Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12 |
T |
A |
2: 150,690,379 (GRCm39) |
|
probably null |
Het |
Adrm1b |
A |
C |
3: 92,336,195 (GRCm39) |
|
probably benign |
Het |
Akap8 |
C |
T |
17: 32,531,272 (GRCm39) |
R380Q |
probably damaging |
Het |
Arhgef12 |
T |
C |
9: 42,886,588 (GRCm39) |
M1131V |
probably damaging |
Het |
Atrn |
T |
C |
2: 130,806,850 (GRCm39) |
|
probably null |
Het |
Btaf1 |
A |
G |
19: 36,963,879 (GRCm39) |
T817A |
probably benign |
Het |
C3 |
C |
T |
17: 57,512,303 (GRCm39) |
D1542N |
possibly damaging |
Het |
Cadm3 |
A |
G |
1: 173,169,236 (GRCm39) |
V293A |
probably benign |
Het |
Cdk11b |
C |
T |
4: 155,724,204 (GRCm39) |
|
probably benign |
Het |
Cdnf |
A |
G |
2: 3,522,060 (GRCm39) |
Y84C |
probably damaging |
Het |
Chdh |
T |
C |
14: 29,757,297 (GRCm39) |
S407P |
probably damaging |
Het |
Cmtr1 |
C |
A |
17: 29,904,949 (GRCm39) |
T300K |
probably damaging |
Het |
Dennd2d |
A |
T |
3: 106,389,939 (GRCm39) |
|
probably benign |
Het |
Diaph1 |
T |
A |
18: 37,986,636 (GRCm39) |
E1116D |
possibly damaging |
Het |
Eif1ad3 |
A |
G |
12: 87,843,401 (GRCm39) |
K16R |
unknown |
Het |
Eif1ad3 |
A |
T |
12: 87,843,710 (GRCm39) |
D119V |
possibly damaging |
Het |
Enpp1 |
A |
G |
10: 24,544,905 (GRCm39) |
|
probably null |
Het |
Erbb4 |
T |
C |
1: 68,079,496 (GRCm39) |
T1195A |
probably benign |
Het |
Ermard |
T |
A |
17: 15,273,638 (GRCm39) |
S408T |
probably benign |
Het |
Etl4 |
A |
T |
2: 20,812,772 (GRCm39) |
R1442S |
probably damaging |
Het |
F13b |
T |
A |
1: 139,429,508 (GRCm39) |
F9I |
unknown |
Het |
Fnbp4 |
C |
T |
2: 90,588,821 (GRCm39) |
R531* |
probably null |
Het |
Gdf6 |
A |
G |
4: 9,844,776 (GRCm39) |
Y100C |
probably damaging |
Het |
Gpr3 |
T |
C |
4: 132,938,226 (GRCm39) |
T149A |
probably damaging |
Het |
Grm8 |
T |
C |
6: 27,760,208 (GRCm39) |
H374R |
probably benign |
Het |
Hbs1l |
T |
C |
10: 21,228,501 (GRCm39) |
V493A |
probably damaging |
Het |
Hgs |
A |
G |
11: 120,368,202 (GRCm39) |
K277E |
probably damaging |
Het |
Hnrnpul1 |
C |
T |
7: 25,426,300 (GRCm39) |
R517Q |
probably damaging |
Het |
Hoxa11 |
A |
T |
6: 52,222,504 (GRCm39) |
Y66N |
probably damaging |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Igdcc4 |
T |
A |
9: 65,039,047 (GRCm39) |
L944Q |
probably damaging |
Het |
Ighv3-1 |
C |
A |
12: 113,928,107 (GRCm39) |
S84I |
probably damaging |
Het |
Iqgap2 |
T |
C |
13: 95,794,375 (GRCm39) |
D1199G |
probably damaging |
Het |
Kcnk10 |
A |
T |
12: 98,401,205 (GRCm39) |
M490K |
probably benign |
Het |
Kirrel1 |
A |
G |
3: 86,992,387 (GRCm39) |
|
probably null |
Het |
Lias |
A |
T |
5: 65,552,768 (GRCm39) |
T124S |
probably benign |
Het |
Lrig3 |
A |
C |
10: 125,845,656 (GRCm39) |
E695A |
probably damaging |
Het |
Lrpap1 |
A |
G |
