Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
A |
10: 100,445,118 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
A |
G |
12: 112,745,216 (GRCm39) |
|
probably benign |
Het |
Akt2 |
T |
C |
7: 27,336,437 (GRCm39) |
|
probably null |
Het |
Aldh1a7 |
A |
T |
19: 20,685,542 (GRCm39) |
L336Q |
possibly damaging |
Het |
Ank2 |
T |
C |
3: 126,740,041 (GRCm39) |
|
probably benign |
Het |
Ank3 |
C |
T |
10: 69,835,209 (GRCm39) |
T680M |
probably damaging |
Het |
Apeh |
T |
C |
9: 107,971,470 (GRCm39) |
E59G |
possibly damaging |
Het |
Arl8a |
G |
C |
1: 135,082,206 (GRCm39) |
E145Q |
probably benign |
Het |
Armc8 |
C |
T |
9: 99,366,018 (GRCm39) |
|
probably null |
Het |
Arsj |
T |
C |
3: 126,158,649 (GRCm39) |
L76P |
probably damaging |
Het |
Atp2b1 |
C |
T |
10: 98,823,172 (GRCm39) |
T244I |
probably damaging |
Het |
Bcl6 |
A |
T |
16: 23,793,611 (GRCm39) |
L112Q |
probably damaging |
Het |
Bfsp1 |
T |
A |
2: 143,668,843 (GRCm39) |
T579S |
possibly damaging |
Het |
Btaf1 |
C |
A |
19: 36,981,869 (GRCm39) |
T1633K |
probably benign |
Het |
Cacng8 |
A |
G |
7: 3,463,819 (GRCm39) |
S324G |
probably benign |
Het |
Cd2ap |
A |
T |
17: 43,109,490 (GRCm39) |
L623Q |
probably damaging |
Het |
Cerkl |
T |
C |
2: 79,171,722 (GRCm39) |
I379V |
probably benign |
Het |
Cndp2 |
T |
A |
18: 84,688,070 (GRCm39) |
H307L |
possibly damaging |
Het |
Derl1 |
A |
G |
15: 57,742,443 (GRCm39) |
|
probably null |
Het |
Dixdc1 |
T |
A |
9: 50,593,864 (GRCm39) |
R254S |
probably benign |
Het |
Dop1b |
T |
A |
16: 93,574,378 (GRCm39) |
D30E |
probably benign |
Het |
Duox2 |
T |
G |
2: 122,110,934 (GRCm39) |
H1513P |
probably damaging |
Het |
Dyrk1a |
G |
A |
16: 94,487,427 (GRCm39) |
V546I |
probably benign |
Het |
E130308A19Rik |
A |
C |
4: 59,719,991 (GRCm39) |
K508Q |
probably damaging |
Het |
Emc8 |
A |
T |
8: 121,385,790 (GRCm39) |
V108E |
probably benign |
Het |
Epb41l1 |
A |
G |
2: 156,371,322 (GRCm39) |
T720A |
probably benign |
Het |
Fcgr4 |
T |
A |
1: 170,847,657 (GRCm39) |
M85K |
probably benign |
Het |
Fem1b |
T |
A |
9: 62,704,310 (GRCm39) |
I317F |
probably damaging |
Het |
Focad |
A |
G |
4: 88,042,874 (GRCm39) |
E36G |
probably benign |
Het |
Fryl |
C |
T |
5: 73,212,951 (GRCm39) |
E2275K |
probably benign |
Het |
Galnt11 |
T |
C |
5: 25,463,811 (GRCm39) |
I361T |
probably damaging |
Het |
Garin3 |
G |
A |
11: 46,298,235 (GRCm39) |
S513N |
|
Het |
Gatad2a |
A |
T |
8: 70,370,644 (GRCm39) |
N114K |
probably damaging |
Het |
Gcnt2 |
CTAATG |
C |
13: 41,041,032 (GRCm39) |
|
probably null |
Het |
Gramd1a |
A |
G |
7: 30,832,181 (GRCm39) |
|
probably null |
Het |
Gsn |
T |
A |
2: 35,182,611 (GRCm39) |
W187R |
probably damaging |
Het |
Hoxc12 |
G |
A |
15: 102,846,795 (GRCm39) |
G229D |
probably damaging |
Het |
Hycc2 |
T |
A |
1: 58,574,696 (GRCm39) |
M282L |
probably benign |
Het |
Ints14 |
T |
C |
9: 64,871,827 (GRCm39) |
V55A |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,527,433 (GRCm39) |
L528P |
probably benign |
Het |
Klf1 |
C |
T |
8: 85,629,379 (GRCm39) |
S68F |
possibly damaging |
Het |
Kmt2e |
A |
G |
5: 23,683,741 (GRCm39) |
E333G |
probably null |
Het |
Krt39 |
A |
C |
11: 99,412,062 (GRCm39) |
V8G |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,646,772 (GRCm39) |
I312T |
probably benign |
Het |
Lrp1b |
T |
C |
2: 41,002,354 (GRCm39) |
D2001G |
possibly damaging |
Het |
Lrrc37 |
T |
A |
11: 103,506,638 (GRCm39) |
|
probably benign |
Het |
Lrrc71 |
T |
C |
3: 87,655,693 (GRCm39) |
T27A |
probably benign |
Het |
Lrrcc1 |
T |
C |
3: 14,628,069 (GRCm39) |
V958A |
possibly damaging |
Het |
Med15 |
