Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk3 |
T |
C |
7: 80,727,757 (GRCm39) |
Y296H |
possibly damaging |
Het |
Armh3 |
T |
G |
19: 45,928,927 (GRCm39) |
H389P |
probably benign |
Het |
Brca2 |
A |
G |
5: 150,464,705 (GRCm39) |
T1490A |
probably benign |
Het |
Btaf1 |
A |
T |
19: 36,987,102 (GRCm39) |
D1732V |
probably damaging |
Het |
Capzb |
T |
C |
4: 139,016,258 (GRCm39) |
I273T |
probably benign |
Het |
Carmil1 |
G |
A |
13: 24,278,474 (GRCm39) |
T165I |
probably damaging |
Het |
Cc2d2a |
A |
G |
5: 43,881,722 (GRCm39) |
|
probably benign |
Het |
Cdh22 |
A |
G |
2: 164,954,521 (GRCm39) |
Y667H |
possibly damaging |
Het |
Celsr1 |
T |
A |
15: 85,815,546 (GRCm39) |
Q1823L |
probably benign |
Het |
Cfap210 |
T |
C |
2: 69,602,328 (GRCm39) |
H361R |
probably benign |
Het |
Cntrl |
T |
C |
2: 35,027,826 (GRCm39) |
|
probably benign |
Het |
Dhx15 |
A |
T |
5: 52,314,924 (GRCm39) |
|
probably benign |
Het |
Dip2c |
A |
T |
13: 9,543,144 (GRCm39) |
D30V |
probably damaging |
Het |
Dyrk2 |
T |
C |
10: 118,695,749 (GRCm39) |
D503G |
probably damaging |
Het |
Enpp1 |
T |
A |
10: 24,521,325 (GRCm39) |
I801F |
possibly damaging |
Het |
Fnbp4 |
A |
C |
2: 90,581,966 (GRCm39) |
|
probably benign |
Het |
Klk1b5 |
T |
A |
7: 43,865,928 (GRCm39) |
W2R |
probably benign |
Het |
Lama2 |
T |
C |
10: 27,064,261 (GRCm39) |
K1240R |
probably benign |
Het |
Matn2 |
A |
G |
15: 34,403,002 (GRCm39) |
N409S |
probably benign |
Het |
Mep1b |
A |
T |
18: 21,217,243 (GRCm39) |
K121* |
probably null |
Het |
Mettl26 |
T |
C |
17: 26,095,098 (GRCm39) |
|
probably null |
Het |
Myh7 |
T |
C |
14: 55,224,845 (GRCm39) |
E574G |
probably damaging |
Het |
Nfkbie |
G |
A |
17: 45,871,139 (GRCm39) |
|
probably null |
Het |
Nlrc4 |
T |
C |
17: 74,753,529 (GRCm39) |
R285G |
probably benign |
Het |
Pax8 |
T |
C |
2: 24,333,144 (GRCm39) |
Y66C |
probably damaging |
Het |
Plxna2 |
A |
G |
1: 194,482,876 (GRCm39) |
D1523G |
probably damaging |
Het |
Pou2f1 |
A |
G |
1: 165,724,159 (GRCm39) |
|
probably benign |
Het |
Prom1 |
A |
G |
5: 44,164,363 (GRCm39) |
|
probably null |
Het |
Ptk6 |
T |
C |
2: 180,837,611 (GRCm39) |
D436G |
probably benign |
Het |
Robo4 |
T |
A |
9: 37,319,525 (GRCm39) |
F592I |
probably damaging |
Het |
Sec24c |
C |
A |
14: 20,743,271 (GRCm39) |
S964R |
probably benign |
Het |
Sgcb |
G |
T |
5: 73,793,021 (GRCm39) |
N260K |
possibly damaging |
Het |
Smarcd2 |
T |
C |
11: 106,156,730 (GRCm39) |
D221G |
probably damaging |
Het |
Zfpl1 |
C |
A |
19: 6,131,137 (GRCm39) |
R285L |
possibly damaging |
Het |
|
Other mutations in Unc13b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00832:Unc13b
|
APN |
4 |
43,258,921 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Unc13b
|
APN |
4 |
43,096,927 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01115:Unc13b
|
APN |
4 |
43,258,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01137:Unc13b
|
APN |
4 |
43,091,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01637:Unc13b
|
APN |
4 |
43,241,066 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01789:Unc13b
|
APN |
4 |
43,239,462 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01792:Unc13b
|
APN |
4 |
43,250,218 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01877:Unc13b
|
APN |
4 |
43,249,583 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01924:Unc13b
|
APN |
4 |
43,239,385 (GRCm39) |
nonsense |
probably null |
|
IGL02087:Unc13b
|
APN |
4 |
43,091,270 (GRCm39) |
missense |
probably null |
1.00 |
IGL02197:Unc13b
|
APN |
4 |
43,165,828 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02504:Unc13b
|
APN |
4 |
43,263,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02659:Unc13b
