Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
G |
A |
19: 3,767,192 (GRCm39) |
D260N |
probably benign |
Het |
Ankef1 |
A |
T |
2: 136,392,078 (GRCm39) |
K422N |
possibly damaging |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Aqp6 |
A |
T |
15: 99,502,188 (GRCm39) |
*294C |
probably null |
Het |
Baz2a |
T |
A |
10: 127,944,877 (GRCm39) |
M38K |
possibly damaging |
Het |
Bcl2l14 |
A |
G |
6: 134,404,265 (GRCm39) |
D151G |
probably damaging |
Het |
Cabp5 |
T |
A |
7: 13,132,267 (GRCm39) |
L12* |
probably null |
Het |
Cachd1 |
T |
C |
4: 100,845,795 (GRCm39) |
V993A |
possibly damaging |
Het |
Cd44 |
G |
A |
2: 102,661,728 (GRCm39) |
T306I |
probably damaging |
Het |
Cdc20 |
A |
T |
4: 118,294,253 (GRCm39) |
N22K |
probably benign |
Het |
Cdc6 |
T |
A |
11: 98,807,807 (GRCm39) |
D433E |
possibly damaging |
Het |
Clhc1 |
A |
G |
11: 29,503,725 (GRCm39) |
D47G |
probably damaging |
Het |
Csf2 |
T |
C |
11: 54,139,389 (GRCm39) |
K65E |
probably benign |
Het |
Cul9 |
T |
C |
17: 46,819,473 (GRCm39) |
E2005G |
probably damaging |
Het |
Dclk3 |
G |
T |
9: 111,296,888 (GRCm39) |
R144L |
possibly damaging |
Het |
Dcpp2 |
C |
T |
17: 24,119,516 (GRCm39) |
T110I |
probably damaging |
Het |
Disp1 |
A |
T |
1: 182,868,038 (GRCm39) |
F1461I |
possibly damaging |
Het |
Dnah1 |
C |
T |
14: 31,016,831 (GRCm39) |
G1562D |
probably damaging |
Het |
Exoc3l2 |
C |
A |
7: 19,229,284 (GRCm39) |
P234Q |
probably damaging |
Het |
F2rl2 |
T |
C |
13: 95,838,047 (GRCm39) |
V364A |
probably benign |
Het |
Fam151a |
T |
C |
4: 106,602,876 (GRCm39) |
L265P |
probably damaging |
Het |
Fam151b |
T |
A |
13: 92,586,674 (GRCm39) |
Q253L |
probably benign |
Het |
Fat1 |
G |
A |
8: 45,406,281 (GRCm39) |
V1011M |
probably benign |
Het |
Fbxo6 |
G |
A |
4: 148,230,441 (GRCm39) |
R274* |
probably null |
Het |
Fgd4 |
G |
T |
16: 16,302,337 (GRCm39) |
Q73K |
probably benign |
Het |
Fth1 |
A |
G |
19: 9,962,217 (GRCm39) |
T154A |
probably benign |
Het |
Hgs |
C |
A |
11: 120,370,866 (GRCm39) |
H572Q |
probably benign |
Het |
Kcnk10 |
G |
A |
12: 98,456,207 (GRCm39) |
T208I |
probably damaging |
Het |
Kdm5b |
G |
A |
1: 134,552,635 (GRCm39) |
V1204M |
probably damaging |
Het |
Keg1 |
A |
C |
19: 12,696,185 (GRCm39) |
H166P |
probably damaging |
Het |
Kifap3 |
A |
T |
1: 163,653,428 (GRCm39) |
N338I |
possibly damaging |
Het |
Llcfc1 |
A |
T |
6: 41,662,218 (GRCm39) |
D74V |
probably damaging |
Het |
Lman2 |
A |
G |
13: 55,499,218 (GRCm39) |
V219A |
possibly damaging |
Het |
Mettl25 |
A |
G |
10: 105,662,451 (GRCm39) |
I173T |
possibly damaging |
Het |
Mov10 |
G |
T |
3: 104,711,862 (GRCm39) |
P170Q |
probably damaging |
Het |
Mtif2 |
G |
T |
11: 29,486,847 (GRCm39) |
A286S |
probably damaging |
Het |
Mtmr10 |
A |
G |
7: 63,963,997 (GRCm39) |
Y244C |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,987,414 (GRCm39) |
C359S |
probably damaging |
Het |
Nbr1 |
C |
T |
11: 101,463,667 (GRCm39) |
T633I |
probably benign |
Het |
Nepn |
A |
T |
10: 52,276,512 (GRCm39) |
T22S |
probably damaging |
Het |
Nup214 |
C |
T |
2: 31,924,478 (GRCm39) |
S1669F |
probably damaging |
Het |
Oacyl |
T |
A |
18: 65,871,043 (GRCm39) |
L342M |
probably damaging |
Het |
Or2ag17 |
A |
G |
7: 106,389,540 (GRCm39) |
F223L |
probably benign |
Het |
Or52b2 |
T |
A |
7: 104,986,463 (GRCm39) |
R153S |
probably damaging |
Het |
Or6c205 |
T |
A |
10: 129,087,012 (GRCm39) |
I203N |
possibly damaging |
Het |
Or7e176 |
G |
A |
9: 20,172,020 (GRCm39) |
V295I |
possibly damaging |
Het |
Oxnad1 |
T |
C |
14: 31,821,590 (GRCm39) |
|
probably null |
Het |
Pard3b |
A |
T |
