Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9230109A22Rik |
T |
C |
15: 25,138,944 (GRCm39) |
|
noncoding transcript |
Het |
Abca15 |
G |
A |
7: 119,934,431 (GRCm39) |
V136M |
probably damaging |
Het |
Abhd3 |
A |
G |
18: 10,645,148 (GRCm39) |
I382T |
probably benign |
Het |
Cux1 |
C |
A |
5: 136,304,169 (GRCm39) |
E1336* |
probably null |
Het |
Cyb5r3 |
T |
C |
15: 83,044,554 (GRCm39) |
I155V |
probably damaging |
Het |
Ddx24 |
T |
C |
12: 103,390,314 (GRCm39) |
T226A |
possibly damaging |
Het |
Dld |
T |
C |
12: 31,382,408 (GRCm39) |
N465S |
probably null |
Het |
Dnmbp |
A |
G |
19: 43,842,566 (GRCm39) |
|
probably benign |
Het |
Dock9 |
T |
C |
14: 121,818,111 (GRCm39) |
H1580R |
probably benign |
Het |
Drd3 |
C |
A |
16: 43,637,319 (GRCm39) |
|
probably benign |
Het |
Gabrb2 |
G |
T |
11: 42,420,322 (GRCm39) |
|
probably null |
Het |
Gbp9 |
T |
C |
5: 105,242,141 (GRCm39) |
|
probably null |
Het |
Inhba |
A |
T |
13: 16,201,664 (GRCm39) |
I409F |
possibly damaging |
Het |
Iqgap2 |
T |
C |
13: 95,764,564 (GRCm39) |
N1560S |
probably damaging |
Het |
Itsn1 |
A |
G |
16: 91,617,606 (GRCm39) |
|
probably benign |
Het |
Kat6b |
T |
C |
14: 21,678,938 (GRCm39) |
F434L |
probably damaging |
Het |
Klra1 |
A |
G |
6: 130,341,278 (GRCm39) |
C232R |
probably damaging |
Het |
Krt18 |
T |
A |
15: 101,938,302 (GRCm39) |
I175N |
probably damaging |
Het |
Lck |
A |
G |
4: 129,450,212 (GRCm39) |
V178A |
probably damaging |
Het |
Mroh4 |
C |
A |
15: 74,481,624 (GRCm39) |
G737V |
probably benign |
Het |
Mug2 |
A |
C |
6: 122,058,285 (GRCm39) |
L1282F |
probably damaging |
Het |
Myo9a |
A |
G |
9: 59,832,187 (GRCm39) |
N2572S |
probably benign |
Het |
Nup88 |
G |
T |
11: 70,834,695 (GRCm39) |
|
probably benign |
Het |
Nxph3 |
G |
T |
11: 95,401,834 (GRCm39) |
H193Q |
possibly damaging |
Het |
Or5b97 |
G |
T |
19: 12,878,221 (GRCm39) |
H308N |
probably benign |
Het |
Orm2 |
A |
G |
4: 63,283,970 (GRCm39) |
T198A |
possibly damaging |
Het |
Pom121 |
T |
C |
5: 135,415,686 (GRCm39) |
I397V |
unknown |
Het |
Prex1 |
C |
A |
2: 166,414,909 (GRCm39) |
E1313D |
probably benign |
Het |
Prkg2 |
T |
A |
5: 99,145,378 (GRCm39) |
|
probably benign |
Het |
Ptpro |
G |
A |
6: 137,355,057 (GRCm39) |
S188N |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,001,209 (GRCm39) |
I1100F |
probably benign |
Het |
Ryr1 |
C |
A |
7: 28,719,188 (GRCm39) |
M4406I |
unknown |
Het |
Sdf4 |
T |
A |
4: 156,093,281 (GRCm39) |
Y204* |
probably null |
Het |
Serinc1 |
A |
T |
10: 57,400,089 (GRCm39) |
|
probably null |
Het |
Slc39a5 |
C |
T |
10: 128,234,324 (GRCm39) |
R193H |
probably damaging |
Het |
Smad9 |
A |
G |
3: 54,689,888 (GRCm39) |
K36R |
probably damaging |
Het |
Spam1 |
T |
A |
6: 24,796,123 (GRCm39) |
L25I |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,686,766 (GRCm39) |
S809R |
possibly damaging |
Het |
Szt2 |
G |
A |
4: 118,231,252 (GRCm39) |
R35C |
probably damaging |
Het |
Tcaf2 |
C |
A |
6: 42,606,058 (GRCm39) |
|
probably benign |
Het |
Tfap2d |
A |
C |
1: 19,174,979 (GRCm39) |
D144A |
probably benign |
Het |
Tmprss11d |
A |
T |
5: 86,479,052 (GRCm39) |
V117D |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,903,913 (GRCm39) |
D1141G |
probably benign |
Het |
Traf6 |
A |
T |
2: 101,527,512 (GRCm39) |
T421S |
possibly damaging |
Het |
Txndc16 |
G |
A |
14: 45,448,607 (GRCm39) |
|
probably benign |
Het |
Utp25 |
G |
A |
1: 192,789,904 (GRCm39) |
Q752* |
probably null |
Het |
Vmn1r73 |
C |
A |
7: 11,490,865 (GRCm39) |
P228T |
probably damaging |
Het |
Vmn2r4 |
A |
G |
3: 64,296,433 (GRCm39) |
I784T |
probably benign |
Het |
Zfp420 |
A |
G |
7: 29,573,795 (GRCm39) |
D5G |
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 |
|
IGL02950:Prl2a1
|
APN |
13 |
27,988,914 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|