Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
G |
T |
7: 45,679,680 (GRCm39) |
T9K |
probably benign |
Het |
Ankrd28 |
T |
C |
14: 31,429,177 (GRCm39) |
H925R |
probably damaging |
Het |
Antxrl |
A |
T |
14: 33,778,556 (GRCm39) |
T128S |
probably damaging |
Het |
Atosa |
A |
G |
9: 74,913,645 (GRCm39) |
M100V |
possibly damaging |
Het |
Bmpr2 |
G |
T |
1: 59,906,595 (GRCm39) |
V563L |
probably benign |
Het |
Btn1a1 |
A |
T |
13: 23,648,521 (GRCm39) |
L104Q |
probably damaging |
Het |
Caskin1 |
C |
G |
17: 24,726,154 (GRCm39) |
D1420E |
probably damaging |
Het |
Cdc14a |
A |
T |
3: 116,144,862 (GRCm39) |
I150N |
probably damaging |
Het |
Cdc26 |
C |
T |
4: 62,321,031 (GRCm39) |
R4Q |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,236,496 (GRCm39) |
D160G |
probably damaging |
Het |
Cxcr4 |
A |
C |
1: 128,519,920 (GRCm39) |
|
probably null |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dgat1 |
T |
C |
15: 76,387,493 (GRCm39) |
N317S |
possibly damaging |
Het |
Disp1 |
G |
A |
1: 182,880,589 (GRCm39) |
T228M |
possibly damaging |
Het |
Dixdc1 |
A |
C |
9: 50,614,656 (GRCm39) |
|
probably null |
Het |
Dnase1l2 |
C |
A |
17: 24,661,492 (GRCm39) |
|
probably benign |
Het |
Dsg2 |
T |
C |
18: 20,727,350 (GRCm39) |
|
probably null |
Het |
Duox2 |
A |
T |
2: 122,117,674 (GRCm39) |
F887I |
probably benign |
Het |
Duxf4 |
A |
G |
10: 58,071,344 (GRCm39) |
M290T |
probably benign |
Het |
Efcab6 |
T |
C |
15: 83,851,825 (GRCm39) |
D351G |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,818,808 (GRCm39) |
V2621A |
probably damaging |
Het |
Epg5 |
G |
T |
18: 77,991,677 (GRCm39) |
V125F |
possibly damaging |
Het |
Ephb1 |
T |
C |
9: 101,800,783 (GRCm39) |
R953G |
probably damaging |
Het |
Etfdh |
G |
T |
3: 79,519,336 (GRCm39) |
Y272* |
probably null |
Het |
Fam117b |
A |
G |
1: 60,008,207 (GRCm39) |
E347G |
probably damaging |
Het |
Gfra3 |
A |
T |
18: 34,828,846 (GRCm39) |
C183S |
probably damaging |
Het |
Gmip |
A |
G |
8: 70,268,773 (GRCm39) |
D466G |
probably damaging |
Het |
Golga5 |
G |
A |
12: 102,450,740 (GRCm39) |
M464I |
probably benign |
Het |
Gpd1 |
A |
T |
15: 99,621,146 (GRCm39) |
Q320L |
possibly damaging |
Het |
H2-Oa |
G |
T |
17: 34,312,851 (GRCm39) |
D43Y |
probably damaging |
Het |
Hecw1 |
T |
A |
13: 14,520,623 (GRCm39) |
I205F |
probably damaging |
Het |
Ighv8-13 |
A |
G |
12: 115,728,973 (GRCm39) |
Y95H |
probably damaging |
Het |
Igkv6-20 |
T |
C |
6: 70,313,081 (GRCm39) |
M31V |
possibly damaging |
Het |
Itih1 |
T |
C |
14: 30,653,217 (GRCm39) |
D737G |
probably benign |
Het |
Kcnc4 |
G |
C |
3: 107,355,693 (GRCm39) |
H252D |
probably damaging |
Het |
Kcnj14 |
T |
A |
7: 45,468,921 (GRCm39) |
T195S |
probably damaging |
Het |
Limch1 |
A |
T |
5: 67,173,845 (GRCm39) |
D642V |
probably damaging |
Het |
Lrp2 |
T |
G |
2: 69,312,710 (GRCm39) |
D2526A |
possibly damaging |
Het |
Lrrc8a |
A |
G |
2: 30,146,565 (GRCm39) |
T460A |
possibly damaging |
Het |
Lrrn4cl |
A |
G |
19: 8,829,135 (GRCm39) |
T38A |
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,277,629 (GRCm39) |
Q137L |
possibly damaging |
Het |
Mapkapk3 |
A |
G |
9: 107,137,262 (GRCm39) |
Y206H |
probably damaging |
Het |
Mrc1 |
G |
A |
2: 14,276,115 (GRCm39) |
G483D |
probably benign |
Het |
Mrpl35 |
C |
A |
6: 71,800,661 (GRCm39) |
|
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,497,665 (GRCm39) |
H936L |
probably benign |
