Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acnat2 |
A |
G |
4: 49,380,269 (GRCm39) |
S370P |
probably damaging |
Het |
Adamts5 |
T |
C |
16: 85,696,363 (GRCm39) |
R265G |
probably benign |
Het |
Cd2ap |
T |
C |
17: 43,156,280 (GRCm39) |
S86G |
possibly damaging |
Het |
Cers3 |
A |
C |
7: 66,435,751 (GRCm39) |
|
probably benign |
Het |
Dnaaf2 |
G |
T |
12: 69,243,376 (GRCm39) |
P562T |
probably damaging |
Het |
Dnajc21 |
A |
C |
15: 10,447,188 (GRCm39) |
V520G |
probably benign |
Het |
Dync1h1 |
A |
G |
12: 110,592,041 (GRCm39) |
|
probably benign |
Het |
Extl3 |
T |
C |
14: 65,304,211 (GRCm39) |
N733D |
probably benign |
Het |
Gm5499 |
T |
A |
17: 87,385,928 (GRCm39) |
|
noncoding transcript |
Het |
Gstm6 |
T |
C |
3: 107,848,379 (GRCm39) |
Q180R |
probably benign |
Het |
Hdlbp |
G |
A |
1: 93,351,524 (GRCm39) |
R460W |
probably damaging |
Het |
Ift81 |
T |
C |
5: 122,749,031 (GRCm39) |
D40G |
probably damaging |
Het |
Igsf3 |
T |
A |
3: 101,334,338 (GRCm39) |
|
probably benign |
Het |
Kcnb2 |
A |
G |
1: 15,383,147 (GRCm39) |
T158A |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,334,567 (GRCm39) |
C4397R |
probably damaging |
Het |
Morc1 |
T |
C |
16: 48,402,825 (GRCm39) |
S583P |
probably benign |
Het |
Mucl3 |
A |
T |
17: 35,947,758 (GRCm39) |
N490K |
probably damaging |
Het |
Nipsnap2 |
T |
A |
5: 129,834,205 (GRCm39) |
*282R |
probably null |
Het |
Or2ag19 |
T |
C |
7: 106,443,956 (GRCm39) |
L46P |
probably damaging |
Het |
Or9m1b |
A |
T |
2: 87,836,589 (GRCm39) |
C178S |
probably damaging |
Het |
Parp14 |
T |
A |
16: 35,676,929 (GRCm39) |
Q1013L |
probably benign |
Het |
Pdzd8 |
A |
C |
19: 59,289,961 (GRCm39) |
S480A |
probably benign |
Het |
Piezo1 |
A |
T |
8: 123,214,339 (GRCm39) |
S1609R |
probably damaging |
Het |
Pkp4 |
G |
A |
2: 59,180,971 (GRCm39) |
|
probably null |
Het |
Plpp2 |
A |
T |
10: 79,363,327 (GRCm39) |
V106D |
probably damaging |
Het |
Rimbp2 |
T |
C |
5: 128,863,816 (GRCm39) |
Y724C |
probably benign |
Het |
Rpgrip1l |
A |
T |
8: 91,987,501 (GRCm39) |
L852* |
probably null |
Het |
Samd9l |
T |
A |
6: 3,376,259 (GRCm39) |
D334V |
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,218,257 (GRCm39) |
T360M |
probably damaging |
Het |
Slc30a2 |
A |
T |
4: 134,070,611 (GRCm39) |
D5V |
probably damaging |
Het |
Spata31 |
T |
C |
13: 65,069,568 (GRCm39) |
I572T |
probably benign |
Het |
Tma16 |
G |
A |
8: 66,929,512 (GRCm39) |
L161F |
probably benign |
Het |
Trappc2b |
A |
T |
11: 51,576,670 (GRCm39) |
V76D |
probably damaging |
Het |
Trim69 |
A |
T |
2: 122,003,765 (GRCm39) |
E238V |
possibly damaging |
Het |
Zfhx4 |
A |
G |
3: 5,307,388 (GRCm39) |
T205A |
probably benign |
Het |
|
Other mutations in Lrrc59 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01525:Lrrc59
|
APN |
11 |
94,525,522 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01929:Lrrc59
|
APN |
11 |
94,534,342 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01958:Lrrc59
|
APN |
11 |
94,529,354 (GRCm39) |
splice site |
probably null |
|
IGL02635:Lrrc59
|
APN |
11 |
94,534,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R0277:Lrrc59
|
UTSW |
11 |
94,534,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R0323:Lrrc59
|
UTSW |
11 |
94,534,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1794:Lrrc59
|
UTSW |
11 |
94,529,421 (GRCm39) |
missense |
probably benign |
|
R4833:Lrrc59
|
UTSW |
11 |
94,525,498 (GRCm39) |
missense |
probably benign |
0.00 |
R6242:Lrrc59
|
UTSW |
11 |
94,525,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6817:Lrrc59
|
UTSW |
11 |
94,520,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Lrrc59
|
UTSW |
11 |
94,525,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7724:Lrrc59
|
UTSW |
11 |
94,534,170 (GRCm39) |
missense |
probably damaging |
0.99 |
R8066:Lrrc59
|
UTSW |
11 |
94,525,426 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9143:Lrrc59
|
UTSW |
11 |
94,525,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R9166:Lrrc59
|
UTSW |
11 |
94,522,959 (GRCm39) |
missense |
probably benign |
0.00 |
R9266:Lrrc59
|
UTSW |
11 |
94,532,044 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Lrrc59
|
UTSW |
11 |
94,534,147 (GRCm39) |
missense |
probably benign |
0.19 |
|