1: 62,205,526 (GRCm39) |
D440V |
probably damaging |
Het |
Pou3f2 |
T |
G |
4: 22,486,960 (GRCm39) |
D391A |
possibly damaging |
Het |
Ptprk |
T |
C |
10: 28,139,512 (GRCm39) |
V79A |
probably benign |
Het |
Rwdd2a |
A |
G |
9: 86,456,331 (GRCm39) |
D169G |
probably damaging |
Het |
Scn3b |
A |
C |
9: 40,190,792 (GRCm39) |
D74A |
probably damaging |
Het |
Setbp1 |
C |
T |
18: 79,130,050 (GRCm39) |
D61N |
probably damaging |
Het |
Setx |
T |
A |
2: 29,053,004 (GRCm39) |
D2089E |
probably damaging |
Het |
Vmn2r69 |
C |
G |
7: 85,056,082 (GRCm39) |
W685C |
probably damaging |
Het |
Vps8 |
A |
G |
16: 21,400,348 (GRCm39) |
Q1272R |
probably benign |
Het |
Wnk4 |
T |
C |
11: 101,160,462 (GRCm39) |
F699L |
probably damaging |
Het |
Zfp616 |
T |
A |
11: 73,974,803 (GRCm39) |
N448K |
possibly damaging |
Het |
Zfp618 |
C |
A |
4: 63,033,685 (GRCm39) |
D307E |
possibly damaging |
Het |
Zfp687 |
A |
G |
3: 94,914,844 (GRCm39) |
F1219S |
probably damaging |
Het |
Zfpm2 |
T |
A |
15: 40,962,687 (GRCm39) |
D248E |
probably damaging |
Het |
|
Other mutations in Ecpas |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00799:Ecpas
|
APN |
4 |
58,828,047 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01145:Ecpas
|
APN |
4 |
58,811,501 (GRCm39) |
missense |
probably null |
0.08 |
IGL01371:Ecpas
|
APN |
4 |
58,809,718 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01445:Ecpas
|
APN |
4 |
58,833,988 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01452:Ecpas
|
APN |
4 |
58,836,181 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01626:Ecpas
|
APN |
4 |
58,832,814 (GRCm39) |
splice site |
probably benign |
|
IGL01672:Ecpas
|
APN |
4 |
58,814,041 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01943:Ecpas
|
APN |
4 |
58,849,937 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01944:Ecpas
|
APN |
4 |
58,861,544 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02190:Ecpas
|
APN |
4 |
58,800,190 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02272:Ecpas
|
APN |
4 |
58,811,731 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02435:Ecpas
|
APN |
4 |
58,830,325 (GRCm39) |
splice site |
probably benign |
|
IGL02516:Ecpas
|
APN |
4 |
58,877,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Ecpas
|
APN |
4 |
58,805,534 (GRCm39) |
splice site |
probably benign |
|
IGL02709:Ecpas
|
APN |
4 |
58,872,699 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02742:Ecpas
|
APN |
4 |
58,840,757 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02812:Ecpas
|
APN |
4 |
58,864,343 (GRCm39) |
splice site |
probably benign |
|
IGL02828:Ecpas
|
APN |
4 |
58,875,512 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL03130:Ecpas
|
APN |
4 |
58,800,288 (GRCm39) |
missense |
probably benign |
|
IGL03179:Ecpas
|
APN |
4 |
58,832,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03237:Ecpas
|
APN |
4 |
58,810,668 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03344:Ecpas
|
APN |
4 |
58,828,538 (GRCm39) |
missense |
probably damaging |
1.00 |
boone
|
UTSW |
4 |
58,877,157 (GRCm39) |
missense |
probably damaging |
1.00 |
Crockett
|
UTSW |
4 |
58,879,100 (GRCm39) |
missense |
probably damaging |
1.00 |
frontiersman
|
UTSW |
4 |
58,832,753 (GRCm39) |
missense |
probably benign |
|
BB006:Ecpas
|
UTSW |
4 |
58,869,554 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Ecpas
|
UTSW |
4 |
58,869,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Ecpas
|
UTSW |
4 |
58,832,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Ecpas
|
UTSW |
4 |
58,832,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0313:Ecpas
