Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
G |
T |
19: 31,895,495 (GRCm39) |
A193S |
probably damaging |
Het |
Adcy4 |
T |
C |
14: 56,006,627 (GRCm39) |
T1069A |
probably benign |
Het |
Arg2 |
A |
T |
12: 79,197,533 (GRCm39) |
I184F |
probably benign |
Het |
Asb18 |
G |
A |
1: 89,942,113 (GRCm39) |
P63S |
probably damaging |
Het |
Cep85 |
T |
C |
4: 133,883,634 (GRCm39) |
H85R |
possibly damaging |
Het |
Chfr |
A |
G |
5: 110,291,413 (GRCm39) |
|
probably null |
Het |
Cog2 |
A |
G |
8: 125,256,698 (GRCm39) |
N148S |
probably benign |
Het |
Csgalnact1 |
T |
C |
8: 68,913,720 (GRCm39) |
T162A |
probably damaging |
Het |
Ddi1 |
C |
T |
9: 6,266,183 (GRCm39) |
G62D |
possibly damaging |
Het |
Dhx33 |
T |
C |
11: 70,878,066 (GRCm39) |
Y435C |
probably damaging |
Het |
Dsc3 |
A |
T |
18: 20,098,885 (GRCm39) |
C765S |
probably benign |
Het |
Egfem1 |
T |
A |
3: 29,722,529 (GRCm39) |
D362E |
probably benign |
Het |
Gm28040 |
A |
T |
1: 133,247,069 (GRCm39) |
I26F |
possibly damaging |
Het |
Gm28778 |
T |
C |
1: 53,338,202 (GRCm39) |
M22T |
probably benign |
Het |
Hipk2 |
A |
G |
6: 38,680,436 (GRCm39) |
I968T |
possibly damaging |
Het |
Hlx |
T |
G |
1: 184,462,948 (GRCm39) |
S235R |
probably damaging |
Het |
Jag1 |
T |
C |
2: 136,933,867 (GRCm39) |
|
probably benign |
Het |
Kdr |
A |
G |
5: 76,125,607 (GRCm39) |
|
probably benign |
Het |
Klhl3 |
T |
C |
13: 58,166,685 (GRCm39) |
E435G |
probably damaging |
Het |
L3mbtl4 |
T |
C |
17: 68,768,607 (GRCm39) |
|
probably benign |
Het |
Large1 |
T |
A |
8: 73,775,042 (GRCm39) |
M223L |
probably benign |
Het |
Lrp1b |
T |
C |
2: 40,760,413 (GRCm39) |
K2838E |
possibly damaging |
Het |
Ncan |
T |
C |
8: 70,561,221 (GRCm39) |
D582G |
probably benign |
Het |
Nedd9 |
T |
C |
13: 41,470,211 (GRCm39) |
D314G |
probably damaging |
Het |
Nip7 |
T |
C |
8: 107,784,825 (GRCm39) |
|
probably benign |
Het |
Or10j27 |
T |
G |
1: 172,957,901 (GRCm39) |
K294N |
probably damaging |
Het |
Or52ae9 |
A |
T |
7: 103,389,710 (GRCm39) |
C246S |
possibly damaging |
Het |
Or7a42 |
C |
A |
10: 78,791,773 (GRCm39) |
H245N |
probably damaging |
Het |
P3h1 |
T |
C |
4: 119,095,053 (GRCm39) |
|
probably benign |
Het |
Pcp4l1 |
C |
T |
1: 171,003,133 (GRCm39) |
|
probably benign |
Het |
Plekhm2 |
C |
T |
4: 141,369,330 (GRCm39) |
G118D |
probably benign |
Het |
Prkg1 |
T |
C |
19: 30,602,134 (GRCm39) |
D374G |
possibly damaging |
Het |
Ptcd1 |
A |
G |
5: 145,091,497 (GRCm39) |
L534P |
possibly damaging |
Het |
Rnf123 |
A |
G |
9: 107,943,547 (GRCm39) |
S563P |
probably damaging |
Het |
Scart1 |
A |
G |
7: 139,800,491 (GRCm39) |
M91V |
probably benign |
Het |
Sdk2 |
A |
T |
11: 113,759,747 (GRCm39) |
I418N |
possibly damaging |
Het |
Slc26a4 |
A |
G |
12: 31,578,688 (GRCm39) |
I655T |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 4,993,618 (GRCm39) |
K524R |
probably damaging |
Het |
Tanc1 |
G |
T |
2: 59,663,602 (GRCm39) |
G1120C |
probably damaging |
Het |
Tbc1d22a |
C |
T |
15: 86,123,372 (GRCm39) |
A135V |
probably benign |
Het |
Tenm3 |
A |
C |
8: 48,751,991 (GRCm39) |
W942G |
probably damaging |
Het |
Thsd7b |
G |
A |
1: 130,092,840 (GRCm39) |
