Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630001G21Rik |
A |
G |
1: 85,652,920 (GRCm39) |
F83L |
probably benign |
Het |
Acsm2 |
T |
A |
7: 119,177,408 (GRCm39) |
C308S |
possibly damaging |
Het |
Ak3 |
A |
G |
19: 29,025,157 (GRCm39) |
S25P |
probably damaging |
Het |
Atp13a2 |
T |
A |
4: 140,721,438 (GRCm39) |
V176E |
unknown |
Het |
Bmper |
A |
T |
9: 23,317,845 (GRCm39) |
H488L |
probably benign |
Het |
Cacna1c |
A |
T |
6: 118,572,933 (GRCm39) |
C2084S |
unknown |
Het |
Ccp110 |
T |
A |
7: 118,321,600 (GRCm39) |
N418K |
probably benign |
Het |
Ddx17 |
C |
A |
15: 79,428,014 (GRCm39) |
G32C |
probably damaging |
Het |
Dennd2b |
G |
A |
7: 109,130,337 (GRCm39) |
A888V |
probably damaging |
Het |
Dusp16 |
G |
A |
6: 134,738,115 (GRCm39) |
|
probably benign |
Het |
Efl1 |
T |
G |
7: 82,307,373 (GRCm39) |
F90V |
probably benign |
Het |
Ell2 |
T |
A |
13: 75,910,011 (GRCm39) |
N252K |
probably damaging |
Het |
Gdf6 |
T |
C |
4: 9,859,569 (GRCm39) |
V217A |
probably damaging |
Het |
H1f4 |
A |
T |
13: 23,806,362 (GRCm39) |
V40E |
probably damaging |
Het |
Hint1 |
T |
A |
11: 54,760,896 (GRCm39) |
S112T |
unknown |
Het |
Kif5c |
T |
C |
2: 49,631,360 (GRCm39) |
V679A |
probably benign |
Het |
Lrrn3 |
A |
T |
12: 41,503,017 (GRCm39) |
D433E |
probably benign |
Het |
Mast4 |
G |
A |
13: 102,941,226 (GRCm39) |
T277M |
probably damaging |
Het |
Naa11 |
A |
G |
5: 97,539,485 (GRCm39) |
|
probably null |
Het |
Pcdh18 |
T |
A |
3: 49,709,518 (GRCm39) |
H599L |
probably benign |
Het |
Pgc |
A |
T |
17: 48,039,680 (GRCm39) |
K25* |
probably null |
Het |
Pramel58 |
T |
A |
5: 94,830,652 (GRCm39) |
V50E |
probably damaging |
Het |
Psd4 |
G |
A |
2: 24,284,306 (GRCm39) |
D57N |
probably benign |
Het |
Pxdn |
G |
A |
12: 30,055,828 (GRCm39) |
R1238Q |
probably benign |
Het |
Smim41 |
T |
C |
15: 101,191,152 (GRCm39) |
V6A |
probably benign |
Het |
Spata32 |
T |
C |
11: 103,100,653 (GRCm39) |
N38S |
probably benign |
Het |
Tpr |
A |
G |
1: 150,279,707 (GRCm39) |
T279A |
probably benign |
Het |
Vmn2r97 |
C |
A |
17: 19,149,878 (GRCm39) |
T422K |
probably benign |
Het |
Zfp474 |
A |
T |
18: 52,771,791 (GRCm39) |
Q148L |
possibly damaging |
Het |
|
Other mutations in Unc13a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00656:Unc13a
|
APN |
8 |
72,095,791 (GRCm39) |
missense |
probably null |
0.70 |
IGL01023:Unc13a
|
APN |
8 |
72,114,469 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01456:Unc13a
|
APN |
8 |
72,097,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01820:Unc13a
|
APN |
8 |
72,107,591 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01909:Unc13a
|
APN |
8 |
72,091,854 (GRCm39) |
splice site |
probably benign |
|
IGL01925:Unc13a
|
APN |
8 |
72,087,187 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02407:Unc13a
|
APN |
8 |
72,101,586 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02622:Unc13a
|
APN |
8 |
72,105,158 (GRCm39) |
splice site |
probably null |
|
IGL02634:Unc13a
|
APN |
8 |
72,108,345 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02724:Unc13a
|
APN |
8 |
72,108,949 (GRCm39) |
splice site |
probably benign |
|
IGL02892:Unc13a
|
APN |
8 |
72,102,554 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02948:Unc13a
|
APN |
8 |
72,103,193 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL03081:Unc13a
|
APN |
8 |
72,102,193 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03372:Unc13a
|
APN |
8 |
