Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankfy1 |
T |
C |
11: 72,631,281 (GRCm39) |
V409A |
probably benign |
Het |
Ap4m1 |
A |
G |
5: 138,171,106 (GRCm39) |
T69A |
probably damaging |
Het |
B3gat2 |
A |
T |
1: 23,884,209 (GRCm39) |
K306* |
probably null |
Het |
Calr |
A |
G |
8: 85,569,479 (GRCm39) |
|
probably benign |
Het |
Ccdc54 |
C |
T |
16: 50,411,215 (GRCm39) |
W17* |
probably null |
Het |
Cd68 |
T |
C |
11: 69,555,927 (GRCm39) |
S204G |
possibly damaging |
Het |
Cep128 |
A |
T |
12: 91,200,984 (GRCm39) |
I342K |
probably damaging |
Het |
Ces1d |
T |
A |
8: 93,904,703 (GRCm39) |
I346L |
probably benign |
Het |
Cfap70 |
T |
A |
14: 20,475,467 (GRCm39) |
D418V |
possibly damaging |
Het |
Cntnap4 |
A |
T |
8: 113,478,866 (GRCm39) |
R197S |
possibly damaging |
Het |
Ddx31 |
G |
T |
2: 28,764,176 (GRCm39) |
V461F |
probably damaging |
Het |
Eps15l1 |
T |
C |
8: 73,121,756 (GRCm39) |
M714V |
possibly damaging |
Het |
Fshb |
A |
T |
2: 106,889,272 (GRCm39) |
F11I |
probably benign |
Het |
Fsip2 |
T |
G |
2: 82,822,482 (GRCm39) |
C6072G |
possibly damaging |
Het |
Fuz |
T |
G |
7: 44,546,383 (GRCm39) |
L93R |
probably damaging |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Gm8991 |
G |
A |
5: 16,935,678 (GRCm39) |
|
noncoding transcript |
Het |
Itga11 |
C |
A |
9: 62,680,278 (GRCm39) |
N973K |
probably benign |
Het |
Lca5 |
T |
A |
9: 83,305,201 (GRCm39) |
T202S |
probably damaging |
Het |
Lrp1 |
G |
A |
10: 127,390,458 (GRCm39) |
L3053F |
probably damaging |
Het |
Mapk13 |
T |
C |
17: 28,994,304 (GRCm39) |
Y129H |
probably damaging |
Het |
Mast1 |
T |
A |
8: 85,647,838 (GRCm39) |
H512L |
probably damaging |
Het |
Mlip |
T |
C |
9: 77,081,281 (GRCm39) |
N213S |
probably damaging |
Het |
Mtcl1 |
C |
T |
17: 66,675,263 (GRCm39) |
G734R |
possibly damaging |
Het |
Myo9a |
T |
A |
9: 59,686,985 (GRCm39) |
I30N |
probably damaging |
Het |
Or4b13 |
A |
G |
2: 90,082,675 (GRCm39) |
I219T |
probably damaging |
Het |
Pctp |
T |
C |
11: 89,878,162 (GRCm39) |
D124G |
probably benign |
Het |
Phc3 |
A |
G |
3: 30,968,565 (GRCm39) |
|
probably null |
Het |
Plat |
T |
A |
8: 23,270,453 (GRCm39) |
F457I |
possibly damaging |
Het |
Snw1 |
T |
C |
12: 87,502,438 (GRCm39) |
K319E |
probably benign |
Het |
Sox8 |
A |
G |
17: 25,789,111 (GRCm39) |
L129P |
probably damaging |
Het |
Sp140l2 |
A |
G |
1: 85,231,907 (GRCm39) |
|
probably benign |
Het |
Stc1 |
A |
T |
14: 69,269,103 (GRCm39) |
|
probably benign |
Het |
Szt2 |
A |
G |
4: 118,241,450 (GRCm39) |
|
probably benign |
Het |
Tmem81 |
T |
A |
1: 132,435,698 (GRCm39) |
V168D |
probably damaging |
Het |
Ttc41 |
C |
A |
10: 86,549,054 (GRCm39) |
Q83K |
probably damaging |
Het |
Ugt1a5 |
T |
C |
1: 88,094,267 (GRCm39) |
V165A |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vps33b |
A |
G |
7: 79,937,560 (GRCm39) |
|
probably null |
Het |
Zap70 |
T |
C |
1: 36,817,868 (GRCm39) |
Y290H |
possibly damaging |
Het |
|
Other mutations in 4933421I07Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01634:4933421I07Rik
|
APN |
7 |
42,097,123 (GRCm39) |
missense |
probably benign |
|
IGL01653:4933421I07Rik
|
APN |
7 |
42,096,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02514:4933421I07Rik
|
APN |
7 |
42,096,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R1330:4933421I07Rik
|
UTSW |
7 |
42,097,018 (GRCm39) |
missense |
probably benign |
0.19 |
R2219:4933421I07Rik
|
UTSW |
7 |
42,095,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R4779:4933421I07Rik
|
UTSW |
7 |
42,097,455 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4952:4933421I07Rik
|
UTSW |
7 |
42,097,083 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6026:4933421I07Rik
|
UTSW |
7 |
42,095,708 (GRCm39) |
missense |
probably benign |
0.06 |
R6141:4933421I07Rik
|
UTSW |
7 |
42,097,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:4933421I07Rik
|
UTSW |
7 |
42,095,667 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6892:4933421I07Rik
|
UTSW |
7 |
42,095,831 (GRCm39) |
missense |
probably benign |
0.35 |
R7284:4933421I07Rik
|
UTSW |
7 |
42,097,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R8684:4933421I07Rik
|
UTSW |
7 |
42,097,413 (GRCm39) |
missense |
probably benign |
0.07 |
|