Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
G |
3: 122,176,123 (GRCm38) |
L2259R |
probably damaging |
Het |
Acd |
A |
G |
8: 105,701,015 (GRCm38) |
S2P |
possibly damaging |
Het |
Acsf3 |
A |
G |
8: 122,780,157 (GRCm38) |
Y63C |
possibly damaging |
Het |
Adam21 |
T |
C |
12: 81,560,974 (GRCm38) |
I5V |
probably benign |
Het |
Adamts6 |
C |
A |
13: 104,444,128 (GRCm38) |
S783* |
probably null |
Het |
Adamtsl1 |
T |
C |
4: 86,243,769 (GRCm38) |
|
probably null |
Het |
Adck2 |
T |
A |
6: 39,576,393 (GRCm38) |
S313T |
probably benign |
Het |
Adgb |
A |
G |
10: 10,357,872 (GRCm38) |
I1285T |
probably benign |
Het |
Angptl1 |
T |
A |
1: 156,860,583 (GRCm38) |
M485K |
possibly damaging |
Het |
Ank3 |
G |
A |
10: 69,858,265 (GRCm38) |
V289I |
probably benign |
Het |
Atp1a1 |
A |
G |
3: 101,583,775 (GRCm38) |
L648P |
probably benign |
Het |
Atp2a3 |
A |
G |
11: 72,973,029 (GRCm38) |
I194V |
probably benign |
Het |
Bglap |
A |
C |
3: 88,384,405 (GRCm38) |
I4S |
unknown |
Het |
Cacna1b |
T |
A |
2: 24,637,487 (GRCm38) |
T1621S |
possibly damaging |
Het |
Ccdc112 |
T |
A |
18: 46,287,672 (GRCm38) |
Q337L |
probably benign |
Het |
Cd34 |
T |
G |
1: 194,951,011 (GRCm38) |
S194A |
probably damaging |
Het |
Cdh20 |
A |
G |
1: 104,941,264 (GRCm38) |
D160G |
probably damaging |
Het |
Clock |
T |
C |
5: 76,265,916 (GRCm38) |
K44R |
probably damaging |
Het |
Commd9 |
A |
G |
2: 101,898,896 (GRCm38) |
N116D |
probably benign |
Het |
Dab2 |
C |
A |
15: 6,429,611 (GRCm38) |
P335T |
probably benign |
Het |
Epb41l3 |
T |
A |
17: 69,248,719 (GRCm38) |
|
probably null |
Het |
Epha2 |
A |
G |
4: 141,322,416 (GRCm38) |
|
probably null |
Het |
Fam78b |
T |
C |
1: 167,078,647 (GRCm38) |
V125A |
probably benign |
Het |
Fars2 |
A |
T |
13: 36,537,426 (GRCm38) |
E448V |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,645,329 (GRCm38) |
A24T |
probably benign |
Het |
Glyr1 |
A |
C |
16: 5,047,758 (GRCm38) |
V44G |
probably benign |
Het |
Gm1527 |
A |
G |
3: 28,920,663 (GRCm38) |
I542V |
possibly damaging |
Het |
Gm18856 |
C |
A |
13: 13,965,208 (GRCm38) |
|
probably benign |
Het |
Gm44501 |
A |
G |
17: 40,578,714 (GRCm38) |
K40E |
probably benign |
Het |
Gm6583 |
A |
G |
5: 112,355,299 (GRCm38) |
S180P |
possibly damaging |
Het |
Hdhd5 |
T |
C |
6: 120,523,446 (GRCm38) |
H97R |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,753,611 (GRCm38) |
V965A |
probably benign |
Het |
Hsf5 |
A |
G |
11: 87,635,620 (GRCm38) |
M373V |
probably benign |
Het |
Igbp1b |
C |
T |
6: 138,657,805 (GRCm38) |
E214K |
probably benign |
Het |
Iigp1 |
T |
A |
18: 60,389,892 (GRCm38) |
F27L |
probably benign |
Het |
Isl1 |
T |
C |
13: 116,305,430 (GRCm38) |
N89S |
probably benign |
