Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad8 |
A |
G |
9: 26,901,923 (GRCm39) |
L147P |
probably damaging |
Het |
Acan |
A |
G |
7: 78,750,890 (GRCm39) |
E464G |
probably benign |
Het |
Agap1 |
A |
G |
1: 89,765,528 (GRCm39) |
|
probably null |
Het |
Akap13 |
A |
G |
7: 75,378,842 (GRCm39) |
T2128A |
probably damaging |
Het |
Ap2a1 |
A |
T |
7: 44,552,343 (GRCm39) |
|
probably benign |
Het |
Arap3 |
T |
C |
18: 38,129,307 (GRCm39) |
D217G |
probably benign |
Het |
Arl2 |
C |
A |
19: 6,184,716 (GRCm39) |
R179L |
probably damaging |
Het |
Atg2a |
T |
A |
19: 6,309,017 (GRCm39) |
|
probably null |
Het |
B3gat1 |
T |
A |
9: 26,663,052 (GRCm39) |
L6Q |
probably benign |
Het |
Bcl10 |
A |
G |
3: 145,636,327 (GRCm39) |
N75S |
probably damaging |
Het |
Bmpr2 |
T |
C |
1: 59,906,875 (GRCm39) |
L656S |
probably damaging |
Het |
Brms1l |
A |
G |
12: 55,888,356 (GRCm39) |
E48G |
possibly damaging |
Het |
C2cd2l |
A |
T |
9: 44,226,322 (GRCm39) |
N414K |
possibly damaging |
Het |
Capn2 |
C |
T |
1: 182,298,345 (GRCm39) |
C640Y |
probably benign |
Het |
Ccdc153 |
G |
T |
9: 44,157,021 (GRCm39) |
R99M |
probably damaging |
Het |
Ccdc51 |
A |
G |
9: 108,920,030 (GRCm39) |
N142S |
probably benign |
Het |
Cdipt |
A |
G |
7: 126,577,578 (GRCm39) |
H108R |
possibly damaging |
Het |
Ceacam20 |
T |
C |
7: 19,719,952 (GRCm39) |
Y495H |
probably damaging |
Het |
Celf2 |
T |
C |
2: 6,726,339 (GRCm39) |
I47V |
probably benign |
Het |
Cts3 |
C |
T |
13: 61,714,637 (GRCm39) |
E223K |
probably benign |
Het |
Cyp2c67 |
T |
A |
19: 39,632,098 (GRCm39) |
H90L |
probably benign |
Het |
Ddx4 |
T |
C |
13: 112,758,778 (GRCm39) |
Y261C |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 117,965,119 (GRCm39) |
T2308A |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,014,671 (GRCm39) |
T3587A |
probably damaging |
Het |
Dpy19l1 |
C |
T |
9: 24,343,664 (GRCm39) |
V494I |
possibly damaging |
Het |
Dse |
T |
G |
10: 34,029,008 (GRCm39) |
Y694S |
probably damaging |
Het |
Emilin3 |
T |
C |
2: 160,752,717 (GRCm39) |
I78V |
probably benign |
Het |
Esam |
T |
A |
9: 37,447,952 (GRCm39) |
Y195* |
probably null |
Het |
Extl3 |
T |
A |
14: 65,313,745 (GRCm39) |
N479I |
possibly damaging |
Het |
Fat2 |
A |
G |
11: 55,202,441 (GRCm39) |
V211A |
probably benign |
Het |
Ganc |
G |
T |
2: 120,261,548 (GRCm39) |
V343F |
probably benign |
Het |
Ggt5 |
T |
C |
10: 75,438,865 (GRCm39) |
L121P |
probably damaging |
Het |
Gnmt |
A |
T |
17: 47,037,225 (GRCm39) |
C186* |
probably null |
Het |
Gpr75 |
A |
T |
11: 30,842,072 (GRCm39) |
I326F |
probably damaging |
Het |
Gsdme |
C |
T |
6: 50,185,102 (GRCm39) |
V451M |
probably damaging |
Het |
H2-T23 |
G |
T |
17: 36,342,690 (GRCm39) |
D149E |
probably damaging |
Het |
Hmcn2 |
G |
T |
2: 31,325,804 (GRCm39) |
R4277L |
probably benign |
Het |
Irf9 |
C |
A |
14: 55,843,223 (GRCm39) |
H94N |
probably benign |
Het |
Jhy |
T |
C |
9: 40,872,449 (GRCm39) |
N20S |
probably benign |
Het |
Klf17 |
C |
A |
4: 117,617,568 (GRCm39) |
C263F |
probably damaging |
Het |
Lama5 |
T |
C |
2: 179,822,430 (GRCm39) |
Y2881C |
probably damaging |
Het |
Lig1 |
T |
G |
7: 13,044,953 (GRCm39) |
I882S |
probably damaging |
Het |
Ltn1 |
A |
T |
16: 87,215,375 (GRCm39) |
M420K |
possibly damaging |
Het |
Mael |
T |
C |
1: 166,063,077 (GRCm39) |
E125G |
probably damaging |
Het |
Mib2 |
C |
T |
4: 155,741,872 (GRCm39) |
D275N |
possibly damaging |
Het |
Mical3 |
C |
T |
6: 120,934,664 (GRCm39) |
R1805Q |
probably damaging |
Het |
Mix23 |
A |
G |
16: 35,903,089 (GRCm39) |
D27G |
probably damaging |
Het |
Mllt10 |
A |
G |
2: 18,208,444 (GRCm39) |