|
UTSW |
4 |
58,811,892 (GRCm39) |
missense |
probably benign |
0.11 |
R0399:Ecpas
|
UTSW |
4 |
58,827,047 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0487:Ecpas
|
UTSW |
4 |
58,819,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Ecpas
|
UTSW |
4 |
58,864,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0705:Ecpas
|
UTSW |
4 |
58,885,366 (GRCm39) |
critical splice donor site |
probably null |
|
R0847:Ecpas
|
UTSW |
4 |
58,841,439 (GRCm39) |
missense |
probably benign |
0.14 |
R1467:Ecpas
|
UTSW |
4 |
58,832,753 (GRCm39) |
missense |
probably benign |
|
R1467:Ecpas
|
UTSW |
4 |
58,832,753 (GRCm39) |
missense |
probably benign |
|
R1529:Ecpas
|
UTSW |
4 |
58,832,701 (GRCm39) |
splice site |
probably null |
|
R1771:Ecpas
|
UTSW |
4 |
58,879,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R1776:Ecpas
|
UTSW |
4 |
58,879,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Ecpas
|
UTSW |
4 |
58,805,539 (GRCm39) |
critical splice donor site |
probably null |
|
R1864:Ecpas
|
UTSW |
4 |
58,849,942 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2029:Ecpas
|
UTSW |
4 |
58,844,165 (GRCm39) |
nonsense |
probably null |
|
R2061:Ecpas
|
UTSW |
4 |
58,824,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Ecpas
|
UTSW |
4 |
58,833,978 (GRCm39) |
missense |
probably benign |
|
R2266:Ecpas
|
UTSW |
4 |
58,830,332 (GRCm39) |
critical splice donor site |
probably null |
|
R2889:Ecpas
|
UTSW |
4 |
58,836,165 (GRCm39) |
missense |
probably benign |
|
R2902:Ecpas
|
UTSW |
4 |
58,809,691 (GRCm39) |
missense |
probably benign |
0.31 |
R2903:Ecpas
|
UTSW |
4 |
58,828,622 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2925:Ecpas
|
UTSW |
4 |
58,833,928 (GRCm39) |
nonsense |
probably null |
|
R4151:Ecpas
|
UTSW |
4 |
58,836,254 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4225:Ecpas
|
UTSW |
4 |
58,847,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4486:Ecpas
|
UTSW |
4 |
58,820,086 (GRCm39) |
intron |
probably benign |
|
R4576:Ecpas
|
UTSW |
4 |
58,834,708 (GRCm39) |
intron |
probably benign |
|
R4580:Ecpas
|
UTSW |
4 |
58,840,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R4654:Ecpas
|
UTSW |
4 |
58,834,523 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4688:Ecpas
|
UTSW |
4 |
58,840,757 (GRCm39) |
missense |
probably damaging |
0.96 |
R4726:Ecpas
|
UTSW |
4 |
58,844,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Ecpas
|
UTSW |
4 |
58,850,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R4928:Ecpas
|
UTSW |
4 |
58,827,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R5098:Ecpas
|
UTSW |
4 |
58,877,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R5284:Ecpas
|
UTSW |
4 |
58,836,172 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5375:Ecpas
|
UTSW |
4 |
58,809,401 (GRCm39) |
nonsense |
probably null |
|
R5382:Ecpas
|
UTSW |
4 |
58,850,934 (GRCm39) |
missense |
probably benign |
0.38 |
R5487:Ecpas
|
UTSW |
4 |
58,809,421 (GRCm39) |
missense |
probably benign |
0.22 |
R5703:Ecpas
|
UTSW |
4 |
58,877,171 (GRCm39) |
splice site |
probably null |
|
R5761:Ecpas
|
UTSW |
4 |
58,853,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R5791:Ecpas
|
UTSW |
4 |
58,822,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R5791:Ecpas
|
UTSW |
4 |
58,814,027 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5928:Ecpas
|
UTSW |
4 |
58,849,948 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6062:Ecpas
|
UTSW |
4 |
58,826,453 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6246:Ecpas
|
UTSW |
4 |
58,811,365 (GRCm39) |
splice site |
probably null |
