Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
G |
A |
1: 156,457,429 (GRCm39) |
V225M |
probably damaging |
Het |
Afmid |
T |
A |
11: 117,726,416 (GRCm39) |
|
probably benign |
Het |
Ccdc191 |
G |
A |
16: 43,735,901 (GRCm39) |
V216I |
probably benign |
Het |
Cep112 |
C |
A |
11: 108,461,258 (GRCm39) |
|
probably benign |
Het |
Dcbld1 |
T |
C |
10: 52,137,910 (GRCm39) |
V58A |
possibly damaging |
Het |
Dop1b |
A |
T |
16: 93,598,481 (GRCm39) |
H1882L |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,479,635 (GRCm39) |
I2894V |
probably benign |
Het |
Focad |
T |
C |
4: 88,196,498 (GRCm39) |
|
probably null |
Het |
Gm45713 |
G |
A |
7: 44,781,788 (GRCm39) |
T203M |
possibly damaging |
Het |
Gstm1 |
T |
C |
3: 107,924,696 (GRCm39) |
Y28C |
probably damaging |
Het |
Gucy1a1 |
T |
C |
3: 82,018,498 (GRCm39) |
D113G |
probably benign |
Het |
Hat1 |
G |
T |
2: 71,250,961 (GRCm39) |
E170* |
probably null |
Het |
Herc1 |
C |
A |
9: 66,340,710 (GRCm39) |
F1686L |
possibly damaging |
Het |
Iffo1 |
A |
G |
6: 125,130,124 (GRCm39) |
E270G |
probably null |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Lrp3 |
A |
T |
7: 34,902,718 (GRCm39) |
Y522N |
probably damaging |
Het |
Lrp6 |
A |
T |
6: 134,484,488 (GRCm39) |
D378E |
probably damaging |
Het |
Mmrn1 |
A |
G |
6: 60,950,103 (GRCm39) |
N351S |
probably benign |
Het |
Or1e16 |
A |
T |
11: 73,285,945 (GRCm39) |
L301Q |
probably damaging |
Het |
Or9q1 |
T |
C |
19: 13,805,220 (GRCm39) |
D180G |
probably damaging |
Het |
Pcnx3 |
T |
C |
19: 5,721,553 (GRCm39) |
K1082E |
possibly damaging |
Het |
Pikfyve |
T |
C |
1: 65,241,989 (GRCm39) |
V243A |
possibly damaging |
Het |
Qdpr |
G |
C |
5: 45,596,728 (GRCm39) |
I145M |
probably benign |
Het |
Rasgrp3 |
G |
T |
17: 75,816,822 (GRCm39) |
|
probably null |
Het |
Rd3l |
G |
T |
12: 111,946,574 (GRCm39) |
Y1* |
probably null |
Het |
Sf3b3 |
A |
G |
8: 111,538,142 (GRCm39) |
|
probably benign |
Het |
Smn1 |
C |
T |
13: 100,264,404 (GRCm39) |
T45I |
probably damaging |
Het |
Sprr3 |
A |
T |
3: 92,364,316 (GRCm39) |
I176N |
probably benign |
Het |
Sv2c |
T |
C |
13: 96,224,763 (GRCm39) |
D182G |
probably damaging |
Het |
Tnni3k |
A |
T |
3: 154,647,316 (GRCm39) |
V397D |
probably damaging |
Het |
Trpt1 |
G |
T |
19: 6,976,308 (GRCm39) |
G235V |
possibly damaging |
Het |
Ttll10 |
A |
T |
4: 156,120,621 (GRCm39) |
C367* |
probably null |
Het |
|
Other mutations in Unc5c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00232:Unc5c
|
APN |
3 |
141,494,701 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01089:Unc5c
|
APN |
3 |
141,523,963 (GRCm39) |
splice site |
probably benign |
|
IGL01478:Unc5c
|
APN |
3 |
141,534,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02083:Unc5c
|
APN |
3 |
141,420,408 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02269:Unc5c
|
APN |
3 |
141,494,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02565:Unc5c
|
APN |
3 |
141,509,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02973:Unc5c
|
APN |
3 |
141,494,651 (GRCm39) |
missense |
probably benign |
0.12 |
R0179:Unc5c
|
UTSW |
3 |
141,523,828 (GRCm39) |
nonsense |
probably null |
|
R0309:Unc5c
|
UTSW |
3 |
141,439,694 (GRCm39) |
missense |
probably benign |
0.01 |
R0371:Unc5c
|
UTSW |
3 |
141,533,283 (GRCm39) |
missense |
probably benign |
0.01 |
R0603:Unc5c
|
UTSW |
3 |
141,476,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0904:Unc5c
|
UTSW |
3 |
141,509,601 (GRCm39) |
missense |
probably benign |
0.08 |
R1300:Unc5c
|
UTSW |
3 |
141,534,304 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1491:Unc5c
|
UTSW |
3 |
141,495,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Unc5c
|
UTSW |
3 |
141,533,310 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1674:Unc5c
|
UTSW |
3 |
141,463,598 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1676:Unc5c
|
UTSW |
3 |
141,463,598 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1726:Unc5c
|
UTSW |
3 |
141,523,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Unc5c
|
UTSW |
