Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Angptl3 |
T |
A |
4: 98,926,171 (GRCm39) |
W434R |
probably damaging |
Het |
B4galt5 |
C |
T |
2: 167,146,982 (GRCm39) |
R284Q |
probably benign |
Het |
Ccdc80 |
T |
G |
16: 44,915,952 (GRCm39) |
V236G |
probably damaging |
Het |
Chd8 |
T |
C |
14: 52,457,191 (GRCm39) |
I926V |
possibly damaging |
Het |
Dgkz |
A |
C |
2: 91,764,542 (GRCm39) |
S1030R |
probably damaging |
Het |
Disp3 |
T |
A |
4: 148,355,906 (GRCm39) |
D318V |
probably damaging |
Het |
Dnaaf10 |
T |
C |
11: 17,162,136 (GRCm39) |
L58P |
possibly damaging |
Het |
Ehd1 |
T |
C |
19: 6,344,330 (GRCm39) |
S197P |
probably damaging |
Het |
Emp1 |
A |
G |
6: 135,356,945 (GRCm39) |
K42R |
probably benign |
Het |
Garin4 |
G |
A |
1: 190,896,067 (GRCm39) |
T192I |
probably damaging |
Het |
Gm4922 |
T |
A |
10: 18,659,423 (GRCm39) |
D433V |
probably benign |
Het |
Gsdma |
T |
C |
11: 98,561,577 (GRCm39) |
|
probably benign |
Het |
Hspbp1 |
G |
T |
7: 4,680,852 (GRCm39) |
A208E |
probably damaging |
Het |
Il5ra |
A |
T |
6: 106,693,712 (GRCm39) |
V342E |
possibly damaging |
Het |
Kif13b |
T |
C |
14: 65,040,880 (GRCm39) |
F1660S |
probably damaging |
Het |
Lvrn |
A |
G |
18: 47,010,016 (GRCm39) |
E388G |
probably damaging |
Het |
Mettl17 |
G |
A |
14: 52,125,504 (GRCm39) |
|
probably null |
Het |
Mgat5b |
T |
C |
11: 116,868,540 (GRCm39) |
Y488H |
probably benign |
Het |
Mtr |
A |
T |
13: 12,214,013 (GRCm39) |
D886E |
possibly damaging |
Het |
Naip6 |
A |
T |
13: 100,435,979 (GRCm39) |
L848* |
probably null |
Het |
Nav3 |
A |
G |
10: 109,702,835 (GRCm39) |
S233P |
probably benign |
Het |
Nme9 |
A |
T |
9: 99,352,908 (GRCm39) |
D286V |
probably benign |
Het |
Nod1 |
C |
A |
6: 54,920,930 (GRCm39) |
A463S |
probably benign |
Het |
Nthl1 |
A |
G |
17: 24,852,949 (GRCm39) |
K51R |
probably benign |
Het |
Or1n2 |
A |
G |
2: 36,797,566 (GRCm39) |
I203V |
probably damaging |
Het |
Or6k14 |
T |
A |
1: 173,927,696 (GRCm39) |
V224D |
possibly damaging |
Het |
Pcnx2 |
G |
A |
8: 126,582,012 (GRCm39) |
A908V |
probably benign |
Het |
Pdcd6 |
A |
G |
13: 74,452,098 (GRCm39) |
Y181H |
probably damaging |
Het |
Pde10a |
A |
C |
17: 9,180,722 (GRCm39) |
I719L |
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,270,014 (GRCm39) |
|
probably null |
Het |
Plekha5 |
G |
T |
6: 140,527,742 (GRCm39) |
A396S |
probably damaging |
Het |
Ppfia2 |
A |
G |
10: 106,664,789 (GRCm39) |
T342A |
probably damaging |
Het |
Rbck1 |
A |
G |
2: 152,164,087 (GRCm39) |
I339T |
possibly damaging |
Het |
Rbms2 |
A |
T |
10: 127,979,309 (GRCm39) |
I140N |
probably damaging |
Het |
Scn1b |
A |
T |
7: 30,822,546 (GRCm39) |
L78Q |
possibly damaging |
Het |
Slc12a6 |
T |
C |
2: 112,188,986 (GRCm39) |
|
probably null |
Het |
Slc25a30 |
A |
T |
14: 76,007,108 (GRCm39) |
|
probably benign |
Het |
Slc30a7 |
C |
T |
3: 115,783,796 (GRCm39) |
|
probably benign |
Het |
Slc5a10 |
C |
A |
11: 61,563,898 (GRCm39) |
R546L |
possibly damaging |
Het |
Stxbp4 |
T |
C |
11: 90,431,095 (GRCm39) |
D405G |
probably damaging |
Het |
Tm4sf19 |
A |
C |
16: 32,226,678 (GRCm39) |
T156P |
possibly damaging |
Het |
Tmem37 |
A |
T |
1: 119,995,719 (GRCm39) |
D119E |
probably damaging |
Het |
Tor1aip1 |
T |
A |
1: 155,889,117 (GRCm39) |
N113I |
probably damaging |
Het |
Ubac2 |
T |
A |
14: 122,144,802 (GRCm39) |
Y87N |
possibly damaging |
Het |
Usp29 |
A |
T |
7: 6,965,617 (GRCm39) |
|
probably null |
Het |
Zfp276 |
A |
G |
8: 123,991,736 (GRCm39) |
E428G |
probably damaging |
Het |
|
Other mutations in Atp7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00932:Atp7b
|
APN |
8 |
22,501,114 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00981:Atp7b
|
APN |
8 |
22,517,543 (GRCm39) |
splice site |
probably null |
|
