Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Als2cl |
T |
C |
9: 110,723,203 (GRCm39) |
S636P |
probably damaging |
Het |
Arhgef4 |
A |
C |
1: 34,763,129 (GRCm39) |
D795A |
unknown |
Het |
Bank1 |
A |
T |
3: 135,948,701 (GRCm39) |
S159T |
possibly damaging |
Het |
Catsperd |
A |
G |
17: 56,967,169 (GRCm39) |
|
probably null |
Het |
Ccdc85a |
A |
G |
11: 28,342,942 (GRCm39) |
|
probably benign |
Het |
Ceacam11 |
T |
C |
7: 17,712,451 (GRCm39) |
I300T |
probably benign |
Het |
Cmtm5 |
A |
G |
14: 55,175,512 (GRCm39) |
|
probably benign |
Het |
Cnn3 |
C |
T |
3: 121,243,702 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
A |
T |
9: 79,585,614 (GRCm39) |
N1254K |
probably damaging |
Het |
Crispld2 |
T |
A |
8: 120,740,828 (GRCm39) |
L107Q |
probably damaging |
Het |
Ctr9 |
C |
T |
7: 110,652,653 (GRCm39) |
R984C |
unknown |
Het |
Cyp1b1 |
T |
C |
17: 80,017,649 (GRCm39) |
N502S |
probably benign |
Het |
Depdc5 |
A |
G |
5: 33,081,515 (GRCm39) |
E559G |
probably damaging |
Het |
Dnai4 |
A |
G |
4: 102,953,858 (GRCm39) |
S114P |
probably benign |
Het |
Dscam |
T |
C |
16: 96,423,915 (GRCm39) |
T1677A |
possibly damaging |
Het |
Dzip1 |
A |
C |
14: 119,159,857 (GRCm39) |
M117R |
possibly damaging |
Het |
Ednrb |
G |
T |
14: 104,059,110 (GRCm39) |
S305R |
probably benign |
Het |
Emilin1 |
A |
G |
5: 31,074,509 (GRCm39) |
D250G |
probably benign |
Het |
Frrs1 |
A |
G |
3: 116,678,778 (GRCm39) |
N200S |
probably benign |
Het |
Fstl5 |
T |
A |
3: 76,337,045 (GRCm39) |
|
probably benign |
Het |
Gmcl1 |
A |
C |
6: 86,703,159 (GRCm39) |
S92A |
probably damaging |
Het |
Gpr62 |
T |
C |
9: 106,341,911 (GRCm39) |
E339G |
probably benign |
Het |
Hspd1 |
A |
T |
1: 55,120,256 (GRCm39) |
D315E |
probably damaging |
Het |
Il19 |
A |
G |
1: 130,863,694 (GRCm39) |
V99A |
possibly damaging |
Het |
Itga9 |
G |
A |
9: 118,465,604 (GRCm39) |
E153K |
probably damaging |
Het |
Itgad |
T |
A |
7: 127,803,732 (GRCm39) |
V42E |
probably benign |
Het |
Krt82 |
T |
C |
15: 101,456,870 (GRCm39) |
Y170C |
probably damaging |
Het |
Map4k4 |
T |
A |
1: 40,039,915 (GRCm39) |
|
probably benign |
Het |
Mdc1 |
T |
A |
17: 36,159,902 (GRCm39) |
V670D |
probably benign |
Het |
Mfsd4b2 |
T |
A |
10: 39,798,119 (GRCm39) |
S79C |
probably benign |
Het |
Mre11a |
A |
G |
9: 14,737,843 (GRCm39) |
E599G |
probably benign |
Het |
Mthfsd |
G |
A |
8: 121,832,512 (GRCm39) |
T60I |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,381,769 (GRCm39) |
F3724I |
probably damaging |
Het |
Nceh1 |
A |
G |
3: 27,295,504 (GRCm39) |
Y255C |
probably damaging |
Het |
Ncoa2 |
C |
T |
1: 13,257,113 (GRCm39) |
V129I |
probably damaging |
Het |
Ndufb5 |
T |
C |
3: 32,800,600 (GRCm39) |
F58L |
probably damaging |
Het |
Npsr1 |
A |
G |
9: 24,221,301 (GRCm39) |
|
probably benign |
Het |
Obscn |
C |
A |
11: 58,920,844 (GRCm39) |
|
probably null |
Het |
Pdzd7 |
C |
G |
19: 45,016,113 (GRCm39) |
V1003L |
probably benign |
Het |
Pias3 |
A |
G |
3: 96,610,853 (GRCm39) |
E377G |
possibly damaging |
Het |
Pilra |
T |
A |
5: 137,834,342 (GRCm39) |
M14L |
probably benign |
Het |
Pkhd1 |
T |
C |
1: 20,128,526 (GRCm39) |
Q4059R |
probably benign |
Het |
Ppa2 |
A |
T |
3: 133,026,764 (GRCm39) |
|
probably null |
Het |
Proser1 |
G |
A |
3: 53,387,966 (GRCm39) |
A885T |
probably benign |
Het |
Robo2 |
A |
G |
16: 73,758,776 (GRCm39) |
I665T |
probably damaging |
Het |
Robo4 |
CGG |
CG |
9: 37,322,786 (GRCm39) |
|
probably null |
Het |
Secisbp2 |
G |
A |
13: 51,808,671 (GRCm39) |
