Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adissp |
A |
T |
2: 130,995,512 (GRCm39) |
|
probably null |
Het |
Anln |
C |
A |
9: 22,293,565 (GRCm39) |
R26M |
probably damaging |
Het |
Capn15 |
A |
T |
17: 26,180,812 (GRCm39) |
S753T |
probably damaging |
Het |
Ccdc62 |
A |
G |
5: 124,092,743 (GRCm39) |
N576S |
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,508,900 (GRCm39) |
D2895G |
probably damaging |
Het |
Dspp |
T |
A |
5: 104,322,814 (GRCm39) |
V37E |
probably damaging |
Het |
Efcab3 |
A |
T |
11: 104,611,919 (GRCm39) |
D587V |
probably benign |
Het |
Efcab6 |
T |
C |
15: 83,752,450 (GRCm39) |
D1473G |
probably damaging |
Het |
Ehhadh |
T |
C |
16: 21,582,090 (GRCm39) |
|
probably benign |
Het |
Fbln1 |
T |
C |
15: 85,116,879 (GRCm39) |
|
probably null |
Het |
Gbp9 |
A |
G |
5: 105,230,652 (GRCm39) |
V424A |
possibly damaging |
Het |
Gda |
T |
C |
19: 21,394,371 (GRCm39) |
Y236C |
possibly damaging |
Het |
Gm4884 |
A |
G |
7: 40,693,969 (GRCm39) |
E646G |
probably damaging |
Het |
Gm4952 |
C |
A |
19: 12,600,960 (GRCm39) |
|
probably benign |
Het |
Gm5422 |
G |
T |
10: 31,126,348 (GRCm39) |
|
noncoding transcript |
Het |
Grin2b |
C |
T |
6: 135,757,253 (GRCm39) |
D403N |
possibly damaging |
Het |
Hsf2bp |
G |
A |
17: 32,226,744 (GRCm39) |
R204C |
probably damaging |
Het |
Kat6b |
G |
T |
14: 21,659,831 (GRCm39) |
D212Y |
possibly damaging |
Het |
Kctd2 |
A |
C |
11: 115,320,208 (GRCm39) |
I247L |
possibly damaging |
Het |
Kel |
T |
A |
6: 41,664,929 (GRCm39) |
|
probably null |
Het |
Krt20 |
A |
T |
11: 99,320,855 (GRCm39) |
|
probably benign |
Het |
Litaf |
T |
C |
16: 10,784,433 (GRCm39) |
T26A |
probably damaging |
Het |
N4bp2l2 |
G |
T |
5: 150,584,931 (GRCm39) |
Q350K |
probably damaging |
Het |
Nav2 |
T |
G |
7: 49,011,847 (GRCm39) |
I26S |
probably damaging |
Het |
Nfya |
A |
G |
17: 48,698,375 (GRCm39) |
Y162H |
probably damaging |
Het |
Or2g25 |
C |
T |
17: 37,970,646 (GRCm39) |
A193T |
probably benign |
Het |
Pbx4 |
A |
T |
8: 70,319,200 (GRCm39) |
S244C |
probably damaging |
Het |
Pcdhb16 |
T |
C |
18: 37,612,285 (GRCm39) |
V415A |
probably benign |
Het |
Rbbp8 |
A |
G |
18: 11,874,133 (GRCm39) |
|
probably benign |
Het |
Sp100 |
T |
C |
1: 85,635,025 (GRCm39) |
|
probably benign |
Het |
Spag16 |
A |
G |
1: 69,883,540 (GRCm39) |
|
probably benign |
Het |
Star |
A |
G |
8: 26,301,082 (GRCm39) |
D138G |
possibly damaging |
Het |
|
Other mutations in Il16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Il16
|
APN |
7 |
83,301,666 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01743:Il16
|
APN |
7 |
83,301,507 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01770:Il16
|
APN |
7 |
83,322,234 (GRCm39) |
splice site |
probably benign |
|
IGL02025:Il16
|
APN |
7 |
83,302,056 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02317:Il16
|
APN |
7 |
83,316,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02412:Il16
|
APN |
7 |
83,301,899 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02550:Il16
|
APN |
7 |
83,323,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02568:Il16
|
APN |
7 |
83,310,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02578:Il16
|
APN |
7 |
83,327,194 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02815:Il16
|
APN |
7 |
83,300,249 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03157:Il16
|
APN |
7 |
83,371,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03161:Il16
|
APN |
7 |
83,371,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03188:Il16
|
APN |
7 |
83,337,371 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03213:Il16
|
APN |
7 |
