Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
G |
T |
10: 28,849,934 (GRCm39) |
D167E |
probably damaging |
Het |
Aadat |
A |
T |
8: 60,979,648 (GRCm39) |
E170V |
probably benign |
Het |
Acsf2 |
T |
C |
11: 94,461,276 (GRCm39) |
E300G |
probably benign |
Het |
Agbl3 |
C |
T |
6: 34,823,911 (GRCm39) |
Q859* |
probably null |
Het |
Arhgap11a |
T |
C |
2: 113,665,118 (GRCm39) |
|
probably benign |
Het |
Arhgef40 |
C |
A |
14: 52,231,803 (GRCm39) |
Q730K |
probably damaging |
Het |
Armc3 |
C |
T |
2: 19,206,616 (GRCm39) |
P13L |
possibly damaging |
Het |
B3gnt2 |
T |
A |
11: 22,786,490 (GRCm39) |
T233S |
probably benign |
Het |
Bnc1 |
G |
A |
7: 81,623,455 (GRCm39) |
Q591* |
probably null |
Het |
Bsn |
A |
T |
9: 107,993,185 (GRCm39) |
F856I |
probably damaging |
Het |
CK137956 |
T |
A |
4: 127,829,643 (GRCm39) |
T558S |
probably benign |
Het |
Coq8b |
G |
A |
7: 26,939,509 (GRCm39) |
V180I |
probably damaging |
Het |
Csmd1 |
A |
T |
8: 17,584,944 (GRCm39) |
L16Q |
possibly damaging |
Het |
Dhx37 |
A |
G |
5: 125,496,152 (GRCm39) |
S769P |
possibly damaging |
Het |
Diras1 |
T |
A |
10: 80,858,249 (GRCm39) |
M1L |
probably damaging |
Het |
Fam161b |
A |
G |
12: 84,404,438 (GRCm39) |
W81R |
probably benign |
Het |
Fat4 |
A |
T |
3: 39,011,418 (GRCm39) |
I2173L |
probably benign |
Het |
Fbn2 |
T |
C |
18: 58,237,153 (GRCm39) |
T617A |
possibly damaging |
Het |
Gabrq |
G |
A |
X: 71,880,439 (GRCm39) |
D311N |
probably benign |
Het |
Isl2 |
G |
T |
9: 55,452,746 (GRCm39) |
G335C |
probably damaging |
Het |
Kbtbd7 |
T |
C |
14: 79,666,052 (GRCm39) |
V628A |
probably damaging |
Het |
Kmt2d |
T |
C |
15: 98,735,029 (GRCm39) |
M5378V |
unknown |
Het |
Lrrc23 |
G |
T |
6: 124,755,782 (GRCm39) |
D75E |
probably benign |
Het |
Mab21l3 |
G |
A |
3: 101,742,446 (GRCm39) |
T38M |
probably benign |
Het |
Matn1 |
T |
C |
4: 130,677,322 (GRCm39) |
I177T |
possibly damaging |
Het |
Mtor |
T |
C |
4: 148,537,494 (GRCm39) |
S60P |
probably benign |
Het |
Naip6 |
T |
C |
13: 100,440,946 (GRCm39) |
E278G |
probably benign |
Het |
Nsun6 |
T |
C |
2: 15,053,789 (GRCm39) |
I7V |
possibly damaging |
Het |
Pabpc6 |
A |
T |
17: 9,887,076 (GRCm39) |
S492T |
probably benign |
Het |
Pakap |
C |
T |
4: 57,757,627 (GRCm39) |
Q188* |
probably null |
Het |
Pom121 |
A |
T |
5: 135,420,560 (GRCm39) |
V287D |
unknown |
Het |
Ptprq |
A |
T |
10: 107,522,079 (GRCm39) |
F624Y |
probably damaging |
Het |
Ptprr |
A |
G |
10: 116,024,222 (GRCm39) |
T178A |
probably benign |
Het |
Pygm |
A |
G |
19: 6,441,424 (GRCm39) |
N473S |
probably benign |
Het |
Ros1 |
A |
T |
10: 51,996,905 (GRCm39) |
Y1256N |
probably damaging |
Het |
Scpep1 |
T |
C |
11: 88,832,154 (GRCm39) |
N192S |
possibly damaging |
Het |
Serpina1f |
A |
G |
12: 103,660,265 (GRCm39) |
S6P |
possibly damaging |
Het |
Sgca |
T |
A |
11: 94,863,113 (GRCm39) |
Q80L |
probably damaging |
Het |
Skint6 |
A |
G |
4: 112,661,879 (GRCm39) |
L1235P |
possibly damaging |
Het |
Slc23a2 |
A |
C |
2: 131,898,736 (GRCm39) |
N600K |
probably benign |
Het |
Spata20 |
T |
C |
11: 94,374,221 (GRCm39) |
T350A |
probably benign |
Het |
Syne1 |
G |
T |
10: 5,294,921 (GRCm39) |
Y1227* |
probably null |
Het |
Usp40 |
G |
A |
1: 87,913,845 (GRCm39) |
T416I |
probably benign |
Het |
Vmn1r200 |
T |
C |
13: 22,579,571 (GRCm39) |
W116R |
probably benign |
Het |
Vps4a |
T |
C |
8: 107,765,851 (GRCm39) |
|
probably benign |
Het |
Zfyve16 |
A |
G |
13: 92,629,030 (GRCm39) |
V1469A |
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 |
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 |
|
IGL03117:Unc13c
|
APN |
9 |
73,441,307 (GRCm39) |
missense |
probably benign |
0.03 |
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 |
|