Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl6a |
G |
T |
3: 32,769,649 (GRCm39) |
A155S |
probably benign |
Het |
Adar |
A |
G |
3: 89,643,045 (GRCm39) |
T309A |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,303,312 (GRCm39) |
W6125R |
probably damaging |
Het |
Adprhl1 |
A |
G |
8: 13,274,352 (GRCm39) |
L802P |
probably benign |
Het |
Ahcy |
A |
G |
2: 154,910,779 (GRCm39) |
L63P |
probably damaging |
Het |
Ang5 |
G |
A |
14: 44,200,352 (GRCm39) |
D139N |
probably damaging |
Het |
Ankrd31 |
A |
G |
13: 96,962,655 (GRCm39) |
D482G |
probably benign |
Het |
Arhgef7 |
A |
G |
8: 11,850,469 (GRCm39) |
N257D |
probably benign |
Het |
Art3 |
C |
A |
5: 92,540,393 (GRCm39) |
S45R |
probably benign |
Het |
Atxn1 |
T |
C |
13: 45,720,891 (GRCm39) |
R335G |
probably damaging |
Het |
Bag6 |
T |
A |
17: 35,363,641 (GRCm39) |
L775H |
probably damaging |
Het |
BC004004 |
T |
G |
17: 29,501,130 (GRCm39) |
H26Q |
possibly damaging |
Het |
Camsap3 |
T |
C |
8: 3,656,575 (GRCm39) |
L986S |
probably benign |
Het |
Cbx5 |
T |
C |
15: 103,121,586 (GRCm39) |
E17G |
probably damaging |
Het |
Cc2d1b |
T |
C |
4: 108,484,617 (GRCm39) |
|
probably null |
Het |
Ccdc59 |
T |
C |
10: 105,683,007 (GRCm39) |
Y231H |
probably damaging |
Het |
Cemip2 |
T |
C |
19: 21,789,986 (GRCm39) |
|
probably null |
Het |
Csnk1g1 |
T |
C |
9: 65,917,854 (GRCm39) |
|
probably null |
Het |
Cybrd1 |
A |
G |
2: 70,967,904 (GRCm39) |
I158M |
possibly damaging |
Het |
Disp2 |
T |
A |
2: 118,621,179 (GRCm39) |
I637N |
probably benign |
Het |
Dll4 |
TC |
T |
2: 119,163,054 (GRCm39) |
|
probably null |
Het |
Dnah7a |
T |
C |
1: 53,512,116 (GRCm39) |
|
probably null |
Het |
Duox2 |
C |
A |
2: 122,110,919 (GRCm39) |
*1518L |
probably null |
Het |
Dym |
A |
G |
18: 75,258,507 (GRCm39) |
I422V |
probably benign |
Het |
Entpd8 |
A |
C |
2: 24,975,144 (GRCm39) |
I492L |
probably benign |
Het |
Fabp12 |
A |
G |
3: 10,317,333 (GRCm39) |
S13P |
probably damaging |
Het |
Fam124b |
A |
G |
1: 80,190,705 (GRCm39) |
I226T |
probably damaging |
Het |
Fer1l6 |
T |
C |
15: 58,455,329 (GRCm39) |
L763P |
probably damaging |
Het |
Git2 |
A |
G |
5: 114,907,676 (GRCm39) |
|
probably null |
Het |
Gltpd2 |
A |
T |
11: 70,410,153 (GRCm39) |
Y37F |
probably benign |
Het |
Gm44511 |
T |
G |
6: 128,797,271 (GRCm39) |
Q72H |
possibly damaging |
Het |
Grid2ip |
A |
T |
5: 143,366,204 (GRCm39) |
T565S |
probably benign |
Het |
Grk6 |
T |
C |
13: 55,606,877 (GRCm39) |
S532P |
possibly damaging |
Het |
Haspin |
A |
T |
11: 73,026,831 (GRCm39) |
F753I |
probably damaging |
Het |
Herpud1 |
T |
A |
8: 95,116,197 (GRCm39) |
S92T |
possibly damaging |
Het |
Heyl |
C |
T |
4: 123,139,768 (GRCm39) |
A109V |
probably damaging |
Het |
Hivep3 |
T |
C |
4: 119,955,304 (GRCm39) |
