Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
C |
T |
3: 137,891,949 (GRCm39) |
|
probably benign |
Het |
Adgra2 |
T |
A |
8: 27,603,465 (GRCm39) |
C417S |
probably damaging |
Het |
Adgra2 |
C |
A |
8: 27,603,464 (GRCm39) |
H416Q |
probably benign |
Het |
Aff3 |
C |
A |
1: 38,445,578 (GRCm39) |
R307L |
possibly damaging |
Het |
Arhgap17 |
T |
C |
7: 122,921,124 (GRCm39) |
D121G |
probably damaging |
Het |
Ascc3 |
G |
T |
10: 50,725,742 (GRCm39) |
R2155I |
probably null |
Het |
Ccdc115 |
C |
T |
1: 34,478,364 (GRCm39) |
S19N |
possibly damaging |
Het |
Ccser2 |
T |
C |
14: 36,662,038 (GRCm39) |
N382S |
probably benign |
Het |
Cct6b |
A |
T |
11: 82,610,785 (GRCm39) |
V500E |
probably damaging |
Het |
Cenpo |
A |
T |
12: 4,266,539 (GRCm39) |
Y190N |
probably damaging |
Het |
Cfh |
T |
A |
1: 140,030,100 (GRCm39) |
K924N |
probably damaging |
Het |
Col4a1 |
A |
G |
8: 11,252,926 (GRCm39) |
|
probably benign |
Het |
Coro1b |
T |
C |
19: 4,200,770 (GRCm39) |
V234A |
probably benign |
Het |
Crot |
T |
C |
5: 9,039,641 (GRCm39) |
K69E |
probably damaging |
Het |
Cyp2d11 |
A |
T |
15: 82,274,339 (GRCm39) |
H347Q |
probably benign |
Het |
Efcab3 |
A |
T |
11: 104,612,284 (GRCm39) |
K636* |
probably null |
Het |
Fbn2 |
T |
A |
18: 58,257,393 (GRCm39) |
I325F |
probably benign |
Het |
Fbxw4 |
T |
A |
19: 45,571,187 (GRCm39) |
R41S |
probably benign |
Het |
Fn1 |
T |
A |
1: 71,653,066 (GRCm39) |
I1308F |
probably benign |
Het |
Frem1 |
C |
A |
4: 82,930,251 (GRCm39) |
E232* |
probably null |
Het |
Gabrg3 |
T |
C |
7: 56,423,059 (GRCm39) |
Q213R |
possibly damaging |
Het |
Garin3 |
G |
A |
11: 46,298,418 (GRCm39) |
G574D |
possibly damaging |
Het |
Gsdme |
A |
T |
6: 50,204,378 (GRCm39) |
V193E |
probably damaging |
Het |
Hadha |
C |
A |
5: 30,352,977 (GRCm39) |
|
probably null |
Het |
Hdgfl2 |
C |
A |
17: 56,406,211 (GRCm39) |
A533E |
probably damaging |
Het |
Hivep2 |
T |
C |
10: 14,006,327 (GRCm39) |
F975S |
probably damaging |
Het |
Htatip2 |
T |
A |
7: 49,420,666 (GRCm39) |
S171T |
probably benign |
Het |
Ift57 |
A |
T |
16: 49,584,167 (GRCm39) |
I307F |
possibly damaging |
Het |
Kcnk13 |
G |
T |
12: 100,027,948 (GRCm39) |
R341L |
probably damaging |
Het |
Kif2b |
G |
A |
11: 91,466,741 (GRCm39) |
T514M |
probably damaging |
Het |
Kmt2c |
A |
C |
5: 25,515,515 (GRCm39) |
I2776S |
probably damaging |
Het |
Ly9 |
T |
C |
1: 171,428,723 (GRCm39) |
D189G |
probably benign |
Het |
Mal2 |
T |
C |
15: 54,451,753 (GRCm39) |
V58A |
probably damaging |
Het |
Mettl21e |
T |
A |
1: 44,245,526 (GRCm39) |
N240I |
probably benign |
Het |
Msantd5f1 |
A |
G |
4: 73,605,621 (GRCm39) |
N344S |
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Nacc1 |
G |
A |
8: 85,399,844 (GRCm39) |
R458C |
probably damaging |
Het |
Ncapd3 |
T |
C |
9: 26,942,105 (GRCm39) |
C14R |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,886,279 (GRCm39) |
|
probably benign |
Het |
Or13c3 |
A |
G |
4: 52,855,695 (GRCm39) |
