Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
C |
A |
8: 73,198,923 (GRCm39) |
A110D |
probably benign |
Het |
4930407I10Rik |
A |
G |
15: 81,947,615 (GRCm39) |
E504G |
probably benign |
Het |
4931406B18Rik |
C |
A |
7: 43,148,702 (GRCm39) |
A170S |
|
Het |
Apbb2 |
T |
C |
5: 66,609,018 (GRCm39) |
K210E |
probably benign |
Het |
Arid4a |
C |
A |
12: 71,122,129 (GRCm39) |
L515I |
probably damaging |
Het |
Atp13a3 |
A |
G |
16: 30,134,716 (GRCm39) |
S1186P |
possibly damaging |
Het |
Brf1 |
A |
G |
12: 112,927,011 (GRCm39) |
Y500H |
probably damaging |
Het |
Btaf1 |
A |
G |
19: 36,964,114 (GRCm39) |
Y895C |
probably benign |
Het |
Cdhr17 |
T |
A |
5: 16,997,909 (GRCm39) |
V47E |
possibly damaging |
Het |
Cenpf |
T |
C |
1: 189,391,571 (GRCm39) |
T737A |
probably benign |
Het |
Cmklr1 |
G |
C |
5: 113,752,043 (GRCm39) |
H319Q |
probably benign |
Het |
Col18a1 |
G |
A |
10: 76,893,204 (GRCm39) |
T1057M |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,515,260 (GRCm39) |
|
probably null |
Het |
Csmd3 |
A |
C |
15: 47,617,187 (GRCm39) |
H1000Q |
|
Het |
Cyp4a29 |
T |
A |
4: 115,108,395 (GRCm39) |
M373K |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,333,173 (GRCm39) |
E215G |
probably damaging |
Het |
Dusp19 |
T |
C |
2: 80,447,729 (GRCm39) |
M1T |
probably null |
Het |
Etv4 |
A |
G |
11: 101,664,492 (GRCm39) |
Y253H |
probably benign |
Het |
Exosc6 |
G |
A |
8: 111,783,513 (GRCm39) |
A171T |
probably damaging |
Het |
Fam219a |
G |
A |
4: 41,521,870 (GRCm39) |
T70M |
probably damaging |
Het |
Fau |
G |
A |
19: 6,108,297 (GRCm39) |
R6H |
probably benign |
Het |
Flrt3 |
T |
C |
2: 140,501,879 (GRCm39) |
D583G |
probably damaging |
Het |
Gm14443 |
A |
T |
2: 175,011,869 (GRCm39) |
C192* |
probably null |
Het |
Gm4353 |
T |
A |
7: 115,682,843 (GRCm39) |
N246I |
probably benign |
Het |
Igfn1 |
A |
G |
1: 135,926,327 (GRCm39) |
L41P |
probably benign |
Het |
Jakmip3 |
A |
T |
7: 138,622,560 (GRCm39) |
I307F |
probably damaging |
Het |
Kcnt2 |
T |
A |
1: 140,353,035 (GRCm39) |
V248D |
probably damaging |
Het |
Kctd14 |
A |
G |
7: 97,107,243 (GRCm39) |
K166R |
probably benign |
Het |
Kdm5b |
T |
C |
1: 134,528,493 (GRCm39) |
|
probably null |
Het |
Kif5c |
A |
G |
2: 49,620,151 (GRCm39) |
D461G |
probably damaging |
Het |
Lpin2 |
T |
C |
17: 71,538,516 (GRCm39) |
|
probably null |
Het |
Mettl22 |
G |
A |
16: 8,305,231 (GRCm39) |
D295N |
probably damaging |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Or10a5 |
A |
T |
7: 106,635,640 (GRCm39) |
I93F |
probably damaging |
Het |
Or5b95 |
T |
A |
19: 12,658,190 (GRCm39) |
C239* |
probably null |
Het |
Or5k8 |
A |
T |
16: 58,644,677 (GRCm39) |
Y132N |
probably damaging |
Het |
Pecam1 |
G |
T |
11: 106,586,587 (GRCm39) |
N309K |
probably damaging |
Het |
Pigc |
C |
T |
1: 161,798,032 (GRCm39) |
R5C |
probably benign |
Het |
Pih1d1 |
T |
C |
7: 44,809,193 (GRCm39) |
V259A |
possibly damaging |
Het |
Ptpre |
A |
G |
7: 135,271,508 (GRCm39) |
I374M |
probably benign |
Het |
Rnps1 |
A |
G |
17: 24,637,573 (GRCm39) |
S72G |
unknown |
Het |
S100pbp |
A |
G |
4: 129,044,847 (GRCm39) |
Y363H |
probably damaging |
Het |
Sema5a |
A |
G |
15: 32,619,040 (GRCm39) |
T523A |
probably benign |
Het |
Slc38a8 |
A |
G |
8: 120,212,851 (GRCm39) |
F270S |
possibly damaging |
Het |
Slc4a1ap |
T |
C |
5: 31,693,538 (GRCm39) |
S491P |
probably damaging |
Het |
Slc66a2 |
T |
C |
18: 80,300,300 (GRCm39) |
L57P |
probably damaging |
Het |
Slc7a6 |
T |
C |
8: 106,922,534 (GRCm39) |
V440A |
probably damaging |
Het |
Sobp |
A |
T |
10: 42,898,902 (GRCm39) |
C228S |
probably damaging |
Het |
Sox8 |
T |
C |
17: 25,787,813 (GRCm39) |
D212G |
possibly damaging |
Het |
Specc1 |
A |
G |
11: 62,102,464 (GRCm39) |
|
probably null |
Het |
Svop |
G |
A |
5: 114,168,231 (GRCm39) |
T456M |
probably benign |
Het |
Synrg |
A |
G |
11: 83,900,278 (GRCm39) |
D750G |
probably damaging |
Het |
Syt14 |
C |
A |
1: 192,612,944 (GRCm39) |
E336* |
probably null |
Het |
Tcp10c |
A |
T |
17: 13,576,650 (GRCm39) |
Q76H |
probably damaging |
Het |
Tcp11l1 |
C |
T |
2: 104,528,897 (GRCm39) |
V134I |
possibly damaging |
Het |
Tex51 |
T |
C |
18: 32,594,029 (GRCm39) |
R110G |
possibly damaging |
Het |
Tle3 |
T |
A |
9: 61,319,562 (GRCm39) |
H443Q |
possibly damaging |
Het |
Vmn2r27 |
T |
C |
6: 124,174,224 (GRCm39) |
Y542C |
possibly damaging |
Het |
Vmn2r5 |
T |
G |
3: 64,411,411 (GRCm39) |
N386H |
possibly damaging |
Het |
Vmn2r91 |
A |
G |
17: 18,327,905 (GRCm39) |
I500V |
probably damaging |
Het |
Wdfy4 |
A |
T |
14: 32,760,704 (GRCm39) |
|
probably null |
Het |
Zfp709 |
A |
T |
8: 72,644,648 (GRCm39) |
E692D |
possibly damaging |
Het |
Zglp1 |
A |
T |
9: 20,977,482 (GRCm39) |
L111Q |
probably benign |
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 |
PIT4469001:Unc13a
|
UTSW |
8 |
72,110,958 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|
|