S1207P |
probably benign |
Het |
Hk1 |
A |
G |
10: 62,105,768 (GRCm39) |
S893P |
probably damaging |
Het |
Itih1 |
C |
A |
14: 30,652,327 (GRCm39) |
V789L |
probably benign |
Het |
Kif12 |
T |
C |
4: 63,090,121 (GRCm39) |
D10G |
possibly damaging |
Het |
Kif16b |
C |
T |
2: 142,554,537 (GRCm39) |
E754K |
possibly damaging |
Het |
Kif20a |
A |
G |
18: 34,760,898 (GRCm39) |
Q191R |
probably benign |
Het |
Lap3 |
A |
G |
5: 45,652,548 (GRCm39) |
D48G |
probably benign |
Het |
Matn3 |
T |
A |
12: 9,002,355 (GRCm39) |
V189E |
probably damaging |
Het |
Mbp |
G |
A |
18: 82,597,067 (GRCm39) |
E143K |
possibly damaging |
Het |
Mrgprd |
A |
G |
7: 144,875,555 (GRCm39) |
H142R |
probably benign |
Het |
Nbea |
A |
T |
3: 55,551,110 (GRCm39) |
C2685S |
possibly damaging |
Het |
Nhsl1 |
A |
C |
10: 18,403,409 (GRCm39) |
I1381L |
possibly damaging |
Het |
Npc1 |
A |
G |
18: 12,346,422 (GRCm39) |
M258T |
probably benign |
Het |
Or2w3 |
T |
C |
11: 58,556,550 (GRCm39) |
L55P |
probably damaging |
Het |
Or7e178 |
T |
A |
9: 20,225,268 (GRCm39) |
N316I |
probably damaging |
Het |
Osbpl10 |
C |
T |
9: 114,807,939 (GRCm39) |
A65V |
unknown |
Het |
Pdia4 |
C |
G |
6: 47,785,149 (GRCm39) |
A73P |
probably benign |
Het |
Plxnb2 |
T |
C |
15: 89,048,471 (GRCm39) |
Y646C |
possibly damaging |
Het |
Pmm1 |
C |
T |
15: 81,839,896 (GRCm39) |
R143H |
probably damaging |
Het |
Pold2 |
T |
C |
11: 5,824,121 (GRCm39) |
D228G |
probably benign |
Het |
Popdc2 |
T |
G |
16: 38,194,508 (GRCm39) |
C310G |
probably benign |
Het |
Prdm10 |
A |
G |
9: 31,268,424 (GRCm39) |
Y791C |
probably benign |
Het |
Psg19 |
C |
T |
7: 18,530,762 (GRCm39) |
V131I |
probably benign |
Het |
Psg19 |
T |
A |
7: 18,531,044 (GRCm39) |
T37S |
probably benign |
Het |
Psme1 |
A |
G |
14: 55,817,271 (GRCm39) |
E39G |
probably damaging |
Het |
Rabep2 |
A |
G |
7: 126,043,719 (GRCm39) |
E472G |
probably damaging |
Het |
Rap1gap |
T |
C |
4: 137,445,309 (GRCm39) |
F297S |
probably damaging |
Het |
Reln |
A |
G |
5: 22,181,613 (GRCm39) |
S1757P |
possibly damaging |
Het |
Rybp |
G |
T |
6: 100,210,074 (GRCm39) |
D95E |
possibly damaging |
Het |
Slc12a8 |
T |
A |
16: 33,466,934 (GRCm39) |
D480E |
probably benign |
Het |
Slc25a1 |
A |
G |
16: 17,745,294 (GRCm39) |
V80A |
probably benign |
Het |
Slc49a4 |
T |
C |
16: 35,570,912 (GRCm39) |
T131A |
probably benign |
Het |
Stab1 |
T |
C |
14: 30,882,226 (GRCm39) |
T490A |
probably benign |
Het |
Stat5b |
A |
T |
11: 100,681,634 (GRCm39) |
I540N |
probably benign |
Het |
Tasor2 |
A |
G |
13: 3,626,659 (GRCm39) |
V1097A |
probably benign |
Het |
Thy1 |
T |
A |
9: 43,957,947 (GRCm39) |
L25Q |
probably damaging |
Het |
Trim30a |
A |
G |
7: 104,084,956 (GRCm39) |
S85P |
probably benign |
Het |
Use1 |
G |
A |
8: 71,819,942 (GRCm39) |