A |
T |
16: 17,516,019 (GRCm39) |
M1K |
probably null |
Het |
Mrgpra3 |
G |
T |
7: 47,239,838 (GRCm39) |
N29K |
possibly damaging |
Het |
Myl1 |
T |
C |
1: 66,969,395 (GRCm39) |
N79S |
probably damaging |
Het |
Naip2 |
A |
T |
13: 100,291,529 (GRCm39) |
D1136E |
probably benign |
Het |
Nat10 |
T |
C |
2: 103,584,453 (GRCm39) |
N108S |
probably benign |
Het |
Ncald |
A |
T |
15: 37,369,122 (GRCm39) |
S178T |
probably benign |
Het |
Ndufs2 |
T |
C |
1: 171,065,877 (GRCm39) |
D256G |
probably benign |
Het |
Nek5 |
T |
C |
8: 22,597,739 (GRCm39) |
N280S |
probably benign |
Het |
Or5ak25 |
A |
G |
2: 85,268,774 (GRCm39) |
S243P |
probably damaging |
Het |
Or5d39 |
T |
A |
2: 87,979,469 (GRCm39) |
D298V |
probably damaging |
Het |
Parp1 |
G |
T |
1: 180,425,817 (GRCm39) |
K849N |
possibly damaging |
Het |
Pcdhb4 |
T |
A |
18: 37,441,835 (GRCm39) |
C382S |
possibly damaging |
Het |
Plce1 |
A |
G |
19: 38,727,801 (GRCm39) |
N1520S |
probably damaging |
Het |
Plcg2 |
G |
A |
8: 118,323,045 (GRCm39) |
R700H |
probably benign |
Het |
Popdc2 |
A |
T |
16: 38,183,173 (GRCm39) |
Y52F |
probably damaging |
Het |
Prrx1 |
T |
A |
1: 163,075,907 (GRCm39) |
M220L |
probably benign |
Het |
Pspc1 |
A |
C |
14: 56,996,085 (GRCm39) |
|
probably null |
Het |
Ptchd1 |
T |
A |
X: 154,357,708 (GRCm39) |
Y499F |
probably damaging |
Het |
Ptpn20 |
A |
G |
14: 33,336,392 (GRCm39) |
*44W |
probably null |
Het |
Qars1 |
T |
A |
9: 108,391,976 (GRCm39) |
V83E |
probably damaging |
Het |
Rrh |
T |
C |
3: 129,609,342 (GRCm39) |
E55G |
possibly damaging |
Het |
Sash1 |
C |
A |
10: 8,605,847 (GRCm39) |
E848* |
probably null |
Het |
Sds |
A |
T |
5: 120,618,912 (GRCm39) |
K125M |
possibly damaging |
Het |
Serpinf2 |
A |
T |
11: 75,329,244 (GRCm39) |
|
probably benign |
Het |
Sh2b2 |
G |
A |
5: 136,247,739 (GRCm39) |
T604I |
probably benign |
Het |
Smug1 |
A |
G |
15: 103,064,369 (GRCm39) |
L184P |
probably damaging |
Het |
Spatc1 |
A |
G |
15: 76,168,080 (GRCm39) |
T180A |
probably benign |
Het |
Ssr1 |
A |
T |
13: 38,178,001 (GRCm39) |
L20Q |
probably null |
Het |
Supt4a |
A |
G |
11: 87,634,084 (GRCm39) |
E100G |
probably damaging |
Het |
Tbx1 |
G |
T |
16: 18,405,551 (GRCm39) |
P38T |
unknown |
Het |
Tcl1 |
T |
C |
12: 105,183,860 (GRCm39) |
|
probably benign |
Het |
Teddm2 |
T |
C |
1: 153,726,320 (GRCm39) |
I132V |
probably benign |
Het |
Tmem131 |
C |
T |
1: 36,832,054 (GRCm39) |
G1861E |
possibly damaging |
Het |
Tpr |
A |
T |
1: 150,299,358 (GRCm39) |
H1186L |
probably benign |
Het |
Trim34b |
A |
T |
7: 103,978,743 (GRCm39) |
|
probably benign |
Het |
Trpm2 |
T |
C |
10: 77,748,426 (GRCm39) |
M1415V |
probably benign |
Het |
Ttll12 |
A |
G |
15: 83,471,086 (GRCm39) |
F264S |
probably benign |
Het |
Vmn2r59 |
T |
C |
7: 41,695,644 (GRCm39) |
E256G |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,546,672 (GRCm39) |
H848L |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,372,315 (GRCm39) |
S290P |
probably damaging |
Het |
Wdr70 |
T |
C |
15: 7,913,855 (GRCm39) |
D598G |
possibly damaging |
Het |
Ybey |
T |
C |
10: 76,304,197 (GRCm39) |
S2G |
possibly damaging |
Het |
Zfp346 |
A |
T |
13: 55,280,200 (GRCm39) |
Q308L |
probably benign |
Het |
Zfp872 |
C |
T |
9: 22,111,856 (GRCm39) |
P445L |
probably benign |
Het |
|
Other mutations in Armh3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Armh3
|
APN |
19 |
45,928,927 (GRCm39) |
missense |
probably benign |
0.19 |
IGL00788:Armh3
|
APN |
19 |
45,920,789 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01356:Armh3
|
APN |
19 |
45,954,742 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01477:Armh3
