Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700062C07Rik |
A |
G |
18: 24,606,013 (GRCm39) |
N36S |
possibly damaging |
Het |
Alox12b |
G |
A |
11: 69,054,431 (GRCm39) |
V250I |
probably benign |
Het |
Armt1 |
T |
C |
10: 4,389,687 (GRCm39) |
F115L |
probably benign |
Het |
Cdh9 |
T |
C |
15: 16,850,474 (GRCm39) |
F536L |
probably benign |
Het |
Fbxo25 |
T |
C |
8: 13,989,617 (GRCm39) |
S355P |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,123,123 (GRCm39) |
K271R |
probably null |
Het |
Gapt |
C |
A |
13: 110,490,289 (GRCm39) |
V125F |
probably damaging |
Het |
Gucd1 |
A |
T |
10: 75,345,662 (GRCm39) |
V131E |
probably damaging |
Het |
Hivep2 |
A |
G |
10: 14,007,299 (GRCm39) |
E1299G |
probably damaging |
Het |
Hnf4g |
A |
G |
3: 3,717,909 (GRCm39) |
D342G |
possibly damaging |
Het |
Kmt2b |
C |
T |
7: 30,273,489 (GRCm39) |
R2349H |
probably benign |
Het |
Lama5 |
C |
T |
2: 179,822,220 (GRCm39) |
R2896Q |
possibly damaging |
Het |
Moxd2 |
A |
C |
6: 40,855,933 (GRCm39) |
I552S |
probably damaging |
Het |
Nkx1-2 |
TGGTGAGAGGGGGCCGCCTTGGCCCCG |
TG |
7: 132,201,209 (GRCm39) |
|
probably null |
Het |
Onecut3 |
A |
G |
10: 80,349,963 (GRCm39) |
T486A |
possibly damaging |
Het |
Or8g36 |
A |
G |
9: 39,422,899 (GRCm39) |
V39A |
probably benign |
Het |
Pik3cb |
T |
C |
9: 98,983,229 (GRCm39) |
|
probably null |
Het |
Pirb |
A |
G |
7: 3,722,297 (GRCm39) |
F182S |
probably damaging |
Het |
Rev1 |
C |
T |
1: 38,146,729 (GRCm39) |
R34H |
possibly damaging |
Het |
Satl1 |
A |
G |
X: 111,316,033 (GRCm39) |
S141P |
probably benign |
Het |
Setx |
GTGGCT |
GT |
2: 29,044,073 (GRCm39) |
1814 |
probably null |
Het |
Snx8 |
A |
G |
5: 140,341,800 (GRCm39) |
L121P |
probably damaging |
Het |
Tep1 |
T |
C |
14: 51,100,351 (GRCm39) |
H389R |
possibly damaging |
Het |
Tnfrsf1b |
G |
A |
4: 144,942,535 (GRCm39) |
A416V |
probably benign |
Het |
Ust |
A |
T |
10: 8,393,982 (GRCm39) |
L61Q |
possibly damaging |
Het |
Vmn2r101 |
A |
T |
17: 19,809,376 (GRCm39) |
K168N |
probably damaging |
Het |
|
Other mutations in Hecw2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Hecw2
|
APN |
1 |
53,869,896 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00338:Hecw2
|
APN |
1 |
53,867,040 (GRCm39) |
splice site |
probably benign |
|
IGL00530:Hecw2
|
APN |
1 |
53,892,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01343:Hecw2
|
APN |
1 |
53,866,135 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01503:Hecw2
|
APN |
1 |
53,866,120 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01989:Hecw2
|
APN |
1 |
53,879,951 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02016:Hecw2
|
APN |
1 |
53,870,702 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02052:Hecw2
|
APN |
1 |
53,965,670 (GRCm39) |
missense |
probably benign |
|
IGL02085:Hecw2
|
APN |
1 |
53,981,961 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02302:Hecw2
|
APN |
1 |
53,972,407 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02310:Hecw2
|
APN |
1 |
53,963,075 (GRCm39) |
missense |
probably null |
0.38 |
IGL02388:Hecw2
|
APN |
1 |
53,964,858 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02499:Hecw2
|
APN |
1 |
53,965,647 (GRCm39) |
missense |
probably benign |
|
IGL02695:Hecw2
|
APN |
1 |
53,965,368 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02732:Hecw2
|
APN |
1 |
53,965,847 (GRCm39) |
splice site |
probably benign |
|
IGL03100:Hecw2
|
APN |
1 |
53,870,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03175:Hecw2
|
APN |
1 |
53,965,416 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03253:Hecw2
|
APN |
1 |
53,871,875 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03356:Hecw2
|
APN |
1 |
53,966,217 (GRCm39) |
splice site |
probably benign |
|
Memoriam
|
UTSW |
1 |
53,965,215 (GRCm39) |
missense |
probably benign |
|
recollect
|
UTSW |
1 |
53,943,581 (GRCm39) |
missense |
possibly damaging |
0.88 |
ANU74:Hecw2
|
UTSW |
1 |
53,964,853 (GRCm39) |
missense |
probably benign |
0.01 |
R0077:Hecw2
|
UTSW |
1 |
53,907,990 (GRCm39) |
splice site |
probably benign |
|
R0133:Hecw2
|
UTSW |
1 |
53,869,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Hecw2
|
UTSW |
1 |
53,965,857 (GRCm39) |
splice site |
probably benign |
|
R1303:Hecw2
|
UTSW |
1 |
54,079,552 (GRCm39) |
missense |
probably benign |
0.00 |
R1460:Hecw2
|
UTSW |