IGL01600:Atp7b
|
APN |
8 |
22,517,541 (GRCm39) |
splice site |
probably null |
|
IGL01713:Atp7b
|
APN |
8 |
22,518,589 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01778:Atp7b
|
APN |
8 |
22,484,844 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01926:Atp7b
|
APN |
8 |
22,501,797 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02312:Atp7b
|
APN |
8 |
22,484,786 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02562:Atp7b
|
APN |
8 |
22,518,101 (GRCm39) |
missense |
probably benign |
|
IGL02603:Atp7b
|
APN |
8 |
22,484,792 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02622:Atp7b
|
APN |
8 |
22,518,454 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02721:Atp7b
|
APN |
8 |
22,512,493 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03145:Atp7b
|
APN |
8 |
22,508,159 (GRCm39) |
missense |
probably damaging |
1.00 |
daffodil
|
UTSW |
8 |
22,488,282 (GRCm39) |
missense |
probably damaging |
1.00 |
menace
|
UTSW |
8 |
22,512,381 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4131001:Atp7b
|
UTSW |
8 |
22,484,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Atp7b
|
UTSW |
8 |
22,501,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Atp7b
|
UTSW |
8 |
22,550,011 (GRCm39) |
missense |
probably benign |
0.00 |
R0128:Atp7b
|
UTSW |
8 |
22,518,188 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0130:Atp7b
|
UTSW |
8 |
22,518,188 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0325:Atp7b
|
UTSW |
8 |
22,518,467 (GRCm39) |
missense |
probably benign |
0.22 |
R0412:Atp7b
|
UTSW |
8 |
22,485,675 (GRCm39) |
splice site |
probably null |
|
R0856:Atp7b
|
UTSW |
8 |
22,487,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R0906:Atp7b
|
UTSW |
8 |
22,517,842 (GRCm39) |
missense |
probably benign |
|
R0989:Atp7b
|
UTSW |
8 |
22,518,710 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1377:Atp7b
|
UTSW |
8 |
22,501,801 (GRCm39) |
missense |
probably benign |
0.17 |
R1517:Atp7b
|
UTSW |
8 |
22,487,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1521:Atp7b
|
UTSW |
8 |
22,517,689 (GRCm39) |
missense |
probably damaging |
0.96 |
R1529:Atp7b
|
UTSW |
8 |
22,518,740 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1691:Atp7b
|
UTSW |
8 |
22,501,039 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1743:Atp7b
|
UTSW |
8 |
22,496,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R1815:Atp7b
|
UTSW |
8 |
22,501,667 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2008:Atp7b
|
UTSW |
8 |
22,517,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Atp7b
|
UTSW |
8 |
22,501,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R2155:Atp7b
|
UTSW |
8 |
22,503,600 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2182:Atp7b
|
UTSW |
8 |
22,504,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R2256:Atp7b
|
UTSW |
8 |
22,488,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Atp7b
|
UTSW |
8 |
22,488,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R2274:Atp7b
|
UTSW |
8 |
22,510,848 (GRCm39) |
missense |
probably benign |
0.20 |
R2475:Atp7b
|
UTSW |
8 |
22,484,792 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2906:Atp7b
|
UTSW |
8 |
22,501,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R2907:Atp7b
|
UTSW |
8 |
22,501,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R3421:Atp7b
|
UTSW |
8 |
22,518,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R3422:Atp7b
|
UTSW |
8 |
22,518,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R3688:Atp7b
|
UTSW |
8 |
22,494,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R3945:Atp7b
|
UTSW |
8 |
22,510,880 (GRCm39) |
missense |
probably benign |
0.02 |
R4235:Atp7b
|
UTSW |
8 |
22,501,039 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4700:Atp7b