Het |
Myh3 |
A |
T |
11: 66,978,312 (GRCm39) |
Y433F |
probably benign |
Het |
Napb |
C |
T |
2: 148,540,098 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
C |
A |
1: 60,335,083 (GRCm39) |
Q2288K |
probably benign |
Het |
Ndst3 |
G |
A |
3: 123,465,301 (GRCm39) |
Q224* |
probably null |
Het |
Nkapd1 |
A |
G |
9: 50,518,971 (GRCm39) |
S214P |
possibly damaging |
Het |
Nkd2 |
A |
G |
13: 73,969,579 (GRCm39) |
S284P |
probably benign |
Het |
Or10a2 |
T |
C |
7: 106,673,343 (GRCm39) |
Y103H |
probably damaging |
Het |
Or5b12 |
A |
T |
19: 12,897,301 (GRCm39) |
V124E |
probably damaging |
Het |
Or6k2 |
G |
A |
1: 173,979,712 (GRCm39) |
S210N |
probably benign |
Het |
Or8h10 |
T |
C |
2: 86,809,035 (GRCm39) |
Y35C |
probably damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,490,037 (GRCm39) |
T572A |
probably benign |
Het |
Pcdhb9 |
A |
G |
18: 37,535,115 (GRCm39) |
I370V |
probably benign |
Het |
Pcsk5 |
T |
G |
19: 17,558,631 (GRCm39) |
E592A |
possibly damaging |
Het |
Pigc |
T |
C |
1: 161,798,036 (GRCm39) |
V6A |
probably benign |
Het |
Pla2g6 |
T |
G |
15: 79,189,924 (GRCm39) |
I389L |
probably benign |
Het |
Pnliprp2 |
T |
C |
19: 58,751,874 (GRCm39) |
|
probably null |
Het |
Psmb11 |
T |
C |
14: 54,863,646 (GRCm39) |
V288A |
probably benign |
Het |
Rapgef5 |
A |
G |
12: 117,685,398 (GRCm39) |
|
probably null |
Het |
Rcn3 |
T |
C |
7: 44,732,720 (GRCm39) |
N316S |
probably damaging |
Het |
Rgs6 |
A |
G |
12: 83,112,738 (GRCm39) |
K183E |
probably damaging |
Het |
Rhoc |
A |
G |
3: 104,700,297 (GRCm39) |
|
probably null |
Het |
Serinc5 |
T |
C |
13: 92,844,616 (GRCm39) |
C453R |
probably damaging |
Het |
Slc14a1 |
A |
C |
18: 78,159,614 (GRCm39) |
M93R |
probably damaging |
Het |
Slc25a3 |
A |
T |
10: 90,958,090 (GRCm39) |
D83E |
probably damaging |
Het |
Slc36a3 |
T |
C |
11: 55,015,777 (GRCm39) |
Y459C |
probably benign |
Het |
Slc44a5 |
A |
T |
3: 153,944,800 (GRCm39) |
Y139F |
probably benign |
Het |
Spag17 |
A |
T |
3: 99,929,918 (GRCm39) |
Q539L |
probably benign |
Het |
Stap2 |
C |
T |
17: 56,306,976 (GRCm39) |
V234M |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,544,231 (GRCm39) |
Y4450C |
probably damaging |
Het |
Taf6l |
C |
T |
19: 8,756,030 (GRCm39) |
R206Q |
probably benign |
Het |
Tbc1d23 |
C |
T |
16: 57,003,266 (GRCm39) |
V501I |
probably damaging |
Het |
Thap2 |
T |
C |
10: 115,208,751 (GRCm39) |
H123R |
probably damaging |
Het |
Tlx3 |
C |
A |
11: 33,152,432 (GRCm39) |
W221L |
probably benign |
Het |
Tmem262 |
T |
A |
19: 6,130,567 (GRCm39) |
|
probably null |
Het |
Tpmt |
C |
A |
13: 47,180,735 (GRCm39) |
R201S |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,831,655 (GRCm39) |
S1507P |
probably damaging |
Het |
Ttc9c |
T |
C |
19: 8,795,847 (GRCm39) |
E64G |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,640,790 (GRCm39) |
S13653T |
probably damaging |
Het |
Ugt3a1 |
G |
T |
15: 9,310,726 (GRCm39) |
W336L |
possibly damaging |
Het |
Vmn1r215 |
C |
A |
13: 23,260,633 (GRCm39) |
N224K |
probably benign |
Het |
Vmn2r59 |
C |
T |
7: 41,691,835 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
G |
5: 102,046,295 (GRCm39) |
S1853P |
possibly damaging |
Het |
Wdr36 |
A |
T |
18: 32,975,059 (GRCm39) |
Y137F |
possibly damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,792,216 (GRCm39) |
D324G |
probably benign |
Het |
Zfp217 |
T |
C |
2: 169,961,497 (GRCm39) |
