCm39) |
I145V |
probably damaging |
Het |
Helz2 |
T |
A |
2: 180,878,245 (GRCm39) |
Y851F |
possibly damaging |
Het |
Hes7 |
C |
A |
11: 69,013,711 (GRCm39) |
P190Q |
probably benign |
Het |
Hivep1 |
T |
C |
13: 42,322,779 (GRCm39) |
C79R |
|
Het |
Hnrnpr |
A |
G |
4: 136,056,681 (GRCm39) |
D227G |
probably damaging |
Het |
Hoxb9 |
C |
A |
11: 96,162,544 (GRCm39) |
F59L |
probably benign |
Het |
Hspb1 |
A |
T |
5: 135,917,930 (GRCm39) |
H135L |
probably benign |
Het |
Igkv1-122 |
T |
A |
6: 67,994,348 (GRCm39) |
F79I |
probably benign |
Het |
Igtp |
G |
C |
11: 58,097,800 (GRCm39) |
V324L |
possibly damaging |
Het |
Il18r1 |
G |
A |
1: 40,528,852 (GRCm39) |
A299T |
probably benign |
Het |
Kat14 |
C |
A |
2: 144,235,527 (GRCm39) |
P329Q |
probably damaging |
Het |
Krt33b |
T |
A |
11: 99,917,315 (GRCm39) |
Q179L |
probably benign |
Het |
Lrrk2 |
C |
T |
15: 91,607,365 (GRCm39) |
A576V |
probably damaging |
Het |
Map3k11 |
A |
G |
19: 5,740,624 (GRCm39) |
E117G |
probably damaging |
Het |
Mgme1 |
C |
T |
2: 144,114,156 (GRCm39) |
A86V |
probably benign |
Het |
Mks1 |
C |
A |
11: 87,753,766 (GRCm39) |
A534E |
probably damaging |
Het |
Mrpl28 |
T |
A |
17: 26,343,594 (GRCm39) |
I118N |
probably damaging |
Het |
Mrps22 |
T |
A |
9: 98,480,219 (GRCm39) |
Y102F |
probably damaging |
Het |
Myt1 |
A |
T |
2: 181,461,991 (GRCm39) |
H1000L |
probably damaging |
Het |
Ncoa5 |
A |
G |
2: 164,854,802 (GRCm39) |
Y107H |
possibly damaging |
Het |
Nipsnap3a |
A |
T |
4: 52,994,039 (GRCm39) |
Y40F |
probably benign |
Het |
Nlrc4 |
T |
A |
17: 74,752,580 (GRCm39) |
Y601F |
probably benign |
Het |
Obsl1 |
A |
G |
1: 75,466,267 (GRCm39) |
L1487P |
probably damaging |
Het |
Oit3 |
A |
T |
10: 59,264,173 (GRCm39) |
N320K |
probably damaging |
Het |
Or1e33 |
T |
C |
11: 73,738,825 (GRCm39) |
N42S |
probably damaging |
Het |
Or7a38 |
A |
G |
10: 78,753,559 (GRCm39) |
N295S |
probably damaging |
Het |
Otud4 |
T |
C |
8: 80,400,480 (GRCm39) |
S1065P |
probably benign |
Het |
P3h1 |
A |
C |
4: 119,094,008 (GRCm39) |
E221A |
possibly damaging |
Het |
Pgpep1 |
C |
A |
8: 71,103,899 (GRCm39) |
A124S |
probably benign |
Het |
Pigg |
T |
A |
5: 108,495,782 (GRCm39) |
S940T |
|
Het |
Proser3 |
G |
T |
7: 30,245,587 (GRCm39) |
T139K |
possibly damaging |
Het |
Prr36 |
C |
T |
8: 4,264,775 (GRCm39) |
R297H |
unknown |
Het |
Rai14 |
A |
T |
15: 10,587,947 (GRCm39) |
F306I |
possibly damaging |
Het |
Rnase13 |
T |
A |
14: 52,159,825 (GRCm39) |
N105Y |
probably damaging |
Het |
Ros1 |
A |
G |
10: 52,000,174 (GRCm39) |
I1138T |
probably benign |
Het |
Rsbn1 |
C |
A |
3: 103,822,146 (GRCm39) |
T127K |
possibly damaging |
Het |
Rsf1 |
G |
GCCGGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Rtca |
T |
C |
3: 116,301,413 (GRCm39) |
T45A |
probably benign |
Het |
Sema6b |
G |
T |
17: 56,439,500 (GRCm39) |
D82E |
probably benign |
Het |
Serpinc1 |
A |
T |
1: 160,821,179 (GRCm39) |
K209* |
probably null |
Het |
Slc4a1 |
C |
A |
11: 102,247,674 (GRCm39) |
R403L |
probably damaging |
Het |
Smtn |
A |
G |
11: 3,482,780 (GRCm39) |
V92A |
possibly damaging |
Het |
Spag9 |
T |
C |
11: 93,959,792 (GRCm39) |
V327A |
probably damaging |
Het |
Spdl1 |
T |
C |
11: 34,713,283 (GRCm39) |
N233S |
possibly damaging |
Het |
Stimate |
A |
G |
14: 30,593,463 (GRCm39) |
N189S |
probably damaging |
Het |
Ston2 |
T |
C |
12: 91,707,424 (GRCm39) |
D62G |
possibly damaging |
Het |
Sult2a5 |
A |
G |
7: 13,359,243 (GRCm39) |
D73G |
probably benign |
Het |
Ticrr |
A |
G |
7: 79,343,597 (GRCm39) |
E1154G |
probably benign |
Het |
Tmem163 |
A |
T |
1: 127,480,529 (GRCm39) |
M111K |
probably damaging |
Het |
Tmem266 |
T |
C |
9: 55,344,973 (GRCm39) |
V535A |
probably damaging |
Het |
Tmprss7 |
T |
A |
16: 45,484,555 (GRCm39) |
D535V |
probably damaging |
Het |
Tmt1a |
T |
C |
15: 100,203,215 (GRCm39) |
V163A |
probably damaging |
Het |
Tpcn1 |
A |
C |
5: 120,698,390 (GRCm39) |
I44S |
probably benign |
Het |
Trhde |
A |
T |
10: 114,636,697 (GRCm39) |
V170E |
probably damaging |
Het |
Trpt1 |
A |
T |
19: 6,975,578 (GRCm39) |
T111S |
probably benign |
Het |
Ttc13 |
T |
C |
8: 125,410,010 (GRCm39) |
T401A |
possibly damaging |
Het |
Ulbp1 |
T |
C |
10: 7,423,260 (GRCm39) |
I28V |
probably benign |
Het |
Vldlr |
A |
T |
19: 27,218,742 (GRCm39) |
D531V |
probably damaging |
Het |
Vmn2r85 |
T |
A |
10: 130,261,387 (GRCm39) |
T317S |
probably damaging |
Het |
Vps33a |
T |
C |
5: 123,696,705 (GRCm39) |
K316R |
probably benign |
Het |
Vwa3b |
A |
G |
1: 37,099,520 (GRCm39) |
N245S |
probably damaging |
Het |
Zfp266 |
A |
T |
9: 20,413,413 (GRCm39) |
C82* |
probably null |
Het |
Zfp746 |
T |
C |
6: 48,041,397 (GRCm39) |
K443R |
probably damaging |
Het |
|