83,295,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R0201:Il16
|
UTSW |
7 |
83,371,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R0309:Il16
|
UTSW |
7 |
83,371,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Il16
|
UTSW |
7 |
83,327,183 (GRCm39) |
splice site |
probably benign |
|
R0942:Il16
|
UTSW |
7 |
83,312,349 (GRCm39) |
missense |
probably benign |
0.01 |
R1018:Il16
|
UTSW |
7 |
83,323,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Il16
|
UTSW |
7 |
83,304,520 (GRCm39) |
missense |
probably benign |
|
R1715:Il16
|
UTSW |
7 |
83,297,936 (GRCm39) |
missense |
probably benign |
0.01 |
R2179:Il16
|
UTSW |
7 |
83,337,287 (GRCm39) |
splice site |
probably null |
|
R2520:Il16
|
UTSW |
7 |
83,301,202 (GRCm39) |
missense |
probably benign |
0.03 |
R3425:Il16
|
UTSW |
7 |
83,293,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3761:Il16
|
UTSW |
7 |
83,300,093 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3943:Il16
|
UTSW |
7 |
83,301,223 (GRCm39) |
missense |
probably damaging |
0.97 |
R4470:Il16
|
UTSW |
7 |
83,300,046 (GRCm39) |
intron |
probably benign |
|
R4530:Il16
|
UTSW |
7 |
83,330,518 (GRCm39) |
intron |
probably benign |
|
R4583:Il16
|
UTSW |
7 |
83,332,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Il16
|
UTSW |
7 |
83,300,104 (GRCm39) |
missense |
probably benign |
0.14 |
R4874:Il16
|
UTSW |
7 |
83,310,153 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4876:Il16
|
UTSW |
7 |
83,322,302 (GRCm39) |
missense |
probably benign |
|
R5677:Il16
|
UTSW |
7 |
83,323,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5686:Il16
|
UTSW |
7 |
83,297,936 (GRCm39) |
missense |
probably benign |
0.36 |
R5920:Il16
|
UTSW |
7 |
83,301,552 (GRCm39) |
missense |
probably benign |
0.03 |
R6115:Il16
|
UTSW |
7 |
83,301,775 (GRCm39) |
nonsense |
probably null |
|
R6459:Il16
|
UTSW |
7 |
83,371,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R6459:Il16
|
UTSW |
7 |
83,371,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Il16
|
UTSW |
7 |
83,371,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6616:Il16
|
UTSW |
7 |
83,295,684 (GRCm39) |
missense |
probably benign |
0.37 |
R6642:Il16
|
UTSW |
7 |
83,337,335 (GRCm39) |
missense |
probably benign |
0.03 |
R6721:Il16
|
UTSW |
7 |
83,312,270 (GRCm39) |
critical splice donor site |
probably null |
|
R7009:Il16
|
UTSW |
7 |
83,295,596 (GRCm39) |
missense |
probably benign |
|
R7144:Il16
|
UTSW |
7 |
83,295,659 (GRCm39) |
missense |
probably damaging |
0.97 |
R7346:Il16
|
UTSW |
7 |
83,293,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7403:Il16
|
UTSW |
7 |
83,319,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7499:Il16
|
UTSW |
7 |
83,323,702 (GRCm39) |
missense |
probably damaging |
0.99 |
R7814:Il16
|
UTSW |
7 |
83,319,348 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7941:Il16
|
UTSW |
7 |
83,332,037 (GRCm39) |
missense |
probably damaging |
0.98 |
R8098:Il16
|
UTSW |
7 |
83,295,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R8317:Il16
|
UTSW |
7 |
83,304,538 (GRCm39) |
missense |
probably benign |
|
R8437:Il16
|
UTSW |
7 |
83,301,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R9094:Il16
|
UTSW |
7 |
83,301,559 (GRCm39) |
missense |
probably benign |
|
R9267:Il16
|
UTSW |
7 |
83,371,757 (GRCm39) |
missense |
probably benign |
0.01 |
R9445:Il16
|
UTSW |
7 |
83,337,380 (GRCm39) |
nonsense |
probably null |
|
R9595:Il16
|
UTSW |
7 |
83,322,273 (GRCm39) |
nonsense |
probably null |
|
R9651:Il16
|
UTSW |
7 |
83,332,064 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Il16
|
UTSW |
7 |
83,302,035 (GRCm39) |
missense |
probably benign |
0.05 |
|