Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp4 |
G |
T |
7: 43,906,399 (GRCm39) |
T51K |
possibly damaging |
Het |
Angel2 |
C |
T |
1: 190,665,332 (GRCm39) |
R88C |
probably damaging |
Het |
Ankrd13b |
G |
A |
11: 77,367,452 (GRCm39) |
R181C |
probably damaging |
Het |
Bmal2 |
T |
C |
6: 146,722,142 (GRCm39) |
C238R |
probably benign |
Het |
Brd3 |
C |
T |
2: 27,354,013 (GRCm39) |
R33Q |
probably damaging |
Het |
Ccdc106 |
T |
A |
7: 5,060,500 (GRCm39) |
L20Q |
probably benign |
Het |
Ccdc117 |
A |
T |
11: 5,491,421 (GRCm39) |
V62D |
possibly damaging |
Het |
Ccnt1 |
T |
C |
15: 98,441,096 (GRCm39) |
|
probably benign |
Het |
Cfap95 |
T |
C |
19: 23,536,385 (GRCm39) |
E174G |
possibly damaging |
Het |
Cmip |
G |
A |
8: 118,138,054 (GRCm39) |
V178I |
probably benign |
Het |
Cnnm3 |
A |
G |
1: 36,558,096 (GRCm39) |
E436G |
probably damaging |
Het |
Dcaf11 |
A |
G |
14: 55,806,761 (GRCm39) |
N488S |
probably benign |
Het |
Dlg2 |
A |
T |
7: 90,501,927 (GRCm39) |
K80* |
probably null |
Het |
Dnase1l2 |
T |
A |
17: 24,661,642 (GRCm39) |
D39V |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,078,945 (GRCm39) |
D708G |
probably benign |
Het |
Enpep |
A |
T |
3: 129,113,090 (GRCm39) |
L278Q |
probably damaging |
Het |
Ephb6 |
C |
T |
6: 41,590,293 (GRCm39) |
A15V |
probably benign |
Het |
Flt3 |
T |
G |
5: 147,303,774 (GRCm39) |
Q388P |
possibly damaging |
Het |
Hltf |
A |
G |
3: 20,136,936 (GRCm39) |
Y329C |
probably damaging |
Het |
Hmcn2 |
C |
T |
2: 31,282,159 (GRCm39) |
P1924S |
probably damaging |
Het |
Iba57 |
A |
G |
11: 59,052,461 (GRCm39) |
V122A |
probably benign |
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Irak2 |
T |
A |
6: 113,624,702 (GRCm39) |
M66K |
probably damaging |
Het |
Mkrn2os |
G |
C |
6: 115,562,317 (GRCm39) |
S215R |
probably benign |
Het |
Mpped1 |
G |
A |
15: 83,676,342 (GRCm39) |
R36Q |
probably damaging |
Het |
Myh1 |
C |
A |
11: 67,102,328 (GRCm39) |
A873E |
probably benign |
Het |
Nedd9 |
G |
T |
13: 41,469,758 (GRCm39) |
A465D |
probably damaging |
Het |
Nr2f1 |
G |
T |
13: 78,337,873 (GRCm39) |
Y257* |
probably null |
Het |
Omd |
A |
G |
13: 49,745,790 (GRCm39) |
E400G |
possibly damaging |
Het |
Or5j1 |
T |
A |
2: 86,879,551 (GRCm39) |
T10S |
possibly damaging |
Het |
Or6c202 |
A |
G |
10: 128,996,484 (GRCm39) |
I123T |
probably damaging |
Het |
Patj |
T |
C |
4: 98,480,212 (GRCm39) |
S1306P |
probably damaging |
Het |
Pdzph1 |
T |
C |
17: 59,281,599 (GRCm39) |
K228E |
probably damaging |
Het |
Rad18 |
T |
C |
6: 112,605,444 (GRCm39) |
E410G |
probably damaging |
Het |
Rp1 |
T |
A |
1: 4,419,650 (GRCm39) |
|
probably benign |
Het |
Runx3 |
C |
T |
4: 134,902,968 (GRCm39) |
S366L |
probably damaging |
Het |
Ssh3 |
T |
A |
19: 4,318,590 (GRCm39) |
R30S |
probably damaging |
Het |
Stxbp5l |
ATTTT |
ATTTTT |
16: 37,036,414 (GRCm39) |
|
probably null |
Het |
Taf6l |
A |
G |
19: 8,750,690 (GRCm39) |
F128S |
possibly damaging |
Het |
Tmc6 |
A |
C |
11: 117,661,293 (GRCm39) |
|
probably null |
Het |
Trpc3 |
T |
G |
3: 36,709,258 (GRCm39) |