|
APN |
4 |
43,235,332 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03031:Unc13b
|
APN |
4 |
43,235,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03036:Unc13b
|
APN |
4 |
43,235,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03209:Unc13b
|
APN |
4 |
43,239,351 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03352:Unc13b
|
APN |
4 |
43,237,110 (GRCm39) |
missense |
possibly damaging |
0.90 |
BB006:Unc13b
|
UTSW |
4 |
43,174,399 (GRCm39) |
missense |
unknown |
|
BB016:Unc13b
|
UTSW |
4 |
43,174,399 (GRCm39) |
missense |
unknown |
|
G1Funyon:Unc13b
|
UTSW |
4 |
43,263,568 (GRCm39) |
missense |
probably benign |
|
P0028:Unc13b
|
UTSW |
4 |
43,256,225 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4585001:Unc13b
|
UTSW |
4 |
43,091,298 (GRCm39) |
missense |
probably benign |
0.03 |
R0019:Unc13b
|
UTSW |
4 |
43,096,990 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0019:Unc13b
|
UTSW |
4 |
43,096,990 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0335:Unc13b
|
UTSW |
4 |
43,236,983 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0504:Unc13b
|
UTSW |
4 |
43,263,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R0631:Unc13b
|
UTSW |
4 |
43,182,849 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0748:Unc13b
|
UTSW |
4 |
43,241,164 (GRCm39) |
splice site |
probably benign |
|
R1275:Unc13b
|
UTSW |
4 |
43,235,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R1293:Unc13b
|
UTSW |
4 |
43,235,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Unc13b
|
UTSW |
4 |
43,239,385 (GRCm39) |
nonsense |
probably null |
|
R1552:Unc13b
|
UTSW |
4 |
43,237,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R1591:Unc13b
|
UTSW |
4 |
43,244,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1628:Unc13b
|
UTSW |
4 |
43,263,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Unc13b
|
UTSW |
4 |
43,240,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1839:Unc13b
|
UTSW |
4 |
43,258,308 (GRCm39) |
splice site |
probably benign |
|
R2045:Unc13b
|
UTSW |
4 |
43,091,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Unc13b
|
UTSW |
4 |
43,245,566 (GRCm39) |
nonsense |
probably null |
|
R2259:Unc13b
|
UTSW |
4 |
43,182,780 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2307:Unc13b
|
UTSW |
4 |
43,239,854 (GRCm39) |
missense |
probably damaging |
0.98 |
R2317:Unc13b
|
UTSW |
4 |
43,245,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R2402:Unc13b
|
UTSW |
4 |
43,095,843 (GRCm39) |
missense |
probably benign |
|
R2847:Unc13b
|
UTSW |
4 |
43,180,404 (GRCm39) |
missense |
probably benign |
0.04 |
R3414:Unc13b
|
UTSW |
4 |
43,234,658 (GRCm39) |
splice site |
probably benign |
|
R3436:Unc13b
|
UTSW |
4 |
43,097,028 (GRCm39) |
splice site |
probably benign |
|
R3955:Unc13b
|
UTSW |
4 |
43,256,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R3957:Unc13b
|
UTSW |
4 |
43,256,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R4015:Unc13b
|
UTSW |
4 |
43,237,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R4650:Unc13b
|
UTSW |
4 |
43,261,035 (GRCm39) |
missense |
probably damaging |
0.97 |
R4836:Unc13b
|
UTSW |
4 |
43,237,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R5041:Unc13b
|
UTSW |
4 |
43,237,836 (GRCm39) |
missense |
probably benign |
0.41 |
R5413:Unc13b
|
UTSW |
4 |
43,257,936 (GRCm39) |
critical splice donor site |
probably null |
|
R5994:Unc13b
|
UTSW |
4 |
43,172,596 (GRCm39) |
intron |
probably benign |
|
R6015:Unc13b
|
UTSW |
4 |
43,177,995 (GRCm39) |
nonsense |
probably null |
|
R6090:Unc13b
|
UTSW |
4 |
43,239,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Unc13b