V36I |
probably benign |
Het |
Vmn1r228 |
T |
A |
17: 20,996,778 (GRCm39) |
I247F |
probably damaging |
Het |
Vmn2r13 |
T |
A |
5: 109,304,242 (GRCm39) |
T730S |
possibly damaging |
Het |
Vmn2r9 |
T |
C |
5: 108,992,923 (GRCm39) |
D529G |
possibly damaging |
Het |
Washc5 |
A |
G |
15: 59,217,233 (GRCm39) |
I778T |
possibly damaging |
Het |
Washc5 |
A |
T |
15: 59,233,069 (GRCm39) |
M294K |
probably damaging |
Het |
Wnt8a |
A |
T |
18: 34,680,298 (GRCm39) |
D221V |
probably damaging |
Het |
Zfp616 |
A |
G |
11: 73,976,539 (GRCm39) |
K936R |
probably damaging |
Het |
Zfp618 |
G |
A |
4: 63,012,687 (GRCm39) |
C133Y |
probably damaging |
Het |
Zfp82 |
A |
G |
7: 29,761,714 (GRCm39) |
S56P |
probably damaging |
Het |
Zkscan16 |
T |
A |
4: 58,957,021 (GRCm39) |
D434E |
probably benign |
Het |
|
Other mutations in Slc25a24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00709:Slc25a24
|
APN |
3 |
109,066,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01065:Slc25a24
|
APN |
3 |
109,065,967 (GRCm39) |
unclassified |
probably benign |
|
IGL01769:Slc25a24
|
APN |
3 |
109,056,816 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02803:Slc25a24
|
APN |
3 |
109,062,387 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03349:Slc25a24
|
APN |
3 |
109,056,865 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0318:Slc25a24
|
UTSW |
3 |
109,064,316 (GRCm39) |
missense |
probably benign |
0.00 |
R0448:Slc25a24
|
UTSW |
3 |
109,064,332 (GRCm39) |
splice site |
probably benign |
|
R1554:Slc25a24
|
UTSW |
3 |
109,043,586 (GRCm39) |
missense |
probably benign |
0.02 |
R1564:Slc25a24
|
UTSW |
3 |
109,070,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Slc25a24
|
UTSW |
3 |
109,043,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R1936:Slc25a24
|
UTSW |
3 |
109,043,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4936:Slc25a24
|
UTSW |
3 |
109,070,864 (GRCm39) |
missense |
probably damaging |
0.98 |
R5299:Slc25a24
|
UTSW |
3 |
109,073,668 (GRCm39) |
missense |
probably benign |
0.03 |
R6480:Slc25a24
|
UTSW |
3 |
109,043,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6748:Slc25a24
|
UTSW |
3 |
109,056,823 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7269:Slc25a24
|
UTSW |
3 |
109,065,960 (GRCm39) |
missense |
probably null |
0.99 |
R7483:Slc25a24
|
UTSW |
3 |
109,066,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Slc25a24
|
UTSW |
3 |
109,065,878 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9017:Slc25a24
|
UTSW |
3 |
109,062,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9178:Slc25a24
|
UTSW |
3 |
109,064,268 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9258:Slc25a24
|
UTSW |
3 |
109,066,751 (GRCm39) |
missense |
probably damaging |
1.00 |
|