Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933405O20Rik |
G |
A |
7: 50,249,284 (GRCm39) |
R106Q |
probably damaging |
Het |
Amhr2 |
T |
C |
15: 102,355,724 (GRCm39) |
V223A |
probably damaging |
Het |
Aqr |
T |
A |
2: 113,943,835 (GRCm39) |
H1101L |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,367,681 (GRCm39) |
|
probably benign |
Het |
Cacnb2 |
G |
A |
2: 14,963,640 (GRCm39) |
V85I |
probably benign |
Het |
Cast |
A |
T |
13: 74,848,806 (GRCm39) |
D727E |
probably damaging |
Het |
Cemip2 |
G |
A |
19: 21,801,207 (GRCm39) |
D775N |
possibly damaging |
Het |
Col5a3 |
A |
G |
9: 20,715,962 (GRCm39) |
S360P |
unknown |
Het |
Cyp4f16 |
T |
C |
17: 32,756,061 (GRCm39) |
I30T |
possibly damaging |
Het |
Dop1b |
T |
C |
16: 93,552,361 (GRCm39) |
F267L |
probably benign |
Het |
Fbxo3 |
A |
G |
2: 103,880,639 (GRCm39) |
T250A |
probably damaging |
Het |
Gm4953 |
C |
T |
1: 158,995,963 (GRCm39) |
|
noncoding transcript |
Het |
Gm9242 |
T |
C |
16: 97,292,279 (GRCm39) |
|
probably benign |
Het |
Gsr |
G |
A |
8: 34,179,453 (GRCm39) |
V354I |
probably damaging |
Het |
H2bc21 |
A |
G |
3: 96,128,732 (GRCm39) |
Y84C |
possibly damaging |
Het |
Hecw1 |
T |
A |
13: 14,552,311 (GRCm39) |
D96V |
probably damaging |
Het |
Il18r1 |
A |
G |
1: 40,537,711 (GRCm39) |
Y492C |
probably damaging |
Het |
Itgb5 |
T |
G |
16: 33,764,465 (GRCm39) |
|
probably benign |
Het |
Lars2 |
T |
G |
9: 123,288,650 (GRCm39) |
L832R |
probably damaging |
Het |
Ms4a6c |
A |
G |
19: 11,448,466 (GRCm39) |
|
probably benign |
Het |
Nrxn1 |
T |
C |
17: 90,515,811 (GRCm39) |
S1227G |
probably damaging |
Het |
Or1j11 |
T |
C |
2: 36,312,132 (GRCm39) |
C241R |
probably damaging |
Het |
Or2c1 |
T |
C |
16: 3,657,680 (GRCm39) |
V281A |
possibly damaging |
Het |
Or52r1c |
A |
G |
7: 102,735,528 (GRCm39) |
T263A |
probably benign |
Het |
Pcdh17 |
A |
G |
14: 84,685,747 (GRCm39) |
Y738C |
probably damaging |
Het |
Pcsk5 |
C |
A |
19: 17,424,865 (GRCm39) |
C1646F |
probably damaging |
Het |
Pirb |
A |
G |
7: 3,720,377 (GRCm39) |
V332A |
probably damaging |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Polrmt |
A |
T |
10: 79,573,092 (GRCm39) |
|
probably benign |
Het |
Saxo1 |
G |
T |
4: 86,363,821 (GRCm39) |
R221S |
probably damaging |
Het |
Specc1l |
A |
G |
10: 75,077,022 (GRCm39) |
I93V |
probably benign |
Het |
St8sia2 |
T |
A |
7: 73,626,397 (GRCm39) |
|
probably benign |
Het |
Tep1 |
A |
T |
14: 51,103,494 (GRCm39) |
N265K |
probably damaging |
Het |
Thbd |
A |
T |
2: 148,248,954 (GRCm39) |
Y305N |
probably damaging |
Het |
Tmem120a |
T |
C |
5: 135,764,605 (GRCm39) |
T325A |
probably damaging |
Het |
Vill |
G |
A |
9: 118,895,955 (GRCm39) |
|
probably benign |
Het |
Wdr35 |
A |
G |
12: 9,077,507 (GRCm39) |
D1060G |
probably damaging |
Het |
Xrn2 |
T |
A |
2: 146,868,444 (GRCm39) |
F166I |
probably damaging |
Het |
Zc3h7a |
T |
G |
16: 10,976,458 (GRCm39) |
|
probably null |
Het |
Zdhhc13 |
G |
A |
7: 48,466,886 (GRCm39) |
|
probably benign |
Het |
Zfp808 |
T |
A |
13: 62,320,944 (GRCm39) |
N724K |
possibly damaging |
Het |
|
Other mutations in Ccdc134 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02746:Ccdc134
|
APN |
15 |
82,015,938 (GRCm39) |
intron |
probably benign |
|
IGL03071:Ccdc134
|
APN |
15 |
82,018,826 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03278:Ccdc134
|
APN |
15 |
82,015,682 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL03308:Ccdc134
|
APN |
15 |
82,015,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03014:Ccdc134
|
UTSW |
15 |
82,014,306 (GRCm39) |
missense |
probably damaging |
0.99 |
R0077:Ccdc134
|
UTSW |
15 |
82,015,938 (GRCm39) |
intron |
probably benign |
|
R0243:Ccdc134
|
UTSW |
15 |
82,025,147 (GRCm39) |
missense |
probably damaging |
0.98 |
R1107:Ccdc134
|
UTSW |
15 |
82,018,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R1107:Ccdc134
|
UTSW |
15 |
82,018,892 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1588:Ccdc134
|
UTSW |
15 |
82,019,337 (GRCm39) |
missense |
probably benign |
0.03 |
R3874:Ccdc134
|
UTSW |
15 |
82,015,643 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6696:Ccdc134
|
UTSW |
15 |
82,015,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Ccdc134
|
UTSW |
15 |
82,025,149 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7814:Ccdc134
|
UTSW |
15 |
82,015,724 (GRCm39) |
missense |
probably damaging |
0.96 |
R8088:Ccdc134
|
UTSW |
15 |
82,015,990 (GRCm39) |
intron |
probably benign |
|
|