|
UTSW |
4 |
43,165,800 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6246:Unc13b
|
UTSW |
4 |
43,216,246 (GRCm39) |
missense |
probably benign |
0.18 |
R6427:Unc13b
|
UTSW |
4 |
43,176,966 (GRCm39) |
unclassified |
probably benign |
|
R6660:Unc13b
|
UTSW |
4 |
43,177,412 (GRCm39) |
unclassified |
probably benign |
|
R6670:Unc13b
|
UTSW |
4 |
43,255,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R6753:Unc13b
|
UTSW |
4 |
43,239,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Unc13b
|
UTSW |
4 |
43,165,828 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6886:Unc13b
|
UTSW |
4 |
43,170,156 (GRCm39) |
intron |
probably benign |
|
R6969:Unc13b
|
UTSW |
4 |
43,263,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6994:Unc13b
|
UTSW |
4 |
43,173,203 (GRCm39) |
intron |
probably benign |
|
R6994:Unc13b
|
UTSW |
4 |
43,171,403 (GRCm39) |
intron |
probably benign |
|
R7080:Unc13b
|
UTSW |
4 |
43,171,926 (GRCm39) |
missense |
unknown |
|
R7117:Unc13b
|
UTSW |
4 |
43,216,544 (GRCm39) |
missense |
probably benign |
0.33 |
R7132:Unc13b
|
UTSW |
4 |
43,215,757 (GRCm39) |
missense |
probably benign |
0.17 |
R7181:Unc13b
|
UTSW |
4 |
43,258,893 (GRCm39) |
missense |
probably damaging |
0.99 |
R7192:Unc13b
|
UTSW |
4 |
43,258,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R7246:Unc13b
|
UTSW |
4 |
43,172,910 (GRCm39) |
missense |
unknown |
|
R7342:Unc13b
|
UTSW |
4 |
43,258,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R7345:Unc13b
|
UTSW |
4 |
43,173,966 (GRCm39) |
missense |
unknown |
|
R7355:Unc13b
|
UTSW |
4 |
43,237,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Unc13b
|
UTSW |
4 |
43,216,459 (GRCm39) |
missense |
probably benign |
0.03 |
R7419:Unc13b
|
UTSW |
4 |
43,174,023 (GRCm39) |
missense |
unknown |
|
R7424:Unc13b
|
UTSW |
4 |
43,172,235 (GRCm39) |
missense |
unknown |
|
R7517:Unc13b
|
UTSW |
4 |
43,215,765 (GRCm39) |
missense |
probably benign |
|
R7532:Unc13b
|
UTSW |
4 |
43,249,565 (GRCm39) |
missense |
probably benign |
0.44 |
R7564:Unc13b
|
UTSW |
4 |
43,091,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Unc13b
|
UTSW |
4 |
43,263,569 (GRCm39) |
missense |
probably benign |
0.20 |
R7604:Unc13b
|
UTSW |
4 |
43,256,776 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7604:Unc13b
|
UTSW |
4 |
43,170,102 (GRCm39) |
missense |
unknown |
|
R7643:Unc13b
|
UTSW |
4 |
43,216,333 (GRCm39) |
missense |
probably benign |
|
R7718:Unc13b
|
UTSW |
4 |
43,173,854 (GRCm39) |
missense |
unknown |
|
R7735:Unc13b
|
UTSW |
4 |
43,165,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7756:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small deletion |
probably benign |
|
R7757:Unc13b
|
UTSW |
4 |
43,177,341 (GRCm39) |
small insertion |
probably benign |
|
R7757:Unc13b
|
UTSW |
4 |
43,177,330 (GRCm39) |
small insertion |
probably benign |
|
R7757:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small deletion |
probably benign |
|
R7758:Unc13b
|
UTSW |
4 |
43,177,344 (GRCm39) |
small insertion |
probably benign |
|
R7758:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small insertion |
probably benign |
|
R7781:Unc13b
|
UTSW |
4 |
43,259,546 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7793:Unc13b
|
UTSW |
4 |
43,172,737 (GRCm39) |
missense |
unknown |
|
R7858:Unc13b
|
UTSW |
4 |
43,176,285 (GRCm39) |
missense |
unknown |
|
R7867:Unc13b
|
UTSW |
4 |
43,232,573 (GRCm39) |
nonsense |
probably null |
|
R7897:Unc13b
|
UTSW |
4 |
43,171,860 (GRCm39) |
missense |
unknown |
|
R7904:Unc13b
|
UTSW |
4 |
43,217,075 (GRCm39) |
missense |
probably benign |
|
R7929:Unc13b
|
UTSW |
4 |
43,174,399 (GRCm39) |
missense |
unknown |
