Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
A |
T |
19: 43,814,406 (GRCm39) |
S1129C |
possibly damaging |
Het |
Afm |
A |
T |
5: 90,679,466 (GRCm39) |
D320V |
probably damaging |
Het |
Ap5m1 |
C |
T |
14: 49,311,392 (GRCm39) |
T154I |
probably benign |
Het |
Bcl11b |
G |
A |
12: 107,956,065 (GRCm39) |
T28I |
probably benign |
Het |
Bhlhe40 |
G |
T |
6: 108,641,503 (GRCm39) |
C149F |
probably damaging |
Het |
Bmper |
A |
T |
9: 23,310,790 (GRCm39) |
D408V |
probably damaging |
Het |
C1rl |
G |
A |
6: 124,485,820 (GRCm39) |
C397Y |
probably damaging |
Het |
C2cd4c |
A |
G |
10: 79,448,665 (GRCm39) |
S161P |
probably damaging |
Het |
Cemip2 |
A |
T |
19: 21,819,564 (GRCm39) |
K1118N |
probably benign |
Het |
Cep290 |
T |
C |
10: 100,376,191 (GRCm39) |
|
probably benign |
Het |
Cp |
T |
C |
3: 20,042,165 (GRCm39) |
Y978H |
probably damaging |
Het |
Csf2ra |
T |
C |
19: 61,215,607 (GRCm39) |
D37G |
probably benign |
Het |
Ddx24 |
A |
G |
12: 103,383,801 (GRCm39) |
V596A |
probably damaging |
Het |
Dnmt3l |
A |
G |
10: 77,886,785 (GRCm39) |
S82G |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,331,753 (GRCm39) |
Y46C |
probably damaging |
Het |
Eno2 |
A |
T |
6: 124,740,081 (GRCm39) |
D318E |
probably damaging |
Het |
Gm43738 |
A |
C |
3: 88,996,355 (GRCm39) |
L120R |
probably damaging |
Het |
Hgsnat |
C |
A |
8: 26,461,729 (GRCm39) |
C29F |
probably damaging |
Het |
Hltf |
T |
A |
3: 20,130,736 (GRCm39) |
V318D |
probably benign |
Het |
Kcnh8 |
A |
G |
17: 53,263,795 (GRCm39) |
H764R |
probably benign |
Het |
Kcnq3 |
A |
G |
15: 65,892,142 (GRCm39) |
F411S |
probably benign |
Het |
Lpcat4 |
C |
A |
2: 112,074,387 (GRCm39) |
N287K |
possibly damaging |
Het |
Ltbp4 |
A |
C |
7: 27,006,143 (GRCm39) |
F1512V |
probably damaging |
Het |
Mctp1 |
A |
T |
13: 77,172,929 (GRCm39) |
L868F |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,713,360 (GRCm39) |
|
probably benign |
Het |
Or5g23 |
A |
T |
2: 85,438,501 (GRCm39) |
L251Q |
possibly damaging |
Het |
Otub2 |
A |
G |
12: 103,369,632 (GRCm39) |
D237G |
probably damaging |
Het |
Pax3 |
A |
G |
1: 78,079,997 (GRCm39) |
V463A |
probably benign |
Het |
Podn |
T |
C |
4: 107,875,048 (GRCm39) |
K573R |
possibly damaging |
Het |
Ppp5c |
A |
C |
7: 16,740,835 (GRCm39) |
S378A |
probably benign |
Het |
Pramel29 |
A |
G |
4: 143,939,531 (GRCm39) |
V2A |
probably benign |
Het |
Ptgir |
A |
G |
7: 16,641,526 (GRCm39) |
T70A |
probably damaging |
Het |
Ralyl |
C |
A |
3: 14,104,781 (GRCm39) |
N15K |
probably damaging |
Het |
Rbck1 |
C |
T |
2: 152,172,997 (GRCm39) |
R17Q |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,796,884 (GRCm39) |
Y973H |
probably damaging |
Het |
Sh2d6 |
A |
G |
6: 72,492,285 (GRCm39) |
V260A |
probably damaging |
Het |
Spen |
G |
A |
4: 141,196,819 (GRCm39) |
P3559S |
probably damaging |
Het |
Tbcd |
T |
A |
11: 121,494,535 (GRCm39) |
V1032D |
probably damaging |
Het |
Trav12-1 |
T |
A |
14: 53,776,024 (GRCm39) |
V59E |
probably damaging |
Het |
Unc93a |
T |
A |
17: 13,344,455 (GRCm39) |
Q29L |
probably damaging |
Het |
Zzef1 |
A |
G |
11: 72,808,525 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Prl2a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00673:Prl2a1
|
APN |
13 |
27,992,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01977:Prl2a1
|
APN |
13 |
27,990,261 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02243:Prl2a1
|
APN |
13 |
27,991,400 (GRCm39) |
splice site |
probably benign |
|
IGL02666:Prl2a1
|
APN |
13 |
27,990,310 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03390:Prl2a1
|
APN |
13 |
27,985,699 (GRCm39) |
missense |
probably benign |
0.00 |
R1795:Prl2a1
|
UTSW |
13 |
27,992,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Prl2a1
|
UTSW |
13 |
27,988,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1868:Prl2a1
|
UTSW |
13 |
27,988,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2221:Prl2a1
|
UTSW |
13 |
27,990,369 (GRCm39) |
critical splice donor site |
probably null |
|
R3969:Prl2a1
|
UTSW |
13 |
27,990,263 (GRCm39) |
missense |
probably benign |
0.00 |
R4772:Prl2a1
|
UTSW |
13 |
27,988,961 (GRCm39) |
missense |
probably benign |
0.02 |
R5604:Prl2a1
|
UTSW |
13 |
27,990,369 (GRCm39) |
critical splice donor site |
probably benign |
|
R7292:Prl2a1
|
UTSW |
13 |
27,991,353 (GRCm39) |
splice site |
probably null |
|
R9110:Prl2a1
|
UTSW |
13 |
27,992,398 (GRCm39) |
missense |
probably benign |
0.03 |
R9193:Prl2a1
|
UTSW |
13 |
27,992,535 (GRCm39) |
missense |
probably damaging |
1.00 |
|