Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
C |
G |
5: 64,055,317 (GRCm39) |
Q18E |
probably damaging |
Het |
Acsf3 |
T |
A |
8: 123,517,411 (GRCm39) |
H402Q |
probably damaging |
Het |
Adam34 |
T |
G |
8: 44,105,098 (GRCm39) |
Q182H |
probably benign |
Het |
Alx1 |
G |
A |
10: 102,864,304 (GRCm39) |
P55L |
possibly damaging |
Het |
Arhgef38 |
A |
T |
3: 132,838,374 (GRCm39) |
|
probably null |
Het |
Corin |
T |
A |
5: 72,518,072 (GRCm39) |
T317S |
probably damaging |
Het |
Ctnna2 |
A |
G |
6: 77,613,822 (GRCm39) |
V256A |
probably benign |
Het |
Dhx29 |
A |
T |
13: 113,089,335 (GRCm39) |
|
probably null |
Het |
Dnah2 |
C |
A |
11: 69,337,475 (GRCm39) |
D3209Y |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,363,194 (GRCm39) |
T3919A |
probably benign |
Het |
F7 |
T |
A |
8: 13,083,958 (GRCm39) |
N214K |
probably benign |
Het |
Fam3b |
T |
G |
16: 97,276,568 (GRCm39) |
Q177H |
possibly damaging |
Het |
Fign |
T |
C |
2: 63,809,654 (GRCm39) |
I539V |
probably benign |
Het |
Hc |
T |
G |
2: 34,903,050 (GRCm39) |
D1067A |
probably damaging |
Het |
Herc6 |
A |
G |
6: 57,560,191 (GRCm39) |
D77G |
probably benign |
Het |
Hmg20a |
A |
T |
9: 56,397,116 (GRCm39) |
E305D |
possibly damaging |
Het |
Il16 |
G |
A |
7: 83,301,775 (GRCm39) |
Q116* |
probably null |
Het |
Kif13a |
T |
A |
13: 46,954,789 (GRCm39) |
I648F |
probably damaging |
Het |
Lactb |
G |
T |
9: 66,874,969 (GRCm39) |
N374K |
possibly damaging |
Het |
Lmx1b |
T |
C |
2: 33,459,118 (GRCm39) |
D145G |
probably damaging |
Het |
Lrfn4 |
T |
C |
19: 4,663,937 (GRCm39) |
D199G |
probably damaging |
Het |
Lrrc49 |
A |
T |
9: 60,522,444 (GRCm39) |
V307E |
possibly damaging |
Het |
Magi1 |
A |
C |
6: 93,685,051 (GRCm39) |
S776A |
possibly damaging |
Het |
Mthfsl |
T |
A |
9: 88,570,807 (GRCm39) |
*147L |
probably null |
Het |
Nsmce4a |
G |
T |
7: 130,148,722 (GRCm39) |
Q95K |
probably benign |
Het |
Or1j15 |
A |
T |
2: 36,458,963 (GRCm39) |
M118L |
probably damaging |
Het |
Or4k37 |
A |
G |
2: 111,159,558 (GRCm39) |
T265A |
probably benign |
Het |
Or4k49 |
A |
T |
2: 111,494,987 (GRCm39) |
K139* |
probably null |
Het |
Or5b24 |
T |
C |
19: 12,912,948 (GRCm39) |
V282A |
possibly damaging |
Het |
Pcdha7 |
A |
G |
18: 37,107,788 (GRCm39) |
E271G |
probably damaging |
Het |
Pcdhga8 |
T |
A |
18: 37,860,596 (GRCm39) |
F551I |
possibly damaging |
Het |
Prpf31 |
T |
C |
7: 3,642,705 (GRCm39) |
|
probably null |
Het |
Qrfpr |
C |
T |
3: 36,236,742 (GRCm39) |
V220I |
possibly damaging |
Het |
Rnf170 |
T |
C |
8: 26,615,994 (GRCm39) |
F95S |
possibly damaging |
Het |
Scn9a |
T |
A |
2: 66,393,973 (GRCm39) |
Y200F |
possibly damaging |
Het |
Sfpq |
A |
T |
4: 126,915,141 (GRCm39) |
|
probably null |
Het |
Slc9c1 |
A |
T |
16: 45,376,132 (GRCm39) |
Y406F |
probably damaging |
Het |
Stk32c |
G |
T |
7: 138,700,628 (GRCm39) |
Y200* |
probably null |
Het |
Svil |
A |
G |
18: 5,108,675 (GRCm39) |
R1938G |
probably damaging |
Het |
Sycp2 |
G |
C |