72,108,353 (GRCm39) |
missense |
probably damaging |
1.00 |
curvy
|
UTSW |
8 |
72,083,148 (GRCm39) |
splice site |
probably null |
|
Greed
|
UTSW |
8 |
72,107,489 (GRCm39) |
missense |
probably damaging |
1.00 |
largesse
|
UTSW |
8 |
72,087,302 (GRCm39) |
missense |
probably damaging |
1.00 |
serpiginous
|
UTSW |
8 |
72,116,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Unc13a
|
UTSW |
8 |
72,087,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Unc13a
|
UTSW |
8 |
72,087,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R0389:Unc13a
|
UTSW |
8 |
72,110,676 (GRCm39) |
missense |
probably benign |
0.01 |
R0457:Unc13a
|
UTSW |
8 |
72,110,645 (GRCm39) |
critical splice donor site |
probably null |
|
R0478:Unc13a
|
UTSW |
8 |
72,103,792 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0483:Unc13a
|
UTSW |
8 |
72,097,557 (GRCm39) |
missense |
probably damaging |
0.96 |
R0609:Unc13a
|
UTSW |
8 |
72,111,111 (GRCm39) |
missense |
probably damaging |
0.96 |
R0611:Unc13a
|
UTSW |
8 |
72,102,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Unc13a
|
UTSW |
8 |
72,108,929 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0883:Unc13a
|
UTSW |
8 |
72,094,817 (GRCm39) |
nonsense |
probably null |
|
R1162:Unc13a
|
UTSW |
8 |
72,100,561 (GRCm39) |
missense |
probably benign |
0.31 |
R1185:Unc13a
|
UTSW |
8 |
72,114,477 (GRCm39) |
missense |
probably benign |
0.13 |
R1185:Unc13a
|
UTSW |
8 |
72,114,477 (GRCm39) |
missense |
probably benign |
0.13 |
R1185:Unc13a
|
UTSW |
8 |
72,114,477 (GRCm39) |
missense |
probably benign |
0.13 |
R1196:Unc13a
|
UTSW |
8 |
72,107,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Unc13a
|
UTSW |
8 |
72,103,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:Unc13a
|
UTSW |
8 |
72,101,625 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1507:Unc13a
|
UTSW |
8 |
72,110,910 (GRCm39) |
missense |
probably benign |
|
R1636:Unc13a
|
UTSW |
8 |
72,106,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Unc13a
|
UTSW |
8 |
72,105,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:Unc13a
|
UTSW |
8 |
72,092,412 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2107:Unc13a
|
UTSW |
8 |
72,108,895 (GRCm39) |
splice site |
probably null |
|
R2286:Unc13a
|
UTSW |
8 |
72,083,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R2334:Unc13a
|
UTSW |
8 |
72,087,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R2924:Unc13a
|
UTSW |
8 |
72,097,596 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3177:Unc13a
|
UTSW |
8 |
72,082,339 (GRCm39) |
missense |
probably benign |
0.01 |
R3277:Unc13a
|
UTSW |
8 |
72,082,339 (GRCm39) |
missense |
probably benign |
0.01 |
R4175:Unc13a
|
UTSW |
8 |
72,120,368 (GRCm39) |
intron |
probably benign |
|
R4279:Unc13a
|
UTSW |
8 |
72,119,311 (GRCm39) |
missense |
probably damaging |
0.98 |
R4629:Unc13a
|
UTSW |
8 |
72,106,097 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4803:Unc13a
|
UTSW |
8 |
72,115,494 (GRCm39) |
splice site |
probably null |
|
R4877:Unc13a
|
UTSW |
8 |
72,111,260 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4927:Unc13a
|
UTSW |
8 |
72,107,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4930:Unc13a
|
UTSW |
8 |
72,083,148 (GRCm39) |
splice site |
probably null |
|
R4994:Unc13a
|
UTSW |
8 |
72,095,816 (GRCm39) |
missense |
probably benign |
0.28 |
R5011:Unc13a
|
UTSW |
8 |
72,094,121 (GRCm39) |
nonsense |
probably null |
|
R5252:Unc13a
|
