Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
A |
T |
8: 25,374,635 (GRCm39) |
H452Q |
probably damaging |
Het |
Adcy8 |
A |
T |
15: 64,792,529 (GRCm39) |
N142K |
possibly damaging |
Het |
Alkbh8 |
T |
A |
9: 3,343,056 (GRCm39) |
S57R |
probably damaging |
Het |
Atp4a |
A |
G |
7: 30,420,192 (GRCm39) |
T780A |
probably benign |
Het |
Atp9b |
A |
T |
18: 80,960,833 (GRCm39) |
|
probably null |
Het |
Ces2a |
C |
T |
8: 105,464,021 (GRCm39) |
R218C |
possibly damaging |
Het |
Cfap57 |
A |
T |
4: 118,446,198 (GRCm39) |
V688E |
probably damaging |
Het |
Clec11a |
T |
C |
7: 43,955,379 (GRCm39) |
T139A |
probably benign |
Het |
Clstn1 |
A |
T |
4: 149,719,373 (GRCm39) |
T411S |
probably benign |
Het |
Commd5 |
A |
T |
15: 76,784,824 (GRCm39) |
S74C |
probably damaging |
Het |
Cyp3a59 |
C |
A |
5: 146,041,560 (GRCm39) |
P368Q |
probably damaging |
Het |
Dennd4b |
A |
G |
3: 90,176,622 (GRCm39) |
M309V |
probably benign |
Het |
Dhrs9 |
T |
A |
2: 69,231,611 (GRCm39) |
V257E |
probably benign |
Het |
Dhx16 |
T |
C |
17: 36,201,952 (GRCm39) |
V993A |
probably damaging |
Het |
Dok5 |
A |
T |
2: 170,712,735 (GRCm39) |
Q247L |
probably benign |
Het |
E330034G19Rik |
A |
T |
14: 24,359,582 (GRCm39) |
E331V |
unknown |
Het |
Efs |
A |
G |
14: 55,157,451 (GRCm39) |
S287P |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,193,667 (GRCm39) |
N1384S |
possibly damaging |
Het |
Flt4 |
A |
G |
11: 49,521,155 (GRCm39) |
E388G |
possibly damaging |
Het |
Fmn2 |
T |
A |
1: 174,331,303 (GRCm39) |
|
probably null |
Het |
Fmo4 |
T |
C |
1: 162,621,672 (GRCm39) |
Y513C |
probably benign |
Het |
Gbp4 |
T |
C |
5: 105,267,419 (GRCm39) |
E500G |
probably damaging |
Het |
Gm29106 |
T |
C |
1: 118,126,982 (GRCm39) |
S225P |
probably damaging |
Het |
Gstt2 |
G |
A |
10: 75,668,354 (GRCm39) |
R134W |
probably damaging |
Het |
Gucy1b2 |
T |
C |
14: 62,630,401 (GRCm39) |
T782A |
probably benign |
Het |
Gzf1 |
G |
T |
2: 148,532,002 (GRCm39) |
R543L |
probably damaging |
Het |
H2-Eb2 |
G |
A |
17: 34,553,321 (GRCm39) |
G169E |
probably damaging |
Het |
Hdhd3 |
T |
A |
4: 62,418,027 (GRCm39) |
R50W |
probably damaging |
Het |
Hdlbp |
T |
C |
1: 93,355,944 (GRCm39) |
K407E |
probably benign |
Het |
Isl2 |
A |
G |
9: 55,452,240 (GRCm39) |
T271A |
probably benign |
Het |
Kbtbd7 |
GTCTCTC |
GTC |
14: 79,665,364 (GRCm39) |
|
probably null |
Het |
Kdm4b |
T |
A |
17: 56,703,319 (GRCm39) |
N671K |
probably damaging |
Het |
Lats1 |
T |
A |
10: 7,586,655 (GRCm39) |
L939H |
probably damaging |
Het |
Map3k1 |
A |
T |
13: 111,892,789 (GRCm39) |
M822K |
probably damaging |
Het |
Mettl18 |
C |
A |
1: 163,824,330 (GRCm39) |
T217N |
probably damaging |
Het |
Nav3 |
A |
T |
10: 109,532,189 (GRCm39) |
Y2083* |
probably null |
Het |
Nckap1l |
T |
C |
15: 103,362,233 (GRCm39) |
|
probably benign |
Het |
Nkx2-3 |
A |
G |
19: 43,600,986 (GRCm39) |
D16G |
probably damaging |
Het |
Nlrx1 |
A |
G |
9: 44,167,807 (GRCm39) |
S697P |
probably benign |
Het |
Or14j4 |
T |
C |
17: 37,921,456 (GRCm39) |
K62R |
possibly damaging |
Het |
Or1e29 |
G |
C |
11: 73,667,652 (GRCm39) |
S167C |
probably benign |
Het |
Or4k6 |
A |
T |
14: 50,475,825 (GRCm39) |
N172K |
probably damaging |
Het |
Or6c75 |
T |
C |
10: 129,337,575 (GRCm39) |
V266A |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,107,503 (GRCm39) |
D638V |
probably damaging |
Het |
Pot1a |
T |
C |
6: 25,771,621 (GRCm39) |
D200G |
probably benign |
Het |
Ptprs |
G |
T |
17: 56,726,502 (GRCm39) |
T1366K |
probably damaging |
Het |
Sass6 |
