Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cacna2d3 |
A |
G |
14: 29,189,909 (GRCm39) |
L109P |
probably damaging |
Het |
Caprin2 |
A |
T |
6: 148,763,964 (GRCm39) |
S568T |
possibly damaging |
Het |
Catip |
A |
G |
1: 74,403,744 (GRCm39) |
T154A |
probably null |
Het |
Ccdc187 |
A |
G |
2: 26,177,980 (GRCm39) |
S270P |
possibly damaging |
Het |
Ccdc88a |
A |
G |
11: 29,324,559 (GRCm39) |
Y39C |
probably damaging |
Het |
Chrdl2 |
A |
T |
7: 99,676,787 (GRCm39) |
H203L |
possibly damaging |
Het |
Chrnb2 |
A |
G |
3: 89,670,552 (GRCm39) |
V62A |
probably damaging |
Het |
Cklf |
T |
A |
8: 104,984,055 (GRCm39) |
S73T |
possibly damaging |
Het |
Clk1 |
A |
G |
1: 58,456,166 (GRCm39) |
|
probably null |
Het |
Ctdp1 |
T |
C |
18: 80,492,716 (GRCm39) |
D593G |
probably damaging |
Het |
Ctsc |
A |
T |
7: 87,958,988 (GRCm39) |
I423F |
probably damaging |
Het |
D130043K22Rik |
T |
A |
13: 25,073,825 (GRCm39) |
V968E |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,696,140 (GRCm39) |
S166G |
possibly damaging |
Het |
Dnah2 |
G |
T |
11: 69,327,117 (GRCm39) |
|
probably benign |
Het |
Dnajb11 |
G |
T |
16: 22,687,888 (GRCm39) |
R206L |
probably benign |
Het |
Dsel |
A |
T |
1: 111,786,908 (GRCm39) |
|
probably benign |
Het |
Ehd2 |
T |
C |
7: 15,684,396 (GRCm39) |
S468G |
possibly damaging |
Het |
Ehmt2 |
T |
A |
17: 35,125,787 (GRCm39) |
V640E |
possibly damaging |
Het |
Elmo2 |
T |
A |
2: 165,140,573 (GRCm39) |
E299D |
probably benign |
Het |
Eps8l1 |
T |
C |
7: 4,473,886 (GRCm39) |
L231P |
probably damaging |
Het |
Esd |
A |
G |
14: 74,978,686 (GRCm39) |
T83A |
probably damaging |
Het |
Flt3 |
A |
G |
5: 147,293,020 (GRCm39) |
F529L |
probably benign |
Het |
Hnrnpu |
G |
A |
1: 178,158,339 (GRCm39) |
|
probably benign |
Het |
Hpx |
G |
T |
7: 105,249,278 (GRCm39) |
A7E |
possibly damaging |
Het |
Ighv6-5 |
C |
T |
12: 114,380,320 (GRCm39) |
V85M |
possibly damaging |
Het |
Itpr3 |
G |
A |
17: 27,338,240 (GRCm39) |
V2503I |
probably damaging |
Het |
Itprid1 |
A |
G |
6: 55,875,114 (GRCm39) |
T355A |
probably benign |
Het |
Matr3 |
G |
T |
18: 35,705,710 (GRCm39) |
G212C |
probably damaging |
Het |
Mrpl35 |
A |
T |
6: 71,793,263 (GRCm39) |
Y129* |
probably null |
Het |
Myh2 |
T |
C |
11: 67,071,710 (GRCm39) |
I509T |
possibly damaging |
Het |
Nat8l |
G |
T |
5: 34,158,288 (GRCm39) |
A233S |
probably damaging |
Het |
Nipbl |
A |
C |
15: 8,361,936 (GRCm39) |
L1447W |
probably damaging |
Het |
Paf1 |
T |
A |
7: 28,094,481 (GRCm39) |
C31S |
possibly damaging |
Het |
Parp4 |
A |
C |
14: 56,840,313 (GRCm39) |
T573P |
probably benign |
Het |
Phf12 |
A |
T |
11: 77,913,846 (GRCm39) |
|
probably benign |
Het |
Pi4k2b |
A |
G |
5: 52,905,765 (GRCm39) |
E102G |
probably benign |
Het |
Pou2f1 |
A |
G |
1: 165,762,382 (GRCm39) |
C7R |
probably benign |
Het |
Prpsap2 |
T |
C |
11: 61,631,815 (GRCm39) |
R181G |
probably benign |
Het |
Psd |
A |
G |
19: 46,311,561 (GRCm39) |
|
probably benign |
Het |
Ptgds |
T |
C |
2: 25,359,622 (GRCm39) |
T22A |
probably benign |
Het |
Rab21 |
A |
T |
10: 115,151,097 (GRCm39) |
|
probably null |
Het |
Relb |
T |
C |
7: 19,346,582 (GRCm39) |
D330G |
probably damaging |
Het |
Rhoc |
A |
T |
3: 104,700,236 (GRCm39) |
T100S |
probably benign |
Het |
Ryr1 |
G |
T |
7: 28,802,389 (GRCm39) |