UTSW |
8 |
72,105,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Unc13a
|
UTSW |
8 |
72,115,158 (GRCm39) |
missense |
probably benign |
0.02 |
R5458:Unc13a
|
UTSW |
8 |
72,116,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R5514:Unc13a
|
UTSW |
8 |
72,095,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R5784:Unc13a
|
UTSW |
8 |
72,108,310 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5853:Unc13a
|
UTSW |
8 |
72,107,773 (GRCm39) |
splice site |
probably null |
|
R6183:Unc13a
|
UTSW |
8 |
72,097,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Unc13a
|
UTSW |
8 |
72,119,283 (GRCm39) |
critical splice donor site |
probably null |
|
R6374:Unc13a
|
UTSW |
8 |
72,094,097 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6392:Unc13a
|
UTSW |
8 |
72,090,453 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6515:Unc13a
|
UTSW |
8 |
72,100,584 (GRCm39) |
missense |
probably benign |
0.44 |
R6576:Unc13a
|
UTSW |
8 |
72,106,122 (GRCm39) |
missense |
probably benign |
0.00 |
R6943:Unc13a
|
UTSW |
8 |
72,105,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Unc13a
|
UTSW |
8 |
72,111,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7062:Unc13a
|
UTSW |
8 |
72,115,881 (GRCm39) |
missense |
probably benign |
0.00 |
R7146:Unc13a
|
UTSW |
8 |
72,083,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Unc13a
|
UTSW |
8 |
72,113,229 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7443:Unc13a
|
UTSW |
8 |
72,083,603 (GRCm39) |
missense |
probably damaging |
0.98 |
R7545:Unc13a
|
UTSW |
8 |
72,094,153 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7644:Unc13a
|
UTSW |
8 |
72,087,182 (GRCm39) |
missense |
probably benign |
0.13 |
R7780:Unc13a
|
UTSW |
8 |
72,110,979 (GRCm39) |
missense |
probably benign |
0.02 |
R7952:Unc13a
|
UTSW |
8 |
72,111,131 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7989:Unc13a
|
UTSW |
8 |
72,104,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R8169:Unc13a
|
UTSW |
8 |
72,108,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R8503:Unc13a
|
UTSW |
8 |
72,098,405 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8504:Unc13a
|
UTSW |
8 |
72,098,405 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8675:Unc13a
|
UTSW |
8 |
72,098,359 (GRCm39) |
missense |
probably benign |
0.00 |
R8929:Unc13a
|
UTSW |
8 |
72,103,835 (GRCm39) |
missense |
probably benign |
0.01 |
R8945:Unc13a
|
UTSW |
8 |
72,100,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R8979:Unc13a
|
UTSW |
8 |
72,113,125 (GRCm39) |
missense |
probably benign |
0.07 |
R9109:Unc13a
|
UTSW |
8 |
72,108,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9136:Unc13a
|
UTSW |
8 |
72,104,994 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9235:Unc13a
|
UTSW |
8 |
72,115,912 (GRCm39) |
missense |
probably benign |
|
R9298:Unc13a
|
UTSW |
8 |
72,108,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9355:Unc13a
|
UTSW |
8 |
72,098,375 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9483:Unc13a
|
UTSW |
8 |
72,103,221 (GRCm39) |
missense |
probably benign |
0.01 |
R9647:Unc13a
|
UTSW |
8 |
72,104,882 (GRCm39) |
missense |
probably damaging |
0.98 |
R9696:Unc13a
|
UTSW |
8 |
72,082,197 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1088:Unc13a
|
UTSW |
8 |
72,107,447 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Unc13a
|
UTSW |
8 |
72,097,516 (GRCm39) |
critical splice donor site |
probably null |
|
|