Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579C12Rik |
A |
G |
9: 89,034,815 (GRCm39) |
|
noncoding transcript |
Het |
9130008F23Rik |
T |
C |
17: 41,191,193 (GRCm39) |
R79G |
probably damaging |
Het |
Acp6 |
C |
T |
3: 97,073,201 (GRCm39) |
R81W |
probably damaging |
Het |
Agbl1 |
A |
C |
7: 76,239,129 (GRCm39) |
Y543S |
probably damaging |
Het |
Anapc7 |
T |
C |
5: 122,571,539 (GRCm39) |
W205R |
probably damaging |
Het |
Ap1g2 |
T |
A |
14: 55,338,886 (GRCm39) |
M532L |
probably damaging |
Het |
Appl1 |
A |
G |
14: 26,647,470 (GRCm39) |
|
probably benign |
Het |
Arhgef19 |
T |
C |
4: 140,976,624 (GRCm39) |
F462S |
probably damaging |
Het |
Astn1 |
A |
G |
1: 158,332,886 (GRCm39) |
|
probably null |
Het |
AU015836 |
T |
C |
X: 93,012,985 (GRCm39) |
|
probably benign |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Cadm2 |
T |
C |
16: 66,679,683 (GRCm39) |
D50G |
probably damaging |
Het |
Ccdc81 |
G |
A |
7: 89,531,502 (GRCm39) |
Q324* |
probably null |
Het |
Cd300lf |
A |
G |
11: 115,011,206 (GRCm39) |
V178A |
probably benign |
Het |
Cdt1 |
T |
C |
8: 123,298,791 (GRCm39) |
V476A |
possibly damaging |
Het |
Cenpj |
A |
G |
14: 56,796,182 (GRCm39) |
V225A |
probably benign |
Het |
Cep295 |
T |
C |
9: 15,243,399 (GRCm39) |
T1686A |
possibly damaging |
Het |
Cfap54 |
A |
G |
10: 92,870,572 (GRCm39) |
S684P |
possibly damaging |
Het |
Clip1 |
C |
A |
5: 123,791,559 (GRCm39) |
V204F |
probably damaging |
Het |
Cnpy4 |
A |
G |
5: 138,191,102 (GRCm39) |
E226G |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,731,433 (GRCm39) |
M1000L |
probably benign |
Het |
Cpsf1 |
T |
C |
15: 76,486,356 (GRCm39) |
M335V |
probably benign |
Het |
Dnmt3b |
C |
A |
2: 153,518,679 (GRCm39) |
A614E |
probably benign |
Het |
Dpm1 |
C |
T |
2: 168,059,655 (GRCm39) |
R147Q |
possibly damaging |
Het |
Dpp7 |
G |
T |
2: 25,243,691 (GRCm39) |
|
probably null |
Het |
Engase |
T |
C |
11: 118,369,759 (GRCm39) |
F57S |
probably damaging |
Het |
Epb41l5 |
T |
C |
1: 119,476,902 (GRCm39) |
D718G |
possibly damaging |
Het |
Fam20a |
T |
C |
11: 109,564,380 (GRCm39) |
K458E |
probably benign |
Het |
Fbxo44 |
C |
G |
4: 148,240,726 (GRCm39) |
R220S |
probably damaging |
Het |
Gkn2 |
T |
A |
6: 87,355,137 (GRCm39) |
Y115* |
probably null |
Het |
Gtdc1 |
A |
G |
2: 44,481,926 (GRCm39) |
S246P |
probably damaging |
Het |
H2-Q2 |
A |
G |
17: 35,564,152 (GRCm39) |
D302G |
probably benign |
Het |
Herc2 |
C |
T |
7: 55,839,561 (GRCm39) |
S3357L |
possibly damaging |
Het |
Herc6 |
T |
A |
6: 57,639,060 (GRCm39) |
Y840* |
probably null |
Het |
Hoxa10 |
GGCTGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTGCTG |
6: 52,211,472 (GRCm39) |
|
probably benign |
Het |
Ift122 |
T |
C |
6: 115,871,382 (GRCm39) |
|
probably null |
Het |
Ilf3 |
T |
A |
9: 21,316,063 (GRCm39) |
|
probably benign |
Het |
Itgb2 |
A |
T |
10: 77,384,457 (GRCm39) |
N193Y |
possibly damaging |
Het |
Itgb5 |
T |
G |
16: 33,730,839 (GRCm39) |
I65S |
probably damaging |
Het |
Jpt2 |
T |
C |
17: 25,179,585 (GRCm39) |
M1V |
probably null |
Het |
Kcnt2 |
A |
T |
1: 140,512,031 (GRCm39) |
H995L |
probably damaging |
Het |
Kif20b |
T |
C |
19: 34,918,608 (GRCm39) |
|
probably benign |
Het |
Kif7 |
T |
C |
7: 79,360,211 (GRCm39) |
Y342C |
probably damaging |
Het |
Klhl21 |
T |
C |
4: 152,099,877 (GRCm39) |
V529A |
possibly damaging |
Het |
Klhl26 |
T |
C |
8: 70,904,383 (GRCm39) |