Het |
Itga1 |
C |
A |
13: 115,035,385 (GRCm38) |
W61C |
probably damaging |
Het |
Itga5 |
T |
C |
15: 103,347,760 (GRCm38) |
R922G |
probably benign |
Het |
Kbtbd3 |
G |
A |
9: 4,331,073 (GRCm38) |
W482* |
probably null |
Het |
Kcnq1 |
A |
G |
7: 143,182,757 (GRCm38) |
T168A |
probably benign |
Het |
Lrch3 |
A |
G |
16: 33,005,704 (GRCm38) |
N631S |
probably damaging |
Het |
Lrrk1 |
T |
A |
7: 66,262,665 (GRCm38) |
I1716F |
possibly damaging |
Het |
Ly75 |
T |
C |
2: 60,349,940 (GRCm38) |
E631G |
probably benign |
Het |
Map4 |
T |
C |
9: 110,035,263 (GRCm38) |
S519P |
probably benign |
Het |
Mkl1 |
C |
T |
15: 81,017,033 (GRCm38) |
S419N |
probably damaging |
Het |
Mroh2a |
A |
G |
1: 88,258,664 (GRCm38) |
S64G |
probably benign |
Het |
Muc5b |
A |
G |
7: 141,849,567 (GRCm38) |
E755G |
unknown |
Het |
Ncaph2 |
T |
G |
15: 89,370,807 (GRCm38) |
V478G |
probably damaging |
Het |
Ncbp1 |
A |
G |
4: 46,152,967 (GRCm38) |
R247G |
possibly damaging |
Het |
Necab1 |
G |
T |
4: 15,111,208 (GRCm38) |
D73E |
possibly damaging |
Het |
Nedd9 |
T |
C |
13: 41,317,900 (GRCm38) |
K208E |
probably benign |
Het |
Nfyb |
A |
T |
10: 82,752,368 (GRCm38) |
|
probably benign |
Het |
Nol4 |
T |
C |
18: 22,921,887 (GRCm38) |
Q162R |
probably damaging |
Het |
Nwd2 |
G |
A |
5: 63,805,433 (GRCm38) |
D787N |
probably benign |
Het |
Olfr2 |
C |
T |
7: 107,001,335 (GRCm38) |
G175D |
probably damaging |
Het |
Olfr205 |
C |
T |
16: 59,328,850 (GRCm38) |
V220I |
probably benign |
Het |
Olfr49 |
A |
G |
14: 54,282,547 (GRCm38) |
M116T |
probably damaging |
Het |
Olfr535 |
A |
G |
7: 140,493,007 (GRCm38) |
D123G |
probably damaging |
Het |
Olfr713 |
A |
T |
7: 107,036,914 (GRCm38) |
Y253F |
probably benign |
Het |
Olfr740 |
A |
C |
14: 50,453,417 (GRCm38) |
M122L |
probably damaging |
Het |
Olfr908 |
T |
A |
9: 38,516,503 (GRCm38) |
M157K |
probably damaging |
Het |
Orai3 |
T |
C |
7: 127,773,888 (GRCm38) |
V187A |
probably benign |
Het |
Parn |
T |
C |
16: 13,606,202 (GRCm38) |
T444A |
probably benign |
Het |
Pcdh11x |
A |
C |
X: 120,400,240 (GRCm38) |
N460T |
probably damaging |
Het |
Pcnt |
C |
T |
10: 76,370,024 (GRCm38) |
R2516H |
probably benign |
Het |
Pde4d |
T |
A |
13: 109,938,171 (GRCm38) |
|
probably benign |
Het |
Pdgfra |
A |
G |
5: 75,189,311 (GRCm38) |
N952S |
probably benign |
Het |
Pgm1 |
A |
G |
5: 64,103,874 (GRCm38) |
Y237C |
probably damaging |
Het |
Plcb2 |
A |
G |
2: 118,711,124 (GRCm38) |
V975A |
probably benign |
Het |
Polk |
T |
C |
13: 96,489,256 (GRCm38) |
T347A |
probably benign |
Het |
Ppp6r1 |
C |
T |
7: 4,641,054 (GRCm38) |
V430M |
possibly damaging |
Het |
Ptges2 |
C |
A |
2: 32,396,322 (GRCm38) |
C16* |
probably null |
Het |
Relb |
