Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
A |
10: 100,609,256 |
|
probably null |
Het |
9030624J02Rik |
T |
C |
7: 118,773,092 |
S290P |
probably damaging |
Het |
9130011E15Rik |
A |
G |
19: 45,965,249 |
I195T |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,778,781 |
|
probably benign |
Het |
Akt2 |
T |
C |
7: 27,637,012 |
|
probably null |
Het |
Aldh1a7 |
A |
T |
19: 20,708,178 |
L336Q |
possibly damaging |
Het |
Ank2 |
T |
C |
3: 126,946,392 |
|
probably benign |
Het |
Ank3 |
C |
T |
10: 69,999,379 |
T680M |
probably damaging |
Het |
Apeh |
T |
C |
9: 108,094,271 |
E59G |
possibly damaging |
Het |
Arl8a |
G |
C |
1: 135,154,468 |
E145Q |
probably benign |
Het |
Armc8 |
C |
T |
9: 99,483,965 |
|
probably null |
Het |
Arsj |
T |
C |
3: 126,365,000 |
L76P |
probably damaging |
Het |
Atp2b1 |
C |
T |
10: 98,987,310 |
T244I |
probably damaging |
Het |
Bcl6 |
A |
T |
16: 23,974,861 |
L112Q |
probably damaging |
Het |
Bfsp1 |
T |
A |
2: 143,826,923 |
T579S |
possibly damaging |
Het |
Btaf1 |
C |
A |
19: 37,004,469 |
T1633K |
probably benign |
Het |
Cacng8 |
A |
G |
7: 3,415,303 |
S324G |
probably benign |
Het |
Cd2ap |
A |
T |
17: 42,798,599 |
L623Q |
probably damaging |
Het |
Cerkl |
T |
C |
2: 79,341,378 |
I379V |
probably benign |
Het |
Cndp2 |
T |
A |
18: 84,669,945 |
H307L |
possibly damaging |
Het |
Derl1 |
A |
G |
15: 57,879,047 |
|
probably null |
Het |
Dixdc1 |
T |
A |
9: 50,682,564 |
R254S |
probably benign |
Het |
Dopey2 |
T |
A |
16: 93,777,490 |
D30E |
probably benign |
Het |
Duox2 |
T |
G |
2: 122,280,453 |
H1513P |
probably damaging |
Het |
Dyrk1a |
G |
A |
16: 94,686,568 |
V546I |
probably benign |
Het |
E130308A19Rik |
A |
C |
4: 59,719,991 |
K508Q |
probably damaging |
Het |
Emc8 |
A |
T |
8: 120,659,051 |
V108E |
probably benign |
Het |
Epb41l1 |
A |
G |
2: 156,529,402 |
T720A |
probably benign |
Het |
Fam126b |
T |
A |
1: 58,535,537 |
M282L |
probably benign |
Het |
Fam71b |
G |
A |
11: 46,407,408 |
S513N |
|
Het |
Fcgr4 |
T |
A |
1: 171,020,088 |
M85K |
probably benign |
Het |
Fem1b |
T |
A |
9: 62,797,028 |
I317F |
probably damaging |
Het |
Focad |
A |
G |
4: 88,124,637 |
E36G |
probably benign |
Het |
Fryl |
C |
T |
5: 73,055,608 |
E2275K |
probably benign |
Het |
Galnt11 |
T |
C |
5: 25,258,813 |
I361T |
probably damaging |
Het |
Gatad2a |
A |
T |
8: 69,917,994 |
N114K |
probably damaging |
Het |
Gcnt2 |
CTAATG |
C |
13: 40,887,556 |
|
probably null |
Het |
Gm884 |
T |
A |
11: 103,615,812 |
|
probably benign |
Het |
Gramd1a |
A |
G |
7: 31,132,756 |
|
probably null |
Het |
Gsn |
T |
A |
2: 35,292,599 |
W187R |
probably damaging |
Het |
Hoxc12 |
G |
A |
15: 102,938,360 |
G229D |
probably damaging |
Het |
Ints14 |
T |
C |
9: 64,964,545 |
V55A |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,698,365 |
L528P |
probably benign |
Het |
Klf1 |
C |
T |
8: 84,902,750 |
S68F |
possibly damaging |
Het |
Kmt2e |
A |
G |
5: 23,478,743 |
E333G |
probably null |
Het |
Krt39 |
A |
C |
11: 99,521,236 |