D475G |
probably damaging |
Het |
Lcor |
T |
C |
19: 41,547,567 (GRCm39) |
Y384H |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,809,179 (GRCm39) |
C2463* |
probably null |
Het |
Marchf6 |
T |
C |
15: 31,459,339 (GRCm39) |
E909G |
possibly damaging |
Het |
Mrc1 |
A |
T |
2: 14,313,488 (GRCm39) |
|
probably null |
Het |
Mtrex |
T |
C |
13: 113,024,024 (GRCm39) |
N707S |
probably benign |
Het |
Nipal4 |
T |
A |
11: 46,041,560 (GRCm39) |
I212F |
probably damaging |
Het |
Nup98 |
T |
A |
7: 101,809,923 (GRCm39) |
T536S |
probably damaging |
Het |
Nwd2 |
A |
G |
5: 63,965,009 (GRCm39) |
E1531G |
possibly damaging |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Oosp1 |
C |
T |
19: 11,645,158 (GRCm39) |
V169I |
possibly damaging |
Het |
Opa1 |
T |
C |
16: 29,444,403 (GRCm39) |
V863A |
possibly damaging |
Het |
Or5ac22 |
T |
G |
16: 59,135,326 (GRCm39) |
Y148S |
probably damaging |
Het |
Pabpc4l |
A |
T |
3: 46,400,798 (GRCm39) |
M282K |
probably benign |
Het |
Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
Pcnx3 |
T |
C |
19: 5,722,684 (GRCm39) |
D1336G |
probably damaging |
Het |
Phlpp1 |
T |
C |
1: 106,246,580 (GRCm39) |
V590A |
possibly damaging |
Het |
Rbck1 |
T |
A |
2: 152,160,276 (GRCm39) |
T468S |
probably damaging |
Het |
Ripor2 |
T |
A |
13: 24,877,870 (GRCm39) |
I290N |
probably damaging |
Het |
Rnf139 |
T |
C |
15: 58,771,346 (GRCm39) |
L457P |
probably damaging |
Het |
Rtn1 |
C |
A |
12: 72,351,184 (GRCm39) |
A342S |
possibly damaging |
Het |
Sema3d |
A |
G |
5: 12,534,988 (GRCm39) |
|
probably null |
Het |
Serpinb2 |
T |
A |
1: 107,452,337 (GRCm39) |
V305D |
probably damaging |
Het |
Sez6l2 |
T |
C |
7: 126,552,668 (GRCm39) |
V148A |
probably damaging |
Het |
Shank2 |
C |
A |
7: 143,740,595 (GRCm39) |
S568* |
probably null |
Het |
Slc10a4 |
T |
C |
5: 73,169,490 (GRCm39) |
S372P |
possibly damaging |
Het |
Slc10a5 |
T |
C |
3: 10,400,550 (GRCm39) |
T37A |
probably benign |
Het |
Slc14a1 |
T |
C |
18: 78,152,912 (GRCm39) |
I276V |
possibly damaging |
Het |
Slc6a20b |
G |
T |
9: 123,461,269 (GRCm39) |
D52E |
probably benign |
Het |
Slc6a5 |
T |
C |
7: 49,601,182 (GRCm39) |
M661T |
probably benign |
Het |
Ssh2 |
C |
G |
11: 77,340,571 (GRCm39) |
D574E |
probably damaging |
Het |
Steap4 |
G |
T |
5: 8,025,892 (GRCm39) |
R151L |
probably damaging |
Het |
Sun5 |
T |
A |
2: 153,707,915 (GRCm39) |
I107L |
probably benign |
Het |
Tacc1 |
C |
T |
8: 25,665,269 (GRCm39) |
V488M |
probably damaging |
Het |
Tgs1 |
A |
G |
4: 3,614,928 (GRCm39) |
T829A |
probably benign |
Het |
Tnxb |
A |
G |
17: 34,914,799 (GRCm39) |
E1929G |
probably damaging |
Het |
Tssc4 |
A |
C |
7: 142,624,292 (GRCm39) |
Q200P |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,588,876 (GRCm39) |
W21398R |
probably damaging |
Het |
Usp50 |
C |
T |
2: 126,619,818 (GRCm39) |
|
probably null |
Het |
Usp9y |
A |
T |
Y: 1,448,829 (GRCm39) |
|
probably null |
Het |
V1rd19 |
T |
A |
7: 23,702,632 (GRCm39) |
F33I |
probably benign |
Het |
Zfat |
T |
C |
15: 67,973,388 (GRCm39) |
T1118A |
probably benign |
Het |
|
Other mutations in Aco1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00813:Aco1
|
APN |
4 |
40,180,290 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01081:Aco1
|
APN |
4 |
40,197,576 (GRCm39) |
missense |
probably benign |
|
IGL01364:Aco1
|
APN |
4 |
40,181,380 (GRCm39) |
splice site |
probably null |