1 |
53,852,404 (GRCm39) |
missense |
probably damaging |
0.96 |
R1524:Hecw2
|
UTSW |
1 |
53,890,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Hecw2
|
UTSW |
1 |
53,965,704 (GRCm39) |
splice site |
probably null |
|
R1828:Hecw2
|
UTSW |
1 |
53,965,182 (GRCm39) |
missense |
probably benign |
|
R2170:Hecw2
|
UTSW |
1 |
53,981,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R2338:Hecw2
|
UTSW |
1 |
53,943,581 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3016:Hecw2
|
UTSW |
1 |
53,869,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R3872:Hecw2
|
UTSW |
1 |
53,871,916 (GRCm39) |
splice site |
probably benign |
|
R3892:Hecw2
|
UTSW |
1 |
53,965,280 (GRCm39) |
missense |
probably benign |
0.01 |
R4086:Hecw2
|
UTSW |
1 |
53,870,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R4247:Hecw2
|
UTSW |
1 |
53,871,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R4249:Hecw2
|
UTSW |
1 |
53,871,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R4545:Hecw2
|
UTSW |
1 |
53,852,381 (GRCm39) |
makesense |
probably null |
|
R4805:Hecw2
|
UTSW |
1 |
53,880,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Hecw2
|
UTSW |
1 |
53,869,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Hecw2
|
UTSW |
1 |
53,990,000 (GRCm39) |
missense |
probably benign |
0.03 |
R4983:Hecw2
|
UTSW |
1 |
53,871,830 (GRCm39) |
missense |
probably benign |
0.42 |
R5168:Hecw2
|
UTSW |
1 |
53,952,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R5482:Hecw2
|
UTSW |
1 |
53,965,360 (GRCm39) |
missense |
probably benign |
0.09 |
R5549:Hecw2
|
UTSW |
1 |
53,964,850 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5623:Hecw2
|
UTSW |
1 |
53,871,782 (GRCm39) |
missense |
probably null |
1.00 |
R5740:Hecw2
|
UTSW |
1 |
53,926,762 (GRCm39) |
missense |
probably benign |
0.12 |
R5919:Hecw2
|
UTSW |
1 |
53,976,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R6058:Hecw2
|
UTSW |
1 |
53,963,135 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6460:Hecw2
|
UTSW |
1 |
53,907,992 (GRCm39) |
splice site |
probably null |
|
R6875:Hecw2
|
UTSW |
1 |
53,976,291 (GRCm39) |
missense |
probably benign |
0.01 |
R7097:Hecw2
|
UTSW |
1 |
53,904,283 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7131:Hecw2
|
UTSW |
1 |
53,904,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7291:Hecw2
|
UTSW |
1 |
53,953,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R7401:Hecw2
|
UTSW |
1 |
53,943,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R7482:Hecw2
|
UTSW |
1 |
54,079,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R7501:Hecw2
|
UTSW |
1 |
53,953,031 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7520:Hecw2
|
UTSW |
1 |
53,965,215 (GRCm39) |
missense |
probably benign |
|
R7611:Hecw2
|
UTSW |
1 |
53,952,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R8184:Hecw2
|
UTSW |
1 |
54,079,546 (GRCm39) |
missense |
probably benign |
0.37 |
R8286:Hecw2
|
UTSW |
1 |
53,879,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R8300:Hecw2
|
UTSW |
1 |
53,926,775 (GRCm39) |
missense |
probably null |
0.07 |
R8354:Hecw2
|
UTSW |
1 |
53,964,467 (GRCm39) |
critical splice donor site |
probably null |
|
R8362:Hecw2
|
UTSW |
1 |
54,079,650 (GRCm39) |
start codon destroyed |
probably null |
0.51 |
R8691:Hecw2
|
UTSW |
1 |
53,904,223 (GRCm39) |
missense |
probably benign |
0.26 |
R8745:Hecw2
|
UTSW |
1 |
53,972,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R8769:Hecw2
|
UTSW |
1 |
53,952,507 (GRCm39) |
missense |
probably benign |
0.00 |
R8830:Hecw2
|
UTSW |
1 |
53,930,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R8842:Hecw2
|
UTSW |
1 |
53,990,033 (GRCm39) |
missense |
|
|
R8874:Hecw2
|
UTSW |
1 |
53,943,608 (GRCm39) |
splice site |
probably benign |
|
R9064:Hecw2
|
UTSW |
1 |
53,866,045 (GRCm39) |
missense |
probably benign |
0.08 |
R9326:Hecw2
|
UTSW |
1 |
54,079,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R9450:Hecw2
|
UTSW |
1 |
53,878,188 (GRCm39) |
nonsense |
probably null |
|
R9486:Hecw2
|
UTSW |
1 |
53,852,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R9763:Hecw2
|
UTSW |
1 |
53,963,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R9766:Hecw2
|
UTSW |
1 |
53,904,287 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Hecw2
|
UTSW |
1 |
53,963,102 (GRCm39) |
missense |
possibly damaging |
0.95 |
|