H744N |
probably damaging |
Het |
Sardh |
C |
T |
2: 27,129,458 (GRCm39) |
G280D |
probably damaging |
Het |
Scyl2 |
A |
C |
10: 89,493,729 (GRCm39) |
N346K |
possibly damaging |
Het |
Sec16b |
T |
C |
1: 157,362,970 (GRCm39) |
F267S |
probably damaging |
Het |
Slc44a5 |
T |
A |
3: 153,956,714 (GRCm39) |
M322K |
probably benign |
Het |
St8sia4 |
T |
A |
1: 95,519,508 (GRCm39) |
N327Y |
probably benign |
Het |
Tbl1xr1 |
T |
A |
3: 22,257,323 (GRCm39) |
Y395* |
probably null |
Het |
Vangl2 |
A |
G |
1: 171,840,415 (GRCm39) |
S58P |
probably damaging |
Het |
Vmn1r17 |
A |
G |
6: 57,337,501 (GRCm39) |
I288T |
probably benign |
Het |
Vmn1r236 |
A |
G |
17: 21,507,508 (GRCm39) |
I209V |
probably benign |
Het |
Zfp809 |
A |
G |
9: 22,149,950 (GRCm39) |
Y149C |
probably damaging |
Het |
|
Other mutations in Unc13c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Unc13c
|
APN |
9 |
73,643,985 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00693:Unc13c
|
APN |
9 |
73,665,884 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01022:Unc13c
|
APN |
9 |
73,424,610 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01088:Unc13c
|
APN |
9 |
73,839,563 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01123:Unc13c
|
APN |
9 |
73,840,479 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01131:Unc13c
|
APN |
9 |
73,471,335 (GRCm39) |
missense |
probably benign |
|
IGL01135:Unc13c
|
APN |
9 |
73,392,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01393:Unc13c
|
APN |
9 |
73,447,552 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01752:Unc13c
|
APN |
9 |
73,839,093 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01893:Unc13c
|
APN |
9 |
73,600,648 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01897:Unc13c
|
APN |
9 |
73,453,309 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01936:Unc13c
|
APN |
9 |
73,600,524 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02122:Unc13c
|
APN |
9 |
73,641,679 (GRCm39) |
splice site |
probably benign |
|
IGL02341:Unc13c
|
APN |
9 |
73,840,492 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02434:Unc13c
|
APN |
9 |
73,839,910 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02545:Unc13c
|
APN |
9 |
73,388,357 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02709:Unc13c
|
APN |
9 |
73,466,238 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02815:Unc13c
|
APN |
9 |
73,447,545 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02904:Unc13c
|
APN |
9 |
73,388,349 (GRCm39) |
nonsense |
probably null |
|
IGL03260:Unc13c
|
APN |
9 |
73,838,626 (GRCm39) |
missense |
probably benign |
0.11 |
Feeling
|
UTSW |
9 |
73,600,553 (GRCm39) |
missense |
possibly damaging |
0.46 |
Inkling
|
UTSW |
9 |
73,839,126 (GRCm39) |
missense |
probably damaging |
1.00 |
notion
|
UTSW |
9 |
73,643,844 (GRCm39) |
missense |
probably damaging |
1.00 |
BB001:Unc13c
|
UTSW |
9 |
73,641,690 (GRCm39) |
missense |
probably benign |
0.05 |
BB011:Unc13c
|
UTSW |
9 |
73,641,690 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4431001:Unc13c
|
UTSW |
9 |
73,656,829 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4651001:Unc13c
|
UTSW |
9 |
73,391,021 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0017:Unc13c
|
UTSW |
9 |
73,600,583 (GRCm39) |
