Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp10b |
T |
C |
11: 43,044,110 (GRCm39) |
V112A |
probably benign |
Het |
Caprin2 |
G |
T |
6: 148,796,505 (GRCm39) |
A36E |
probably damaging |
Het |
Castor1 |
A |
T |
11: 4,170,278 (GRCm39) |
T119S |
probably damaging |
Het |
Dnase1l2 |
T |
C |
17: 24,661,226 (GRCm39) |
M28V |
possibly damaging |
Het |
Eci1 |
T |
A |
17: 24,655,300 (GRCm39) |
|
probably null |
Het |
Edil3 |
T |
A |
13: 89,279,855 (GRCm39) |
S178T |
probably damaging |
Het |
Epha5 |
A |
G |
5: 84,479,085 (GRCm39) |
|
probably null |
Het |
Exoc3l4 |
A |
G |
12: 111,388,547 (GRCm39) |
E12G |
probably damaging |
Het |
Frmd7 |
G |
A |
X: 49,984,835 (GRCm39) |
T445I |
probably benign |
Het |
Golga4 |
A |
G |
9: 118,365,953 (GRCm39) |
E344G |
probably damaging |
Het |
H2-M10.4 |
A |
G |
17: 36,772,812 (GRCm39) |
Y57H |
probably damaging |
Het |
Hnmt |
T |
C |
2: 23,909,171 (GRCm39) |
I81V |
probably benign |
Het |
Hsd17b7 |
C |
T |
1: 169,780,649 (GRCm39) |
E320K |
probably damaging |
Het |
Htra3 |
C |
T |
5: 35,823,477 (GRCm39) |
V280I |
probably damaging |
Het |
Impg2 |
G |
T |
16: 56,087,485 (GRCm39) |
E992D |
probably damaging |
Het |
Kctd4 |
T |
C |
14: 76,200,418 (GRCm39) |
W130R |
possibly damaging |
Het |
Kdm3b |
T |
A |
18: 34,942,544 (GRCm39) |
|
probably null |
Het |
Kmt2d |
G |
A |
15: 98,759,652 (GRCm39) |
T1202M |
unknown |
Het |
Lrp11 |
A |
T |
10: 7,478,689 (GRCm39) |
D326V |
probably damaging |
Het |
Lrrcc1 |
A |
T |
3: 14,601,144 (GRCm39) |
I59F |
probably damaging |
Het |
Lyg2 |
G |
A |
1: 37,954,845 (GRCm39) |
|
probably benign |
Het |
Med16 |
A |
G |
10: 79,732,667 (GRCm39) |
V699A |
probably damaging |
Het |
Myo18b |
G |
T |
5: 113,022,804 (GRCm39) |
|
probably benign |
Het |
Nrxn2 |
A |
G |
19: 6,531,767 (GRCm39) |
T744A |
probably damaging |
Het |
Or1e1f |
T |
A |
11: 73,855,812 (GRCm39) |
I126N |
probably damaging |
Het |
Oser1 |
A |
T |
2: 163,253,309 (GRCm39) |
|
probably benign |
Het |
Pcdhgc5 |
T |
C |
18: 37,952,966 (GRCm39) |
V80A |
probably benign |
Het |
Pi4ka |
C |
T |
16: 17,100,539 (GRCm39) |
G1857D |
possibly damaging |
Het |
Pitpnc1 |
C |
T |
11: 107,228,237 (GRCm39) |
|
probably null |
Het |
Pofut2 |
A |
G |
10: 77,102,844 (GRCm39) |
E137G |
probably benign |
Het |
Rgsl1 |
A |
T |
1: 153,701,687 (GRCm39) |
W291R |
probably damaging |
Het |
Rnf113a2 |
T |
C |
12: 84,465,050 (GRCm39) |
I314T |
probably benign |
Het |
Rps2 |
C |
T |
17: 24,939,263 (GRCm39) |
|
probably benign |
Het |
Setbp1 |
T |
C |
18: 78,900,224 (GRCm39) |
K1148E |
probably damaging |
Het |
Slc45a2 |
A |
G |
15: 11,012,741 (GRCm39) |
D248G |
probably benign |
Het |
Slit2 |
G |
T |
5: 48,368,681 (GRCm39) |
R352L |
probably damaging |
Het |
Smg1 |
A |
G |
7: 117,756,404 (GRCm39) |
|
probably benign |
Het |
Sycp2 |
A |
T |
2: 177,994,272 (GRCm39) |
C1217* |
probably null |
Het |
Tbcb |
A |
G |
7: 29,926,261 (GRCm39) |
|
probably benign |
Het |
Tinf2 |
T |
C |
14: 55,918,346 (GRCm39) |