|
UTSW |
8 |
22,490,137 (GRCm39) |
missense |
probably benign |
0.00 |
R4701:Atp7b
|
UTSW |
8 |
22,490,137 (GRCm39) |
missense |
probably benign |
0.00 |
R4877:Atp7b
|
UTSW |
8 |
22,518,617 (GRCm39) |
missense |
probably damaging |
0.98 |
R4962:Atp7b
|
UTSW |
8 |
22,510,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Atp7b
|
UTSW |
8 |
22,517,714 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5016:Atp7b
|
UTSW |
8 |
22,505,885 (GRCm39) |
splice site |
probably null |
|
R5038:Atp7b
|
UTSW |
8 |
22,518,472 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5438:Atp7b
|
UTSW |
8 |
22,504,570 (GRCm39) |
missense |
probably benign |
|
R5467:Atp7b
|
UTSW |
8 |
22,501,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Atp7b
|
UTSW |
8 |
22,549,986 (GRCm39) |
critical splice donor site |
probably null |
|
R5512:Atp7b
|
UTSW |
8 |
22,502,755 (GRCm39) |
missense |
probably benign |
0.20 |
R5563:Atp7b
|
UTSW |
8 |
22,518,730 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5751:Atp7b
|
UTSW |
8 |
22,508,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Atp7b
|
UTSW |
8 |
22,517,879 (GRCm39) |
missense |
probably benign |
|
R5941:Atp7b
|
UTSW |
8 |
22,487,512 (GRCm39) |
missense |
probably damaging |
0.98 |
R6227:Atp7b
|
UTSW |
8 |
22,510,841 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6265:Atp7b
|
UTSW |
8 |
22,505,943 (GRCm39) |
nonsense |
probably null |
|
R6290:Atp7b
|
UTSW |
8 |
22,510,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6368:Atp7b
|
UTSW |
8 |
22,510,771 (GRCm39) |
splice site |
probably null |
|
R6647:Atp7b
|
UTSW |
8 |
22,518,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Atp7b
|
UTSW |
8 |
22,494,391 (GRCm39) |
missense |
probably benign |
0.37 |
R6830:Atp7b
|
UTSW |
8 |
22,512,381 (GRCm39) |
missense |
probably damaging |
0.97 |
R6886:Atp7b
|
UTSW |
8 |
22,518,706 (GRCm39) |
missense |
probably benign |
0.01 |
R6928:Atp7b
|
UTSW |
8 |
22,484,828 (GRCm39) |
missense |
probably benign |
|
R6965:Atp7b
|
UTSW |
8 |
22,518,101 (GRCm39) |
missense |
probably benign |
|
R7203:Atp7b
|
UTSW |
8 |
22,487,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R7222:Atp7b
|
UTSW |
8 |
22,512,394 (GRCm39) |
nonsense |
probably null |
|
R7344:Atp7b
|
UTSW |
8 |
22,487,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7384:Atp7b
|
UTSW |
8 |
22,512,331 (GRCm39) |
missense |
probably benign |
0.01 |
R7449:Atp7b
|
UTSW |
8 |
22,501,865 (GRCm39) |
missense |
probably damaging |
0.98 |
R7451:Atp7b
|
UTSW |
8 |
22,504,700 (GRCm39) |
nonsense |
probably null |
|
R7607:Atp7b
|
UTSW |
8 |
22,501,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R8140:Atp7b
|
UTSW |
8 |
22,518,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R8160:Atp7b
|
UTSW |
8 |
22,487,575 (GRCm39) |
missense |
probably damaging |
0.98 |
R8349:Atp7b
|
UTSW |
8 |
22,503,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R8421:Atp7b
|
UTSW |
8 |
22,518,487 (GRCm39) |
missense |
probably benign |
0.01 |
R8449:Atp7b
|
UTSW |
8 |
22,503,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R8749:Atp7b
|
UTSW |
8 |
22,518,334 (GRCm39) |
missense |
probably damaging |
0.96 |
R8989:Atp7b
|
UTSW |
8 |
22,510,911 (GRCm39) |
missense |
probably benign |
0.06 |
R9210:Atp7b
|
UTSW |
8 |
22,487,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R9353:Atp7b
|
UTSW |
8 |
22,517,890 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9462:Atp7b
|
UTSW |
8 |
22,490,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R9485:Atp7b
|
UTSW |
8 |
22,502,778 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Atp7b
|
UTSW |
8 |
22,518,730 (GRCm39) |
missense |
probably benign |
0.07 |
Z1177:Atp7b
|
UTSW |
8 |
22,484,893 (GRCm39) |
missense |
probably benign |
|
|