5: 35,253,381 (GRCm39) |
I261T |
possibly damaging |
Het |
Lrrc37a |
T |
A |
11: 103,388,808 (GRCm39) |
T2206S |
unknown |
Het |
Macf1 |
T |
A |
4: 123,365,884 (GRCm39) |
Q2959L |
probably benign |
Het |
Mis12 |
A |
G |
11: 70,916,134 (GRCm39) |
T56A |
probably benign |
Het |
Or10ag56 |
T |
A |
2: 87,139,208 (GRCm39) |
M25K |
probably null |
Het |
Or1l4 |
T |
A |
2: 37,092,024 (GRCm39) |
I257N |
possibly damaging |
Het |
Or4k41 |
A |
G |
2: 111,279,848 (GRCm39) |
D121G |
probably damaging |
Het |
Or5b99 |
T |
C |
19: 12,977,235 (GRCm39) |
V295A |
probably damaging |
Het |
Otof |
A |
T |
5: 30,576,850 (GRCm39) |
L134Q |
possibly damaging |
Het |
Pds5b |
T |
A |
5: 150,717,824 (GRCm39) |
V1155E |
possibly damaging |
Het |
Pdss2 |
A |
T |
10: 43,278,518 (GRCm39) |
M342L |
probably benign |
Het |
Phyhipl |
C |
T |
10: 70,404,903 (GRCm39) |
V57I |
probably damaging |
Het |
Plekha5 |
T |
A |
6: 140,501,647 (GRCm39) |
|
probably null |
Het |
Pnck |
A |
T |
X: 72,701,761 (GRCm39) |
V93E |
probably damaging |
Het |
Proser1 |
A |
G |
3: 53,385,962 (GRCm39) |
T615A |
probably damaging |
Het |
Ptprk |
G |
A |
10: 28,139,508 (GRCm39) |
V78I |
probably benign |
Het |
Ptprv |
A |
G |
1: 135,038,168 (GRCm39) |
|
noncoding transcript |
Het |
Ranbp3l |
A |
G |
15: 9,060,838 (GRCm39) |
N233S |
probably damaging |
Het |
Rassf2 |
G |
A |
2: 131,854,522 (GRCm39) |
P7S |
probably benign |
Het |
Sart1 |
A |
T |
19: 5,432,771 (GRCm39) |
L521Q |
possibly damaging |
Het |
Scgb1b21 |
T |
A |
7: 33,227,118 (GRCm39) |
|
noncoding transcript |
Het |
Scyl2 |
A |
T |
10: 89,476,458 (GRCm39) |
M889K |
probably benign |
Het |
Secisbp2l |
A |
G |
2: 125,593,785 (GRCm39) |
|
probably benign |
Het |
Svil |
A |
G |
18: 5,063,522 (GRCm39) |
E931G |
probably benign |
Het |
Syce1 |
C |
A |
7: 140,359,809 (GRCm39) |
L83F |
probably damaging |
Het |
Tdrd1 |
A |
G |
19: 56,819,505 (GRCm39) |
M2V |
probably benign |
Het |
Tjp2 |
A |
T |
19: 24,086,182 (GRCm39) |
V780E |
possibly damaging |
Het |
Tram1 |
A |
G |
1: 13,636,599 (GRCm39) |
V358A |
probably benign |
Het |
Unc13c |
C |
T |
9: 73,643,821 (GRCm39) |
W1214* |
probably null |
Het |
Vps13b |
T |
C |
15: 35,455,274 (GRCm39) |
C728R |
probably damaging |
Het |
Wwox |
A |
G |
8: 115,166,481 (GRCm39) |
|
probably benign |
Het |
Zbtb41 |
G |
A |
1: 139,357,064 (GRCm39) |
V440I |
probably benign |
Het |
Zfp777 |
T |
C |
6: 48,002,456 (GRCm39) |
S589G |
probably benign |
Het |
Zfp955a |
A |
G |
17: 33,460,675 (GRCm39) |
Y486H |
probably benign |
Het |
|
Other mutations in Adam33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Adam33
|
APN |
2 |
130,896,183 (GRCm39) |
splice site |
probably benign |
|
IGL01586:Adam33
|
APN |
2 |
130,895,970 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02156:Adam33
|