missense |
probably benign |
0.07 |
R0039:Unc13c
|
UTSW |
9 |
73,576,847 (GRCm39) |
splice site |
probably benign |
|
R0164:Unc13c
|
UTSW |
9 |
73,602,174 (GRCm39) |
missense |
probably benign |
0.01 |
R0164:Unc13c
|
UTSW |
9 |
73,602,174 (GRCm39) |
missense |
probably benign |
0.01 |
R0308:Unc13c
|
UTSW |
9 |
73,388,400 (GRCm39) |
missense |
probably benign |
0.04 |
R0344:Unc13c
|
UTSW |
9 |
73,838,067 (GRCm39) |
missense |
probably benign |
0.39 |
R0421:Unc13c
|
UTSW |
9 |
73,840,492 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0606:Unc13c
|
UTSW |
9 |
73,438,265 (GRCm39) |
splice site |
probably benign |
|
R0655:Unc13c
|
UTSW |
9 |
73,838,235 (GRCm39) |
missense |
probably damaging |
0.96 |
R1013:Unc13c
|
UTSW |
9 |
73,840,614 (GRCm39) |
missense |
probably benign |
0.45 |
R1293:Unc13c
|
UTSW |
9 |
73,481,356 (GRCm39) |
missense |
probably benign |
0.06 |
R1493:Unc13c
|
UTSW |
9 |
73,546,350 (GRCm39) |
missense |
probably benign |
0.27 |
R1675:Unc13c
|
UTSW |
9 |
73,546,332 (GRCm39) |
critical splice donor site |
probably null |
|
R1789:Unc13c
|
UTSW |
9 |
73,663,621 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2001:Unc13c
|
UTSW |
9 |
73,390,897 (GRCm39) |
splice site |
probably null |
|
R2055:Unc13c
|
UTSW |
9 |
73,643,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Unc13c
|
UTSW |
9 |
73,572,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R2420:Unc13c
|
UTSW |
9 |
73,838,829 (GRCm39) |
missense |
probably damaging |
0.97 |
R2421:Unc13c
|
UTSW |
9 |
73,838,829 (GRCm39) |
missense |
probably damaging |
0.97 |
R2422:Unc13c
|
UTSW |
9 |
73,838,829 (GRCm39) |
missense |
probably damaging |
0.97 |
R3415:Unc13c
|
UTSW |
9 |
73,839,868 (GRCm39) |
missense |
probably benign |
0.00 |
R3423:Unc13c
|
UTSW |
9 |
73,837,935 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3820:Unc13c
|
UTSW |
9 |
73,838,240 (GRCm39) |
missense |
probably benign |
0.00 |
R3857:Unc13c
|
UTSW |
9 |
73,606,390 (GRCm39) |
nonsense |
probably null |
|
R3859:Unc13c
|
UTSW |
9 |
73,606,390 (GRCm39) |
nonsense |
probably null |
|
R3895:Unc13c
|
UTSW |
9 |
73,840,805 (GRCm39) |
missense |
probably benign |
|
R4038:Unc13c
|
UTSW |
9 |
73,441,188 (GRCm39) |
critical splice donor site |
probably null |
|
R4077:Unc13c
|
UTSW |
9 |
73,643,821 (GRCm39) |
nonsense |
probably null |
|
R4125:Unc13c
|
UTSW |
9 |
73,481,289 (GRCm39) |
critical splice donor site |
probably null |
|
R4128:Unc13c
|
UTSW |
9 |
73,641,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Unc13c
|
UTSW |
9 |
73,438,234 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4295:Unc13c
|
UTSW |
9 |
73,641,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4307:Unc13c
|
UTSW |
9 |
73,600,649 (GRCm39) |
missense |
probably benign |
0.06 |
R4658:Unc13c
|
UTSW |
9 |
73,840,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R4694:Unc13c
|
UTSW |
9 |
73,479,636 (GRCm39) |
missense |
probably benign |
0.00 |
R4735:Unc13c
|
UTSW |
9 |
73,600,620 (GRCm39) |
missense |
probably benign |
0.00 |
R4744:Unc13c
|
UTSW |
9 |
73,839,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Unc13c
|
UTSW |
9 |
73,839,469 (GRCm39) |
missense |
probably damaging |
0.97 |
R4827:Unc13c
|
UTSW |
9 |
73,838,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Unc13c
|
