Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34 |
T |
C |
8: 44,103,854 (GRCm39) |
H597R |
probably damaging |
Het |
Adgrf4 |
G |
T |
17: 42,978,568 (GRCm39) |
H258Q |
probably benign |
Het |
Ankrd1 |
T |
A |
19: 36,095,273 (GRCm39) |
K138N |
probably damaging |
Het |
Arg1 |
T |
C |
10: 24,798,575 (GRCm39) |
E25G |
probably damaging |
Het |
Arhgef19 |
T |
C |
4: 140,973,660 (GRCm39) |
I49T |
possibly damaging |
Het |
Bsn |
A |
G |
9: 107,990,145 (GRCm39) |
V1869A |
possibly damaging |
Het |
Cep350 |
G |
A |
1: 155,808,621 (GRCm39) |
R652W |
probably damaging |
Het |
Cyp19a1 |
G |
A |
9: 54,093,980 (GRCm39) |
T94I |
probably damaging |
Het |
Dnajc13 |
G |
A |
9: 104,067,641 (GRCm39) |
L1173F |
probably damaging |
Het |
Dse |
A |
G |
10: 34,029,330 (GRCm39) |
F587L |
probably damaging |
Het |
Efcab14 |
A |
C |
4: 115,597,594 (GRCm39) |
D63A |
probably damaging |
Het |
Eomes |
A |
G |
9: 118,308,031 (GRCm39) |
T35A |
probably benign |
Het |
Fbxl20 |
T |
C |
11: 97,986,220 (GRCm39) |
|
probably benign |
Het |
Flcn |
T |
C |
11: 59,691,947 (GRCm39) |
N234S |
probably benign |
Het |
Gm20939 |
A |
T |
17: 95,184,162 (GRCm39) |
Y270F |
possibly damaging |
Het |
Ikzf4 |
A |
T |
10: 128,479,605 (GRCm39) |
|
probably benign |
Het |
Kcne4 |
A |
G |
1: 78,795,819 (GRCm39) |
N156D |
probably benign |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Lrrc45 |
A |
T |
11: 120,609,272 (GRCm39) |
D377V |
possibly damaging |
Het |
Magi3 |
T |
C |
3: 103,958,277 (GRCm39) |
K603E |
probably damaging |
Het |
Mocos |
T |
C |
18: 24,807,303 (GRCm39) |
I345T |
probably damaging |
Het |
Nox4 |
A |
T |
7: 87,046,032 (GRCm39) |
H557L |
possibly damaging |
Het |
Oasl1 |
A |
G |
5: 115,075,073 (GRCm39) |
K378E |
possibly damaging |
Het |
Pla2r1 |
A |
T |
2: 60,252,966 (GRCm39) |
I1375K |
probably damaging |
Het |
Ppp6r3 |
T |
A |
19: 3,562,037 (GRCm39) |
H208L |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,001,683 (GRCm39) |
K1258* |
probably null |
Het |
Ptprz1 |
T |
C |
6: 23,022,204 (GRCm39) |
I844T |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 142,100,154 (GRCm39) |
I1395V |
probably benign |
Het |
Sec31b |
T |
C |
19: 44,513,625 (GRCm39) |
N470S |
probably benign |
Het |
Slc26a7 |
T |
C |
4: 14,544,197 (GRCm39) |
T369A |
probably benign |
Het |
Tex14 |
T |
G |
11: 87,407,595 (GRCm39) |
S900R |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,460,907 (GRCm39) |
V2723M |
probably damaging |
Het |
Vat1l |
T |
A |
8: 115,098,469 (GRCm39) |
M413K |
probably benign |
Het |
Zfp981 |
C |
A |
4: 146,622,080 (GRCm39) |
P335Q |
probably benign |
Het |
Zfp981 |
T |
A |
4: 146,622,339 (GRCm39) |
H421Q |
probably benign |
Het |
|
Other mutations in Il22b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01796:Il22b
|
APN |
10 |
118,126,069 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02149:Il22b
|
APN |
10 |
118,130,902 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02965:Il22b
|
APN |
10 |
118,130,762 (GRCm39) |
missense |
probably damaging |
0.98 |
R0310:Il22b
|
UTSW |
10 |
118,129,090 (GRCm39) |
missense |
probably benign |
0.41 |
R0730:Il22b
|
UTSW |
10 |
118,130,142 (GRCm39) |
missense |
probably benign |
0.01 |
R1078:Il22b
|
UTSW |
10 |
118,126,056 (GRCm39) |
makesense |
probably null |
|
R4067:Il22b
|
UTSW |
10 |
118,126,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R4911:Il22b
|
UTSW |
10 |
118,130,894 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R5433:Il22b
|
UTSW |
10 |
118,130,789 (GRCm39) |
missense |
probably damaging |
0.96 |
R5778:Il22b
|
UTSW |
10 |
118,130,768 (GRCm39) |
nonsense |
probably null |
|
R7295:Il22b
|
UTSW |
10 |
118,130,848 (GRCm39) |
nonsense |
probably null |
|
R9313:Il22b
|
UTSW |
10 |
118,130,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R9485:Il22b
|
UTSW |
10 |
118,130,314 (GRCm39) |
missense |
probably benign |
|
R9566:Il22b
|
UTSW |
10 |
118,130,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9796:Il22b
|
UTSW |
10 |
118,130,081 (GRCm39) |
missense |
probably benign |
0.19 |
|