|
probably null |
Het |
Setbp1 |
T |
A |
18: 78,967,211 (GRCm39) |
Q171L |
probably benign |
Het |
Spata1 |
A |
G |
3: 146,193,295 (GRCm39) |
L96P |
possibly damaging |
Het |
Srprb |
G |
A |
9: 103,076,038 (GRCm39) |
Q800* |
probably null |
Het |
Stk11ip |
A |
G |
1: 75,505,911 (GRCm39) |
|
probably benign |
Het |
Tbl3 |
T |
C |
17: 24,921,557 (GRCm39) |
T445A |
probably damaging |
Het |
Tdrd12 |
G |
A |
7: 35,184,798 (GRCm39) |
T705M |
probably damaging |
Het |
Tek |
A |
G |
4: 94,708,461 (GRCm39) |
T340A |
probably benign |
Het |
Timm22 |
G |
A |
11: 76,304,925 (GRCm39) |
A188T |
probably damaging |
Het |
Tmeff1 |
T |
A |
4: 48,604,692 (GRCm39) |
|
probably null |
Het |
Tmprss12 |
C |
A |
15: 100,180,296 (GRCm39) |
T112K |
possibly damaging |
Het |
U2surp |
A |
G |
9: 95,382,735 (GRCm39) |
|
probably null |
Het |
Vmn2r84 |
T |
A |
10: 130,230,036 (GRCm39) |
E25D |
probably benign |
Het |
Wdr62 |
A |
T |
7: 29,960,862 (GRCm39) |
N22K |
possibly damaging |
Het |
Zfp653 |
A |
T |
9: 21,968,862 (GRCm39) |
D426E |
probably benign |
Het |
Zfyve28 |
G |
A |
5: 34,354,006 (GRCm39) |
P834L |
probably damaging |
Het |
Zkscan16 |
A |
G |
4: 58,957,364 (GRCm39) |
T549A |
possibly damaging |
Het |
|
Other mutations in Cyp51 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02045:Cyp51
|
APN |
5 |
4,133,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02047:Cyp51
|
APN |
5 |
4,149,244 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02191:Cyp51
|
APN |
5 |
4,150,147 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02492:Cyp51
|
APN |
5 |
4,154,304 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03209:Cyp51
|
APN |
5 |
4,154,195 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4515001:Cyp51
|
UTSW |
5 |
4,149,122 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4520001:Cyp51
|
UTSW |
5 |
4,151,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0535:Cyp51
|
UTSW |
5 |
4,149,202 (GRCm39) |
missense |
probably benign |
0.00 |
R2048:Cyp51
|
UTSW |
5 |
4,136,636 (GRCm39) |
splice site |
probably benign |
|
R2165:Cyp51
|
UTSW |
5 |
4,136,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R3975:Cyp51
|
UTSW |
5 |
4,141,877 (GRCm39) |
missense |
probably damaging |
0.97 |
R4799:Cyp51
|
UTSW |
5 |
4,133,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5699:Cyp51
|
UTSW |
5 |
4,151,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Cyp51
|
UTSW |
5 |
4,150,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R6484:Cyp51
|
UTSW |
5 |
4,136,627 (GRCm39) |
missense |
probably benign |
0.07 |
R7046:Cyp51
|
UTSW |
5 |
4,150,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Cyp51
|
UTSW |
5 |
4,137,846 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7877:Cyp51
|
UTSW |
5 |
4,152,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Cyp51
|
UTSW |
5 |
4,150,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R8094:Cyp51
|
UTSW |
5 |
4,136,490 (GRCm39) |
missense |
probably benign |
0.08 |
R8095:Cyp51
|
UTSW |
5 |
4,136,490 (GRCm39) |
missense |
probably benign |
0.08 |
R8938:Cyp51
|
UTSW |
5 |
4,150,202 (GRCm39) |
missense |
probably benign |
0.00 |
R8963:Cyp51
|
UTSW |
5 |
4,136,519 (GRCm39) |
missense |
probably damaging |
0.98 |
R9097:Cyp51
|
UTSW |
5 |
4,149,172 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9173:Cyp51
|
UTSW |
5 |
4,136,504 (GRCm39) |
missense |
probably benign |
|
R9416:Cyp51
|
UTSW |
5 |
4,150,198 (GRCm39) |
missense |
probably damaging |
0.98 |
|