Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810024B03Rik |
T |
C |
2: 127,028,873 (GRCm39) |
T109A |
probably damaging |
Het |
A430005L14Rik |
GCC |
G |
4: 154,045,410 (GRCm39) |
|
probably null |
Het |
Actr1a |
T |
C |
19: 46,384,103 (GRCm39) |
D5G |
possibly damaging |
Het |
Adra2c |
A |
G |
5: 35,438,217 (GRCm39) |
T330A |
probably benign |
Het |
Ahcyl2 |
C |
T |
6: 29,859,697 (GRCm39) |
|
probably benign |
Het |
Ahnak |
T |
C |
19: 8,984,539 (GRCm39) |
V1941A |
probably damaging |
Het |
Akr1b7 |
G |
A |
6: 34,389,411 (GRCm39) |
|
probably null |
Het |
Anapc15 |
C |
T |
7: 101,547,810 (GRCm39) |
P68L |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,746,875 (GRCm39) |
V570A |
probably damaging |
Het |
Ano4 |
T |
C |
10: 88,948,702 (GRCm39) |
E302G |
probably damaging |
Het |
Bop1 |
A |
T |
15: 76,339,489 (GRCm39) |
H285Q |
probably damaging |
Het |
Btbd19 |
G |
A |
4: 116,980,957 (GRCm39) |
A104V |
probably damaging |
Het |
Catsperb |
A |
T |
12: 101,560,543 (GRCm39) |
I845L |
possibly damaging |
Het |
Ccdc28b |
G |
T |
4: 129,513,238 (GRCm39) |
Q184K |
probably damaging |
Het |
Cd101 |
A |
G |
3: 100,926,126 (GRCm39) |
S198P |
probably damaging |
Het |
Cdc7 |
A |
T |
5: 107,117,163 (GRCm39) |
|
probably null |
Het |
Cdhr2 |
A |
G |
13: 54,884,269 (GRCm39) |
D1268G |
probably benign |
Het |
Celsr3 |
C |
T |
9: 108,705,781 (GRCm39) |
R755W |
probably damaging |
Het |
Chrnb1 |
T |
A |
11: 69,684,979 (GRCm39) |
N117I |
probably damaging |
Het |
Chst11 |
C |
A |
10: 83,027,083 (GRCm39) |
P170Q |
probably damaging |
Het |
Clca3b |
A |
G |
3: 144,552,932 (GRCm39) |
Y98H |
probably damaging |
Het |
Crnkl1 |
A |
G |
2: 145,770,132 (GRCm39) |
V237A |
possibly damaging |
Het |
Ctnnbl1 |
G |
A |
2: 157,659,752 (GRCm39) |
|
probably null |
Het |
Dbndd1 |
C |
A |
8: 124,236,582 (GRCm39) |
R95S |
probably damaging |
Het |
Ddx3y |
A |
G |
Y: 1,265,965 (GRCm39) |
V344A |
probably damaging |
Het |
Defb30 |
A |
T |
14: 63,273,559 (GRCm39) |
|
probably null |
Het |
Dennd10 |
T |
C |
19: 60,823,274 (GRCm39) |
L303P |
probably benign |
Het |
Dnah17 |
C |
T |
11: 118,018,108 (GRCm39) |
R129Q |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,362,891 (GRCm39) |
M3818L |
probably benign |
Het |
Dusp4 |
G |
T |
8: 35,284,458 (GRCm39) |
D258Y |
probably damaging |
Het |
E2f1 |
A |
T |
2: 154,406,368 (GRCm39) |
F103I |
probably benign |
Het |
Elavl2 |
T |
C |
4: 91,149,055 (GRCm39) |
Y248C |
probably damaging |
Het |
Ephb3 |
T |
C |
16: 21,037,855 (GRCm39) |
V310A |
possibly damaging |
Het |
Erbin |
A |
G |
13: 103,993,917 (GRCm39) |
|
probably null |
Het |
Etv4 |
A |
T |
11: 101,666,167 (GRCm39) |
H120Q |
probably damaging |
Het |
Fcgbpl1 |
T |
C |
7: 27,839,608 (GRCm39) |
F474L |
probably benign |
Het |
Flot2 |
T |
A |
11: 77,940,314 (GRCm39) |
C20* |
probably null |
Het |
Fsip2 |
G |
A |
2: 82,821,262 (GRCm39) |
G5665D |
probably benign |
Het |
Gad1-ps |
G |
A |
10: 99,281,009 (GRCm39) |
|
noncoding transcript |
Het |
Glrp1 |
TTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGTTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGTTGGTGCTGCTGGTGCTGCTG |
TTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGTTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGCTGGTGCTGTTGGTGCTGCTGGTGCTGCTG |
1: 88,431,066 (GRCm39) |
|
probably benign |
Het |
Gm43302 |
A |
T |
5: 105,427,955 (GRCm39) |
L202* |
probably null |
Het |
Gm4787 |
G |
C |
12: 81,424,604 (GRCm39) |