|
IGL01733:Aco1
|
APN |
4 |
40,175,738 (GRCm39) |
splice site |
probably benign |
|
IGL02232:Aco1
|
APN |
4 |
40,175,996 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02709:Aco1
|
APN |
4 |
40,180,199 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03164:Aco1
|
APN |
4 |
40,167,116 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03208:Aco1
|
APN |
4 |
40,186,424 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03324:Aco1
|
APN |
4 |
40,186,363 (GRCm39) |
missense |
probably benign |
|
IGL03353:Aco1
|
APN |
4 |
40,175,893 (GRCm39) |
missense |
probably damaging |
0.99 |
krebs
|
UTSW |
4 |
40,180,210 (GRCm39) |
nonsense |
probably null |
|
R0002:Aco1
|
UTSW |
4 |
40,176,649 (GRCm39) |
splice site |
probably benign |
|
R0486:Aco1
|
UTSW |
4 |
40,177,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Aco1
|
UTSW |
4 |
40,175,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R1344:Aco1
|
UTSW |
4 |
40,179,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R1844:Aco1
|
UTSW |
4 |
40,197,566 (GRCm39) |
missense |
probably benign |
0.00 |
R1932:Aco1
|
UTSW |
4 |
40,176,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Aco1
|
UTSW |
4 |
40,167,193 (GRCm39) |
critical splice donor site |
probably null |
|
R1965:Aco1
|
UTSW |
4 |
40,175,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Aco1
|
UTSW |
4 |
40,175,845 (GRCm39) |
missense |
probably benign |
0.37 |
R2072:Aco1
|
UTSW |
4 |
40,183,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R2073:Aco1
|
UTSW |
4 |
40,183,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Aco1
|
UTSW |
4 |
40,183,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R3155:Aco1
|
UTSW |
4 |
40,182,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R4595:Aco1
|
UTSW |
4 |
40,167,139 (GRCm39) |
missense |
probably benign |
0.43 |
R4999:Aco1
|
UTSW |
4 |
40,176,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R5131:Aco1
|
UTSW |
4 |
40,163,797 (GRCm39) |
missense |
probably benign |
|
R5354:Aco1
|
UTSW |
4 |
40,180,290 (GRCm39) |
critical splice donor site |
probably null |
|
R5380:Aco1
|
UTSW |
4 |
40,177,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Aco1
|
UTSW |
4 |
40,186,367 (GRCm39) |
missense |
probably benign |
0.10 |
R6353:Aco1
|
UTSW |
4 |
40,186,367 (GRCm39) |
missense |
probably benign |
0.10 |
R6380:Aco1
|
UTSW |
4 |
40,185,028 (GRCm39) |
missense |
probably benign |
0.02 |
R6540:Aco1
|
UTSW |
4 |
40,186,367 (GRCm39) |
missense |
probably benign |
0.10 |
R6751:Aco1
|
UTSW |
4 |
40,188,330 (GRCm39) |
splice site |
probably null |
|
R6760:Aco1
|
UTSW |
4 |
40,180,210 (GRCm39) |
nonsense |
probably null |
|
R6833:Aco1
|
UTSW |
4 |
40,164,747 (GRCm39) |
missense |
probably benign |
0.00 |
R6834:Aco1
|
UTSW |
4 |
40,164,747 (GRCm39) |
missense |
probably benign |
0.00 |
R7019:Aco1
|
UTSW |
4 |
40,186,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R7852:Aco1
|
UTSW |
4 |
40,180,263 (GRCm39) |
missense |
probably benign |
0.00 |
R7912:Aco1
|
UTSW |
4 |
40,184,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R8188:Aco1
|
UTSW |
4 |
40,180,284 (GRCm39) |
missense |
probably benign |
0.00 |
R8329:Aco1
|
UTSW |
4 |
40,186,376 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8346:Aco1
|
UTSW |
4 |
40,177,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Aco1
|
UTSW |
4 |
40,179,037 (GRCm39) |
missense |
probably benign |
|
|