Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa1b |
T |
A |
9: 118,977,462 (GRCm39) |
M407L |
possibly damaging |
Het |
Acsf2 |
T |
C |
11: 94,460,768 (GRCm39) |
|
probably benign |
Het |
Apob |
A |
G |
12: 8,060,353 (GRCm39) |
D2945G |
probably benign |
Het |
Atg2a |
T |
C |
19: 6,307,490 (GRCm39) |
Y1475H |
probably damaging |
Het |
Capn5 |
A |
G |
7: 97,778,593 (GRCm39) |
L342P |
possibly damaging |
Het |
Ccdc7b |
A |
G |
8: 129,799,195 (GRCm39) |
M91V |
possibly damaging |
Het |
Cd3g |
T |
C |
9: 44,884,929 (GRCm39) |
E105G |
possibly damaging |
Het |
Cdadc1 |
A |
G |
14: 59,834,360 (GRCm39) |
L44P |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,167,096 (GRCm39) |
V1852A |
possibly damaging |
Het |
Cdx2 |
T |
C |
5: 147,238,833 (GRCm39) |
Q252R |
possibly damaging |
Het |
Cps1 |
A |
T |
1: 67,196,923 (GRCm39) |
I325F |
probably benign |
Het |
Dctn1 |
G |
A |
6: 83,174,931 (GRCm39) |
|
probably null |
Het |
Dcun1d3 |
T |
C |
7: 119,457,256 (GRCm39) |
K152R |
probably benign |
Het |
Dhx35 |
G |
A |
2: 158,673,705 (GRCm39) |
V379M |
probably damaging |
Het |
Fam171a2 |
T |
C |
11: 102,330,807 (GRCm39) |
E224G |
possibly damaging |
Het |
Flt1 |
G |
T |
5: 147,571,293 (GRCm39) |
Y671* |
probably null |
Het |
Fndc3b |
T |
C |
3: 27,515,922 (GRCm39) |
Y628C |
probably damaging |
Het |
Foxj3 |
A |
T |
4: 119,443,008 (GRCm39) |
D144V |
probably damaging |
Het |
Gp2 |
A |
G |
7: 119,048,331 (GRCm39) |
V429A |
probably damaging |
Het |
Hydin |
T |
A |
8: 111,178,690 (GRCm39) |
I1095N |
probably benign |
Het |
Kat2a |
A |
G |
11: 100,599,066 (GRCm39) |
F571S |
probably damaging |
Het |
Kcnq1 |
C |
A |
7: 142,702,493 (GRCm39) |
|
probably benign |
Het |
Letm2 |
A |
C |
8: 26,077,341 (GRCm39) |
S250A |
possibly damaging |
Het |
Llgl1 |
T |
C |
11: 60,600,286 (GRCm39) |
V545A |
probably benign |
Het |
Lrfn3 |
T |
C |
7: 30,059,031 (GRCm39) |
D398G |
probably benign |
Het |
Lrig1 |
G |
T |
6: 94,676,520 (GRCm39) |
C49* |
probably null |
Het |
Mug1 |
A |
G |
6: 121,855,452 (GRCm39) |
I929V |
probably benign |
Het |
Naaa |
G |
A |
5: 92,411,314 (GRCm39) |
T291I |
probably damaging |
Het |
Ndufaf1 |
G |
A |
2: 119,490,521 (GRCm39) |
Q180* |
probably null |
Het |
Nr3c1 |
A |
T |
18: 39,548,752 (GRCm39) |
H741Q |
probably damaging |
Het |
Nsun5 |
T |
C |
5: 135,400,204 (GRCm39) |
L109P |
probably damaging |
Het |
Pacsin3 |
A |
G |
2: 91,090,605 (GRCm39) |
E18G |
probably damaging |
Het |
Rpgr |
G |
A |
X: 10,032,511 (GRCm39) |
P857L |
probably benign |
Het |
Siglec1 |
G |
A |
2: 130,916,188 (GRCm39) |
T1254M |
probably benign |
Het |
Slc35a4 |
A |
T |
18: 36,815,394 (GRCm39) |
T75S |
probably benign |
Het |
Slc52a2 |
T |
C |
15: 76,425,274 (GRCm39) |
I434T |
probably benign |
Het |
Slco2a1 |
C |
T |
9: 102,927,455 (GRCm39) |
T116I |
probably damaging |
Het |
Snrpd2 |
T |
C |
7: 18,886,538 (GRCm39) |
|
probably null |
Het |
Tbc1d32 |
T |
A |
10: 55,964,489 (GRCm39) |
L903F |
probably damaging |
Het |
Tex10 |
G |
T |
4: 48,460,046 (GRCm39) |
T435K |
probably damaging |
Het |
Tmem266 |
T |
C |
9: 55,288,120 (GRCm39) |
S66P |
probably damaging |
Het |
Top2b |
A |
T |
14: 16,400,106 (GRCm38) |
E581D |
possibly damaging |
Het |
Uggt1 |
A |
T |
1: 36,200,852 (GRCm39) |
|
probably null |
Het |
Wdr47 |
T |
A |
3: 108,540,472 (GRCm39) |
Y622* |
probably null |
Het |
Zfp644 |
A |
T |
5: 106,784,989 (GRCm39) |
H519Q |
probably damaging |
Het |
Zfp687 |
T |
C |
3: 94,918,528 (GRCm39) |
M415V |
possibly damaging |
Het |
|
Other mutations in Ccdc152 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01466:Ccdc152
|
APN |
15 |
3,323,329 (GRCm39) |
splice site |
probably benign |
|
IGL01543:Ccdc152
|
APN |
15 |
3,327,606 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0622:Ccdc152
|
UTSW |
15 |
3,327,660 (GRCm39) |
missense |
probably damaging |
0.96 |
R1605:Ccdc152
|
UTSW |
15 |
3,327,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R2875:Ccdc152
|
UTSW |
15 |
3,327,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R2876:Ccdc152
|
UTSW |
15 |
3,327,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R4990:Ccdc152
|
UTSW |
15 |
3,330,639 (GRCm39) |
missense |
probably benign |
0.00 |
R5114:Ccdc152
|
UTSW |
15 |
3,312,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R6336:Ccdc152
|
UTSW |
15 |
3,330,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R6704:Ccdc152
|
UTSW |
15 |
3,310,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Ccdc152
|
UTSW |
15 |
3,310,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R8300:Ccdc152
|
UTSW |
15 |
3,327,634 (GRCm39) |
missense |
probably benign |
0.00 |
R9061:Ccdc152
|
UTSW |
15 |
3,330,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|