V8G |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,738,337 |
I312T |
probably benign |
Het |
Lrp1b |
T |
C |
2: 41,112,342 |
D2001G |
possibly damaging |
Het |
Lrrc71 |
T |
C |
3: 87,748,386 |
T27A |
probably benign |
Het |
Lrrcc1 |
T |
C |
3: 14,563,009 |
V958A |
possibly damaging |
Het |
Mrgpra3 |
G |
T |
7: 47,590,090 |
N29K |
possibly damaging |
Het |
Myl1 |
T |
C |
1: 66,930,236 |
N79S |
probably damaging |
Het |
Naip2 |
A |
T |
13: 100,155,021 |
D1136E |
probably benign |
Het |
Nat10 |
T |
C |
2: 103,754,108 |
N108S |
probably benign |
Het |
Ncald |
A |
T |
15: 37,368,878 |
S178T |
probably benign |
Het |
Ndufs2 |
T |
C |
1: 171,238,308 |
D256G |
probably benign |
Het |
Nek5 |
T |
C |
8: 22,107,723 |
N280S |
probably benign |
Het |
Olfr1167 |
T |
A |
2: 88,149,125 |
D298V |
probably damaging |
Het |
Olfr995 |
A |
G |
2: 85,438,430 |
S243P |
probably damaging |
Het |
Parp1 |
G |
T |
1: 180,598,252 |
K849N |
possibly damaging |
Het |
Pcdhb4 |
T |
A |
18: 37,308,782 |
C382S |
possibly damaging |
Het |
Plce1 |
A |
G |
19: 38,739,357 |
N1520S |
probably damaging |
Het |
Plcg2 |
G |
A |
8: 117,596,306 |
R700H |
probably benign |
Het |
Popdc2 |
A |
T |
16: 38,362,811 |
Y52F |
probably damaging |
Het |
Prrx1 |
T |
A |
1: 163,248,338 |
M220L |
probably benign |
Het |
Pspc1 |
A |
C |
14: 56,758,628 |
|
probably null |
Het |
Ptchd1 |
T |
A |
X: 155,574,712 |
Y499F |
probably damaging |
Het |
Ptpn20 |
A |
G |
14: 33,614,435 |
*44W |
probably null |
Het |
Qars |
T |
A |
9: 108,514,777 |
V83E |
probably damaging |
Het |
Rrh |
T |
C |
3: 129,815,693 |
E55G |
possibly damaging |
Het |
Sash1 |
C |
A |
10: 8,730,083 |
E848* |
probably null |
Het |
Sds |
A |
T |
5: 120,480,847 |
K125M |
possibly damaging |
Het |
Serpinf2 |
A |
T |
11: 75,438,418 |
|
probably benign |
Het |
Sh2b2 |
G |
A |
5: 136,218,885 |
T604I |
probably benign |
Het |
Smug1 |
A |
G |
15: 103,155,942 |
L184P |
probably damaging |
Het |
Spatc1 |
A |
G |
15: 76,283,880 |
T180A |
probably benign |
Het |
Ssr1 |
A |
T |
13: 37,994,025 |
L20Q |
probably null |
Het |
Supt4a |
A |
G |
11: 87,743,258 |
E100G |
probably damaging |
Het |
Tbx1 |
G |
T |
16: 18,586,801 |
P38T |
unknown |
Het |
Tcl1 |
T |
C |
12: 105,217,601 |
|
probably benign |
Het |
Teddm2 |
T |
C |
1: 153,850,574 |
I132V |
probably benign |
Het |
Tmem131 |
C |
T |
1: 36,792,973 |
G1861E |
possibly damaging |
Het |
Tpr |
A |
T |
1: 150,423,607 |
H1186L |
probably benign |
Het |
Trim34b |
A |
T |
7: 104,329,536 |
|
probably benign |
Het |
Trpm2 |
T |
C |
10: 77,912,592 |
M1415V |
probably benign |
Het |
Ttll12 |
A |
G |
15: 83,586,885 |
F264S |
probably benign |
Het |
Vmn2r59 |
T |
C |
7: 42,046,220 |
E256G |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,326,410 |
H848L |
probably benign |
Het |
Wdr70 |
T |
C |
15: 7,884,374 |
D598G |
possibly damaging |
Het |
Ybey |
T |
C |
10: 76,468,363 |
S2G |
possibly damaging |
Het |
Zfp346 |
A |
T |
13: 55,132,387 |
Q308L |
probably benign |
Het |
Zfp872 |
C |
T |
9: 22,200,560 |
P445L |
probably benign |
Het |
|