Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503B20Rik |
T |
C |
3: 146,356,716 (GRCm39) |
D64G |
possibly damaging |
Het |
Amtn |
T |
C |
5: 88,525,956 (GRCm39) |
L40P |
probably damaging |
Het |
Ano6 |
A |
G |
15: 95,792,342 (GRCm39) |
R90G |
probably damaging |
Het |
Arfgef3 |
A |
C |
10: 18,540,637 (GRCm39) |
|
probably null |
Het |
Asxl3 |
C |
T |
18: 22,658,445 (GRCm39) |
P2152S |
probably benign |
Het |
Bik |
T |
A |
15: 83,428,409 (GRCm39) |
Y146N |
probably benign |
Het |
C1qtnf7 |
A |
T |
5: 43,766,436 (GRCm39) |
I12F |
possibly damaging |
Het |
Cacna1e |
A |
G |
1: 154,289,720 (GRCm39) |
|
probably null |
Het |
Ccdc168 |
A |
G |
1: 44,095,890 (GRCm39) |
V1736A |
probably benign |
Het |
Ccnj |
A |
G |
19: 40,833,636 (GRCm39) |
E231G |
probably damaging |
Het |
Cd101 |
T |
C |
3: 100,901,012 (GRCm39) |
K1020R |
probably benign |
Het |
Cdh6 |
C |
A |
15: 13,044,860 (GRCm39) |
V421L |
probably benign |
Het |
Cplane1 |
T |
C |
15: 8,205,668 (GRCm39) |
S135P |
probably benign |
Het |
Decr1 |
T |
C |
4: 15,924,355 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
C |
T |
18: 50,054,091 (GRCm39) |
P2566S |
probably damaging |
Het |
Dock9 |
G |
A |
14: 121,860,330 (GRCm39) |
P866L |
probably damaging |
Het |
Epx |
A |
G |
11: 87,759,452 (GRCm39) |
F546L |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,035,966 (GRCm39) |
M3206K |
probably benign |
Het |
Fgb |
T |
C |
3: 82,952,332 (GRCm39) |
D179G |
probably benign |
Het |
Gbgt1 |
A |
G |
2: 28,395,220 (GRCm39) |
D286G |
probably damaging |
Het |
Gpn1 |
T |
A |
5: 31,664,832 (GRCm39) |
S285R |
probably benign |
Het |
Htt |
T |
A |
5: 34,991,670 (GRCm39) |
Y1212N |
possibly damaging |
Het |
Kcnj13 |
T |
C |
1: 87,314,745 (GRCm39) |
K159R |
probably damaging |
Het |
Ldb2 |
T |
A |
5: 44,699,199 (GRCm39) |
I80F |
probably damaging |
Het |
Macrod2 |
T |
A |
2: 140,294,602 (GRCm39) |
N89K |
probably damaging |
Het |
Mdga2 |
G |
A |
12: 66,769,775 (GRCm39) |
R173C |
probably damaging |
Het |
Mroh9 |
A |
G |
1: 162,903,935 (GRCm39) |
F26L |
probably benign |
Het |
Neil3 |
G |
T |
8: 54,052,514 (GRCm39) |
N361K |
probably benign |
Het |
Nepro |
A |
G |
16: 44,551,720 (GRCm39) |
R193G |
probably damaging |
Het |
Or52d3 |
T |
A |
7: 104,229,447 (GRCm39) |
I198N |
probably damaging |
Het |
Pclo |
A |
T |
5: 14,731,113 (GRCm39) |
Q3205L |
unknown |
Het |
Plekhm1 |
A |
T |
11: 103,267,715 (GRCm39) |
I752N |
probably damaging |
Het |
Podn |
T |
C |
4: 107,878,614 (GRCm39) |
T273A |
possibly damaging |
Het |
Prep |
T |
A |
10: 44,973,597 (GRCm39) |
M235K |
probably benign |
Het |
Ptprc |
A |
T |
1: 137,999,993 (GRCm39) |
|
probably null |
Het |
Reg2 |
A |
G |
6: 78,384,625 (GRCm39) |
H119R |
possibly damaging |
Het |
Rpe65 |
T |
C |
3: 159,319,805 (GRCm39) |
V225A |
probably benign |
Het |
Scn9a |
T |
C |
2: 66,398,373 (GRCm39) |
D79G |
probably damaging |
Het |
Slc25a23 |
G |
A |
17: 57,360,804 (GRCm39) |
R9* |
probably null |
Het |
Snai3 |
A |
G |
8: 123,183,212 (GRCm39) |
L111P |
probably damaging |
Het |
Stk38 |
A |
G |
17: 29,218,981 (GRCm39) |
|
probably null |
Het |
Stk38l |
A |
T |
6: 146,668,269 (GRCm39) |
I115F |
possibly damaging |
Het |
Tmco6 |
T |
A |
18: 36,871,406 (GRCm39) |
|
probably null |
Het |
Tollip |
A |
T |
7: 141,452,451 (GRCm39) |
M1K |
probably null |
Het |
Trim40 |
T |
C |
17: 37,199,742 (GRCm39) |
Y112C |
possibly damaging |
Het |
Ttc27 |
T |
A |
17: 75,163,550 (GRCm39) |
Y719* |
probably null |
Het |
Ubald1 |
T |
C |
16: 4,697,584 (GRCm39) |
D6G |
probably damaging |
Het |
Vmn2r59 |
A |
T |
7: 41,693,171 (GRCm39) |
S476R |
probably benign |
Het |
Wfdc3 |
C |
T |
2: 164,576,178 (GRCm39) |
G38R |
possibly damaging |
Het |
Zbtb21 |
C |
T |
16: 97,753,161 (GRCm39) |
G402D |
probably damaging |
Het |
Zfp84 |
A |
G |
7: 29,475,911 (GRCm39) |
Y201C |
probably benign |
Het |
Zswim2 |
T |
A |
2: 83,770,028 (GRCm39) |
H62L |
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 |
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 |
|
|