Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
A |
C |
3: 59,945,893 (GRCm39) |
S188R |
probably damaging |
Het |
Aars1 |
T |
A |
8: 111,768,289 (GRCm39) |
I220N |
probably damaging |
Het |
Abca15 |
A |
G |
7: 119,931,440 (GRCm39) |
N16S |
probably damaging |
Het |
Adck1 |
A |
T |
12: 88,423,570 (GRCm39) |
M358L |
probably benign |
Het |
Adck5 |
A |
T |
15: 76,478,748 (GRCm39) |
Q345L |
probably benign |
Het |
Adgrl2 |
A |
G |
3: 148,542,094 (GRCm39) |
F876S |
probably damaging |
Het |
Aebp2 |
T |
A |
6: 140,569,584 (GRCm39) |
L55Q |
unknown |
Het |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Aox3 |
T |
C |
1: 58,215,676 (GRCm39) |
V1036A |
possibly damaging |
Het |
Aox4 |
A |
G |
1: 58,279,866 (GRCm39) |
D494G |
probably benign |
Het |
Cacna1a |
C |
A |
8: 85,286,023 (GRCm39) |
H889Q |
probably benign |
Het |
Cacna1c |
T |
C |
6: 119,029,587 (GRCm39) |
D151G |
|
Het |
Car8 |
A |
G |
4: 8,237,939 (GRCm39) |
V92A |
possibly damaging |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 116,370,013 (GRCm39) |
I877V |
probably benign |
Het |
Copa |
A |
T |
1: 171,939,509 (GRCm39) |
D582V |
probably damaging |
Het |
Cpne2 |
T |
G |
8: 95,295,312 (GRCm39) |
S466A |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 133,816,156 (GRCm39) |
K1311R |
possibly damaging |
Het |
Csmd1 |
A |
G |
8: 15,982,461 (GRCm39) |
|
probably null |
Het |
Dnah2 |
A |
T |
11: 69,342,144 (GRCm39) |
C2947* |
probably null |
Het |
Exoc1 |
A |
T |
5: 76,709,359 (GRCm39) |
K656* |
probably null |
Het |
Exoc8 |
T |
C |
8: 125,622,558 (GRCm39) |
N603S |
probably benign |
Het |
Fam171a1 |
T |
A |
2: 3,226,483 (GRCm39) |
C539S |
possibly damaging |
Het |
Fastkd5 |
A |
T |
2: 130,456,988 (GRCm39) |
I534K |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,145,115 (GRCm39) |
D2708G |
probably benign |
Het |
Fhad1 |
A |
G |
4: 141,618,250 (GRCm39) |
L1392P |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,874,754 (GRCm39) |
T2306S |
probably benign |
Het |
Gdf7 |
G |
T |
12: 8,351,854 (GRCm39) |
A27E |
unknown |
Het |
Hnrnph1 |
A |
T |
11: 50,270,324 (GRCm39) |
I43F |
probably damaging |
Het |
Igkv8-27 |
T |
A |
6: 70,148,999 (GRCm39) |
S52C |
probably benign |
Het |
Jmjd1c |
T |
C |
10: 67,052,824 (GRCm39) |
F24L |
probably damaging |
Het |
Knl1 |
T |
G |
2: 118,902,037 (GRCm39) |
L1246R |
probably benign |
Het |
Limk2 |
C |
T |
11: 3,305,896 (GRCm39) |
S191N |
probably damaging |
Het |
Mdga2 |
C |
A |
12: 66,736,125 (GRCm39) |
A368S |
possibly damaging |
Het |
Mdga2 |
G |
A |
12: 66,736,124 (GRCm39) |
A368V |
probably damaging |
Het |
Med24 |
A |
T |
11: 98,595,793 (GRCm39) |
L966Q |
probably damaging |
Het |
Mgll |
T |
C |
6: 88,702,770 (GRCm39) |
V23A |
possibly damaging |
Het |
Nedd1 |
C |
T |
10: 92,550,034 (GRCm39) |
D84N |
probably benign |
Het |
Obscn |
A |
C |
11: 58,951,681 (GRCm39) |
L4024R |
probably damaging |
Het |