Q406P |
probably benign |
Het |
Uncx |
C |
A |
5: 139,529,826 (GRCm39) |
Y26* |
probably null |
Het |
Urb1 |
T |
C |
16: 90,571,005 (GRCm39) |
D1268G |
probably benign |
Het |
Wif1 |
T |
C |
10: 120,931,957 (GRCm39) |
C294R |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,979,137 (GRCm39) |
L425F |
probably damaging |
Het |
Zfp78 |
A |
G |
7: 6,382,380 (GRCm39) |
R477G |
probably damaging |
Het |
|
Other mutations in Prl2c5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00910:Prl2c5
|
APN |
13 |
13,364,061 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01874:Prl2c5
|
APN |
13 |
13,365,362 (GRCm39) |
missense |
probably benign |
|
IGL01878:Prl2c5
|
APN |
13 |
13,360,402 (GRCm39) |
missense |
probably benign |
0.00 |
R0178:Prl2c5
|
UTSW |
13 |
13,366,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R0276:Prl2c5
|
UTSW |
13 |
13,357,634 (GRCm39) |
intron |
probably benign |
|
R0373:Prl2c5
|
UTSW |
13 |
13,357,609 (GRCm39) |
intron |
probably benign |
|
R0539:Prl2c5
|
UTSW |
13 |
13,363,906 (GRCm39) |
splice site |
probably null |
|
R1037:Prl2c5
|
UTSW |
13 |
13,360,492 (GRCm39) |
nonsense |
probably null |
|
R1296:Prl2c5
|
UTSW |
13 |
13,364,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Prl2c5
|
UTSW |
13 |
13,365,310 (GRCm39) |
missense |
probably benign |
0.40 |
R1557:Prl2c5
|
UTSW |
13 |
13,365,265 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1850:Prl2c5
|
UTSW |
13 |
13,360,377 (GRCm39) |
missense |
probably benign |
0.40 |
R1866:Prl2c5
|
UTSW |
13 |
13,365,358 (GRCm39) |
splice site |
probably null |
|
R1894:Prl2c5
|
UTSW |
13 |
13,366,263 (GRCm39) |
missense |
probably benign |
0.04 |
R2060:Prl2c5
|
UTSW |
13 |
13,365,238 (GRCm39) |
missense |
probably damaging |
0.99 |
R2330:Prl2c5
|
UTSW |
13 |
13,366,378 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4755:Prl2c5
|
UTSW |
13 |
13,363,970 (GRCm39) |
missense |
probably benign |
|
R5229:Prl2c5
|
UTSW |
13 |
13,360,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R5364:Prl2c5
|
UTSW |
13 |
13,357,627 (GRCm39) |
missense |
probably benign |
0.01 |
R6307:Prl2c5
|
UTSW |
13 |
13,365,175 (GRCm39) |
missense |
probably benign |
0.01 |
R6350:Prl2c5
|
UTSW |
13 |
13,357,631 (GRCm39) |
critical splice donor site |
probably null |
|
R6927:Prl2c5
|
UTSW |
13 |
13,357,503 (GRCm39) |
splice site |
probably null |
|
R7397:Prl2c5
|
UTSW |
13 |
13,366,327 (GRCm39) |
missense |
probably benign |
0.01 |
R7965:Prl2c5
|
UTSW |
13 |
13,360,469 (GRCm39) |
missense |
probably benign |
0.01 |
R8084:Prl2c5
|
UTSW |
13 |
13,360,539 (GRCm39) |
missense |
probably benign |
0.20 |
R8980:Prl2c5
|
UTSW |
13 |
13,360,470 (GRCm39) |
missense |
probably benign |
0.12 |
R9258:Prl2c5
|
UTSW |
13 |
13,365,297 (GRCm39) |
missense |
probably damaging |
0.97 |
R9465:Prl2c5
|
UTSW |
13 |
13,360,531 (GRCm39) |
missense |
probably benign |
0.42 |
RF020:Prl2c5
|
UTSW |
13 |
13,360,497 (GRCm39) |
missense |
probably benign |
0.28 |
X0025:Prl2c5
|
UTSW |
13 |
13,366,339 (GRCm39) |
missense |
probably benign |
0.03 |
|