A |
T |
7: 19,619,839 (GRCm38) |
I38N |
probably damaging |
Het |
Runx1t1 |
T |
A |
4: 13,837,767 (GRCm38) |
N51K |
probably damaging |
Het |
Samsn1 |
A |
G |
16: 75,883,845 (GRCm38) |
|
probably benign |
Het |
Scrn1 |
A |
G |
6: 54,520,769 (GRCm38) |
V279A |
possibly damaging |
Het |
Sec31b |
A |
G |
19: 44,531,746 (GRCm38) |
S200P |
probably benign |
Het |
Selp |
A |
G |
1: 164,144,906 (GRCm38) |
T705A |
probably benign |
Het |
Slc2a1 |
G |
A |
4: 119,132,445 (GRCm38) |
R61Q |
probably damaging |
Het |
Slit3 |
G |
A |
11: 35,651,820 (GRCm38) |
|
probably null |
Het |
Smo |
T |
A |
6: 29,755,574 (GRCm38) |
V415E |
probably damaging |
Het |
Spag8 |
C |
A |
4: 43,652,035 (GRCm38) |
V350L |
possibly damaging |
Het |
Tbck |
T |
G |
3: 132,707,798 (GRCm38) |
L132R |
possibly damaging |
Het |
Thnsl1 |
T |
A |
2: 21,212,045 (GRCm38) |
C203* |
probably null |
Het |
Tm9sf2 |
T |
A |
14: 122,149,840 (GRCm38) |
|
probably null |
Het |
Tmem131 |
A |
G |
1: 36,841,676 (GRCm38) |
V171A |
probably damaging |
Het |
Tmem209 |
T |
C |
6: 30,501,955 (GRCm38) |
T83A |
probably benign |
Het |
Tmem63a |
T |
C |
1: 180,954,851 (GRCm38) |
Y138H |
probably damaging |
Het |
Trim80 |
A |
G |
11: 115,447,943 (GRCm38) |
Y533C |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,581,180 (GRCm38) |
D66G |
possibly damaging |
Het |
Trrap |
T |
A |
5: 144,832,488 (GRCm38) |
I2620N |
probably benign |
Het |
Ttyh3 |
A |
T |
5: 140,634,786 (GRCm38) |
I232N |
probably damaging |
Het |
Ube2dnl1 |
G |
A |
X: 114,905,785 (GRCm38) |
C119Y |
possibly damaging |
Het |
Unc13c |
T |
A |
9: 73,932,187 (GRCm38) |
S461C |
probably damaging |
Het |
Unc80 |
T |
G |
1: 66,527,941 (GRCm38) |
I902S |
probably damaging |
Het |
Usp42 |
C |
A |
5: 143,723,937 (GRCm38) |
G170W |
probably damaging |
Het |
Vldlr |
T |
C |
19: 27,238,852 (GRCm38) |
|
probably null |
Het |
Ywhab |
A |
G |
2: 164,015,345 (GRCm38) |
Y180C |
probably damaging |
Het |
Zan |
A |
T |
5: 137,380,850 (GRCm38) |
C5329* |
probably null |
Het |
Zbtb40 |
C |
T |
4: 136,998,642 (GRCm38) |
M535I |
probably benign |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 105,483,744 (GRCm38) |
|
probably null |
Het |
Zfp318 |
A |
G |
17: 46,412,062 (GRCm38) |
T1664A |
probably benign |
Het |
Zfp7 |
T |
A |
15: 76,891,346 (GRCm38) |
C529* |
probably null |
Het |
Zfp768 |
T |
C |
7: 127,343,375 (GRCm38) |
Q527R |
possibly damaging |
Het |
Zfp975 |
T |
A |
7: 42,665,146 (GRCm38) |
|
probably null |
Het |
|
Other mutations in Atp13a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00563:Atp13a4
|
APN |
16 |
29,403,778 (GRCm38) |
splice site |
probably benign |
|
IGL01577:Atp13a4
|
APN |
16 |
29,441,284 (GRCm38) |
missense |