D158G |
probably damaging |
Het |
Mocs1 |
A |
G |
17: 49,761,613 (GRCm39) |
D569G |
possibly damaging |
Het |
Msh6 |
T |
C |
17: 88,292,234 (GRCm39) |
S330P |
possibly damaging |
Het |
Mtmr2 |
T |
C |
9: 13,707,260 (GRCm39) |
S199P |
probably damaging |
Het |
Ndufaf5 |
T |
C |
2: 140,029,675 (GRCm39) |
V164A |
probably benign |
Het |
Nek9 |
T |
C |
12: 85,360,978 (GRCm39) |
E518G |
probably benign |
Het |
Nfatc2 |
T |
C |
2: 168,413,410 (GRCm39) |
I72V |
probably benign |
Het |
Nlrp9c |
C |
T |
7: 26,074,793 (GRCm39) |
A746T |
possibly damaging |
Het |
Nup42 |
A |
G |
5: 24,387,415 (GRCm39) |
R402G |
probably benign |
Het |
Ogdh |
G |
T |
11: 6,290,600 (GRCm39) |
C406F |
probably benign |
Het |
Or3a1d |
A |
G |
11: 74,237,789 (GRCm39) |
V207A |
probably benign |
Het |
Or4c120 |
G |
A |
2: 89,001,245 (GRCm39) |
H104Y |
probably damaging |
Het |
Or8b35 |
A |
T |
9: 37,904,381 (GRCm39) |
I198F |
possibly damaging |
Het |
Or8g17 |
T |
A |
9: 38,930,675 (GRCm39) |
Y54F |
probably benign |
Het |
Or8j3 |
A |
T |
2: 86,028,277 (GRCm39) |
M273K |
possibly damaging |
Het |
Otof |
A |
G |
5: 30,578,318 (GRCm39) |
|
probably null |
Het |
Pcdhb17 |
T |
C |
18: 37,619,259 (GRCm39) |
S350P |
probably damaging |
Het |
Phf3 |
T |
C |
1: 30,869,027 (GRCm39) |
T674A |
probably damaging |
Het |
Pikfyve |
T |
A |
1: 65,289,432 (GRCm39) |
C1235S |
probably damaging |
Het |
Ppfia3 |
T |
C |
7: 45,001,517 (GRCm39) |
E465G |
probably damaging |
Het |
Prkg1 |
T |
A |
19: 31,641,639 (GRCm39) |
I15F |
probably damaging |
Het |
Rab5c |
A |
G |
11: 100,610,843 (GRCm39) |
F22L |
probably damaging |
Het |
Raf1 |
A |
G |
6: 115,609,880 (GRCm39) |
S220P |
probably damaging |
Het |
Rgl1 |
T |
G |
1: 152,397,122 (GRCm39) |
R716S |
probably damaging |
Het |
Rhbg |
C |
A |
3: 88,153,273 (GRCm39) |
W205L |
probably damaging |
Het |
Rimbp3 |
A |
G |
16: 17,027,053 (GRCm39) |
E159G |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,759,256 (GRCm39) |
D3338G |
probably null |
Het |
Sash1 |
T |
C |
10: 8,606,149 (GRCm39) |
N747S |
probably benign |
Het |
Serpina3g |
A |
T |
12: 104,205,479 (GRCm39) |
I73F |
probably damaging |
Het |
Sfxn2 |
C |
A |
19: 46,574,213 (GRCm39) |
N134K |
probably damaging |
Het |
Slc12a6 |
A |
G |
2: 112,184,640 (GRCm39) |
H853R |
probably damaging |
Het |
Slc16a12 |
C |
T |
19: 34,649,965 (GRCm39) |
D357N |
probably damaging |
Het |
Slc39a8 |
T |
C |
3: 135,561,772 (GRCm39) |
Y164H |
probably benign |
Het |
Snx9 |
A |
G |
17: 5,977,499 (GRCm39) |
K518E |
probably damaging |
Het |
Spdye4c |
G |
A |
2: 128,434,273 (GRCm39) |
V5I |
possibly damaging |
Het |
Spef2 |
A |
G |
15: 9,676,459 (GRCm39) |
V704A |
probably benign |
Het |
Stard3nl |
T |
A |
13: 19,560,689 (GRCm39) |
N29Y |
probably damaging |
Het |
Strap |
C |
A |
6: 137,712,384 (GRCm39) |
S11* |
probably null |
Het |
Synpo2 |
A |
G |
3: 122,906,712 (GRCm39) |
L868P |
probably damaging |
Het |
Tenm2 |
A |
G |
11: 35,901,314 (GRCm39) |
V2474A |
probably damaging |
Het |
Tm9sf4 |
T |
A |
2: 153,029,228 (GRCm39) |
V92D |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,147,388 (GRCm39) |
M526K |
probably benign |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Ttc39d |
A |
G |
17: 80,525,068 (GRCm39) |
I576V |
probably benign |
Het |
Upk1a |
T |
G |
7: 30,304,554 (GRCm39) |
T193P |
probably benign |
Het |
Vmn2r67 |
A |
T |
7: 84,799,732 (GRCm39) |
V502E |
probably benign |
Het |
Wdr17 |
A |
G |
8: 55,143,083 (GRCm39) |
V189A |
possibly damaging |
Het |
Wrap73 |
A |
T |
4: 154,236,153 (GRCm39) |
S161C |
probably benign |
Het |
Zfp568 |
A |
G |
