Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atr |
T |
A |
9: 95,744,916 (GRCm39) |
S78T |
probably damaging |
Het |
B2m |
T |
C |
2: 121,981,465 (GRCm39) |
L60P |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Cep350 |
A |
C |
1: 155,724,373 (GRCm39) |
I3075S |
probably damaging |
Het |
Cep97 |
A |
G |
16: 55,725,935 (GRCm39) |
S651P |
probably damaging |
Het |
Chrna5 |
C |
T |
9: 54,888,985 (GRCm39) |
|
probably benign |
Het |
Cog5 |
T |
C |
12: 31,715,468 (GRCm39) |
V80A |
possibly damaging |
Het |
Col9a2 |
G |
A |
4: 120,906,913 (GRCm39) |
|
probably null |
Het |
Cop1 |
C |
T |
1: 159,077,647 (GRCm39) |
L161F |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,814,205 (GRCm39) |
D1474G |
possibly damaging |
Het |
Dgkb |
A |
C |
12: 38,150,492 (GRCm39) |
S100R |
probably benign |
Het |
Dnah17 |
A |
G |
11: 118,016,212 (GRCm39) |
V309A |
probably benign |
Het |
Dner |
C |
A |
1: 84,558,457 (GRCm39) |
R169L |
possibly damaging |
Het |
Dus1l |
T |
C |
11: 120,682,120 (GRCm39) |
E362G |
probably benign |
Het |
Eed |
A |
T |
7: 89,619,564 (GRCm39) |
S168T |
possibly damaging |
Het |
Eif3a |
T |
A |
19: 60,751,500 (GRCm39) |
|
probably null |
Het |
Fam234b |
A |
G |
6: 135,205,450 (GRCm39) |
S472G |
probably benign |
Het |
Fbn2 |
T |
A |
18: 58,209,798 (GRCm39) |
T1028S |
probably benign |
Het |
Fbxw16 |
A |
G |
9: 109,265,352 (GRCm39) |
V393A |
possibly damaging |
Het |
Fig4 |
A |
T |
10: 41,096,928 (GRCm39) |
L838Q |
probably benign |
Het |
Gm13941 |
T |
G |
2: 110,927,147 (GRCm39) |
S137R |
unknown |
Het |
Gm9938 |
T |
G |
19: 23,701,981 (GRCm39) |
|
probably benign |
Het |
Igsf10 |
T |
G |
3: 59,238,501 (GRCm39) |
D560A |
probably damaging |
Het |
Lrrk2 |
T |
A |
15: 91,659,198 (GRCm39) |
L1870* |
probably null |
Het |
Mep1b |
T |
A |
18: 21,224,247 (GRCm39) |
Y347N |
probably damaging |
Het |
Mepce |
T |
C |
5: 137,780,968 (GRCm39) |
N613D |
probably damaging |
Het |
Mgat3 |
T |
G |
15: 80,096,097 (GRCm39) |
L308R |
probably damaging |
Het |
Morc2a |
A |
G |
11: 3,625,925 (GRCm39) |
Y175C |
probably damaging |
Het |
Necab2 |
A |
G |
8: 120,178,878 (GRCm39) |
N98S |
probably benign |
Het |
Net1 |
T |
C |
13: 3,934,845 (GRCm39) |
M394V |
probably benign |
Het |
Nfat5 |
G |
A |
8: 108,094,738 (GRCm39) |
G993D |
probably damaging |
Het |
Obscn |
C |
A |
11: 58,887,122 (GRCm39) |
|
probably benign |
Het |
Olr1 |
T |
C |
6: 129,465,904 (GRCm39) |
H34R |
probably damaging |
Het |
Or2ab1 |
A |
G |
11: 58,489,044 (GRCm39) |
Y274C |
probably damaging |
Het |
Or4f60 |
T |
C |
2: 111,902,662 (GRCm39) |
N89D |
probably benign |
Het |
Pmm2 |
T |
A |
16: 8,460,628 (GRCm39) |
F27L |
probably damaging |
Het |
Ptpdc1 |
C |
A |
13: 48,740,466 (GRCm39) |
V261F |
possibly damaging |
Het |
Pyroxd1 |
G |
T |
6: 142,304,808 (GRCm39) |
R345L |
probably benign |
Het |
Radil |
A |
T |
5: 142,480,109 (GRCm39) |
C670* |
probably null |
Het |
Rasgrf2 |
C |
T |
13: 92,167,203 (GRCm39) |
S290N |
probably damaging |
Het |
Rbm33 |
T |
C |
5: 28,599,001 (GRCm39) |
|
probably benign |
Het |
Rnf111 |
A |
T |
9: 70,360,957 (GRCm39) |
S501R |
possibly damaging |
Het |
Sel1l2 |
T |
A |
2: 140,087,334 (GRCm39) |
I446F |
probably benign |
Het |
Sh3pxd2b |
T |
C |
11: 32,372,737 (GRCm39) |
S635P |
probably benign |
Het |
Slc30a2 |
G |
A |
4: 134,074,726 (GRCm39) |
R161Q |
probably damaging |
Het |
Smg1 |
T |
C |
7: 117,745,623 (GRCm39) |
|
probably benign |
Het |
Sorcs2 |
C |
A |
5: 36,225,474 (GRCm39) |
D132Y |
probably damaging |
Het |
Sox18 |
T |
C |
2: 181,313,280 (GRCm39) |
D12G |
probably damaging |
Het |
Srsf4 |
G |
T |
4: 131,628,004 (GRCm39) |
|
probably benign |
Het |
Susd4 |
C |
A |
1: 182,660,721 (GRCm39) |
T81N |
probably benign |
Het |
Tmem256 |
G |
T |
