Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
8430423G03Rik |
A |
G |
5: 148,887,472 (GRCm39) |
|
probably benign |
Het |
Adam4 |
C |
T |
12: 81,468,102 (GRCm39) |
R173H |
probably benign |
Het |
Akap12 |
A |
G |
10: 4,306,034 (GRCm39) |
E948G |
possibly damaging |
Het |
Avil |
T |
C |
10: 126,854,316 (GRCm39) |
V761A |
probably benign |
Het |
Bahd1 |
T |
A |
2: 118,749,645 (GRCm39) |
F480L |
probably benign |
Het |
Bicral |
T |
C |
17: 47,119,380 (GRCm39) |
T714A |
probably benign |
Het |
Cert1 |
T |
C |
13: 96,746,390 (GRCm39) |
I263T |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cyp2d34 |
C |
T |
15: 82,502,480 (GRCm39) |
V219I |
probably benign |
Het |
Dsn1 |
A |
G |
2: 156,838,667 (GRCm39) |
V316A |
probably damaging |
Het |
Errfi1 |
T |
A |
4: 150,950,813 (GRCm39) |
F80L |
probably benign |
Het |
Fam221b |
A |
G |
4: 43,660,642 (GRCm39) |
|
probably null |
Het |
Fgd6 |
G |
A |
10: 93,910,064 (GRCm39) |
G790R |
probably benign |
Het |
Fn1 |
T |
C |
1: 71,680,302 (GRCm39) |
|
probably benign |
Het |
Gldn |
T |
A |
9: 54,246,005 (GRCm39) |
Y519N |
probably damaging |
Het |
Il18r1 |
T |
C |
1: 40,530,381 (GRCm39) |
|
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,292,819 (GRCm39) |
V380A |
probably damaging |
Het |
Kcnab1 |
T |
C |
3: 65,209,600 (GRCm39) |
Y154H |
possibly damaging |
Het |
Lama1 |
T |
C |
17: 68,118,480 (GRCm39) |
V2564A |
probably benign |
Het |
Lca5 |
T |
C |
9: 83,281,774 (GRCm39) |
T337A |
probably damaging |
Het |
Lrp1 |
A |
G |
10: 127,407,756 (GRCm39) |
|
probably null |
Het |
Moxd1 |
A |
G |
10: 24,155,334 (GRCm39) |
N245S |
probably benign |
Het |
Napepld |
T |
C |
5: 21,888,440 (GRCm39) |
E3G |
probably benign |
Het |
Nr1d2 |
T |
C |
14: 18,222,011 (GRCm38) |
T87A |
probably benign |
Het |
Nudt4 |
T |
A |
10: 95,385,245 (GRCm39) |
T149S |
probably benign |
Het |
Rad18 |
A |
T |
6: 112,597,859 (GRCm39) |
D219E |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,760,560 (GRCm39) |
I1508V |
probably damaging |
Het |
Setx |
G |
A |
2: 29,038,420 (GRCm39) |
S1635N |
probably benign |
Het |
Slc6a19 |
A |
G |
13: 73,839,919 (GRCm39) |
V121A |
probably benign |
Het |
Snapc4 |
T |
C |
2: 26,258,212 (GRCm39) |
D736G |
probably damaging |
Het |
Spink5 |
T |
C |
18: 44,123,811 (GRCm39) |
|
probably null |
Het |
Strip1 |
T |
C |
3: 107,521,962 (GRCm39) |
I739V |
probably benign |
Het |
Tmem161a |
T |
C |
8: 70,629,577 (GRCm39) |
|
probably null |
Het |
Top1mt |
T |
C |
15: 75,547,970 (GRCm39) |
T39A |
probably benign |
Het |
Trpm1 |
T |
C |
7: 63,890,175 (GRCm39) |
M926T |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,587,624 (GRCm39) |
K19744* |
probably null |
Het |
Vmn2r26 |
A |
G |
6: 124,038,777 (GRCm39) |
E784G |
probably damaging |
Het |
Wnk1 |
A |
G |
6: 119,940,415 (GRCm39) |
F774S |
probably damaging |
Het |
Zfp317 |
T |
A |
9: 19,554,909 (GRCm39) |
Y101* |
probably null |
Het |
|
Other mutations in Akr1c12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01479:Akr1c12
|
APN |
13 |
4,322,934 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01603:Akr1c12
|
APN |
13 |
4,322,926 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01935:Akr1c12
|
APN |
13 |
4,322,244 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02066:Akr1c12
|
APN |
13 |
4,326,236 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02224:Akr1c12
|
APN |
13 |
4,329,289 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02277:Akr1c12
|
APN |
13 |
4,322,268 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02884:Akr1c12
|
APN |
13 |
4,322,211 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02959:Akr1c12
|
APN |
13 |
4,329,331 (GRCm39) |
missense |
probably benign |
|
IGL03075:Akr1c12
|
APN |
13 |
4,322,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Akr1c12
|
UTSW |
13 |
4,326,322 (GRCm39) |
missense |
probably benign |
0.10 |
R1302:Akr1c12
|
UTSW |
13 |
4,322,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R1520:Akr1c12
|
UTSW |
13 |
4,326,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R2213:Akr1c12
|
UTSW |
13 |
4,326,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R3944:Akr1c12
|
UTSW |
13 |
4,329,339 (GRCm39) |
missense |
probably benign |
|
R4671:Akr1c12
|
UTSW |
13 |
4,323,816 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6237:Akr1c12
|
UTSW |
13 |
4,325,767 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6266:Akr1c12
|
UTSW |
13 |
4,320,206 (GRCm39) |
missense |
probably benign |
|
R6467:Akr1c12
|
UTSW |
13 |
4,325,772 (GRCm39) |
missense |
probably benign |
0.10 |
R6826:Akr1c12
|
UTSW |
13 |
4,325,733 (GRCm39) |
missense |
probably benign |
0.06 |
R6865:Akr1c12
|
UTSW |
13 |
4,320,212 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6874:Akr1c12
|
UTSW |
13 |
4,322,959 (GRCm39) |
missense |
probably benign |
0.22 |
R7574:Akr1c12
|
UTSW |
13 |
4,329,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Akr1c12
|
UTSW |
13 |
4,322,244 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8242:Akr1c12
|
UTSW |
13 |
4,322,269 (GRCm39) |
nonsense |
probably null |
|
R8295:Akr1c12
|
UTSW |
13 |
4,322,355 (GRCm39) |
missense |
probably benign |
0.02 |
R8530:Akr1c12
|
UTSW |
13 |
4,320,160 (GRCm39) |
missense |
probably benign |
|
R8749:Akr1c12
|
UTSW |
13 |
4,320,155 (GRCm39) |
splice site |
probably benign |
|
R9420:Akr1c12
|
UTSW |
13 |
4,325,796 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Akr1c12
|
UTSW |
13 |
4,322,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|