Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1bg |
G |
A |
15: 60,792,244 (GRCm39) |
P128L |
probably damaging |
Het |
Acsm3 |
T |
C |
7: 119,377,678 (GRCm39) |
V401A |
probably damaging |
Het |
Arhgef11 |
C |
A |
3: 87,594,227 (GRCm39) |
N93K |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,489,760 (GRCm39) |
|
probably null |
Het |
Camk2a |
A |
G |
18: 61,091,226 (GRCm39) |
E236G |
probably damaging |
Het |
Cav2 |
C |
A |
6: 17,281,410 (GRCm39) |
D17E |
possibly damaging |
Het |
Ccdc149 |
T |
C |
5: 52,533,607 (GRCm39) |
S520G |
probably benign |
Het |
Chd4 |
C |
A |
6: 125,083,501 (GRCm39) |
H674Q |
probably damaging |
Het |
Clrn2 |
A |
T |
5: 45,611,096 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
A |
C |
11: 101,077,337 (GRCm39) |
I1000L |
probably damaging |
Het |
Cyp2c67 |
T |
C |
19: 39,631,778 (GRCm39) |
T140A |
possibly damaging |
Het |
D7Ertd443e |
T |
C |
7: 133,966,208 (GRCm39) |
|
probably null |
Het |
Dcdc2c |
G |
T |
12: 28,591,496 (GRCm39) |
Q131K |
probably benign |
Het |
Dmpk |
T |
A |
7: 18,822,149 (GRCm39) |
V369E |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,070,297 (GRCm39) |
W1503R |
probably damaging |
Het |
Dnai7 |
A |
G |
6: 145,120,945 (GRCm39) |
F625L |
possibly damaging |
Het |
Dok2 |
T |
C |
14: 71,013,045 (GRCm39) |
V71A |
probably benign |
Het |
Dqx1 |
A |
T |
6: 83,036,446 (GRCm39) |
Q150L |
probably damaging |
Het |
Extl3 |
A |
G |
14: 65,304,189 (GRCm39) |
I740T |
possibly damaging |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fat2 |
C |
T |
11: 55,143,300 (GRCm39) |
W4183* |
probably null |
Het |
Fkrp |
C |
T |
7: 16,545,751 (GRCm39) |
R37Q |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,341,774 (GRCm39) |
K1356E |
probably benign |
Het |
Fus |
A |
T |
7: 127,571,741 (GRCm39) |
|
probably benign |
Het |
Gabarapl2 |
C |
A |
8: 112,669,201 (GRCm39) |
S53* |
probably null |
Het |
Gjd3 |
A |
C |
11: 102,691,733 (GRCm39) |
M90R |
probably damaging |
Het |
Gm30083 |
C |
T |
14: 33,725,557 (GRCm39) |
|
probably null |
Het |
Gm7356 |
T |
A |
17: 14,221,387 (GRCm39) |
Y214F |
probably benign |
Het |
Hexd |
A |
T |
11: 121,113,164 (GRCm39) |
D533V |
probably benign |
Het |
Ift172 |
G |
A |
5: 31,414,930 (GRCm39) |
A1364V |
probably damaging |
Het |
Ighmbp2 |
A |
T |
19: 3,326,907 (GRCm39) |
F186Y |
probably damaging |
Het |
Inpp5e |
C |
A |
2: 26,297,774 (GRCm39) |
|
probably null |
Het |
Iqcb1 |
A |
G |
16: 36,660,274 (GRCm39) |
T146A |
possibly damaging |
Het |
Kcnmb2 |
A |
G |
3: 32,252,465 (GRCm39) |
Y222C |
probably damaging |
Het |
Kdm6b |
A |
G |
11: 69,297,588 (GRCm39) |
W284R |
probably damaging |
Het |
Khdc4 |
T |
A |
3: 88,593,824 (GRCm39) |
M71K |
probably damaging |
Het |
Ksr2 |
T |
A |
5: 117,903,626 (GRCm39) |
*952R |
probably null |
Het |
Ldlrap1 |
C |
A |
4: 134,495,285 (GRCm39) |
|
probably benign |
Het |
Mpdu1 |
G |
A |
11: 69,548,881 (GRCm39) |
|
probably benign |
Het |
Mrgprh |
A |
T |
17: 13,095,822 (GRCm39) |
T21S |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,549,833 (GRCm39) |
T5487S |
probably benign |
Het |
Mydgf |
A |
G |
17: 56,490,737 (GRCm39) |
|
probably null |
Het |
Napa |
T |
C |
7: 15,849,182 (GRCm39) |
C241R |
possibly damaging |
Het |
Or10ab4 |
C |
A |
7: 107,654,312 (GRCm39) |
A41E |
possibly damaging |
Het |
Or10n7-ps1 |
T |
C |
9: 39,598,187 (GRCm39) |
T18A |
possibly damaging |
Het |
Or5k17 |
A |
T |
16: 58,746,648 (GRCm39) |
Y95* |
probably null |
Het |
Pla2g4f |
A |
T |
2: 120,137,782 (GRCm39) |
L326Q |
probably damaging |
Het |
Pramel16 |
T |
C |
4: 143,675,366 (GRCm39) |
T487A |
probably benign |
Het |
Psme4 |
T |
A |
11: 30,787,291 (GRCm39) |
Y1029N |
probably damaging |
Het |
Ptprj |
T |
C |
2: 90,289,858 (GRCm39) |
T707A |
possibly damaging |
Het |
Raet1e |
T |
A |
10: 22,050,256 (GRCm39) |
M13K |
possibly damaging |
Het |
Rftn2 |
T |
C |
1: 55,233,508 (GRCm39) |
|
probably null |
Het |
Rmi1 |
A |
G |
13: 58,557,169 (GRCm39) |
I473V |
probably benign |
Het |
Ryr1 |
T |
A |
7: 28,751,751 (GRCm39) |
M3672L |
possibly damaging |
Het |
Smarca5 |
A |
T |
8: 81,431,949 (GRCm39) |
C890S |
possibly damaging |
Het |