11: 69,729,416 (GRCm39) |
|
probably benign |
Het |
Tor4a |
T |
C |
2: 25,084,853 (GRCm39) |
H350R |
probably benign |
Het |
Ugt2a3 |
T |
A |
5: 87,484,953 (GRCm39) |
S24C |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r77 |
C |
T |
7: 86,451,023 (GRCm39) |
T303I |
probably benign |
Het |
Wdr70 |
T |
A |
15: 7,913,877 (GRCm39) |
I591F |
possibly damaging |
Het |
Wdr93 |
T |
C |
7: 79,399,088 (GRCm39) |
I74T |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,809,784 (GRCm39) |
C1087S |
probably damaging |
Het |
Zfp592 |
T |
A |
7: 80,673,067 (GRCm39) |
D10E |
probably damaging |
Het |
Zfp69 |
A |
G |
4: 120,788,295 (GRCm39) |
V340A |
probably benign |
Het |
Zswim2 |
C |
T |
2: 83,751,092 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cyp4f17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Cyp4f17
|
APN |
17 |
32,743,849 (GRCm39) |
nonsense |
probably null |
|
IGL01767:Cyp4f17
|
APN |
17 |
32,725,956 (GRCm39) |
missense |
probably benign |
|
IGL01867:Cyp4f17
|
APN |
17 |
32,747,057 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02009:Cyp4f17
|
APN |
17 |
32,743,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02423:Cyp4f17
|
APN |
17 |
32,725,923 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02503:Cyp4f17
|
APN |
17 |
32,743,940 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02571:Cyp4f17
|
APN |
17 |
32,743,878 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03328:Cyp4f17
|
APN |
17 |
32,739,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03047:Cyp4f17
|
UTSW |
17 |
32,743,023 (GRCm39) |
missense |
possibly damaging |
0.88 |
PIT4810001:Cyp4f17
|
UTSW |
17 |
32,743,574 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0486:Cyp4f17
|
UTSW |
17 |
32,743,797 (GRCm39) |
splice site |
probably benign |
|
R0606:Cyp4f17
|
UTSW |
17 |
32,746,817 (GRCm39) |
missense |
probably damaging |
0.98 |
R0655:Cyp4f17
|
UTSW |
17 |
32,743,871 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1781:Cyp4f17
|
UTSW |
17 |
32,742,993 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1795:Cyp4f17
|
UTSW |
17 |
32,736,943 (GRCm39) |
missense |
probably benign |
0.00 |
R1833:Cyp4f17
|
UTSW |
17 |
32,743,184 (GRCm39) |
missense |
probably benign |
0.01 |
R2268:Cyp4f17
|
UTSW |
17 |
32,736,928 (GRCm39) |
missense |
probably benign |
0.44 |
R3030:Cyp4f17
|
UTSW |
17 |
32,725,950 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3861:Cyp4f17
|
UTSW |
17 |
32,747,078 (GRCm39) |
missense |
probably damaging |
0.97 |
R5236:Cyp4f17
|
UTSW |
17 |
32,739,606 (GRCm39) |
critical splice donor site |
probably null |
|
R5450:Cyp4f17
|
UTSW |
17 |
32,747,860 (GRCm39) |
missense |
probably benign |
|
R5866:Cyp4f17
|
UTSW |
17 |
32,725,887 (GRCm39) |
missense |
probably benign |
0.03 |
R5886:Cyp4f17
|
UTSW |
17 |
32,743,013 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5965:Cyp4f17
|
UTSW |
17 |
32,743,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R6692:Cyp4f17
|
UTSW |
17 |
32,725,950 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7968:Cyp4f17
|
UTSW |
17 |
32,743,116 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8458:Cyp4f17
|
UTSW |
17 |
32,739,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R8550:Cyp4f17
|
UTSW |
17 |
32,746,936 (GRCm39) |
missense |
probably benign |
0.01 |
R8818:Cyp4f17
|
UTSW |
17 |
32,743,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Cyp4f17
|
UTSW |
17 |
32,743,868 (GRCm39) |
nonsense |
probably null |
|
R9360:Cyp4f17
|
UTSW |
17 |
32,743,880 (GRCm39) |
missense |
probably benign |
0.25 |
R9375:Cyp4f17
|
UTSW |
17 |
32,747,746 (GRCm39) |
missense |
probably damaging |
0.97 |
R9690:Cyp4f17
|
UTSW |
17 |
32,725,950 (GRCm39) |
missense |
probably benign |
0.00 |
|