UTSW |
9 |
73,839,354 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4869:Unc13c
|
UTSW |
9 |
73,587,716 (GRCm39) |
missense |
probably benign |
0.02 |
R4873:Unc13c
|
UTSW |
9 |
73,424,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R4875:Unc13c
|
UTSW |
9 |
73,424,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R4876:Unc13c
|
UTSW |
9 |
73,656,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4905:Unc13c
|
UTSW |
9 |
73,587,674 (GRCm39) |
missense |
probably benign |
|
R4912:Unc13c
|
UTSW |
9 |
73,481,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R5026:Unc13c
|
UTSW |
9 |
73,838,185 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5127:Unc13c
|
UTSW |
9 |
73,840,654 (GRCm39) |
missense |
probably benign |
0.26 |
R5151:Unc13c
|
UTSW |
9 |
73,838,757 (GRCm39) |
missense |
probably benign |
0.02 |
R5171:Unc13c
|
UTSW |
9 |
73,665,236 (GRCm39) |
missense |
probably benign |
|
R5244:Unc13c
|
UTSW |
9 |
73,433,233 (GRCm39) |
critical splice donor site |
probably null |
|
R5342:Unc13c
|
UTSW |
9 |
73,838,105 (GRCm39) |
missense |
probably benign |
0.00 |
R5399:Unc13c
|
UTSW |
9 |
73,656,970 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5409:Unc13c
|
UTSW |
9 |
73,485,672 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5460:Unc13c
|
UTSW |
9 |
73,453,271 (GRCm39) |
missense |
probably benign |
|
R5680:Unc13c
|
UTSW |
9 |
73,839,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R5681:Unc13c
|
UTSW |
9 |
73,453,357 (GRCm39) |
splice site |
probably null |
|
R5728:Unc13c
|
UTSW |
9 |
73,466,238 (GRCm39) |
missense |
probably benign |
0.01 |
R5762:Unc13c
|
UTSW |
9 |
73,719,649 (GRCm39) |
missense |
probably benign |
0.00 |
R5764:Unc13c
|
UTSW |
9 |
73,441,185 (GRCm39) |
splice site |
probably null |
|
R5829:Unc13c
|
UTSW |
9 |
73,600,650 (GRCm39) |
missense |
probably benign |
0.15 |
R5894:Unc13c
|
UTSW |
9 |
73,600,486 (GRCm39) |
critical splice donor site |
probably null |
|
R5936:Unc13c
|
UTSW |
9 |
73,485,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R6043:Unc13c
|
UTSW |
9 |
73,643,933 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6046:Unc13c
|
UTSW |
9 |
73,838,166 (GRCm39) |
missense |
probably benign |
|
R6148:Unc13c
|
UTSW |
9 |
73,600,648 (GRCm39) |
missense |
probably benign |
0.15 |
R6207:Unc13c
|
UTSW |
9 |
73,665,910 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6277:Unc13c
|
UTSW |
9 |
73,606,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6338:Unc13c
|
UTSW |
9 |
73,641,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R6615:Unc13c
|
UTSW |
9 |
73,837,890 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6978:Unc13c
|
UTSW |
9 |
73,839,259 (GRCm39) |
missense |
probably benign |
0.39 |
R7053:Unc13c
|
UTSW |
9 |
73,839,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7223:Unc13c
|
UTSW |
9 |
73,536,473 (GRCm39) |
missense |
probably benign |
0.44 |
R7259:Unc13c
|
UTSW |
9 |
73,424,645 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Unc13c
|
UTSW |
9 |
73,481,355 (GRCm39) |
missense |
probably benign |
0.00 |
R7357:Unc13c
|
UTSW |
9 |
73,840,811 (GRCm39) |
small insertion |
probably benign |
|
R7357:Unc13c
|
UTSW |
9 |
73,840,810 (GRCm39) |
small insertion |
probably benign |
|
R7607:Unc13c
|
UTSW |
9 |
73,576,817 (GRCm39) |