F273L |
probably benign |
Het |
Or1j4 |
A |
T |
2: 36,740,234 (GRCm39) |
M59L |
possibly damaging |
Het |
Or8d23 |
T |
A |
9: 38,841,772 (GRCm39) |
F102I |
possibly damaging |
Het |
Parp12 |
T |
C |
6: 39,088,670 (GRCm39) |
I189V |
probably benign |
Het |
Pde4dip |
C |
A |
3: 97,674,340 (GRCm39) |
R192L |
possibly damaging |
Het |
Pdlim4 |
C |
A |
11: 53,946,674 (GRCm39) |
E204D |
probably damaging |
Het |
Phf3 |
T |
C |
1: 30,853,063 (GRCm39) |
Q1049R |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,985,103 (GRCm39) |
L1464P |
probably damaging |
Het |
Psg25 |
C |
T |
7: 18,255,323 (GRCm39) |
V398I |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,522,086 (GRCm39) |
N622Y |
probably damaging |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Tex36 |
A |
G |
7: 133,189,002 (GRCm39) |
L190P |
probably benign |
Het |
Tk1 |
A |
G |
11: 117,707,320 (GRCm39) |
C156R |
probably damaging |
Het |
Tmem144 |
T |
A |
3: 79,739,406 (GRCm39) |
M126L |
probably benign |
Het |
Tmem208 |
G |
A |
8: 106,054,862 (GRCm39) |
|
probably null |
Het |
Trappc13 |
T |
C |
13: 104,286,660 (GRCm39) |
Q199R |
probably damaging |
Het |
Trim30b |
T |
A |
7: 104,012,960 (GRCm39) |
K156N |
probably damaging |
Het |
Trps1 |
A |
G |
15: 50,695,001 (GRCm39) |
|
probably null |
Het |
Washc4 |
T |
A |
10: 83,394,757 (GRCm39) |
F329Y |
possibly damaging |
Het |
Zbed5 |
T |
G |
5: 129,932,026 (GRCm39) |
D658E |
probably benign |
Het |
Zfyve28 |
T |
G |
5: 34,445,449 (GRCm39) |
K11N |
probably benign |
Het |
Zp1 |
C |
T |
19: 10,893,877 (GRCm39) |
V443I |
possibly damaging |
Het |
|
Other mutations in Il22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03204:Il22
|
APN |
10 |
118,041,085 (GRCm39) |
splice site |
probably benign |
|
IGL03290:Il22
|
APN |
10 |
118,041,785 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4651001:Il22
|
UTSW |
10 |
118,041,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Il22
|
UTSW |
10 |
118,041,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R3905:Il22
|
UTSW |
10 |
118,041,529 (GRCm39) |
nonsense |
probably null |
|
R3908:Il22
|
UTSW |
10 |
118,041,529 (GRCm39) |
nonsense |
probably null |
|
R4703:Il22
|
UTSW |
10 |
118,041,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R4797:Il22
|
UTSW |
10 |
118,041,058 (GRCm39) |
missense |
probably damaging |
0.98 |
R4799:Il22
|
UTSW |
10 |
118,041,058 (GRCm39) |
missense |
probably damaging |
0.98 |
R5439:Il22
|
UTSW |
10 |
118,045,366 (GRCm39) |
nonsense |
probably null |
|
R5496:Il22
|
UTSW |
10 |
118,041,002 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5957:Il22
|
UTSW |
10 |
118,041,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6584:Il22
|
UTSW |
10 |
118,040,932 (GRCm39) |
missense |
probably benign |
0.00 |
R7381:Il22
|
UTSW |
10 |
118,041,069 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8095:Il22
|
UTSW |
10 |
118,041,028 (GRCm39) |
missense |
possibly damaging |
0.95 |
|