Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
G |
A |
4: 144,344,490 (GRCm39) |
V89I |
probably damaging |
Het |
Abhd5 |
T |
C |
9: 122,206,980 (GRCm39) |
F89L |
possibly damaging |
Het |
Akr1c13 |
T |
A |
13: 4,248,593 (GRCm39) |
V266E |
probably damaging |
Het |
B4galt2 |
C |
T |
4: 117,738,602 (GRCm39) |
A72T |
probably benign |
Het |
Ccdc141 |
T |
C |
2: 76,857,938 (GRCm39) |
Y1081C |
probably damaging |
Het |
Coq8b |
T |
C |
7: 26,956,038 (GRCm39) |
V405A |
possibly damaging |
Het |
Ddah2 |
A |
G |
17: 35,280,776 (GRCm39) |
K251E |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,272,331 (GRCm39) |
V1045A |
probably benign |
Het |
Dpy19l1 |
A |
T |
9: 24,332,476 (GRCm39) |
M662K |
probably benign |
Het |
Dpys |
A |
G |
15: 39,690,279 (GRCm39) |
V358A |
probably damaging |
Het |
H2-D1 |
A |
G |
17: 35,483,064 (GRCm39) |
N198S |
probably benign |
Het |
Hnrnpa1 |
T |
C |
15: 103,150,538 (GRCm39) |
V163A |
probably damaging |
Het |
Hr |
C |
T |
14: 70,797,225 (GRCm39) |
R543C |
possibly damaging |
Het |
Lct |
C |
T |
1: 128,240,869 (GRCm39) |
V245M |
probably benign |
Het |
Lpl |
G |
A |
8: 69,345,400 (GRCm39) |
V135M |
probably damaging |
Het |
Mblac1 |
T |
A |
5: 138,193,119 (GRCm39) |
C154S |
probably benign |
Het |
Mmp9 |
T |
C |
2: 164,793,039 (GRCm39) |
F396S |
probably damaging |
Het |
Mroh1 |
A |
T |
15: 76,293,168 (GRCm39) |
H314L |
probably damaging |
Het |
Nol8 |
A |
G |
13: 49,815,878 (GRCm39) |
D662G |
probably benign |
Het |
Nynrin |
G |
A |
14: 56,109,837 (GRCm39) |
S1648N |
probably damaging |
Het |
Or52a20 |
A |
G |
7: 103,366,427 (GRCm39) |
I209V |
probably benign |
Het |
Plcb2 |
C |
T |
2: 118,549,590 (GRCm39) |
|
probably null |
Het |
Scyl2 |
T |
A |
10: 89,496,163 (GRCm39) |
N229I |
possibly damaging |
Het |
Spryd3 |
C |
T |
15: 102,026,544 (GRCm39) |
E376K |
probably benign |
Het |
Srr |
T |
G |
11: 74,799,563 (GRCm39) |
E304A |
probably benign |
Het |
Srsf1 |
A |
G |
11: 87,940,352 (GRCm39) |
|
probably benign |
Het |
Txnrd2 |
T |
G |
16: 18,296,456 (GRCm39) |
S473A |
probably benign |
Het |
Wdr18 |
T |
A |
10: 79,800,889 (GRCm39) |
C151S |
probably benign |
Het |
Zfp282 |
C |
T |
6: 47,874,848 (GRCm39) |
T351I |
probably damaging |
Het |
|
Other mutations in Msantd4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02021:Msantd4
|
APN |
9 |
4,385,163 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02347:Msantd4
|
APN |
9 |
4,384,734 (GRCm39) |
splice site |
probably benign |
|
IGL02947:Msantd4
|
APN |
9 |
4,384,787 (GRCm39) |
missense |
probably damaging |
0.97 |
FR4548:Msantd4
|
UTSW |
9 |
4,384,937 (GRCm39) |
missense |
possibly damaging |
0.50 |
FR4976:Msantd4
|
UTSW |
9 |
4,384,937 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0006:Msantd4
|
UTSW |
9 |
4,384,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R0436:Msantd4
|
UTSW |
9 |
4,385,180 (GRCm39) |
missense |
probably damaging |
0.98 |
R1403:Msantd4
|
UTSW |
9 |
4,384,023 (GRCm39) |
missense |
probably benign |
0.19 |
R1403:Msantd4
|
UTSW |
9 |
4,384,023 (GRCm39) |
missense |
probably benign |
0.19 |
R1512:Msantd4
|
UTSW |
9 |
4,384,138 (GRCm39) |
missense |
probably benign |
0.02 |
R1639:Msantd4
|
UTSW |
9 |
4,385,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R3819:Msantd4
|
UTSW |
9 |
4,385,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R6021:Msantd4
|
UTSW |
9 |
4,384,063 (GRCm39) |
missense |
probably benign |
0.34 |
R6982:Msantd4
|
UTSW |
9 |
4,384,061 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8166:Msantd4
|
UTSW |
9 |
4,384,095 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8753:Msantd4
|
UTSW |
9 |
4,385,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R9510:Msantd4
|
UTSW |
9 |
4,385,007 (GRCm39) |
missense |
probably benign |
0.00 |
|