|
R7984:Unc13b
|
UTSW |
4 |
43,173,973 (GRCm39) |
missense |
unknown |
|
R8069:Unc13b
|
UTSW |
4 |
43,177,597 (GRCm39) |
missense |
unknown |
|
R8101:Unc13b
|
UTSW |
4 |
43,239,918 (GRCm39) |
missense |
probably benign |
0.08 |
R8246:Unc13b
|
UTSW |
4 |
43,175,954 (GRCm39) |
missense |
unknown |
|
R8289:Unc13b
|
UTSW |
4 |
43,172,524 (GRCm39) |
nonsense |
probably null |
|
R8301:Unc13b
|
UTSW |
4 |
43,263,568 (GRCm39) |
missense |
probably benign |
|
R8397:Unc13b
|
UTSW |
4 |
43,217,290 (GRCm39) |
missense |
probably benign |
0.12 |
R8421:Unc13b
|
UTSW |
4 |
43,178,304 (GRCm39) |
missense |
unknown |
|
R8738:Unc13b
|
UTSW |
4 |
43,177,564 (GRCm39) |
missense |
unknown |
|
R8746:Unc13b
|
UTSW |
4 |
43,176,120 (GRCm39) |
missense |
unknown |
|
R8766:Unc13b
|
UTSW |
4 |
43,174,722 (GRCm39) |
missense |
unknown |
|
R8825:Unc13b
|
UTSW |
4 |
43,237,683 (GRCm39) |
splice site |
probably benign |
|
R8834:Unc13b
|
UTSW |
4 |
43,175,954 (GRCm39) |
missense |
unknown |
|
R8862:Unc13b
|
UTSW |
4 |
43,235,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Unc13b
|
UTSW |
4 |
43,174,724 (GRCm39) |
missense |
unknown |
|
R8889:Unc13b
|
UTSW |
4 |
43,176,484 (GRCm39) |
missense |
unknown |
|
R8892:Unc13b
|
UTSW |
4 |
43,176,484 (GRCm39) |
missense |
unknown |
|
R8904:Unc13b
|
UTSW |
4 |
43,178,531 (GRCm39) |
intron |
probably benign |
|
R9089:Unc13b
|
UTSW |
4 |
43,095,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R9144:Unc13b
|
UTSW |
4 |
43,173,649 (GRCm39) |
missense |
unknown |
|
R9149:Unc13b
|
UTSW |
4 |
43,176,186 (GRCm39) |
missense |
unknown |
|
R9173:Unc13b
|
UTSW |
4 |
43,177,421 (GRCm39) |
missense |
unknown |
|
R9200:Unc13b
|
UTSW |
4 |
43,257,352 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9232:Unc13b
|
UTSW |
4 |
43,240,321 (GRCm39) |
missense |
probably benign |
0.03 |
R9269:Unc13b
|
UTSW |
4 |
43,171,955 (GRCm39) |
missense |
unknown |
|
R9320:Unc13b
|
UTSW |
4 |
43,171,044 (GRCm39) |
missense |
unknown |
|
R9335:Unc13b
|
UTSW |
4 |
43,255,551 (GRCm39) |
missense |
probably damaging |
0.99 |
R9335:Unc13b
|
UTSW |
4 |
43,216,123 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9352:Unc13b
|
UTSW |
4 |
43,177,313 (GRCm39) |
nonsense |
probably null |
|
R9352:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small insertion |
probably benign |
|
R9378:Unc13b
|
UTSW |
4 |
43,173,282 (GRCm39) |
missense |
unknown |
|
R9382:Unc13b
|
UTSW |
4 |
43,172,512 (GRCm39) |
missense |
unknown |
|
R9569:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small deletion |
probably benign |
|
R9622:Unc13b
|
UTSW |
4 |
43,172,513 (GRCm39) |
missense |
|
|
R9687:Unc13b
|
UTSW |
4 |
43,174,920 (GRCm39) |
missense |
unknown |
|
R9704:Unc13b
|
UTSW |
4 |
43,237,102 (GRCm39) |
missense |
probably benign |
0.31 |
R9721:Unc13b
|
UTSW |
4 |
43,101,869 (GRCm39) |
missense |
probably benign |
|
R9753:Unc13b
|
UTSW |
4 |
43,182,842 (GRCm39) |
nonsense |
probably null |
|
RF016:Unc13b
|
UTSW |
4 |
43,177,350 (GRCm39) |
small insertion |
probably benign |
|
RF016:Unc13b
|
UTSW |
4 |
43,177,347 (GRCm39) |
small insertion |
probably benign |
|
RF041:Unc13b
|
UTSW |
4 |
43,177,338 (GRCm39) |
small insertion |
probably benign |
|
RF056:Unc13b
|
UTSW |
4 |
43,177,359 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Unc13b
|
UTSW |
4 |
43,177,764 (GRCm39) |
missense |
unknown |
|
Z1176:Unc13b
|
UTSW |
4 |
43,177,191 (GRCm39) |
missense |
unknown |
|
Z1176:Unc13b
|
UTSW |
4 |
43,171,419 (GRCm39) |
missense |
unknown |
|
Z1176:Unc13b
|
UTSW |
4 |
43,261,043 (GRCm39) |
missense |
probably benign |
0.11 |
Z1177:Unc13b
|
UTSW |
4 |
43,173,669 (GRCm39) |
missense |
unknown |
|
|