T277A |
probably benign |
Het |
Zfp451 |
A |
G |
1: 33,842,219 (GRCm39) |
|
probably benign |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zfp871 |
T |
C |
17: 32,994,858 (GRCm39) |
S106G |
possibly damaging |
Het |
|
Other mutations in Atp8b5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00885:Atp8b5
|
APN |
4 |
43,355,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00970:Atp8b5
|
APN |
4 |
43,311,938 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01335:Atp8b5
|
APN |
4 |
43,302,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01462:Atp8b5
|
APN |
4 |
43,368,010 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01657:Atp8b5
|
APN |
4 |
43,291,693 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01935:Atp8b5
|
APN |
4 |
43,366,638 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01977:Atp8b5
|
APN |
4 |
43,320,590 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02102:Atp8b5
|
APN |
4 |
43,364,167 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02369:Atp8b5
|
APN |
4 |
43,334,205 (GRCm39) |
missense |
probably benign |
|
IGL02456:Atp8b5
|
APN |
4 |
43,365,578 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02696:Atp8b5
|
APN |
4 |
43,369,634 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02826:Atp8b5
|
APN |
4 |
43,366,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Atp8b5
|
APN |
4 |
43,305,774 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0128:Atp8b5
|
UTSW |
4 |
43,369,715 (GRCm39) |
critical splice donor site |
probably null |
|
R0130:Atp8b5
|
UTSW |
4 |
43,369,715 (GRCm39) |
critical splice donor site |
probably null |
|
R0243:Atp8b5
|
UTSW |
4 |
43,366,057 (GRCm39) |
missense |
probably benign |
|
R0256:Atp8b5
|
UTSW |
4 |
43,302,576 (GRCm39) |
intron |
probably benign |
|
R0379:Atp8b5
|
UTSW |
4 |
43,361,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R0671:Atp8b5
|
UTSW |
4 |
43,291,672 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1109:Atp8b5
|
UTSW |
4 |
43,305,719 (GRCm39) |
intron |
probably benign |
|
R1442:Atp8b5
|
UTSW |
4 |
43,334,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R1454:Atp8b5
|
UTSW |
4 |
43,302,590 (GRCm39) |
missense |
probably benign |
|
R1469:Atp8b5
|
UTSW |
4 |
43,291,733 (GRCm39) |
critical splice donor site |
probably null |
|
R1469:Atp8b5
|
UTSW |
4 |
43,291,733 (GRCm39) |
critical splice donor site |
probably null |
|
R1503:Atp8b5
|
UTSW |
4 |
43,344,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1580:Atp8b5
|
UTSW |
4 |
43,355,673 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1677:Atp8b5
|
UTSW |
4 |
43,372,903 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1861:Atp8b5
|
UTSW |
4 |
43,372,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Atp8b5
|
UTSW |
4 |
43,361,804 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1903:Atp8b5
|
UTSW |
4 |
43,357,063 (GRCm39) |
missense |
probably damaging |
0.98 |
R1961:Atp8b5
|
UTSW |
4 |
43,369,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R2131:Atp8b5
|
UTSW |
4 |
43,370,726 (GRCm39) |
missense |
probably benign |
0.33 |
R2971:Atp8b5
|
UTSW |
4 |
43,361,953 (GRCm39) |
splice site |
probably benign |
|
R3023:Atp8b5
|
UTSW |
4 |
43,311,957 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3433:Atp8b5
|
UTSW |
4 |
43,372,697 (GRCm39) |
missense |
probably benign |
|
R3690:Atp8b5
|
UTSW |
4 |
43,368,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Atp8b5
