Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
T |
17: 46,635,361 (GRCm39) |
V214E |
probably damaging |
Het |
Adh1 |
A |
G |
3: 137,992,556 (GRCm39) |
D224G |
probably damaging |
Het |
Arhgap28 |
C |
A |
17: 68,164,459 (GRCm39) |
Q554H |
probably damaging |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Brat1 |
G |
A |
5: 140,703,768 (GRCm39) |
V674I |
probably benign |
Het |
Brd2 |
ATCTTCTTC |
ATCTTC |
17: 34,332,981 (GRCm39) |
|
probably benign |
Het |
Ccdc162 |
T |
C |
10: 41,429,178 (GRCm39) |
D438G |
possibly damaging |
Het |
Cyp4x1 |
T |
A |
4: 114,969,988 (GRCm39) |
|
probably benign |
Het |
Dip2a |
T |
C |
10: 76,115,654 (GRCm39) |
|
probably benign |
Het |
Eif2s1 |
A |
G |
12: 78,927,942 (GRCm39) |
D206G |
probably benign |
Het |
Gsto1 |
A |
G |
19: 47,846,381 (GRCm39) |
E76G |
probably damaging |
Het |
Hspa14 |
A |
T |
2: 3,509,858 (GRCm39) |
W12R |
probably damaging |
Het |
L3mbtl2 |
T |
A |
15: 81,560,518 (GRCm39) |
C260S |
possibly damaging |
Het |
Lama3 |
G |
T |
18: 12,614,155 (GRCm39) |
|
probably null |
Het |
Lrrc34 |
T |
A |
3: 30,697,728 (GRCm39) |
|
probably benign |
Het |
Lrrc45 |
A |
T |
11: 120,610,839 (GRCm39) |
Q525L |
probably benign |
Het |
Lss |
T |
C |
10: 76,372,137 (GRCm39) |
I164T |
probably damaging |
Het |
Myh11 |
T |
A |
16: 14,023,795 (GRCm39) |
K1527* |
probably null |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Ncoa1 |
T |
A |
12: 4,320,737 (GRCm39) |
|
probably benign |
Het |
Or5an1c |
G |
T |
19: 12,218,546 (GRCm39) |
Q160K |
possibly damaging |
Het |
Or6c38 |
A |
T |
10: 128,929,559 (GRCm39) |
C95S |
probably damaging |
Het |
Pafah1b3 |
T |
C |
7: 24,996,560 (GRCm39) |
E41G |
possibly damaging |
Het |
Pnma8a |
C |
T |
7: 16,694,909 (GRCm39) |
P255S |
possibly damaging |
Het |
Prkar2b |
A |
T |
12: 32,012,987 (GRCm39) |
|
probably benign |
Het |
Rbck1 |
A |
T |
2: 152,169,161 (GRCm39) |
|
probably benign |
Het |
Rcor2 |
A |
G |
19: 7,248,395 (GRCm39) |
S137G |
possibly damaging |
Het |
Slc25a48 |
T |
A |
13: 56,596,804 (GRCm39) |
|
probably benign |
Het |
Slc7a4 |
A |
G |
16: 17,391,808 (GRCm39) |
|
probably null |
Het |
Tert |
T |
C |
13: 73,790,472 (GRCm39) |
|
probably benign |
Het |
Traf7 |
A |
T |
17: 24,730,655 (GRCm39) |
I344N |
probably damaging |
Het |
Vmn1r194 |
T |
A |
13: 22,429,236 (GRCm39) |
F284L |
probably damaging |
Het |
Xpc |
A |
G |
6: 91,470,220 (GRCm39) |
M699T |
probably damaging |
Het |
Zbtb5 |
T |
C |
4: 44,993,968 (GRCm39) |
H472R |
possibly damaging |
Het |
Zfp786 |
A |
G |
6: 47,802,013 (GRCm39) |
V88A |
probably benign |
Het |
Zkscan7 |
T |
C |
9: 122,724,228 (GRCm39) |
I399T |
probably benign |
Het |
Zyg11b |
G |
A |
4: 108,108,009 (GRCm39) |
R466C |
probably damaging |
Het |
|
Other mutations in Elovl7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01819:Elovl7
|
APN |
13 |
108,410,854 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01901:Elovl7
|
APN |
13 |
108,410,927 (GRCm39) |
critical splice donor site |
probably null |
|
R1346:Elovl7
|
UTSW |
13 |
108,410,883 (GRCm39) |
missense |
probably benign |
0.02 |
R1677:Elovl7
|
UTSW |
13 |
108,419,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4163:Elovl7
|
UTSW |
13 |
108,403,904 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4207:Elovl7
|
UTSW |
13 |
108,419,040 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5000:Elovl7
|
UTSW |
13 |
108,410,915 (GRCm39) |
missense |
probably benign |
0.38 |
R5467:Elovl7
|
UTSW |
13 |
108,416,156 (GRCm39) |
missense |
probably benign |
0.12 |
R7186:Elovl7
|
UTSW |
13 |
108,408,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8736:Elovl7
|
UTSW |
13 |
108,393,320 (GRCm39) |
missense |
probably benign |
0.00 |
R8956:Elovl7
|
UTSW |
13 |
108,393,320 (GRCm39) |
missense |
probably benign |
0.00 |
R9401:Elovl7
|
UTSW |
13 |
108,419,188 (GRCm39) |
missense |
probably benign |
0.00 |
R9695:Elovl7
|
UTSW |
13 |
108,416,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|