Spata31d1e |
T |
A |
13: 59,889,872 (GRCm39) |
K231N |
possibly damaging |
Het |
Tdrd12 |
C |
T |
7: 35,185,024 (GRCm39) |
|
probably null |
Het |
Tecta |
T |
C |
9: 42,259,293 (GRCm39) |
N1530S |
probably damaging |
Het |
Tenm4 |
G |
A |
7: 96,202,703 (GRCm39) |
R106H |
probably benign |
Het |
Tmem94 |
A |
G |
11: 115,676,656 (GRCm39) |
S54G |
possibly damaging |
Het |
Tnk2 |
T |
C |
16: 32,482,696 (GRCm39) |
V41A |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 63,918,045 (GRCm39) |
T462A |
probably benign |
Het |
Tsg101 |
T |
C |
7: 46,556,847 (GRCm39) |
T61A |
probably benign |
Het |
Usp42 |
T |
C |
5: 143,713,724 (GRCm39) |
N17D |
probably damaging |
Het |
Zfp607a |
T |
A |
7: 27,578,473 (GRCm39) |
C514* |
probably null |
Het |
Zfp866 |
G |
T |
8: 70,218,871 (GRCm39) |
Q250K |
probably damaging |
Het |
|
Other mutations in Rps6ka4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01146:Rps6ka4
|
APN |
19 |
6,808,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01548:Rps6ka4
|
APN |
19 |
6,809,691 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02536:Rps6ka4
|
APN |
19 |
6,809,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02902:Rps6ka4
|
APN |
19 |
6,809,623 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03299:Rps6ka4
|
APN |
19 |
6,809,615 (GRCm39) |
splice site |
probably benign |
|
R0510:Rps6ka4
|
UTSW |
19 |
6,817,866 (GRCm39) |
missense |
probably benign |
0.13 |
R1104:Rps6ka4
|
UTSW |
19 |
6,808,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R1620:Rps6ka4
|
UTSW |
19 |
6,815,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Rps6ka4
|
UTSW |
19 |
6,816,730 (GRCm39) |
missense |
probably benign |
0.15 |
R1648:Rps6ka4
|
UTSW |
19 |
6,816,730 (GRCm39) |
missense |
probably benign |
0.15 |
R1939:Rps6ka4
|
UTSW |
19 |
6,816,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R2370:Rps6ka4
|
UTSW |
19 |
6,807,468 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2412:Rps6ka4
|
UTSW |
19 |
6,807,309 (GRCm39) |
makesense |
probably null |
|
R2571:Rps6ka4
|
UTSW |
19 |
6,815,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2698:Rps6ka4
|
UTSW |
19 |
6,814,720 (GRCm39) |
missense |
probably benign |
0.08 |
R3427:Rps6ka4
|
UTSW |
19 |
6,815,123 (GRCm39) |
critical splice donor site |
probably null |
|
R3721:Rps6ka4
|
UTSW |
19 |
6,816,645 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3844:Rps6ka4
|
UTSW |
19 |
6,815,171 (GRCm39) |
nonsense |
probably null |
|
R4092:Rps6ka4
|
UTSW |
19 |
6,809,623 (GRCm39) |
critical splice donor site |
probably null |
|
R4169:Rps6ka4
|
UTSW |
19 |
6,809,188 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4677:Rps6ka4
|
UTSW |
19 |
6,816,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Rps6ka4
|
UTSW |
19 |
6,815,467 (GRCm39) |
missense |
probably benign |
0.02 |
R4975:Rps6ka4
|
UTSW |
19 |
6,817,678 (GRCm39) |
splice site |
probably null |
|
R5631:Rps6ka4
|
UTSW |
19 |
6,808,345 (GRCm39) |
splice site |
probably benign |
|
R6462:Rps6ka4
|
UTSW |
19 |
6,814,957 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6643:Rps6ka4
|
UTSW |
19 |
6,809,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7030:Rps6ka4
|
UTSW |
19 |
6,816,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R7902:Rps6ka4
|
UTSW |
19 |
6,808,679 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8021:Rps6ka4
|
UTSW |
19 |
6,807,777 (GRCm39) |
missense |
probably benign |
0.01 |
R8166:Rps6ka4
|
UTSW |
19 |
6,814,811 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8988:Rps6ka4
|
UTSW |
19 |
6,808,667 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9481:Rps6ka4
|
UTSW |
19 |
6,809,372 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9664:Rps6ka4
|
UTSW |
19 |
6,809,354 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9723:Rps6ka4
|
UTSW |
19 |
6,816,663 (GRCm39) |
missense |
probably damaging |
0.99 |
U24488:Rps6ka4
|
UTSW |
19 |
6,809,724 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Rps6ka4
|
UTSW |
19 |
6,815,508 (GRCm39) |
missense |
probably damaging |
0.97 |
X0027:Rps6ka4
|
UTSW |
19 |
6,815,140 (GRCm39) |
missense |
probably benign |
0.37 |
|