possibly damaging |
0.77 |
IGL01834:Atp13a4
|
APN |
16 |
29,415,777 (GRCm38) |
splice site |
probably benign |
|
IGL02165:Atp13a4
|
APN |
16 |
29,434,010 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02194:Atp13a4
|
APN |
16 |
29,456,629 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02322:Atp13a4
|
APN |
16 |
29,440,102 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02553:Atp13a4
|
APN |
16 |
29,422,703 (GRCm38) |
missense |
probably benign |
0.03 |
IGL02821:Atp13a4
|
APN |
16 |
29,441,307 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03349:Atp13a4
|
APN |
16 |
29,456,671 (GRCm38) |
missense |
probably benign |
0.01 |
G5030:Atp13a4
|
UTSW |
16 |
29,455,488 (GRCm38) |
missense |
probably damaging |
1.00 |
R0091:Atp13a4
|
UTSW |
16 |
29,455,395 (GRCm38) |
missense |
probably damaging |
1.00 |
R0100:Atp13a4
|
UTSW |
16 |
29,421,724 (GRCm38) |
missense |
probably damaging |
1.00 |
R0278:Atp13a4
|
UTSW |
16 |
29,454,834 (GRCm38) |
missense |
probably damaging |
1.00 |
R1263:Atp13a4
|
UTSW |
16 |
29,471,953 (GRCm38) |
missense |
possibly damaging |
0.60 |
R1378:Atp13a4
|
UTSW |
16 |
29,420,428 (GRCm38) |
missense |
probably damaging |
1.00 |
R1575:Atp13a4
|
UTSW |
16 |
29,409,710 (GRCm38) |
missense |
probably benign |
0.01 |
R1720:Atp13a4
|
UTSW |
16 |
29,408,928 (GRCm38) |
missense |
probably damaging |
0.99 |
R1759:Atp13a4
|
UTSW |
16 |
29,456,611 (GRCm38) |
missense |
probably damaging |
0.99 |
R1967:Atp13a4
|
UTSW |
16 |
29,479,854 (GRCm38) |
missense |
probably damaging |
0.99 |
R2030:Atp13a4
|
UTSW |
16 |
29,422,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R2113:Atp13a4
|
UTSW |
16 |
29,441,284 (GRCm38) |
missense |
possibly damaging |
0.77 |
R3409:Atp13a4
|
UTSW |
16 |
29,413,749 (GRCm38) |
missense |
probably damaging |
1.00 |
R3410:Atp13a4
|
UTSW |
16 |
29,413,749 (GRCm38) |
missense |
probably damaging |
1.00 |
R4032:Atp13a4
|
UTSW |
16 |
29,418,571 (GRCm38) |
missense |
probably damaging |
1.00 |
R4163:Atp13a4
|
UTSW |
16 |
29,541,250 (GRCm38) |
missense |
possibly damaging |
0.87 |
R4652:Atp13a4
|
UTSW |
16 |
29,452,603 (GRCm38) |
missense |
probably damaging |
1.00 |
R4772:Atp13a4
|
UTSW |
16 |
29,420,835 (GRCm38) |
intron |
probably benign |
|
R4898:Atp13a4
|
UTSW |
16 |
29,408,961 (GRCm38) |
nonsense |
probably null |
|
R4996:Atp13a4
|
UTSW |
16 |
29,472,004 (GRCm38) |
missense |
probably damaging |
1.00 |
R5112:Atp13a4
|
UTSW |
16 |
29,409,868 (GRCm38) |
missense |
possibly damaging |
0.87 |
R5259:Atp13a4
|
UTSW |
16 |
29,456,610 (GRCm38) |
missense |
probably damaging |
1.00 |
R5395:Atp13a4
|
UTSW |
16 |
29,456,604 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5395:Atp13a4
|
UTSW |
16 |
