Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
G |
2: 68,575,749 (GRCm39) |
R683G |
possibly damaging |
Het |
Abca9 |
A |
G |
11: 110,036,463 (GRCm39) |
S549P |
probably damaging |
Het |
Adgrd1 |
T |
C |
5: 129,174,273 (GRCm39) |
S17P |
possibly damaging |
Het |
Ankrd36 |
C |
A |
11: 5,578,348 (GRCm39) |
H546N |
probably benign |
Het |
Aopep |
C |
T |
13: 63,338,290 (GRCm39) |
|
probably benign |
Het |
Bivm |
T |
G |
1: 44,165,907 (GRCm39) |
I119S |
possibly damaging |
Het |
Ccdc88a |
G |
T |
11: 29,453,915 (GRCm39) |
D1693Y |
probably damaging |
Het |
Clcn6 |
G |
A |
4: 148,103,423 (GRCm39) |
R242C |
probably damaging |
Het |
Clec4a2 |
A |
C |
6: 123,104,947 (GRCm39) |
K79T |
probably damaging |
Het |
Cspp1 |
G |
A |
1: 10,186,905 (GRCm39) |
R129H |
probably damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,801,027 (GRCm39) |
M47K |
probably benign |
Het |
Dmxl1 |
A |
G |
18: 49,990,401 (GRCm39) |
D280G |
probably benign |
Het |
Fbxo38 |
A |
G |
18: 62,655,487 (GRCm39) |
S400P |
probably damaging |
Het |
Fsd1 |
C |
T |
17: 56,303,733 (GRCm39) |
S491F |
probably damaging |
Het |
Gen1 |
T |
C |
12: 11,305,242 (GRCm39) |
I184M |
probably benign |
Het |
Gm9949 |
A |
T |
18: 62,317,089 (GRCm39) |
|
probably benign |
Het |
Grtp1 |
A |
T |
8: 13,229,629 (GRCm39) |
V253E |
probably damaging |
Het |
Irag1 |
A |
G |
7: 110,525,708 (GRCm39) |
V148A |
possibly damaging |
Het |
Lamb1 |
T |
A |
12: 31,370,930 (GRCm39) |
M1327K |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,313,846 (GRCm39) |
D2295V |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,284,156 (GRCm39) |
D3874G |
probably null |
Het |
Muc5b |
A |
T |
7: 141,400,555 (GRCm39) |
I509F |
unknown |
Het |
Mug1 |
A |
C |
6: 121,826,433 (GRCm39) |
|
probably benign |
Het |
Myh7 |
A |
T |
14: 55,208,916 (GRCm39) |
L1903Q |
probably damaging |
Het |
Mylk |
G |
T |
16: 34,759,322 (GRCm39) |
A1229S |
probably benign |
Het |
Myorg |
G |
T |
4: 41,498,151 (GRCm39) |
A493E |
probably damaging |
Het |
Ncam1 |
A |
T |
9: 49,421,152 (GRCm39) |
I721N |
possibly damaging |
Het |
Or8b101 |
T |
A |
9: 38,020,858 (GRCm39) |
I287N |
probably damaging |
Het |
Pla2g2c |
A |
G |
4: 138,471,012 (GRCm39) |
K131R |
probably benign |
Het |
Rpgrip1l |
A |
T |
8: 92,000,268 (GRCm39) |
I557N |
probably benign |
Het |
Sirpb1b |
T |
A |
3: 15,613,789 (GRCm39) |
N98Y |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,872,365 (GRCm39) |
V1182A |
probably benign |
Het |
Tiam2 |
T |
A |
17: 3,477,477 (GRCm39) |
F567I |
probably benign |
Het |
Ush2a |
A |
T |
1: 188,285,425 (GRCm39) |
D1987V |
possibly damaging |
Het |
Vmn1r36 |
A |
T |
6: 66,693,446 (GRCm39) |
I37N |
probably damaging |
Het |
Wif1 |
A |
T |
10: 120,920,855 (GRCm39) |
T226S |
possibly damaging |
Het |
Zfp428 |
A |
G |
7: 24,210,167 (GRCm39) |
D22G |
possibly damaging |
Het |
Zfp521 |
A |
T |
18: 13,976,980 (GRCm39) |
N1144K |
probably benign |
Het |
|
Other mutations in Tagap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02138:Tagap1
|
APN |
17 |
7,223,485 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02475:Tagap1
|
APN |
17 |
7,223,826 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02955:Tagap1
|
APN |
17 |
7,223,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Tagap1
|
UTSW |
17 |
7,224,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Tagap1
|
UTSW |
17 |
7,223,425 (GRCm39) |
missense |
probably benign |
0.02 |
R1990:Tagap1
|
UTSW |
17 |
7,224,285 (GRCm39) |
missense |
probably benign |
0.00 |
R2067:Tagap1
|
UTSW |
17 |
7,224,259 (GRCm39) |
missense |
probably benign |
0.00 |
R2086:Tagap1
|
UTSW |
17 |
7,224,102 (GRCm39) |
missense |
probably benign |
0.00 |
R2111:Tagap1
|
UTSW |
17 |
7,224,259 (GRCm39) |
missense |
probably benign |
0.00 |
R4425:Tagap1
|
UTSW |
17 |
7,223,511 (GRCm39) |
missense |
probably benign |
0.00 |
R5271:Tagap1
|
UTSW |
17 |
7,223,495 (GRCm39) |
nonsense |
probably null |
|
R5728:Tagap1
|
UTSW |
17 |
7,224,420 (GRCm39) |
missense |
probably benign |
0.30 |
R7100:Tagap1
|
UTSW |
17 |
7,224,111 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8145:Tagap1
|
UTSW |
17 |
7,223,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Tagap1
|
UTSW |
17 |
7,224,327 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:Tagap1
|
UTSW |
17 |
7,228,477 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Tagap1
|
UTSW |
17 |
7,224,016 (GRCm39) |
missense |
probably benign |
0.01 |
|