Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bhmt1b |
A |
G |
18: 87,774,954 (GRCm39) |
E159G |
probably damaging |
Het |
Cc2d2a |
T |
C |
5: 43,860,691 (GRCm39) |
|
probably null |
Het |
Ccdc88a |
A |
G |
11: 29,427,433 (GRCm39) |
D1046G |
probably damaging |
Het |
Ccl12 |
A |
T |
11: 81,993,437 (GRCm39) |
D25V |
possibly damaging |
Het |
Cdh23 |
G |
A |
10: 60,143,306 (GRCm39) |
A3005V |
possibly damaging |
Het |
Ces3a |
G |
T |
8: 105,776,547 (GRCm39) |
R45L |
probably benign |
Het |
Cntln |
G |
T |
4: 84,802,597 (GRCm39) |
|
probably benign |
Het |
Crybg3 |
C |
A |
16: 59,421,107 (GRCm39) |
|
probably null |
Het |
Cxxc4 |
G |
T |
3: 133,945,913 (GRCm39) |
G165C |
unknown |
Het |
Dab2ip |
G |
A |
2: 35,598,851 (GRCm39) |
C181Y |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 118,143,434 (GRCm39) |
V403A |
probably benign |
Het |
Dnah12 |
T |
C |
14: 26,578,507 (GRCm39) |
S3089P |
probably damaging |
Het |
Dnajc13 |
A |
T |
9: 104,067,571 (GRCm39) |
I1196N |
probably benign |
Het |
Faiml |
T |
C |
9: 99,116,462 (GRCm39) |
Y76C |
probably damaging |
Het |
Fam171b |
T |
A |
2: 83,707,028 (GRCm39) |
H299Q |
probably benign |
Het |
Fbxo36 |
A |
G |
1: 84,874,259 (GRCm39) |
N85S |
probably benign |
Het |
Filip1 |
A |
G |
9: 79,725,623 (GRCm39) |
F999L |
possibly damaging |
Het |
Gtf3c3 |
A |
T |
1: 54,445,211 (GRCm39) |
S614R |
possibly damaging |
Het |
Il18rap |
A |
G |
1: 40,587,088 (GRCm39) |
T457A |
probably benign |
Het |
Inmt |
C |
T |
6: 55,151,984 (GRCm39) |
|
probably benign |
Het |
Kcnb1 |
C |
T |
2: 166,947,007 (GRCm39) |
G614S |
probably benign |
Het |
Kdm2a |
C |
T |
19: 4,393,141 (GRCm39) |
D405N |
|
Het |
Kdm5a |
T |
A |
6: 120,404,730 (GRCm39) |
V1324E |
probably benign |
Het |
Lyn |
A |
T |
4: 3,746,804 (GRCm39) |
Y194F |
possibly damaging |
Het |
Mdn1 |
A |
G |
4: 32,693,504 (GRCm39) |
D1043G |
probably damaging |
Het |
Mier1 |
T |
A |
4: 103,012,800 (GRCm39) |
H397Q |
probably damaging |
Het |
Mov10l1 |
T |
A |
15: 88,872,622 (GRCm39) |
D105E |
possibly damaging |
Het |
Muc21 |
T |
C |
17: 35,930,545 (GRCm39) |
T1214A |
unknown |
Het |
Nav3 |
A |
G |
10: 109,554,065 (GRCm39) |
S1766P |
probably damaging |
Het |
Ncdn |
T |
A |
4: 126,644,464 (GRCm39) |
E119D |
probably benign |
Het |
Nckipsd |
C |
A |
9: 108,691,471 (GRCm39) |
A416E |
probably damaging |
Het |
Nek5 |
A |
G |
8: 22,563,961 (GRCm39) |
V623A |
probably benign |
Het |
Oas1g |
A |
G |
5: 121,023,986 (GRCm39) |
Y108H |
possibly damaging |
Het |
Or13n4 |
T |
C |
7: 106,423,062 (GRCm39) |
T224A |
probably benign |
Het |
P2ry1 |
T |
C |
3: 60,911,916 (GRCm39) |
S352P |
probably damaging |
Het |
Pde6a |
T |
C |
18: 61,390,382 (GRCm39) |
F535S |
probably damaging |
Het |
Pitpnb |
T |
C |
5: 111,530,891 (GRCm39) |
L228P |
probably damaging |
Het |
Rbck1 |
G |
T |
2: 152,161,145 (GRCm39) |
H368N |
probably damaging |
Het |
Snrnp35 |
T |
A |
5: 124,628,559 (GRCm39) |
V124E |
probably damaging |
Het |
Spdye4a |
C |
T |
5: 143,204,793 (GRCm39) |
M224I |
probably benign |
Het |
Stau1 |
A |
G |
2: 166,792,267 (GRCm39) |
Y424H |
probably damaging |
Het |
Sult1c2 |
A |
T |
17: 54,271,060 (GRCm39) |
D190E |
probably benign |
Het |
Thbs1 |
A |
G |
2: 117,953,051 (GRCm39) |
D887G |
probably damaging |
Het |
Tiam2 |
C |
T |
17: 3,558,074 (GRCm39) |
Q1233* |
probably null |
Het |
Tmem88 |
A |
G |
11: 69,288,939 (GRCm39) |
V38A |
probably damaging |
Het |
Vmn1r219 |
G |
A |
13: 23,346,902 (GRCm39) |
M30I |
probably benign |
Het |
Zswim3 |
A |
G |
2: 164,662,261 (GRCm39) |
H247R |
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 |
|
IGL02573:Atp7b
|
APN |
8 |
22,512,486 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|
|