Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp2a3 |
C |
A |
11: 72,866,165 (GRCm39) |
H262N |
probably benign |
Het |
C2cd6 |
T |
C |
1: 59,133,997 (GRCm39) |
N8S |
probably benign |
Het |
Cdh8 |
G |
A |
8: 99,757,387 (GRCm39) |
T737M |
probably damaging |
Het |
Celsr3 |
T |
C |
9: 108,711,920 (GRCm39) |
|
probably benign |
Het |
Cenph |
T |
A |
13: 100,909,269 (GRCm39) |
Q46L |
probably benign |
Het |
Dlg5 |
A |
G |
14: 24,200,277 (GRCm39) |
C1395R |
probably damaging |
Het |
Dnah8 |
C |
T |
17: 31,037,025 (GRCm39) |
|
probably benign |
Het |
Dolk |
T |
C |
2: 30,175,740 (GRCm39) |
N102D |
probably benign |
Het |
Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
Farp2 |
G |
A |
1: 93,505,372 (GRCm39) |
R368Q |
probably damaging |
Het |
Fermt3 |
A |
T |
19: 6,996,183 (GRCm39) |
M4K |
probably benign |
Het |
Galc |
G |
A |
12: 98,173,672 (GRCm39) |
T630I |
probably damaging |
Het |
Gm21970 |
T |
G |
16: 91,211,545 (GRCm39) |
S128A |
possibly damaging |
Het |
Gpr146 |
T |
C |
5: 139,378,533 (GRCm39) |
S112P |
probably damaging |
Het |
Grip2 |
A |
G |
6: 91,764,276 (GRCm39) |
S51P |
probably damaging |
Het |
Htra2 |
G |
T |
6: 83,031,280 (GRCm39) |
T43N |
possibly damaging |
Het |
Lnpep |
T |
C |
17: 17,799,445 (GRCm39) |
Y70C |
possibly damaging |
Het |
Med17 |
G |
A |
9: 15,188,963 (GRCm39) |
R101* |
probably null |
Het |
Mtdh |
A |
T |
15: 34,099,723 (GRCm39) |
N158Y |
probably damaging |
Het |
Neo1 |
A |
T |
9: 58,833,094 (GRCm39) |
H550Q |
possibly damaging |
Het |
Or2h1b |
C |
T |
17: 37,461,979 (GRCm39) |
V295I |
probably benign |
Het |
Or5p57 |
A |
C |
7: 107,665,710 (GRCm39) |
F68L |
probably benign |
Het |
Pex1 |
C |
T |
5: 3,655,952 (GRCm39) |
Q260* |
probably null |
Het |
Pex6 |
T |
C |
17: 47,034,425 (GRCm39) |
V758A |
probably damaging |
Het |
Qsox1 |
T |
C |
1: 155,688,346 (GRCm39) |
E67G |
probably damaging |
Het |
Rimbp2 |
C |
T |
5: 128,848,861 (GRCm39) |
S895N |
probably benign |
Het |
Rnls |
A |
G |
19: 33,180,012 (GRCm39) |
V28A |
possibly damaging |
Het |
Spidr |
T |
C |
16: 15,707,494 (GRCm39) |
*934W |
probably null |
Het |
Spta1 |
A |
T |
1: 174,046,380 (GRCm39) |
M1654L |
probably damaging |
Het |
Srbd1 |
C |
A |
17: 86,295,801 (GRCm39) |
V870F |
probably benign |
Het |
Suco |
A |
T |
1: 161,662,136 (GRCm39) |
M765K |
probably benign |
Het |
Taok1 |
A |
G |
11: 77,440,178 (GRCm39) |
Y610H |
probably benign |
Het |
Thbs1 |
A |
G |
2: 117,945,141 (GRCm39) |
N238S |
probably benign |
Het |
Them7 |
T |
A |
2: 105,209,220 (GRCm39) |
L180* |
probably null |
Het |
Trim45 |
A |
G |
3: 100,832,621 (GRCm39) |
I285V |
probably benign |
Het |
Trim66 |
T |
C |
7: 109,059,481 (GRCm39) |
K921R |
probably benign |
Het |
Ttn |
A |
G |
2: 76,601,887 (GRCm39) |
S10265P |
probably damaging |
Het |
Vgll3 |
A |
T |
16: 65,612,556 (GRCm39) |
Y13F |
probably damaging |
Het |
Ylpm1 |
T |
A |
12: 85,061,731 (GRCm39) |
M544K |
unknown |
Het |
Ypel1 |
T |
C |
16: 16,906,702 (GRCm39) |
T500A |
probably benign |
Het |
Zmym1 |
T |
A |
4: 126,942,256 (GRCm39) |
S711C |
probably damaging |
Het |
|
Other mutations in Fndc8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0066:Fndc8
|
UTSW |
11 |
82,788,398 (GRCm39) |
missense |
probably benign |
0.38 |
R0066:Fndc8
|
UTSW |
11 |
82,788,398 (GRCm39) |
missense |
probably benign |
0.38 |
R1827:Fndc8
|
UTSW |
11 |
82,790,355 (GRCm39) |
missense |
probably damaging |
0.97 |
R2179:Fndc8
|
UTSW |
11 |
82,789,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R4504:Fndc8
|
UTSW |
11 |
82,783,226 (GRCm39) |
missense |
probably benign |
0.21 |
R5401:Fndc8
|
UTSW |
11 |
82,788,676 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5889:Fndc8
|
UTSW |
11 |
82,789,555 (GRCm39) |
missense |
probably damaging |
0.99 |
R5960:Fndc8
|
UTSW |
11 |
82,788,398 (GRCm39) |
missense |
probably benign |
0.15 |
R6793:Fndc8
|
UTSW |
11 |
82,788,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Fndc8
|
UTSW |
11 |
82,783,217 (GRCm39) |
missense |
probably benign |
|
R7210:Fndc8
|
UTSW |
11 |
82,788,692 (GRCm39) |
missense |
probably damaging |
0.99 |
R7224:Fndc8
|
UTSW |
11 |
82,783,151 (GRCm39) |
missense |
probably benign |
0.05 |
R7341:Fndc8
|
UTSW |
11 |
82,789,603 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7576:Fndc8
|
UTSW |
11 |
82,788,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R8190:Fndc8
|
UTSW |
11 |
82,788,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Fndc8
|
UTSW |
11 |
82,789,522 (GRCm39) |
missense |
probably benign |
0.03 |
R9399:Fndc8
|
UTSW |
11 |
82,788,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|