Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aff1 |
A |
G |
5: 103,988,926 (GRCm39) |
D831G |
possibly damaging |
Het |
Amer2 |
A |
G |
14: 60,617,331 (GRCm39) |
K509E |
possibly damaging |
Het |
Ankrd6 |
T |
C |
4: 32,808,771 (GRCm39) |
K449E |
probably damaging |
Het |
Atp8b2 |
G |
A |
3: 89,855,828 (GRCm39) |
P459L |
probably benign |
Het |
Atr |
C |
T |
9: 95,802,875 (GRCm39) |
R1846* |
probably null |
Het |
Brd10 |
C |
T |
19: 29,694,676 (GRCm39) |
G1606R |
probably damaging |
Het |
Ccdc159 |
C |
A |
9: 21,842,992 (GRCm39) |
|
probably null |
Het |
Ccna1 |
A |
C |
3: 54,954,698 (GRCm39) |
Y338D |
probably damaging |
Het |
Cpq |
A |
T |
15: 33,213,089 (GRCm39) |
E36V |
probably damaging |
Het |
Cyp2c23 |
A |
G |
19: 44,003,371 (GRCm39) |
I268T |
probably damaging |
Het |
Dctn2 |
G |
T |
10: 127,114,057 (GRCm39) |
Q332H |
probably damaging |
Het |
Dnah17 |
T |
A |
11: 117,972,769 (GRCm39) |
I2055F |
probably damaging |
Het |
Dnmt3b |
A |
G |
2: 153,528,279 (GRCm39) |
H764R |
probably damaging |
Het |
Gphn |
T |
A |
12: 78,528,087 (GRCm39) |
I135K |
probably damaging |
Het |
Hnrnpul1 |
A |
G |
7: 25,450,409 (GRCm39) |
M1T |
probably null |
Het |
Htra4 |
T |
C |
8: 25,519,714 (GRCm39) |
D406G |
probably benign |
Het |
Klk10 |
G |
T |
7: 43,433,883 (GRCm39) |
|
probably benign |
Het |
Lilrb4a |
T |
A |
10: 51,367,616 (GRCm39) |
W53R |
probably benign |
Het |
Magel2 |
T |
C |
7: 62,028,461 (GRCm39) |
V455A |
probably benign |
Het |
Mrgprb5 |
T |
C |
7: 47,818,442 (GRCm39) |
T98A |
probably benign |
Het |
Mrps35 |
T |
A |
6: 146,951,373 (GRCm39) |
C76* |
probably null |
Het |
Myh7b |
C |
T |
2: 155,465,399 (GRCm39) |
R701C |
probably damaging |
Het |
Nbeal1 |
G |
A |
1: 60,300,745 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,215,720 (GRCm39) |
M196L |
probably benign |
Het |
Nmd3 |
A |
G |
3: 69,642,421 (GRCm39) |
K207R |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,179,129 (GRCm39) |
R962Q |
probably benign |
Het |
Psme4 |
A |
G |
11: 30,757,788 (GRCm39) |
D307G |
possibly damaging |
Het |
Rnf41 |
T |
G |
10: 128,274,149 (GRCm39) |
M267R |
possibly damaging |
Het |
Sis |
T |
C |
3: 72,836,052 (GRCm39) |
N846D |
probably benign |
Het |
Slc22a19 |
T |
A |
19: 7,659,227 (GRCm39) |
I463L |
probably benign |
Het |
Slc25a39 |
A |
T |
11: 102,297,030 (GRCm39) |
|
probably null |
Het |
Slc35b2 |
C |
T |
17: 45,877,571 (GRCm39) |
R233C |
probably damaging |
Het |
Slc4a4 |
T |
C |
5: 89,376,695 (GRCm39) |
L983P |
probably damaging |
Het |
Sp110 |
A |
C |
1: 85,505,050 (GRCm39) |
F434C |
probably benign |
Het |
Tbc1d10a |
A |
G |
11: 4,159,984 (GRCm39) |
Y123C |
probably damaging |
Het |
Thbs4 |
A |
C |
13: 92,906,056 (GRCm39) |
I395S |
probably benign |
Het |
Triml2 |
A |
G |
8: 43,646,776 (GRCm39) |
T422A |
probably benign |
Het |
Ubn2 |
T |
C |
6: 38,417,382 (GRCm39) |
|
probably benign |
Het |
Vmn1r15 |
T |
A |
6: 57,235,555 (GRCm39) |
M141K |
probably benign |
Het |
Vmn2r80 |
A |
G |
10: 79,005,362 (GRCm39) |
E333G |
probably damaging |
Het |
Zfp169 |
T |
C |
13: 48,644,639 (GRCm39) |
|
probably benign |
Het |
Zfp942 |
G |
A |
17: 22,148,083 (GRCm39) |
P182L |
probably benign |
Het |
|
Other mutations in Pom121 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Pom121
|
APN |
5 |
135,420,560 (GRCm39) |
missense |
unknown |
|
IGL01537:Pom121
|
APN |
5 |
135,421,389 (GRCm39) |
splice site |
probably benign |
|
IGL01611:Pom121
|
APN |
5 |
135,412,526 (GRCm39) |
missense |
unknown |
|
IGL01803:Pom121
|
APN |
5 |
135,410,463 (GRCm39) |
unclassified |
probably benign |
|
IGL02666:Pom121
|
APN |
5 |
135,415,686 (GRCm39) |
missense |
unknown |
|
IGL03134:Pom121
|
UTSW |
5 |
135,410,935 (GRCm39) |
missense |
unknown |
|
R0511:Pom121
|
UTSW |
5 |
135,410,686 (GRCm39) |
missense |
unknown |
|
R1935:Pom121
|
UTSW |
5 |
135,412,740 (GRCm39) |
missense |
unknown |
|
R1967:Pom121
|
UTSW |
5 |
135,420,608 (GRCm39) |
missense |
unknown |
|
R2024:Pom121
|
UTSW |
5 |
135,410,404 (GRCm39) |
unclassified |
probably benign |
|
R4082:Pom121
|
UTSW |
5 |
135,417,491 (GRCm39) |
missense |
unknown |
|
R4477:Pom121
|
UTSW |
5 |
135,410,842 (GRCm39) |
missense |
unknown |
|
R5655:Pom121
|
UTSW |
5 |
135,421,171 (GRCm39) |
missense |
unknown |
|
R6460:Pom121
|
UTSW |
5 |
135,420,537 (GRCm39) |
missense |
unknown |
|
R6807:Pom121
|
UTSW |
5 |
135,409,978 (GRCm39) |
unclassified |
probably benign |
|
R6914:Pom121
|
UTSW |
5 |
135,407,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Pom121
|
UTSW |
5 |
135,409,941 (GRCm39) |
missense |
unknown |
|
R7726:Pom121
|
UTSW |
5 |
135,407,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R7886:Pom121
|
UTSW |
5 |
135,410,848 (GRCm39) |
missense |
unknown |
|
R7956:Pom121
|
UTSW |
5 |
135,412,815 (GRCm39) |
missense |
unknown |
|
R8356:Pom121
|
UTSW |
5 |
135,410,032 (GRCm39) |
missense |
unknown |
|
R8456:Pom121
|
UTSW |
5 |
135,410,032 (GRCm39) |
missense |
unknown |
|
R8503:Pom121
|
UTSW |
5 |
135,410,398 (GRCm39) |
missense |
unknown |
|
R9776:Pom121
|
UTSW |
5 |
135,420,554 (GRCm39) |
missense |
unknown |
|
|