|
APN |
19 |
45,967,043 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01660:Armh3
|
APN |
19 |
45,928,915 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02193:Armh3
|
APN |
19 |
45,961,323 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02863:Armh3
|
APN |
19 |
45,946,850 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03108:Armh3
|
APN |
19 |
45,808,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R0035:Armh3
|
UTSW |
19 |
45,879,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0791:Armh3
|
UTSW |
19 |
45,922,307 (GRCm39) |
splice site |
probably null |
|
R0792:Armh3
|
UTSW |
19 |
45,922,307 (GRCm39) |
splice site |
probably null |
|
R1487:Armh3
|
UTSW |
19 |
45,928,882 (GRCm39) |
critical splice donor site |
probably null |
|
R1843:Armh3
|
UTSW |
19 |
45,963,691 (GRCm39) |
missense |
probably benign |
0.17 |
R2061:Armh3
|
UTSW |
19 |
45,967,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Armh3
|
UTSW |
19 |
45,879,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Armh3
|
UTSW |
19 |
45,953,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2073:Armh3
|
UTSW |
19 |
45,953,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2074:Armh3
|
UTSW |
19 |
45,953,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2091:Armh3
|
UTSW |
19 |
45,941,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R2263:Armh3
|
UTSW |
19 |
45,920,788 (GRCm39) |
critical splice donor site |
probably null |
|
R2863:Armh3
|
UTSW |
19 |
45,874,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Armh3
|
UTSW |
19 |
45,963,722 (GRCm39) |
splice site |
probably benign |
|
R3796:Armh3
|
UTSW |
19 |
45,910,049 (GRCm39) |
splice site |
probably benign |
|
R4044:Armh3
|
UTSW |
19 |
45,808,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Armh3
|
UTSW |
19 |
45,948,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Armh3
|
UTSW |
19 |
45,808,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Armh3
|
UTSW |
19 |
45,939,146 (GRCm39) |
missense |
probably benign |
|
R5063:Armh3
|
UTSW |
19 |
45,874,394 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5313:Armh3
|
UTSW |
19 |
45,807,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R5782:Armh3
|
UTSW |
19 |
45,874,466 (GRCm39) |
missense |
probably benign |
0.08 |
R5985:Armh3
|
UTSW |
19 |
45,808,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Armh3
|
UTSW |
19 |
45,834,554 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6379:Armh3
|
UTSW |
19 |
45,910,136 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6674:Armh3
|
UTSW |
19 |
45,963,437 (GRCm39) |
missense |
probably benign |
0.06 |
R6842:Armh3
|
UTSW |
19 |
45,807,416 (GRCm39) |
missense |
probably benign |
0.05 |
R6890:Armh3
|
UTSW |
19 |
45,948,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Armh3
|
UTSW |
19 |
45,953,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R7305:Armh3
|
UTSW |
19 |
45,880,560 (GRCm39) |
missense |
probably benign |
0.35 |
R7411:Armh3
|
UTSW |
19 |
45,953,874 (GRCm39) |
missense |
probably benign |
0.00 |
R7762:Armh3
|
UTSW |
19 |
45,928,882 (GRCm39) |
critical splice donor site |
probably null |
|
R8021:Armh3
|
UTSW |
19 |
45,945,180 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8366:Armh3
|
UTSW |
19 |
45,920,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Armh3
|
UTSW |
19 |
45,945,120 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Armh3
|
UTSW |
19 |
45,920,832 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Armh3
|
UTSW |
19 |
45,807,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|