V1247I |
probably benign |
Het |
Treml1 |
A |
G |
17: 48,667,459 (GRCm39) |
T115A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,540,306 (GRCm39) |
T34227A |
probably benign |
Het |
Ugt2b38 |
T |
A |
5: 87,571,342 (GRCm39) |
D230V |
probably benign |
Het |
Vmn1r203 |
G |
A |
13: 22,709,074 (GRCm39) |
G285D |
probably damaging |
Het |
Vmn2r76 |
A |
G |
7: 85,879,356 (GRCm39) |
S315P |
probably benign |
Het |
Vmn2r98 |
T |
G |
17: 19,286,083 (GRCm39) |
S194A |
probably benign |
Het |
Wdr1 |
G |
A |
5: 38,703,165 (GRCm39) |
S137F |
probably damaging |
Het |
Wnt7b |
C |
T |
15: 85,443,097 (GRCm39) |
|
probably benign |
Het |
Zfp668 |
A |
T |
7: 127,467,494 (GRCm39) |
C27* |
probably null |
Het |
|
Other mutations in Hdac1-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01936:Hdac1-ps
|
APN |
17 |
78,799,558 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01983:Hdac1-ps
|
APN |
17 |
78,800,282 (GRCm39) |
missense |
probably benign |
|
buttress
|
UTSW |
17 |
78,800,343 (GRCm39) |
missense |
possibly damaging |
0.91 |
Chartre
|
UTSW |
17 |
78,799,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R1174:Hdac1-ps
|
UTSW |
17 |
78,799,507 (GRCm39) |
missense |
probably benign |
0.01 |
R1605:Hdac1-ps
|
UTSW |
17 |
78,799,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R2416:Hdac1-ps
|
UTSW |
17 |
78,799,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Hdac1-ps
|
UTSW |
17 |
78,800,275 (GRCm39) |
missense |
probably damaging |
0.98 |
R2920:Hdac1-ps
|
UTSW |
17 |
78,800,275 (GRCm39) |
missense |
probably damaging |
0.98 |
R3846:Hdac1-ps
|
UTSW |
17 |
78,800,401 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4544:Hdac1-ps
|
UTSW |
17 |
78,800,388 (GRCm39) |
missense |
probably benign |
0.02 |
R4546:Hdac1-ps
|
UTSW |
17 |
78,800,388 (GRCm39) |
missense |
probably benign |
0.02 |
R5223:Hdac1-ps
|
UTSW |
17 |
78,799,867 (GRCm39) |
missense |
probably benign |
0.02 |
R5297:Hdac1-ps
|
UTSW |
17 |
78,800,187 (GRCm39) |
missense |
probably benign |
|
R6164:Hdac1-ps
|
UTSW |
17 |
78,799,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R6568:Hdac1-ps
|
UTSW |
17 |
78,800,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R6726:Hdac1-ps
|
UTSW |
17 |
78,800,287 (GRCm39) |
missense |
probably damaging |
0.99 |
R6901:Hdac1-ps
|
UTSW |
17 |
78,800,089 (GRCm39) |
missense |
probably benign |
0.07 |
R6923:Hdac1-ps
|
UTSW |
17 |
78,800,343 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7838:Hdac1-ps
|
UTSW |
17 |
78,799,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Hdac1-ps
|
UTSW |
17 |
78,799,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R8728:Hdac1-ps
|
UTSW |
17 |
78,800,332 (GRCm39) |
missense |
probably benign |
0.01 |
R8821:Hdac1-ps
|
UTSW |
17 |
78,799,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R8920:Hdac1-ps
|
UTSW |
17 |
78,799,171 (GRCm39) |
missense |
probably benign |
0.37 |
R9618:Hdac1-ps
|
UTSW |
17 |
78,799,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Hdac1-ps
|
UTSW |
17 |
78,799,075 (GRCm39) |
missense |
probably benign |
0.03 |
X0060:Hdac1-ps
|
UTSW |
17 |
78,799,557 (GRCm39) |
missense |
probably damaging |
0.99 |
|