Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930474N05Rik |
C |
T |
14: 35,817,306 (GRCm39) |
P69S |
probably benign |
Het |
Adam17 |
A |
G |
12: 21,405,694 (GRCm39) |
|
probably benign |
Het |
Bcl7a |
T |
A |
5: 123,482,757 (GRCm39) |
M22K |
probably benign |
Het |
C6 |
T |
A |
15: 4,826,432 (GRCm39) |
C672S |
probably damaging |
Het |
Capn11 |
C |
T |
17: 45,954,738 (GRCm39) |
R133H |
probably damaging |
Het |
Cfhr4 |
T |
C |
1: 139,667,436 (GRCm39) |
|
probably null |
Het |
Cotl1 |
T |
G |
8: 120,537,040 (GRCm39) |
I125L |
probably benign |
Het |
Dennd5a |
A |
T |
7: 109,504,906 (GRCm39) |
M868K |
probably damaging |
Het |
Depdc5 |
T |
C |
5: 33,136,852 (GRCm39) |
I1374T |
probably damaging |
Het |
Dhx36 |
T |
C |
3: 62,386,814 (GRCm39) |
Y646C |
probably benign |
Het |
Ecpas |
T |
C |
4: 58,834,593 (GRCm39) |
K762E |
probably benign |
Het |
Egln2 |
A |
G |
7: 26,864,310 (GRCm39) |
V205A |
probably damaging |
Het |
Eri2 |
T |
A |
7: 119,386,009 (GRCm39) |
M229L |
probably benign |
Het |
Fancf |
C |
A |
7: 51,511,452 (GRCm39) |
R184L |
probably damaging |
Het |
Fancl |
A |
T |
11: 26,353,363 (GRCm39) |
E86D |
probably damaging |
Het |
Fignl2 |
T |
C |
15: 100,951,259 (GRCm39) |
D341G |
unknown |
Het |
Gm14410 |
A |
T |
2: 176,885,648 (GRCm39) |
H205Q |
probably damaging |
Het |
Haus1 |
T |
C |
18: 77,848,666 (GRCm39) |
N181D |
probably benign |
Het |
Hmbox1 |
T |
C |
14: 65,066,115 (GRCm39) |
Y285C |
probably damaging |
Het |
Igkv3-9 |
A |
G |
6: 70,565,739 (GRCm39) |
M113V |
probably benign |
Het |
Ivd |
T |
C |
2: 118,701,985 (GRCm39) |
V139A |
probably benign |
Het |
Limch1 |
A |
T |
5: 67,116,942 (GRCm39) |
Y119F |
probably benign |
Het |
Lrp1 |
C |
T |
10: 127,374,856 (GRCm39) |
R4534Q |
probably benign |
Het |
Mbd3l2 |
G |
A |
9: 18,355,738 (GRCm39) |
S21N |
probably benign |
Het |
Mob1b |
A |
G |
5: 88,901,036 (GRCm39) |
N148D |
probably benign |
Het |
Mylk4 |
A |
T |
13: 32,904,548 (GRCm39) |
D195E |
probably benign |
Het |
Ndufa7 |
T |
C |
17: 34,048,687 (GRCm39) |
S50P |
probably benign |
Het |
Nectin4 |
G |
T |
1: 171,214,203 (GRCm39) |
E453* |
probably null |
Het |
Nell1 |
T |
G |
7: 50,506,017 (GRCm39) |
F741L |
probably benign |
Het |
Ntng1 |
T |
A |
3: 109,739,933 (GRCm39) |
H369L |
possibly damaging |
Het |
Plin4 |
T |
A |
17: 56,409,330 (GRCm39) |
M1297L |
probably benign |
Het |
Pnp |
G |
A |
14: 51,188,404 (GRCm39) |
V193M |
probably damaging |
Het |
Ppp1r10 |
T |
G |
17: 36,241,773 (GRCm39) |
S849R |
unknown |
Het |
Rpgrip1 |
A |
G |
14: 52,387,012 (GRCm39) |
E981G |
unknown |
Het |
Sbsn |
T |
C |
7: 30,451,309 (GRCm39) |
F108S |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,636,017 (GRCm39) |
M310T |
probably benign |
Het |
Sf3b1 |
A |
G |
1: 55,055,949 (GRCm39) |
S97P |
probably benign |
Het |
Sgsh |
A |
G |
11: 119,238,525 (GRCm39) |
V313A |
probably benign |
Het |
Slc25a10 |
G |
T |
11: 120,382,782 (GRCm39) |
|
probably benign |
Het |
Slc9a2 |
T |
A |
1: 40,806,828 (GRCm39) |
V705E |
possibly damaging |
Het |
Surf2 |
G |
T |
2: 26,808,894 (GRCm39) |
C116F |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 84,882,698 (GRCm39) |
I175T |
probably benign |
Het |
Tnxb |
C |
T |
17: 34,897,875 (GRCm39) |
T841I |
probably benign |
Het |
Ttll3 |
A |
G |
6: 113,386,246 (GRCm39) |
D693G |
probably damaging |
Het |
Ust |
A |
G |
10: 8,393,973 (GRCm39) |
L64P |
probably damaging |
Het |
Vmn1r77 |
C |
T |
7: 11,775,983 (GRCm39) |
S253F |
possibly damaging |
Het |
Vmn2r66 |
A |
G |
7: 84,654,423 (GRCm39) |
M512T |
probably benign |
Het |
Zfp13 |
C |
T |
17: 23,800,036 (GRCm39) |
G89D |
probably damaging |
Het |
Zfp616 |
T |
A |
11: 73,976,205 (GRCm39) |
Y825N |
probably benign |
Het |
Zfp865 |
A |
G |
7: 5,032,252 (GRCm39) |
Y79C |
possibly damaging |
Het |
Zfyve26 |
A |
T |
12: 79,297,942 (GRCm39) |
F1916I |
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 |
|
R6115:Ccdc102a
|
UTSW |
8 |
95,629,999 (GRCm39) |
missense |
probably benign |
|
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 |
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 |
|