missense |
probably damaging |
0.98 |
R7626:Unc13c
|
UTSW |
9 |
73,641,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7639:Unc13c
|
UTSW |
9 |
73,840,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R7657:Unc13c
|
UTSW |
9 |
73,441,185 (GRCm39) |
splice site |
probably null |
|
R7665:Unc13c
|
UTSW |
9 |
73,587,756 (GRCm39) |
missense |
probably benign |
0.28 |
R7704:Unc13c
|
UTSW |
9 |
73,606,494 (GRCm39) |
missense |
probably benign |
0.27 |
R7776:Unc13c
|
UTSW |
9 |
73,602,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Unc13c
|
UTSW |
9 |
73,600,553 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7833:Unc13c
|
UTSW |
9 |
73,388,391 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7839:Unc13c
|
UTSW |
9 |
73,840,596 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7869:Unc13c
|
UTSW |
9 |
73,602,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R7924:Unc13c
|
UTSW |
9 |
73,641,690 (GRCm39) |
missense |
probably benign |
0.05 |
R8047:Unc13c
|
UTSW |
9 |
73,719,636 (GRCm39) |
nonsense |
probably null |
|
R8167:Unc13c
|
UTSW |
9 |
73,643,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R8202:Unc13c
|
UTSW |
9 |
73,643,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R8210:Unc13c
|
UTSW |
9 |
73,392,220 (GRCm39) |
missense |
probably benign |
0.13 |
R8352:Unc13c
|
UTSW |
9 |
73,838,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R8368:Unc13c
|
UTSW |
9 |
73,838,070 (GRCm39) |
missense |
probably benign |
0.15 |
R8452:Unc13c
|
UTSW |
9 |
73,838,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R8535:Unc13c
|
UTSW |
9 |
73,447,653 (GRCm39) |
missense |
probably benign |
|
R8677:Unc13c
|
UTSW |
9 |
73,840,243 (GRCm39) |
missense |
probably benign |
0.00 |
R8700:Unc13c
|
UTSW |
9 |
73,479,679 (GRCm39) |
missense |
probably benign |
0.44 |
R8848:Unc13c
|
UTSW |
9 |
73,433,263 (GRCm39) |
missense |
probably benign |
|
R8902:Unc13c
|
UTSW |
9 |
73,656,830 (GRCm39) |
missense |
probably damaging |
0.97 |
R8953:Unc13c
|
UTSW |
9 |
73,840,044 (GRCm39) |
missense |
probably benign |
0.00 |
R8961:Unc13c
|
UTSW |
9 |
73,839,524 (GRCm39) |
missense |
probably benign |
0.06 |
R9015:Unc13c
|
UTSW |
9 |
73,453,322 (GRCm39) |
missense |
probably benign |
|
R9114:Unc13c
|
UTSW |
9 |
73,719,665 (GRCm39) |
missense |
probably benign |
0.02 |
R9217:Unc13c
|
UTSW |
9 |
73,485,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R9252:Unc13c
|
UTSW |
9 |
73,424,553 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9273:Unc13c
|
UTSW |
9 |
73,839,862 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9317:Unc13c
|
UTSW |
9 |
73,447,662 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9412:Unc13c
|
UTSW |
9 |
73,839,772 (GRCm39) |
missense |
probably benign |
|
R9505:Unc13c
|
UTSW |
9 |
73,838,824 (GRCm39) |
missense |
probably benign |
0.22 |
R9516:Unc13c
|
UTSW |
9 |
73,392,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R9528:Unc13c
|
UTSW |
9 |
73,837,960 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9567:Unc13c
|
UTSW |
9 |
73,536,485 (GRCm39) |
missense |
probably damaging |
0.99 |
R9756:Unc13c
|
UTSW |
9 |
73,839,526 (GRCm39) |
missense |
probably benign |
0.23 |
R9783:Unc13c
|
UTSW |
9 |
73,392,227 (GRCm39) |
missense |
probably benign |
0.09 |
|