T518S |
probably benign |
Het |
Hnf1b |
A |
T |
11: 83,746,863 (GRCm39) |
M160L |
probably damaging |
Het |
Inhbe |
T |
C |
10: 127,186,470 (GRCm39) |
T237A |
possibly damaging |
Het |
Kdm5b |
G |
A |
1: 134,549,836 (GRCm39) |
|
probably null |
Het |
Kmt2c |
A |
T |
5: 25,499,732 (GRCm39) |
|
probably null |
Het |
Kyat3 |
A |
G |
3: 142,440,367 (GRCm39) |
K364E |
probably benign |
Het |
Lars1 |
T |
A |
18: 42,350,024 (GRCm39) |
T927S |
probably benign |
Het |
Mroh8 |
G |
A |
2: 157,070,576 (GRCm39) |
P592S |
possibly damaging |
Het |
Myo3b |
A |
T |
2: 69,957,329 (GRCm39) |
I185L |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or1x6 |
C |
T |
11: 50,939,297 (GRCm39) |
A121V |
probably damaging |
Het |
Or4c110 |
A |
T |
2: 88,832,540 (GRCm39) |
L31M |
probably benign |
Het |
Or51a24 |
T |
C |
7: 103,734,098 (GRCm39) |
Y63C |
probably benign |
Het |
Pcdha8 |
T |
A |
18: 37,126,787 (GRCm39) |
V423E |
probably damaging |
Het |
Pcdhb21 |
G |
T |
18: 37,648,772 (GRCm39) |
V634L |
probably benign |
Het |
Pde8a |
T |
C |
7: 80,983,170 (GRCm39) |
V791A |
probably damaging |
Het |
Pds5a |
A |
G |
5: 65,795,920 (GRCm39) |
S657P |
probably benign |
Het |
Pes1 |
CGGAGGAGGAGGAGGAGGAGGAGG |
CGGAGGAGGAGGAGGAGGAGG |
11: 3,927,719 (GRCm39) |
|
probably benign |
Het |
Rad51d |
A |
G |
11: 82,781,196 (GRCm39) |
V17A |
possibly damaging |
Het |
Sdc1 |
A |
T |
12: 8,841,743 (GRCm39) |
|
probably null |
Het |
Sdcbp2 |
T |
A |
2: 151,429,057 (GRCm39) |
I152N |
probably damaging |
Het |
Slc4a4 |
G |
T |
5: 89,194,076 (GRCm39) |
M141I |
probably benign |
Het |
Sntb1 |
C |
G |
15: 55,506,191 (GRCm39) |
G461R |
probably damaging |
Het |
Spata6 |
T |
C |
4: 111,656,315 (GRCm39) |
C320R |
probably damaging |
Het |
Spata6l |
T |
C |
19: 28,905,089 (GRCm39) |
H325R |
possibly damaging |
Het |
Ssu2 |
T |
A |
6: 112,357,957 (GRCm39) |
T129S |
probably damaging |
Het |
Stat5a |
T |
A |
11: 100,771,409 (GRCm39) |
W631R |
probably damaging |
Het |
Sult1c2 |
T |
A |
17: 54,143,939 (GRCm39) |
N122I |
possibly damaging |
Het |
Synpo2 |
G |
A |
3: 122,911,331 (GRCm39) |
Q105* |
probably null |
Het |
Tert |
G |
A |
13: 73,787,362 (GRCm39) |
V783I |
probably damaging |
Het |
Ticam1 |
G |
T |
17: 56,578,117 (GRCm39) |
T326K |
probably benign |
Het |
Tmem63b |
T |
C |
17: 45,980,888 (GRCm39) |
M269V |
possibly damaging |
Het |
Tmem86a |
T |
A |
7: 46,702,794 (GRCm39) |
V73E |
possibly damaging |
Het |
Trpv4 |
G |
A |
5: 114,761,675 (GRCm39) |
R818C |
possibly damaging |
Het |
Tstd2 |
A |
G |
4: 46,135,542 (GRCm39) |
S4P |
probably benign |
Het |
Ttn |
A |
T |
2: 76,644,715 (GRCm39) |
V4686E |
probably damaging |
Het |
Ubash3b |
A |
G |
9: 40,954,769 (GRCm39) |
|
probably null |
Het |
Usp31 |
A |
G |
7: 121,267,005 (GRCm39) |
|
probably null |
Het |
Usp33 |
A |
G |
3: 152,089,824 (GRCm39) |
E780G |
possibly damaging |
Het |
Vapb |
T |
A |
2: 173,613,336 (GRCm39) |
Y78* |
probably null |
Het |
Vps13b |
G |
A |
15: 35,887,094 (GRCm39) |
R3227Q |
probably damaging |
Het |
Vps33a |
A |
T |
5: 123,696,693 (GRCm39) |
I320N |
probably damaging |
Het |
Wnt5a |
T |
C |
14: 28,244,727 (GRCm39) |
C305R |
probably damaging |
Het |
Zbtb38 |
A |
G |
9: 96,569,696 (GRCm39) |
C463R |
probably damaging |
Het |
Zc3h12d |
G |
A |
10: 7,742,090 (GRCm39) |
C263Y |
probably damaging |
Het |
Zfp971 |
G |
A |
2: 177,675,526 (GRCm39) |
R375Q |
probably damaging |
Het |
Znrf1 |
T |
A |
8: 112,345,826 (GRCm39) |
|
probably null |
Het |
|