Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
A |
T |
11: 110,107,374 (GRCm39) |
I747N |
probably benign |
Het |
Adamtsl2 |
A |
G |
2: 26,973,268 (GRCm39) |
Y97C |
probably damaging |
Het |
Alox12e |
A |
G |
11: 70,212,007 (GRCm39) |
|
probably benign |
Het |
Alpk2 |
A |
T |
18: 65,414,075 (GRCm39) |
S2014T |
probably damaging |
Het |
Ankrd36 |
A |
T |
11: 5,639,340 (GRCm39) |
|
probably null |
Het |
Apobec1 |
T |
C |
6: 122,558,356 (GRCm39) |
D133G |
probably damaging |
Het |
Arfgef1 |
A |
T |
1: 10,283,366 (GRCm39) |
I181N |
probably damaging |
Het |
Cilp2 |
A |
G |
8: 70,335,060 (GRCm39) |
V646A |
probably damaging |
Het |
Clasrp |
A |
G |
7: 19,318,389 (GRCm39) |
|
probably null |
Het |
Cnot2 |
T |
C |
10: 116,330,751 (GRCm39) |
T423A |
probably benign |
Het |
Crtap |
T |
C |
9: 114,213,874 (GRCm39) |
D227G |
probably benign |
Het |
Ddx60 |
A |
G |
8: 62,440,455 (GRCm39) |
M1036V |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 117,973,860 (GRCm39) |
I2818N |
probably benign |
Het |
Dok6 |
T |
A |
18: 89,492,071 (GRCm39) |
I169F |
possibly damaging |
Het |
Duox2 |
T |
A |
2: 122,112,207 (GRCm39) |
R1326S |
probably benign |
Het |
Epha10 |
A |
G |
4: 124,796,361 (GRCm39) |
T357A |
unknown |
Het |
Ephb2 |
A |
C |
4: 136,383,251 (GRCm39) |
F942C |
probably damaging |
Het |
Fscn3 |
T |
A |
6: 28,430,634 (GRCm39) |
|
probably null |
Het |
Gabrb2 |
A |
G |
11: 42,484,744 (GRCm39) |
N267S |
possibly damaging |
Het |
Gabrr3 |
A |
T |
16: 59,282,001 (GRCm39) |
Y452F |
probably benign |
Het |
Gen1 |
A |
G |
12: 11,292,419 (GRCm39) |
S457P |
probably damaging |
Het |
Gm1993 |
C |
T |
X: 25,515,656 (GRCm39) |
R77H |
probably damaging |
Het |
Gm5592 |
G |
A |
7: 40,865,583 (GRCm39) |
|
probably benign |
Het |
Hmbox1 |
A |
G |
14: 65,140,682 (GRCm39) |
|
probably null |
Het |
Hus1 |
A |
T |
11: 8,957,617 (GRCm39) |
|
probably null |
Het |
Ino80 |
G |
A |
2: 119,232,839 (GRCm39) |
R1160W |
probably damaging |
Het |
Kalrn |
A |
T |
16: 34,212,412 (GRCm39) |
F27L |
probably damaging |
Het |
Kri1 |
A |
T |
9: 21,191,680 (GRCm39) |
F187L |
probably damaging |
Het |
Lekr1 |
A |
T |
3: 65,691,336 (GRCm39) |
|
noncoding transcript |
Het |
Mapk15 |
T |
C |
15: 75,870,599 (GRCm39) |
|
probably benign |
Het |
Mrgpre |
G |
A |
7: 143,334,841 (GRCm39) |
L221F |
probably damaging |
Het |
Mrpl50 |
A |
T |
4: 49,514,399 (GRCm39) |
S91T |
possibly damaging |
Het |
Muc4 |
T |
C |
16: 32,753,802 (GRCm38) |
I1226T |
probably benign |
Het |
Mup15 |
A |
G |
4: 61,356,454 (GRCm39) |
|
probably null |
Het |
Ncapd3 |
A |
G |
9: 27,005,911 (GRCm39) |
D1469G |
probably damaging |
Het |
Nlrp9b |
G |
A |
7: 19,760,606 (GRCm39) |
|
probably null |
Het |
Npy6r |
A |
T |
18: 44,408,984 (GRCm39) |
Y135F |
probably benign |
Het |
Or7e170 |
A |
C |
9: 19,795,275 (GRCm39) |
C109G |
probably benign |
Het |
Phf14 |
G |
A |
6: 12,006,823 (GRCm39) |
R825Q |
probably damaging |
Het |
Pigg |
A |
G |
5: 108,480,751 (GRCm39) |
M379V |
probably benign |
Het |
Plppr3 |
T |
A |
10: 79,701,897 (GRCm39) |
Q315L |
probably benign |
Het |
Plxnd1 |
C |
A |
6: 115,932,717 (GRCm39) |
C1921F |
probably damaging |
Het |
Ptger4 |
A |
C |
15: 5,272,614 (GRCm39) |
S2A |
probably benign |
Het |
Qrfprl |
A |
T |
6: 65,431,975 (GRCm39) |
M293L |
probably benign |
Het |
Rab4a |
A |
T |
8: 124,560,799 (GRCm39) |
D196V |
probably benign |
Het |
Rbck1 |
G |
A |
2: 152,160,653 (GRCm39) |
Q428* |
probably null |
Het |
Rgs14 |
A |
T |
13: 55,527,875 (GRCm39) |
N266I |
probably damaging |
Het |
Serpina1c |
A |
T |
12: 103,864,967 (GRCm39) |
|
probably benign |
Het |
Sesn3 |
G |
A |
9: 14,232,516 (GRCm39) |
R263H |
probably benign |
Het |
Slfn1 |
A |
T |
11: 83,012,289 (GRCm39) |
D135V |
probably benign |
Het |
Spata17 |
T |
C |
1: 186,926,193 (GRCm39) |
K46E |
possibly damaging |
Het |
Srcin1 |
A |
C |