29,420,888 (GRCm38) |
nonsense |
probably null |
|
R5640:Atp13a4
|
UTSW |
16 |
29,415,831 (GRCm38) |
missense |
probably damaging |
0.98 |
R5809:Atp13a4
|
UTSW |
16 |
29,433,987 (GRCm38) |
missense |
possibly damaging |
0.56 |
R5856:Atp13a4
|
UTSW |
16 |
29,433,987 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5912:Atp13a4
|
UTSW |
16 |
29,456,571 (GRCm38) |
missense |
probably benign |
0.33 |
R6282:Atp13a4
|
UTSW |
16 |
29,434,004 (GRCm38) |
missense |
probably benign |
0.00 |
R6404:Atp13a4
|
UTSW |
16 |
29,471,901 (GRCm38) |
nonsense |
probably null |
|
R6497:Atp13a4
|
UTSW |
16 |
29,479,901 (GRCm38) |
missense |
probably damaging |
1.00 |
R6577:Atp13a4
|
UTSW |
16 |
29,479,841 (GRCm38) |
missense |
probably benign |
0.03 |
R6806:Atp13a4
|
UTSW |
16 |
29,469,280 (GRCm38) |
missense |
probably damaging |
1.00 |
R7229:Atp13a4
|
UTSW |
16 |
29,420,905 (GRCm38) |
missense |
probably benign |
0.05 |
R7438:Atp13a4
|
UTSW |
16 |
29,441,196 (GRCm38) |
missense |
|
|
R7493:Atp13a4
|
UTSW |
16 |
29,471,956 (GRCm38) |
missense |
|
|
R7712:Atp13a4
|
UTSW |
16 |
29,459,487 (GRCm38) |
missense |
|
|
R7739:Atp13a4
|
UTSW |
16 |
29,456,601 (GRCm38) |
missense |
|
|
R7897:Atp13a4
|
UTSW |
16 |
29,396,466 (GRCm38) |
missense |
|
|
R7950:Atp13a4
|
UTSW |
16 |
29,449,917 (GRCm38) |
missense |
|
|
R8217:Atp13a4
|
UTSW |
16 |
29,403,801 (GRCm38) |
missense |
|
|
R8227:Atp13a4
|
UTSW |
16 |
29,403,845 (GRCm38) |
missense |
|
|
R8273:Atp13a4
|
UTSW |
16 |
29,471,902 (GRCm38) |
missense |
|
|
R8488:Atp13a4
|
UTSW |
16 |
29,417,836 (GRCm38) |
missense |
possibly damaging |
0.63 |
R8508:Atp13a4
|
UTSW |
16 |
29,454,769 (GRCm38) |
nonsense |
probably null |
|
R8773:Atp13a4
|
UTSW |
16 |
29,441,580 (GRCm38) |
missense |
|
|
R8921:Atp13a4
|
UTSW |
16 |
29,454,774 (GRCm38) |
missense |
|
|
R8940:Atp13a4
|
UTSW |
16 |
29,454,690 (GRCm38) |
critical splice donor site |
probably null |
|
R9056:Atp13a4
|
UTSW |
16 |
29,471,888 (GRCm38) |
critical splice donor site |
probably null |
|
R9272:Atp13a4
|
UTSW |
16 |
29,449,979 (GRCm38) |
missense |
|
|
R9292:Atp13a4
|
UTSW |
16 |
29,422,682 (GRCm38) |
missense |
|
|
R9415:Atp13a4
|
UTSW |
16 |
29,409,003 (GRCm38) |
missense |
|
|
R9453:Atp13a4
|
UTSW |
16 |
29,420,841 (GRCm38) |
missense |
unknown |
|
R9497:Atp13a4
|
UTSW |
16 |
29,469,312 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9541:Atp13a4
|
UTSW |
16 |
29,422,726 (GRCm38) |
missense |
|
|
R9614:Atp13a4
|
UTSW |
16 |
29,441,580 (GRCm38) |
missense |
|
|
R9622:Atp13a4
|
UTSW |
16 |
29,420,459 (GRCm38) |
missense |
|
|
R9727:Atp13a4
|
UTSW |
16 |
29,409,771 (GRCm38) |
missense |
|
|
Z1176:Atp13a4
|
UTSW |
16 |
29,422,587 (GRCm38) |
missense |
probably null |
|
|