3 |
141,533,278 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1815:Unc5c
|
UTSW |
3 |
141,463,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R2381:Unc5c
|
UTSW |
3 |
141,383,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R2394:Unc5c
|
UTSW |
3 |
141,383,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R2945:Unc5c
|
UTSW |
3 |
141,495,735 (GRCm39) |
missense |
probably damaging |
0.97 |
R4284:Unc5c
|
UTSW |
3 |
141,420,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R4285:Unc5c
|
UTSW |
3 |
141,420,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R4287:Unc5c
|
UTSW |
3 |
141,420,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R4681:Unc5c
|
UTSW |
3 |
141,474,374 (GRCm39) |
critical splice donor site |
probably null |
|
R4736:Unc5c
|
UTSW |
3 |
141,522,692 (GRCm39) |
missense |
probably benign |
0.00 |
R4740:Unc5c
|
UTSW |
3 |
141,522,692 (GRCm39) |
missense |
probably benign |
0.00 |
R4774:Unc5c
|
UTSW |
3 |
141,534,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R4862:Unc5c
|
UTSW |
3 |
141,495,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R4905:Unc5c
|
UTSW |
3 |
141,507,071 (GRCm39) |
missense |
probably benign |
0.19 |
R4921:Unc5c
|
UTSW |
3 |
141,494,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5150:Unc5c
|
UTSW |
3 |
141,463,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R5559:Unc5c
|
UTSW |
3 |
141,509,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5562:Unc5c
|
UTSW |
3 |
141,474,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Unc5c
|
UTSW |
3 |
141,383,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Unc5c
|
UTSW |
3 |
141,383,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Unc5c
|
UTSW |
3 |
141,534,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Unc5c
|
UTSW |
3 |
141,494,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R6154:Unc5c
|
UTSW |
3 |
141,383,914 (GRCm39) |
missense |
probably damaging |
0.97 |
R6547:Unc5c
|
UTSW |
3 |
141,495,780 (GRCm39) |
missense |
probably benign |
0.16 |
R6558:Unc5c
|
UTSW |
3 |
141,495,490 (GRCm39) |
missense |
probably damaging |
0.98 |
R7104:Unc5c
|
UTSW |
3 |
141,439,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R7113:Unc5c
|
UTSW |
3 |
141,507,054 (GRCm39) |
missense |
probably benign |
0.00 |
R7282:Unc5c
|
UTSW |
3 |
141,383,751 (GRCm39) |
missense |
probably damaging |
0.98 |
R7317:Unc5c
|
UTSW |
3 |
141,495,703 (GRCm39) |
missense |
probably benign |
0.00 |
R7787:Unc5c
|
UTSW |
3 |
141,474,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R7873:Unc5c
|
UTSW |
3 |
141,533,310 (GRCm39) |
missense |
probably benign |
0.04 |
R7896:Unc5c
|
UTSW |
3 |
141,476,922 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7936:Unc5c
|
UTSW |
3 |
141,534,238 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8041:Unc5c
|
UTSW |
3 |
141,171,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8277:Unc5c
|
UTSW |
3 |
141,474,373 (GRCm39) |
critical splice donor site |
probably null |
|
R8669:Unc5c
|
UTSW |
3 |
141,509,704 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8886:Unc5c
|
UTSW |
3 |
141,509,581 (GRCm39) |
missense |
probably benign |
0.02 |
R8989:Unc5c
|
UTSW |
3 |
141,509,467 (GRCm39) |
splice site |
probably benign |
|
R9244:Unc5c
|
UTSW |
3 |
141,533,370 (GRCm39) |
missense |
probably benign |
0.00 |
R9444:Unc5c
|
UTSW |
3 |
141,507,209 (GRCm39) |
critical splice donor site |
probably null |
|
R9508:Unc5c
|
UTSW |
3 |
141,494,736 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9524:Unc5c
|
UTSW |
3 |
141,494,683 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9633:Unc5c
|
UTSW |
3 |
141,495,654 (GRCm39) |
missense |
probably damaging |
0.99 |
X0018:Unc5c
|
UTSW |
3 |
141,420,500 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Unc5c
|
UTSW |
3 |
141,533,422 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Unc5c
|
UTSW |
3 |
141,439,661 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Unc5c
|
UTSW |
3 |
141,383,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|