D128G |
probably damaging |
Het |
Traf3ip2 |
A |
G |
10: 39,515,218 (GRCm39) |
D332G |
possibly damaging |
Het |
Tram1 |
A |
G |
1: 13,659,829 (GRCm39) |
F40L |
probably benign |
Het |
Trank1 |
A |
T |
9: 111,196,475 (GRCm39) |
I1500L |
probably damaging |
Het |
Wdfy4 |
G |
A |
14: 32,884,827 (GRCm39) |
P25L |
probably benign |
Het |
Wnt5a |
G |
T |
14: 28,244,882 (GRCm39) |
Q376H |
probably damaging |
Het |
Zfp526 |
A |
C |
7: 24,924,049 (GRCm39) |
T103P |
probably benign |
Het |
|
Other mutations in Ap5m1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Ap5m1
|
APN |
14 |
49,311,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01806:Ap5m1
|
APN |
14 |
49,317,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02011:Ap5m1
|
APN |
14 |
49,318,592 (GRCm39) |
unclassified |
probably benign |
|
IGL02165:Ap5m1
|
APN |
14 |
49,316,185 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02203:Ap5m1
|
APN |
14 |
49,317,715 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02950:Ap5m1
|
APN |
14 |
49,311,392 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03368:Ap5m1
|
APN |
14 |
49,318,593 (GRCm39) |
unclassified |
probably benign |
|
R1688:Ap5m1
|
UTSW |
14 |
49,318,291 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2113:Ap5m1
|
UTSW |
14 |
49,323,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R2184:Ap5m1
|
UTSW |
14 |
49,323,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R2220:Ap5m1
|
UTSW |
14 |
49,318,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2971:Ap5m1
|
UTSW |
14 |
49,321,339 (GRCm39) |
nonsense |
probably null |
|
R3425:Ap5m1
|
UTSW |
14 |
49,311,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R4506:Ap5m1
|
UTSW |
14 |
49,311,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4679:Ap5m1
|
UTSW |
14 |
49,316,285 (GRCm39) |
missense |
probably benign |
0.00 |
R4799:Ap5m1
|
UTSW |
14 |
49,318,527 (GRCm39) |
missense |
probably benign |
0.08 |
R6365:Ap5m1
|
UTSW |
14 |
49,316,285 (GRCm39) |
missense |
probably benign |
0.00 |
R6834:Ap5m1
|
UTSW |
14 |
49,311,194 (GRCm39) |
missense |
probably damaging |
0.99 |
R7115:Ap5m1
|
UTSW |
14 |
49,323,727 (GRCm39) |
nonsense |
probably null |
|
R7224:Ap5m1
|
UTSW |
14 |
49,318,384 (GRCm39) |
missense |
unknown |
|
R7383:Ap5m1
|
UTSW |
14 |
49,311,653 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7539:Ap5m1
|
UTSW |
14 |
49,311,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7866:Ap5m1
|
UTSW |
14 |
49,311,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R7897:Ap5m1
|
UTSW |
14 |
49,311,232 (GRCm39) |
missense |
probably benign |
0.11 |
R8853:Ap5m1
|
UTSW |
14 |
49,311,337 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9236:Ap5m1
|
UTSW |
14 |
49,311,064 (GRCm39) |
missense |
probably benign |
0.00 |
R9545:Ap5m1
|
UTSW |
14 |
49,311,271 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9750:Ap5m1
|
UTSW |
14 |
49,317,756 (GRCm39) |
missense |
probably benign |
0.00 |
|