2: 177,990,038 (GRCm39) |
R1403G |
probably benign |
Het |
Tm9sf4 |
T |
C |
2: 153,024,409 (GRCm39) |
|
probably null |
Het |
Tmc3 |
A |
T |
7: 83,264,170 (GRCm39) |
M633L |
possibly damaging |
Het |
Tmem163 |
T |
C |
1: 127,605,185 (GRCm39) |
D61G |
possibly damaging |
Het |
Unc5b |
C |
A |
10: 60,613,325 (GRCm39) |
A304S |
probably benign |
Het |
Vmn2r106 |
G |
A |
17: 20,488,638 (GRCm39) |
P587L |
probably benign |
Het |
Vmn2r18 |
A |
T |
5: 151,508,462 (GRCm39) |
S221T |
possibly damaging |
Het |
Vmn2r85 |
T |
G |
10: 130,258,672 (GRCm39) |
Y461S |
probably damaging |
Het |
Yod1 |
T |
C |
1: 130,646,800 (GRCm39) |
F226L |
possibly damaging |
Het |
Zbtb4 |
T |
C |
11: 69,667,148 (GRCm39) |
I151T |
probably damaging |
Het |
Zfp110 |
A |
T |
7: 12,583,701 (GRCm39) |
Q783L |
probably damaging |
Het |
|
Other mutations in Ccdc102a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Ccdc102a
|
APN |
8 |
95,638,266 (GRCm39) |
splice site |
probably null |
|
IGL01921:Ccdc102a
|
APN |
8 |
95,640,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Ccdc102a
|
APN |
8 |
95,629,978 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0413:Ccdc102a
|
UTSW |
8 |
95,629,914 (GRCm39) |
missense |
probably benign |
0.23 |
R0423:Ccdc102a
|
UTSW |
8 |
95,632,554 (GRCm39) |
splice site |
probably benign |
|
R0437:Ccdc102a
|
UTSW |
8 |
95,640,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Ccdc102a
|
UTSW |
8 |
95,632,714 (GRCm39) |
missense |
probably benign |
0.06 |
R1468:Ccdc102a
|
UTSW |
8 |
95,632,714 (GRCm39) |
missense |
probably benign |
0.06 |
R1540:Ccdc102a
|
UTSW |
8 |
95,634,341 (GRCm39) |
critical splice donor site |
probably null |
|
R1893:Ccdc102a
|
UTSW |
8 |
95,640,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2317:Ccdc102a
|
UTSW |
8 |
95,634,957 (GRCm39) |
missense |
probably null |
1.00 |
R4280:Ccdc102a
|
UTSW |
8 |
95,634,444 (GRCm39) |
nonsense |
probably null |
|
R6331:Ccdc102a
|
UTSW |
8 |
95,638,144 (GRCm39) |
missense |
probably benign |
|
R6650:Ccdc102a
|
UTSW |
8 |
95,639,892 (GRCm39) |
missense |
probably benign |
0.23 |
R7019:Ccdc102a
|
UTSW |
8 |
95,636,431 (GRCm39) |
missense |
probably benign |
0.42 |
R7302:Ccdc102a
|
UTSW |
8 |
95,640,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Ccdc102a
|
UTSW |
8 |
95,629,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R7949:Ccdc102a
|
UTSW |
8 |
95,631,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Ccdc102a
|
UTSW |
8 |
95,634,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R8166:Ccdc102a
|
UTSW |
8 |
95,639,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8537:Ccdc102a
|
UTSW |
8 |
95,632,684 (GRCm39) |
missense |
probably benign |
0.00 |
R9179:Ccdc102a
|
UTSW |
8 |
95,639,748 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9297:Ccdc102a
|
UTSW |
8 |
95,638,120 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9599:Ccdc102a
|
UTSW |
8 |
95,639,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|