Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c20 |
A |
G |
13: 4,562,664 (GRCm39) |
|
probably null |
Het |
Alg5 |
T |
C |
3: 54,652,140 (GRCm39) |
|
probably benign |
Het |
App |
A |
T |
16: 84,762,599 (GRCm39) |
F675I |
probably damaging |
Het |
Atp2a3 |
A |
C |
11: 72,873,613 (GRCm39) |
I829L |
probably damaging |
Het |
B3galt1 |
C |
T |
2: 67,949,050 (GRCm39) |
S255L |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,964,754 (GRCm39) |
V1417A |
possibly damaging |
Het |
Cast |
T |
A |
13: 74,885,093 (GRCm39) |
T219S |
probably damaging |
Het |
Cep95 |
A |
T |
11: 106,709,043 (GRCm39) |
I705F |
probably damaging |
Het |
Cnot3 |
C |
T |
7: 3,653,854 (GRCm39) |
A2V |
probably damaging |
Het |
Col1a1 |
A |
G |
11: 94,840,204 (GRCm39) |
D1084G |
unknown |
Het |
Col5a3 |
G |
A |
9: 20,697,685 (GRCm39) |
Q873* |
probably null |
Het |
Cubn |
C |
T |
2: 13,386,738 (GRCm39) |
G1509D |
probably damaging |
Het |
Defb10 |
T |
A |
8: 22,351,952 (GRCm39) |
C66S |
possibly damaging |
Het |
Dennd4b |
T |
C |
3: 90,186,993 (GRCm39) |
|
probably null |
Het |
Dido1 |
G |
A |
2: 180,331,319 (GRCm39) |
T43M |
possibly damaging |
Het |
Hmcn1 |
C |
T |
1: 150,506,091 (GRCm39) |
V3812I |
probably benign |
Het |
Islr2 |
T |
C |
9: 58,107,069 (GRCm39) |
T64A |
probably benign |
Het |
Kif2b |
A |
T |
11: 91,467,206 (GRCm39) |
I359N |
probably damaging |
Het |
Kit |
A |
C |
5: 75,806,619 (GRCm39) |
N704T |
probably damaging |
Het |
Ksr1 |
A |
G |
11: 78,918,343 (GRCm39) |
F604L |
probably damaging |
Het |
Lrp5 |
A |
T |
19: 3,699,404 (GRCm39) |
F294I |
probably benign |
Het |
Lrrn1 |
A |
G |
6: 107,545,269 (GRCm39) |
T356A |
probably benign |
Het |
Mrps17 |
G |
A |
5: 129,793,829 (GRCm39) |
V8I |
probably benign |
Het |
Nop56 |
T |
A |
2: 130,117,915 (GRCm39) |
H130Q |
possibly damaging |
Het |
Plg |
T |
A |
17: 12,630,380 (GRCm39) |
L639Q |
probably damaging |
Het |
Ppcdc |
A |
G |
9: 57,322,423 (GRCm39) |
F159L |
probably benign |
Het |
Ppp1ca |
A |
G |
19: 4,244,519 (GRCm39) |
T193A |
probably benign |
Het |
Prpf39 |
A |
G |
12: 65,090,037 (GRCm39) |
D117G |
probably damaging |
Het |
Ranbp2 |
C |
A |
10: 58,289,145 (GRCm39) |
T51K |
possibly damaging |
Het |
Sytl2 |
A |
G |
7: 90,031,844 (GRCm39) |
|
probably benign |
Het |
Tenm2 |
T |
A |
11: 35,915,085 (GRCm39) |
I2150F |
probably damaging |
Het |
Wdr11 |
T |
G |
7: 129,194,817 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Atad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02128:Atad1
|
APN |
19 |
32,664,727 (GRCm39) |
splice site |
probably benign |
|
IGL02441:Atad1
|
APN |
19 |
32,684,348 (GRCm39) |
missense |
probably benign |
|
R0332:Atad1
|
UTSW |
19 |
32,679,934 (GRCm39) |
splice site |
probably benign |
|
R0433:Atad1
|
UTSW |
19 |
32,675,877 (GRCm39) |
missense |
probably benign |
0.00 |
R1529:Atad1
|
UTSW |
19 |
32,684,321 (GRCm39) |
missense |
probably benign |
0.01 |
R1981:Atad1
|
UTSW |
19 |
32,673,210 (GRCm39) |
missense |
probably benign |
0.00 |
R3156:Atad1
|
UTSW |
19 |
32,684,355 (GRCm39) |
missense |
probably benign |
0.11 |
R4490:Atad1
|
UTSW |
19 |
32,673,197 (GRCm39) |
missense |
probably benign |
0.17 |
R4866:Atad1
|
UTSW |
19 |
32,679,964 (GRCm39) |
missense |
probably benign |
0.00 |
R5253:Atad1
|
UTSW |
19 |
32,651,702 (GRCm39) |
missense |
probably benign |
0.16 |
R5284:Atad1
|
UTSW |
19 |
32,664,671 (GRCm39) |
missense |
probably benign |
0.00 |
R6118:Atad1
|
UTSW |
19 |
32,664,697 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6224:Atad1
|
UTSW |
19 |
32,676,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Atad1
|
UTSW |
19 |
32,678,987 (GRCm39) |
missense |
probably benign |
0.00 |
R9523:Atad1
|
UTSW |
19 |
32,684,323 (GRCm39) |
missense |
possibly damaging |
0.55 |
|