|
UTSW |
4 |
43,365,591 (GRCm39) |
missense |
probably damaging |
0.97 |
R4484:Atp8b5
|
UTSW |
4 |
43,357,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Atp8b5
|
UTSW |
4 |
43,320,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4511:Atp8b5
|
UTSW |
4 |
43,320,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4679:Atp8b5
|
UTSW |
4 |
43,365,955 (GRCm39) |
missense |
probably benign |
0.16 |
R4753:Atp8b5
|
UTSW |
4 |
43,372,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R4761:Atp8b5
|
UTSW |
4 |
43,308,504 (GRCm39) |
makesense |
probably null |
|
R4784:Atp8b5
|
UTSW |
4 |
43,356,980 (GRCm39) |
missense |
probably damaging |
0.97 |
R4785:Atp8b5
|
UTSW |
4 |
43,356,980 (GRCm39) |
missense |
probably damaging |
0.97 |
R4855:Atp8b5
|
UTSW |
4 |
43,344,449 (GRCm39) |
missense |
probably benign |
|
R5422:Atp8b5
|
UTSW |
4 |
43,366,644 (GRCm39) |
missense |
probably benign |
0.10 |
R5915:Atp8b5
|
UTSW |
4 |
43,370,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Atp8b5
|
UTSW |
4 |
43,371,003 (GRCm39) |
missense |
probably benign |
0.03 |
R6708:Atp8b5
|
UTSW |
4 |
43,334,249 (GRCm39) |
missense |
probably benign |
|
R6931:Atp8b5
|
UTSW |
4 |
43,364,108 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7021:Atp8b5
|
UTSW |
4 |
43,355,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R7085:Atp8b5
|
UTSW |
4 |
43,361,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R7207:Atp8b5
|
UTSW |
4 |
43,357,018 (GRCm39) |
missense |
probably damaging |
0.97 |
R7404:Atp8b5
|
UTSW |
4 |
43,342,640 (GRCm39) |
missense |
probably benign |
0.10 |
R7448:Atp8b5
|
UTSW |
4 |
43,366,021 (GRCm39) |
missense |
probably benign |
|
R7465:Atp8b5
|
UTSW |
4 |
43,271,269 (GRCm39) |
missense |
probably benign |
0.00 |
R7526:Atp8b5
|
UTSW |
4 |
43,366,609 (GRCm39) |
missense |
probably damaging |
0.99 |
R7616:Atp8b5
|
UTSW |
4 |
43,370,823 (GRCm39) |
critical splice donor site |
probably null |
|
R7698:Atp8b5
|
UTSW |
4 |
43,366,735 (GRCm39) |
missense |
probably benign |
0.27 |
R7883:Atp8b5
|
UTSW |
4 |
43,342,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R8052:Atp8b5
|
UTSW |
4 |
43,356,982 (GRCm39) |
nonsense |
probably null |
|
R8218:Atp8b5
|
UTSW |
4 |
43,372,728 (GRCm39) |
critical splice donor site |
probably null |
|
R8248:Atp8b5
|
UTSW |
4 |
43,366,072 (GRCm39) |
missense |
probably damaging |
0.97 |
R8345:Atp8b5
|
UTSW |
4 |
43,291,714 (GRCm39) |
missense |
probably benign |
0.01 |
R8756:Atp8b5
|
UTSW |
4 |
43,342,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R8888:Atp8b5
|
UTSW |
4 |
43,304,687 (GRCm39) |
missense |
|
|
R8942:Atp8b5
|
UTSW |
4 |
43,353,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R9153:Atp8b5
|
UTSW |
4 |
43,308,493 (GRCm39) |
utr 3 prime |
probably benign |
|
R9154:Atp8b5
|
UTSW |
4 |
43,372,630 (GRCm39) |
missense |
probably benign |
0.19 |
R9211:Atp8b5
|
UTSW |
4 |
43,367,960 (GRCm39) |
missense |
probably damaging |
0.97 |
R9361:Atp8b5
|
UTSW |
4 |
43,369,658 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9786:Atp8b5
|
UTSW |
4 |
43,305,798 (GRCm39) |
missense |
probably damaging |
0.97 |
X0025:Atp8b5
|
UTSW |
4 |
43,366,774 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Atp8b5
|
UTSW |
4 |
43,361,903 (GRCm39) |
missense |
probably benign |
0.40 |
Z1177:Atp8b5
|
UTSW |
4 |
43,370,669 (GRCm39) |
missense |
probably benign |
0.12 |
|