|
R6298:Ecpas
|
UTSW |
4 |
58,877,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Ecpas
|
UTSW |
4 |
58,827,068 (GRCm39) |
missense |
probably benign |
0.34 |
R6478:Ecpas
|
UTSW |
4 |
58,810,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R6707:Ecpas
|
UTSW |
4 |
58,879,101 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6846:Ecpas
|
UTSW |
4 |
58,814,081 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6857:Ecpas
|
UTSW |
4 |
58,814,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6951:Ecpas
|
UTSW |
4 |
58,853,114 (GRCm39) |
critical splice donor site |
probably null |
|
R7088:Ecpas
|
UTSW |
4 |
58,849,766 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7302:Ecpas
|
UTSW |
4 |
58,834,593 (GRCm39) |
missense |
probably benign |
0.43 |
R7337:Ecpas
|
UTSW |
4 |
58,827,047 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7341:Ecpas
|
UTSW |
4 |
58,809,415 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7344:Ecpas
|
UTSW |
4 |
58,824,770 (GRCm39) |
missense |
probably benign |
0.08 |
R7525:Ecpas
|
UTSW |
4 |
58,847,038 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7530:Ecpas
|
UTSW |
4 |
58,815,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R7533:Ecpas
|
UTSW |
4 |
58,809,411 (GRCm39) |
missense |
probably benign |
0.12 |
R7557:Ecpas
|
UTSW |
4 |
58,849,691 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7698:Ecpas
|
UTSW |
4 |
58,832,660 (GRCm39) |
missense |
unknown |
|
R7793:Ecpas
|
UTSW |
4 |
58,853,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Ecpas
|
UTSW |
4 |
58,828,593 (GRCm39) |
missense |
probably benign |
|
R7894:Ecpas
|
UTSW |
4 |
58,853,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R7929:Ecpas
|
UTSW |
4 |
58,869,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Ecpas
|
UTSW |
4 |
58,832,681 (GRCm39) |
missense |
unknown |
|
R8082:Ecpas
|
UTSW |
4 |
58,807,852 (GRCm39) |
missense |
probably benign |
0.00 |
R8175:Ecpas
|
UTSW |
4 |
58,872,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Ecpas
|
UTSW |
4 |
58,872,587 (GRCm39) |
critical splice donor site |
probably null |
|
R8326:Ecpas
|
UTSW |
4 |
58,847,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R8459:Ecpas
|
UTSW |
4 |
58,821,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Ecpas
|
UTSW |
4 |
58,834,515 (GRCm39) |
missense |
probably benign |
0.31 |
R8747:Ecpas
|
UTSW |
4 |
58,828,632 (GRCm39) |
missense |
probably damaging |
0.98 |
R8981:Ecpas
|
UTSW |
4 |
58,801,796 (GRCm39) |
missense |
probably benign |
|
R9206:Ecpas
|
UTSW |
4 |
58,875,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Ecpas
|
UTSW |
4 |
58,875,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Ecpas
|
UTSW |
4 |
58,875,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R9249:Ecpas
|
UTSW |
4 |
58,869,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R9355:Ecpas
|
UTSW |
4 |
58,844,114 (GRCm39) |
missense |
probably benign |
0.23 |
R9534:Ecpas
|
UTSW |
4 |
58,807,867 (GRCm39) |
missense |
probably benign |
|
R9555:Ecpas
|
UTSW |
4 |
58,879,083 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9570:Ecpas
|
UTSW |
4 |
58,832,796 (GRCm39) |
nonsense |
probably null |
|
R9673:Ecpas
|
UTSW |
4 |
58,822,060 (GRCm39) |
missense |
probably benign |
|
R9707:Ecpas
|
UTSW |
4 |
58,824,816 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9721:Ecpas
|
UTSW |
4 |
58,850,938 (GRCm39) |
missense |
probably benign |
0.39 |
X0060:Ecpas
|
UTSW |
4 |
58,840,752 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Ecpas
|
UTSW |
4 |
58,861,614 (GRCm39) |
missense |
probably damaging |
0.99 |
|