7: 29,722,702 (GRCm39) |
H549R |
probably damaging |
Het |
Zfp605 |
T |
A |
5: 110,275,227 (GRCm39) |
M115K |
possibly damaging |
Het |
Zp1 |
T |
A |
19: 10,896,269 (GRCm39) |
H152L |
probably benign |
Het |
|
Other mutations in Cyp2a22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Cyp2a22
|
APN |
7 |
26,637,163 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01111:Cyp2a22
|
APN |
7 |
26,635,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01388:Cyp2a22
|
APN |
7 |
26,637,217 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01449:Cyp2a22
|
APN |
7 |
26,632,978 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01642:Cyp2a22
|
APN |
7 |
26,638,184 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02253:Cyp2a22
|
APN |
7 |
26,637,662 (GRCm39) |
splice site |
probably benign |
|
IGL02327:Cyp2a22
|
APN |
7 |
26,634,206 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02673:Cyp2a22
|
APN |
7 |
26,637,525 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02813:Cyp2a22
|
APN |
7 |
26,635,859 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02896:Cyp2a22
|
APN |
7 |
26,635,886 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03193:Cyp2a22
|
APN |
7 |
26,635,846 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03350:Cyp2a22
|
APN |
7 |
26,634,279 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1648:Cyp2a22
|
UTSW |
7 |
26,631,793 (GRCm39) |
missense |
probably damaging |
0.98 |
R1679:Cyp2a22
|
UTSW |
7 |
26,635,736 (GRCm39) |
nonsense |
probably null |
|
R1733:Cyp2a22
|
UTSW |
7 |
26,634,187 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2001:Cyp2a22
|
UTSW |
7 |
26,634,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R2858:Cyp2a22
|
UTSW |
7 |
26,633,687 (GRCm39) |
missense |
probably damaging |
0.99 |
R3054:Cyp2a22
|
UTSW |
7 |
26,638,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R4528:Cyp2a22
|
UTSW |
7 |
26,634,194 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4623:Cyp2a22
|
UTSW |
7 |
26,632,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R4690:Cyp2a22
|
UTSW |
7 |
26,638,634 (GRCm39) |
nonsense |
probably null |
|
R4840:Cyp2a22
|
UTSW |
7 |
26,631,949 (GRCm39) |
missense |
probably benign |
0.13 |
R4915:Cyp2a22
|
UTSW |
7 |
26,637,195 (GRCm39) |
missense |
probably benign |
0.33 |
R5071:Cyp2a22
|
UTSW |
7 |
26,631,906 (GRCm39) |
missense |
probably benign |
0.01 |
R5072:Cyp2a22
|
UTSW |
7 |
26,631,906 (GRCm39) |
missense |
probably benign |
0.01 |
R5074:Cyp2a22
|
UTSW |
7 |
26,631,906 (GRCm39) |
missense |
probably benign |
0.01 |
R5147:Cyp2a22
|
UTSW |
7 |
26,635,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Cyp2a22
|
UTSW |
7 |
26,635,858 (GRCm39) |
missense |
probably damaging |
0.99 |
R5705:Cyp2a22
|
UTSW |
7 |
26,638,640 (GRCm39) |
missense |
probably benign |
0.05 |
R6014:Cyp2a22
|
UTSW |
7 |
26,638,605 (GRCm39) |
splice site |
probably null |
|
R6042:Cyp2a22
|
UTSW |
7 |
26,633,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6253:Cyp2a22
|
UTSW |
7 |
26,633,657 (GRCm39) |
missense |
probably benign |
0.18 |
R6757:Cyp2a22
|
UTSW |
7 |
26,638,629 (GRCm39) |
missense |
probably benign |
0.00 |
R6994:Cyp2a22
|
UTSW |
7 |
26,638,606 (GRCm39) |
critical splice donor site |
probably null |
|
R7581:Cyp2a22
|
UTSW |
7 |
26,637,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8212:Cyp2a22
|
UTSW |
7 |
26,637,205 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9225:Cyp2a22
|
UTSW |
7 |
26,637,202 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9749:Cyp2a22
|
UTSW |
7 |
26,638,715 (GRCm39) |
missense |
probably null |
0.41 |
|