A |
T |
3: 116,413,813 (GRCm39) |
R505S |
probably benign |
Het |
Slc30a6 |
T |
C |
17: 74,714,233 (GRCm39) |
I84T |
probably benign |
Het |
Sox10 |
A |
T |
15: 79,040,339 (GRCm39) |
F400L |
probably benign |
Het |
Spata31d1b |
A |
T |
13: 59,864,723 (GRCm39) |
I624F |
probably damaging |
Het |
Stpg4 |
A |
G |
17: 87,735,006 (GRCm39) |
|
probably null |
Het |
Tbc1d9 |
G |
T |
8: 83,963,309 (GRCm39) |
K340N |
probably damaging |
Het |
Tspan12 |
T |
A |
6: 21,772,682 (GRCm39) |
H289L |
probably benign |
Het |
Ubr1 |
T |
A |
2: 120,748,309 (GRCm39) |
T809S |
probably benign |
Het |
Vmn1r43 |
C |
T |
6: 89,847,172 (GRCm39) |
V105M |
probably damaging |
Het |
Vmn1r49 |
A |
G |
6: 90,049,534 (GRCm39) |
V156A |
probably benign |
Het |
Wnt5a |
A |
G |
14: 28,240,236 (GRCm39) |
|
probably null |
Het |
Wwp2 |
T |
A |
8: 108,244,592 (GRCm39) |
S255T |
probably benign |
Het |
Zbtb10 |
A |
G |
3: 9,316,538 (GRCm39) |
T117A |
possibly damaging |
Het |
Zfp800 |
C |
T |
6: 28,244,228 (GRCm39) |
V246I |
probably benign |
Het |
Zfp955a |
G |
T |
17: 33,463,025 (GRCm39) |
Y35* |
probably null |
Het |
|
Other mutations in Cdyl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00953:Cdyl2
|
APN |
8 |
117,321,928 (GRCm39) |
splice site |
probably benign |
|
IGL01670:Cdyl2
|
APN |
8 |
117,351,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01964:Cdyl2
|
APN |
8 |
117,350,768 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02148:Cdyl2
|
APN |
8 |
117,315,983 (GRCm39) |
splice site |
probably benign |
|
IGL02186:Cdyl2
|
APN |
8 |
117,306,025 (GRCm39) |
missense |
possibly damaging |
0.78 |
Allein
|
UTSW |
8 |
117,305,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Cdyl2
|
UTSW |
8 |
117,309,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Cdyl2
|
UTSW |
8 |
117,350,774 (GRCm39) |
missense |
probably benign |
0.03 |
R1430:Cdyl2
|
UTSW |
8 |
117,306,056 (GRCm39) |
splice site |
probably benign |
|
R1883:Cdyl2
|
UTSW |
8 |
117,321,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R2326:Cdyl2
|
UTSW |
8 |
117,350,537 (GRCm39) |
missense |
probably benign |
|
R4194:Cdyl2
|
UTSW |
8 |
117,305,903 (GRCm39) |
splice site |
probably null |
|
R4916:Cdyl2
|
UTSW |
8 |
117,305,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R4977:Cdyl2
|
UTSW |
8 |
117,302,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R5092:Cdyl2
|
UTSW |
8 |
117,350,679 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5320:Cdyl2
|
UTSW |
8 |
117,321,794 (GRCm39) |
nonsense |
probably null |
|
R5727:Cdyl2
|
UTSW |
8 |
117,309,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R5830:Cdyl2
|
UTSW |
8 |
117,321,823 (GRCm39) |
missense |
probably benign |
0.23 |
R6077:Cdyl2
|
UTSW |
8 |
117,316,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R6086:Cdyl2
|
UTSW |
8 |
117,316,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Cdyl2
|
UTSW |
8 |
117,321,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6380:Cdyl2
|
UTSW |
8 |
117,309,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7152:Cdyl2
|
UTSW |
8 |
117,351,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Cdyl2
|
UTSW |
8 |
117,350,733 (GRCm39) |
missense |
probably benign |
0.09 |
R7244:Cdyl2
|
UTSW |
8 |
117,301,999 (GRCm39) |
nonsense |
probably null |
|
R7394:Cdyl2
|
UTSW |
8 |
117,350,790 (GRCm39) |
missense |
not run |
|
R8770:Cdyl2
|
UTSW |
8 |
117,321,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R9574:Cdyl2
|
UTSW |
8 |
117,350,669 (GRCm39) |
missense |
probably benign |
0.00 |
|