APN |
2 |
130,895,078 (GRCm39) |
splice site |
probably benign |
|
IGL02498:Adam33
|
APN |
2 |
130,895,157 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Adam33
|
UTSW |
2 |
130,896,041 (GRCm39) |
splice site |
probably null |
|
R0012:Adam33
|
UTSW |
2 |
130,894,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R0471:Adam33
|
UTSW |
2 |
130,896,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R1401:Adam33
|
UTSW |
2 |
130,893,391 (GRCm39) |
unclassified |
probably benign |
|
R2071:Adam33
|
UTSW |
2 |
130,897,266 (GRCm39) |
missense |
probably benign |
0.01 |
R2095:Adam33
|
UTSW |
2 |
130,895,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R2383:Adam33
|
UTSW |
2 |
130,893,282 (GRCm39) |
missense |
probably benign |
0.01 |
R4403:Adam33
|
UTSW |
2 |
130,895,190 (GRCm39) |
missense |
probably benign |
0.03 |
R4821:Adam33
|
UTSW |
2 |
130,903,115 (GRCm39) |
missense |
probably benign |
0.03 |
R5110:Adam33
|
UTSW |
2 |
130,895,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5150:Adam33
|
UTSW |
2 |
130,895,117 (GRCm39) |
intron |
probably benign |
|
R5364:Adam33
|
UTSW |
2 |
130,896,392 (GRCm39) |
critical splice donor site |
probably null |
|
R5632:Adam33
|
UTSW |
2 |
130,895,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R5818:Adam33
|
UTSW |
2 |
130,896,278 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6226:Adam33
|
UTSW |
2 |
130,897,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Adam33
|
UTSW |
2 |
130,893,266 (GRCm39) |
missense |
probably benign |
0.01 |
R6755:Adam33
|
UTSW |
2 |
130,895,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:Adam33
|
UTSW |
2 |
130,895,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Adam33
|
UTSW |
2 |
130,895,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Adam33
|
UTSW |
2 |
130,903,089 (GRCm39) |
missense |
probably benign |
0.00 |
R7650:Adam33
|
UTSW |
2 |
130,903,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:Adam33
|
UTSW |
2 |
130,900,257 (GRCm39) |
missense |
unknown |
|
R7809:Adam33
|
UTSW |
2 |
130,893,266 (GRCm39) |
missense |
probably benign |
|
R7932:Adam33
|
UTSW |
2 |
130,905,617 (GRCm39) |
unclassified |
probably benign |
|
R8210:Adam33
|
UTSW |
2 |
130,898,250 (GRCm39) |
missense |
probably benign |
|
R8969:Adam33
|
UTSW |
2 |
130,894,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R9102:Adam33
|
UTSW |
2 |
130,897,737 (GRCm39) |
missense |
probably benign |
0.01 |
R9449:Adam33
|
UTSW |
2 |
130,895,606 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9650:Adam33
|
UTSW |
2 |
130,894,989 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9720:Adam33
|
UTSW |
2 |
130,900,236 (GRCm39) |
missense |
|
|
Z1177:Adam33
|
UTSW |
2 |
130,900,582 (GRCm39) |
missense |
possibly damaging |
0.89 |
|