Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A330008L17Rik |
T |
C |
8: 100,148,586 (GRCm39) |
|
noncoding transcript |
Het |
Acp4 |
C |
T |
7: 43,902,876 (GRCm39) |
V331I |
probably benign |
Het |
Aen |
G |
A |
7: 78,557,050 (GRCm39) |
M299I |
probably damaging |
Het |
Alg6 |
T |
C |
4: 99,629,807 (GRCm39) |
V128A |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,686,026 (GRCm39) |
K280E |
probably damaging |
Het |
Bfar |
T |
C |
16: 13,503,105 (GRCm39) |
C36R |
probably damaging |
Het |
Car14 |
A |
G |
3: 95,806,128 (GRCm39) |
I311T |
probably damaging |
Het |
Cd300c |
T |
C |
11: 114,851,253 (GRCm39) |
|
probably benign |
Het |
Cfap100 |
T |
A |
6: 90,383,096 (GRCm39) |
E513V |
probably damaging |
Het |
Clip1 |
C |
A |
5: 123,768,867 (GRCm39) |
K612N |
probably damaging |
Het |
Depdc5 |
A |
G |
5: 33,056,411 (GRCm39) |
|
probably null |
Het |
Dock3 |
A |
T |
9: 106,959,572 (GRCm39) |
|
probably null |
Het |
Dph6 |
A |
T |
2: 114,478,290 (GRCm39) |
M17K |
probably damaging |
Het |
Enkur |
T |
C |
2: 21,194,042 (GRCm39) |
Q177R |
probably benign |
Het |
Faap100 |
T |
C |
11: 120,262,958 (GRCm39) |
H800R |
probably damaging |
Het |
Fastkd2 |
T |
G |
1: 63,776,930 (GRCm39) |
|
probably benign |
Het |
Fcgr2b |
A |
T |
1: 170,795,622 (GRCm39) |
N102K |
possibly damaging |
Het |
Fezf1 |
C |
T |
6: 23,247,842 (GRCm39) |
V78I |
possibly damaging |
Het |
Fmn2 |
A |
T |
1: 174,330,885 (GRCm39) |
D425V |
unknown |
Het |
Fnta |
G |
A |
8: 26,497,229 (GRCm39) |
Q207* |
probably null |
Het |
Fpr3 |
T |
A |
17: 18,190,828 (GRCm39) |
V33D |
probably benign |
Het |
Fshr |
C |
T |
17: 89,292,821 (GRCm39) |
C619Y |
possibly damaging |
Het |
Gbp3 |
T |
C |
3: 142,272,358 (GRCm39) |
|
probably null |
Het |
Gjb2 |
A |
G |
14: 57,337,629 (GRCm39) |
V193A |
possibly damaging |
Het |
Il4ra |
A |
G |
7: 125,174,333 (GRCm39) |
T292A |
probably benign |
Het |
Lama5 |
A |
G |
2: 179,818,336 (GRCm39) |
|
probably benign |
Het |
Marveld3 |
G |
T |
8: 110,688,596 (GRCm39) |
D48E |
possibly damaging |
Het |
Meox1 |
A |
T |
11: 101,784,599 (GRCm39) |
I78N |
probably benign |
Het |
Ncor1 |
A |
T |
11: 62,283,354 (GRCm39) |
H444Q |
probably damaging |
Het |
Ndst3 |
T |
C |
3: 123,340,466 (GRCm39) |
Q784R |
probably damaging |
Het |
Or10ag2 |
A |
G |
2: 87,248,714 (GRCm39) |
I107M |
probably benign |
Het |
Or4k44 |
T |
A |
2: 111,368,359 (GRCm39) |
I92F |
probably damaging |
Het |
Pld5 |
A |
T |
1: 176,102,445 (GRCm39) |
|
probably benign |
Het |
Plk1 |
G |
A |
7: 121,768,148 (GRCm39) |
R456H |
probably damaging |
Het |
Polr2a |
T |
A |
11: 69,638,840 (GRCm39) |
I65F |
possibly damaging |
Het |
Ptprd |
T |
A |
4: 75,977,922 (GRCm39) |
I196F |
probably damaging |
Het |
Qsox2 |
T |
C |
2: 26,118,408 (GRCm39) |
N121S |
probably damaging |
Het |
Reln |
A |
G |
5: 22,184,664 (GRCm39) |
L1617S |
probably damaging |
Het |
Rragc |
T |
C |
4: 123,823,761 (GRCm39) |
F345L |
probably benign |
Het |
Sass6 |
A |
T |
3: 116,407,605 (GRCm39) |
E240D |
possibly damaging |
Het |
Shcbp1l |
A |
C |
1: 153,311,770 (GRCm39) |
S308R |
possibly damaging |
Het |
Slc1a5 |
T |
A |
7: 16,520,804 (GRCm39) |
C224* |
probably null |
Het |
Slc27a5 |
T |
C |
7: 12,722,999 (GRCm39) |
E567G |
probably damaging |
Het |
Synj2 |
T |
A |
17: 6,088,201 (GRCm39) |
N1417K |
possibly damaging |
Het |
Tbc1d9 |
A |
G |
8: 83,960,791 (GRCm39) |
T214A |
probably damaging |
Het |
Tjp3 |
C |
A |
10: 81,109,699 (GRCm39) |
V835L |
probably benign |
Het |
Trpc4 |
C |
A |
3: 54,129,983 (GRCm39) |
Q250K |
probably benign |
Het |
Ttn |
A |
T |
2: 76,575,506 (GRCm39) |
I25129N |
probably damaging |
Het |
Ube4a |
T |
A |
9: 44,856,163 (GRCm39) |
Y523F |
probably damaging |
Het |
Zfp971 |
G |
A |
2: 177,665,175 (GRCm39) |
|
probably null |
Het |
|
Other mutations in 1110038F14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01060:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01063:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01065:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01069:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01070:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01128:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01131:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01132:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01133:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01135:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01154:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01155:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02472:1110038F14Rik
|
APN |
15 |
76,834,578 (GRCm39) |
missense |
probably damaging |
0.98 |
ANU05:1110038F14Rik
|
UTSW |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:1110038F14Rik
|
UTSW |
15 |
76,833,863 (GRCm39) |
small insertion |
probably benign |
|
R4023:1110038F14Rik
|
UTSW |
15 |
76,833,863 (GRCm39) |
small insertion |
probably benign |
|
|