11: 97,425,760 (GRCm39) |
D432E |
probably damaging |
Het |
Stxbp5 |
T |
C |
10: 9,713,888 (GRCm39) |
E217G |
probably damaging |
Het |
Terf2ip |
A |
G |
8: 112,738,649 (GRCm39) |
D179G |
probably damaging |
Het |
Tll1 |
A |
G |
8: 64,509,343 (GRCm39) |
F556L |
possibly damaging |
Het |
Tmed4 |
CTCTTTCT |
CTCT |
11: 6,224,461 (GRCm39) |
|
probably null |
Het |
Trappc9 |
G |
T |
15: 72,808,916 (GRCm39) |
Q537K |
possibly damaging |
Het |
Trim30a |
G |
T |
7: 104,060,395 (GRCm39) |
C460* |
probably null |
Het |
Trim35 |
T |
C |
14: 66,545,322 (GRCm39) |
Y298H |
probably damaging |
Het |
Ugt3a1 |
T |
A |
15: 9,306,479 (GRCm39) |
H209Q |
probably benign |
Het |
Ulk4 |
T |
C |
9: 121,021,830 (GRCm39) |
K627R |
probably damaging |
Het |
Wnk1 |
T |
C |
6: 119,928,872 (GRCm39) |
T1319A |
possibly damaging |
Het |
Wnt9b |
G |
A |
11: 103,622,981 (GRCm39) |
R141C |
probably damaging |
Het |
Zfp735 |
A |
G |
11: 73,580,611 (GRCm39) |
M37V |
probably benign |
Het |
Zmym1 |
A |
T |
4: 126,944,628 (GRCm39) |
N186K |
probably benign |
Het |
|
Other mutations in Cyp17a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01524:Cyp17a1
|
APN |
19 |
46,659,495 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01839:Cyp17a1
|
APN |
19 |
46,659,110 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01901:Cyp17a1
|
APN |
19 |
46,659,531 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02033:Cyp17a1
|
APN |
19 |
46,661,046 (GRCm39) |
nonsense |
probably null |
|
IGL02349:Cyp17a1
|
APN |
19 |
46,655,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02663:Cyp17a1
|
APN |
19 |
46,661,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02883:Cyp17a1
|
APN |
19 |
46,657,790 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03092:Cyp17a1
|
APN |
19 |
46,661,050 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03239:Cyp17a1
|
APN |
19 |
46,655,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03336:Cyp17a1
|
APN |
19 |
46,659,474 (GRCm39) |
missense |
probably benign |
0.00 |
R3773:Cyp17a1
|
UTSW |
19 |
46,658,162 (GRCm39) |
missense |
probably damaging |
0.97 |
R4445:Cyp17a1
|
UTSW |
19 |
46,656,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R4446:Cyp17a1
|
UTSW |
19 |
46,656,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R5544:Cyp17a1
|
UTSW |
19 |
46,661,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R5730:Cyp17a1
|
UTSW |
19 |
46,661,095 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6163:Cyp17a1
|
UTSW |
19 |
46,657,761 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6271:Cyp17a1
|
UTSW |
19 |
46,661,159 (GRCm39) |
missense |
probably benign |
0.17 |
R6728:Cyp17a1
|
UTSW |
19 |
46,657,673 (GRCm39) |
missense |
probably benign |
|
R6729:Cyp17a1
|
UTSW |
19 |
46,659,020 (GRCm39) |
missense |
probably benign |
|
R7025:Cyp17a1
|
UTSW |
19 |
46,659,419 (GRCm39) |
missense |
probably damaging |
0.98 |
R7395:Cyp17a1
|
UTSW |
19 |
46,659,134 (GRCm39) |
missense |
probably benign |
|
R8056:Cyp17a1
|
UTSW |
19 |
46,659,030 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8308:Cyp17a1
|
UTSW |
19 |
46,656,516 (GRCm39) |
missense |
probably benign |
0.09 |
R8735:Cyp17a1
|
UTSW |
19 |
46,659,533 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8737:Cyp17a1
|
UTSW |
19 |
46,658,166 (GRCm39) |
missense |
probably benign |
0.09 |
R9091:Cyp17a1
|
UTSW |
19 |
46,656,030 (GRCm39) |
missense |
probably benign |
0.00 |
R9270:Cyp17a1
|
UTSW |
19 |
46,656,030 (GRCm39) |
missense |
probably benign |
0.00 |
R9364:Cyp17a1
|
UTSW |
19 |
46,657,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Cyp17a1
|
UTSW |
19 |
46,657,165 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Cyp17a1
|
UTSW |
19 |
46,659,459 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1177:Cyp17a1
|
UTSW |
19 |
46,661,098 (GRCm39) |
missense |
possibly damaging |
0.95 |
|