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 |
Rps6ka4 |
A |
G |
19: 6,815,437 (GRCm39) |
F186L |
probably damaging |
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 |
Zfp866 |
G |
T |
8: 70,218,871 (GRCm39) |
Q250K |
probably damaging |
Het |
|
Other mutations in Zfp607a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00164:Zfp607a
|
APN |
7 |
27,577,214 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01019:Zfp607a
|
APN |
7 |
27,578,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01412:Zfp607a
|
APN |
7 |
27,578,109 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03206:Zfp607a
|
APN |
7 |
27,577,248 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0071:Zfp607a
|
UTSW |
7 |
27,577,694 (GRCm39) |
missense |
probably damaging |
0.96 |
R0304:Zfp607a
|
UTSW |
7 |
27,578,637 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0685:Zfp607a
|
UTSW |
7 |
27,577,901 (GRCm39) |
missense |
probably damaging |
0.97 |
R0726:Zfp607a
|
UTSW |
7 |
27,578,574 (GRCm39) |
missense |
probably benign |
0.00 |
R1201:Zfp607a
|
UTSW |
7 |
27,578,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1304:Zfp607a
|
UTSW |
7 |
27,565,000 (GRCm39) |
missense |
probably benign |
0.00 |
R1648:Zfp607a
|
UTSW |
7 |
27,578,493 (GRCm39) |
missense |
probably benign |
0.02 |
R1732:Zfp607a
|
UTSW |
7 |
27,577,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R2194:Zfp607a
|
UTSW |
7 |
27,578,805 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3793:Zfp607a
|
UTSW |
7 |
27,578,331 (GRCm39) |
missense |
probably benign |
0.01 |
R3808:Zfp607a
|
UTSW |
7 |
27,578,826 (GRCm39) |
missense |
probably benign |
0.01 |
R4296:Zfp607a
|
UTSW |
7 |
27,565,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Zfp607a
|
UTSW |
7 |
27,578,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Zfp607a
|
UTSW |
7 |
27,578,078 (GRCm39) |
missense |
probably benign |
0.23 |
R4915:Zfp607a
|
UTSW |
7 |
27,577,985 (GRCm39) |
missense |
probably benign |
0.00 |
R4950:Zfp607a
|
UTSW |
7 |
27,578,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R5123:Zfp607a
|
UTSW |
7 |
27,578,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Zfp607a
|
UTSW |
7 |
27,577,269 (GRCm39) |
missense |
probably damaging |
0.97 |
R5270:Zfp607a
|
UTSW |
7 |
27,577,730 (GRCm39) |
nonsense |
probably null |
|
R5403:Zfp607a
|
UTSW |
7 |
27,578,744 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6010:Zfp607a
|
UTSW |
7 |
27,577,254 (GRCm39) |
nonsense |
probably null |
|
R6224:Zfp607a
|
UTSW |
7 |
27,578,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R6953:Zfp607a
|
UTSW |
7 |
27,577,790 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7082:Zfp607a
|
UTSW |
7 |
27,578,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Zfp607a
|
UTSW |
7 |
27,565,000 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7909:Zfp607a
|
UTSW |
7 |
27,578,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Zfp607a
|
UTSW |
7 |
27,578,868 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8224:Zfp607a
|
UTSW |
7 |
27,577,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R8949:Zfp607a
|
UTSW |
7 |
27,577,944 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8962:Zfp607a
|
UTSW |
7 |
27,578,786 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9178:Zfp607a
|
UTSW |
7 |
27,577,382 (GRCm39) |
missense |
probably benign |
0.00 |
R9802:Zfp607a
|
UTSW |
7 |
27,578,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|