Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
T |
C |
15: 81,949,748 (GRCm39) |
L1215P |
probably benign |
Het |
Angptl7 |
T |
C |
4: 148,584,601 (GRCm39) |
N49S |
possibly damaging |
Het |
Asns |
A |
G |
6: 7,685,411 (GRCm39) |
|
probably benign |
Het |
Atr |
T |
A |
9: 95,781,194 (GRCm39) |
Y1419* |
probably null |
Het |
Bptf |
A |
T |
11: 106,964,178 (GRCm39) |
I1672N |
probably benign |
Het |
Cgas |
G |
A |
9: 78,341,667 (GRCm39) |
T370I |
probably benign |
Het |
Chd1 |
A |
G |
17: 17,610,315 (GRCm39) |
T490A |
probably damaging |
Het |
Cyfip2 |
A |
T |
11: 46,167,732 (GRCm39) |
C223* |
probably null |
Het |
Ddr1 |
G |
A |
17: 35,994,372 (GRCm39) |
A801V |
probably damaging |
Het |
Dnah12 |
T |
C |
14: 26,430,316 (GRCm39) |
V308A |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,158,926 (GRCm39) |
V703A |
probably damaging |
Het |
Fgd3 |
A |
G |
13: 49,440,802 (GRCm39) |
F210L |
probably damaging |
Het |
Gm6526 |
T |
G |
14: 43,988,262 (GRCm39) |
V171G |
probably damaging |
Het |
Grin3a |
A |
G |
4: 49,702,805 (GRCm39) |
Y894H |
probably damaging |
Het |
Grm3 |
C |
A |
5: 9,561,660 (GRCm39) |
C730F |
probably damaging |
Het |
Hdac4 |
A |
G |
1: 91,886,171 (GRCm39) |
|
probably benign |
Het |
Ints5 |
A |
G |
19: 8,872,959 (GRCm39) |
D306G |
probably benign |
Het |
Mid2 |
T |
A |
X: 139,637,245 (GRCm39) |
I273N |
probably damaging |
Het |
Ndufs2 |
A |
T |
1: 171,066,934 (GRCm39) |
Y114* |
probably null |
Het |
Neu4 |
G |
T |
1: 93,952,213 (GRCm39) |
R194L |
probably damaging |
Het |
Ntng1 |
A |
T |
3: 110,042,829 (GRCm39) |
|
probably null |
Het |
Nub1 |
A |
G |
5: 24,894,392 (GRCm39) |
M1V |
probably null |
Het |
Olfml2a |
A |
G |
2: 38,844,680 (GRCm39) |
T379A |
probably benign |
Het |
Or9e1 |
A |
T |
11: 58,732,338 (GRCm39) |
I133F |
probably benign |
Het |
Pex3 |
G |
T |
10: 13,400,643 (GRCm39) |
Q303K |
probably benign |
Het |
Pmp2 |
A |
T |
3: 10,247,560 (GRCm39) |
I43N |
probably damaging |
Het |
Pnliprp1 |
T |
A |
19: 58,726,601 (GRCm39) |
D319E |
probably benign |
Het |
Rap1gap2 |
A |
T |
11: 74,288,181 (GRCm39) |
|
probably null |
Het |
Rpl15-ps6 |
T |
C |
15: 52,341,368 (GRCm39) |
|
noncoding transcript |
Het |
Rwdd3 |
A |
G |
3: 120,952,679 (GRCm39) |
V104A |
probably damaging |
Het |
Sbf1 |
A |
T |
15: 89,191,775 (GRCm39) |
V157E |
probably damaging |
Het |
Slc4a11 |
T |
A |
2: 130,526,879 (GRCm39) |
I750F |
probably damaging |
Het |
Tcea1 |
G |
A |
1: 4,948,356 (GRCm39) |
|
probably null |
Het |
Ush2a |
A |
T |
1: 188,516,943 (GRCm39) |
M3218L |
probably benign |
Het |
Utp20 |
G |
A |
10: 88,607,715 (GRCm39) |
|
probably benign |
Het |
Zfp493 |
T |
A |
13: 67,935,089 (GRCm39) |
Y347* |
probably null |
Het |
Zswim6 |
T |
C |
13: 107,880,637 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Habp4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00924:Habp4
|
APN |
13 |
64,321,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Habp4
|
UTSW |
13 |
64,332,420 (GRCm39) |
missense |
probably benign |
0.09 |
R2012:Habp4
|
UTSW |
13 |
64,317,995 (GRCm39) |
splice site |
probably null |
|
R2884:Habp4
|
UTSW |
13 |
64,330,080 (GRCm39) |
missense |
probably benign |
0.40 |
R3800:Habp4
|
UTSW |
13 |
64,321,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R6404:Habp4
|
UTSW |
13 |
64,330,000 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7029:Habp4
|
UTSW |
13 |
64,309,939 (GRCm39) |
missense |
probably benign |
0.08 |
R7985:Habp4
|
UTSW |
13 |
64,323,860 (GRCm39) |
missense |
probably benign |
0.05 |
R8025:Habp4
|
UTSW |
13 |
64,322,645 (GRCm39) |
missense |
probably benign |
0.08 |
R8046:Habp4
|
UTSW |
13 |
64,322,656 (GRCm39) |
missense |
probably benign |
0.11 |
R8138:Habp4
|
UTSW |
13 |
64,323,884 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8314:Habp4
|
UTSW |
13 |
64,332,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R9571:Habp4
|
UTSW |
13 |
64,322,615 (GRCm39) |
missense |
probably benign |
0.02 |
RF038:Habp4
|
UTSW |
13 |
64,309,976 (GRCm39) |
small deletion |
probably benign |
|
Z1177:Habp4
|
UTSW |
13 |
64,321,884 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Habp4
|
UTSW |
13 |
64,321,882 (GRCm39) |
missense |
probably benign |
0.00 |
|