Or5k1b |
A |
T |
16: 58,580,782 (GRCm39) |
Y252* |
probably null |
Het |
Pcnx2 |
T |
C |
8: 126,577,846 (GRCm39) |
I944V |
probably benign |
Het |
Pecr |
T |
C |
1: 72,306,157 (GRCm39) |
|
probably null |
Het |
Phf3 |
A |
T |
1: 30,843,305 (GRCm39) |
W1885R |
probably damaging |
Het |
Pitpnm2 |
C |
G |
5: 124,266,768 (GRCm39) |
A697P |
probably benign |
Het |
Piwil2 |
T |
A |
14: 70,631,638 (GRCm39) |
H602L |
probably benign |
Het |
Pprc1 |
T |
C |
19: 46,053,781 (GRCm39) |
S1104P |
unknown |
Het |
Prkar1a |
T |
A |
11: 109,544,673 (GRCm39) |
Y21* |
probably null |
Het |
Prl2c3 |
A |
T |
13: 12,813,186 (GRCm39) |
Y9* |
probably null |
Het |
Rhbdl3 |
T |
A |
11: 80,214,405 (GRCm39) |
L172Q |
possibly damaging |
Het |
Rsph3a |
T |
G |
17: 8,198,075 (GRCm39) |
L484W |
probably damaging |
Het |
Sbno1 |
A |
T |
5: 124,530,962 (GRCm39) |
S809T |
probably benign |
Het |
Stmnd1 |
T |
A |
13: 46,453,077 (GRCm39) |
V251E |
possibly damaging |
Het |
Stt3a |
A |
T |
9: 36,662,535 (GRCm39) |
C241* |
probably null |
Het |
Tas2r114 |
A |
T |
6: 131,666,401 (GRCm39) |
M209K |
probably damaging |
Het |
Tchh |
G |
T |
3: 93,352,084 (GRCm39) |
R508L |
unknown |
Het |
Tgfbr3l |
T |
C |
8: 4,300,622 (GRCm39) |
S267P |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,598,144 (GRCm39) |
I19590F |
probably damaging |
Het |
Vmn1r171 |
A |
G |
7: 23,332,035 (GRCm39) |
T87A |
probably benign |
Het |
|
Other mutations in Ccdc8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00333:Ccdc8
|
APN |
7 |
16,729,967 (GRCm39) |
missense |
unknown |
|
R0255:Ccdc8
|
UTSW |
7 |
16,729,582 (GRCm39) |
missense |
unknown |
|
R0504:Ccdc8
|
UTSW |
7 |
16,729,939 (GRCm39) |
missense |
unknown |
|
R3843:Ccdc8
|
UTSW |
7 |
16,729,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R5054:Ccdc8
|
UTSW |
7 |
16,728,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:Ccdc8
|
UTSW |
7 |
16,730,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R6045:Ccdc8
|
UTSW |
7 |
16,729,956 (GRCm39) |
missense |
unknown |
|
R6244:Ccdc8
|
UTSW |
7 |
16,730,176 (GRCm39) |
missense |
probably benign |
0.04 |
R6753:Ccdc8
|
UTSW |
7 |
16,730,562 (GRCm39) |
nonsense |
probably null |
|
R7299:Ccdc8
|
UTSW |
7 |
16,729,956 (GRCm39) |
missense |
unknown |
|
R7567:Ccdc8
|
UTSW |
7 |
16,728,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R7623:Ccdc8
|
UTSW |
7 |
16,730,537 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8310:Ccdc8
|
UTSW |
7 |
16,729,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R8707:Ccdc8
|
UTSW |
7 |
16,729,975 (GRCm39) |
missense |
unknown |
|
R8840:Ccdc8
|
UTSW |
7 |
16,728,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Ccdc8
|
UTSW |
7 |
16,728,800 (GRCm39) |
nonsense |
probably null |
|
R9630:Ccdc8
|
UTSW |
7 |
16,728,733 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9696:Ccdc8
|
UTSW |
7 |
16,730,087 (GRCm39) |
missense |
unknown |
|
|