Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
A |
T |
17: 84,966,091 (GRCm39) |
M423K |
probably benign |
Het |
Adamtsl1 |
T |
A |
4: 86,255,246 (GRCm39) |
W780R |
probably damaging |
Het |
Ago3 |
A |
G |
4: 126,311,165 (GRCm39) |
I16T |
probably benign |
Het |
Amph |
T |
A |
13: 19,297,316 (GRCm39) |
L354* |
probably null |
Het |
Ankk1 |
G |
A |
9: 49,338,267 (GRCm39) |
L9F |
probably benign |
Het |
Brdt |
A |
G |
5: 107,525,011 (GRCm39) |
T851A |
probably damaging |
Het |
Bzw2 |
A |
C |
12: 36,170,788 (GRCm39) |
|
probably null |
Het |
Capn7 |
A |
T |
14: 31,081,167 (GRCm39) |
I395F |
probably damaging |
Het |
Ccdc146 |
T |
C |
5: 21,499,591 (GRCm39) |
R864G |
possibly damaging |
Het |
Ccdc50 |
G |
T |
16: 27,228,139 (GRCm39) |
R102L |
possibly damaging |
Het |
Cep83 |
T |
C |
10: 94,622,700 (GRCm39) |
V592A |
probably damaging |
Het |
Cgn |
G |
A |
3: 94,685,792 (GRCm39) |
|
probably benign |
Het |
Cidec |
C |
A |
6: 113,405,086 (GRCm39) |
V195L |
probably benign |
Het |
Cntln |
A |
G |
4: 84,923,289 (GRCm39) |
|
probably benign |
Het |
Cntrob |
A |
T |
11: 69,213,526 (GRCm39) |
L88* |
probably null |
Het |
Dnah17 |
C |
T |
11: 117,931,912 (GRCm39) |
V3687M |
probably damaging |
Het |
Dst |
T |
C |
1: 34,328,729 (GRCm39) |
I4599T |
probably damaging |
Het |
Dtl |
A |
T |
1: 191,285,175 (GRCm39) |
Y320* |
probably null |
Het |
Fam98b |
A |
G |
2: 117,098,408 (GRCm39) |
T293A |
probably damaging |
Het |
Farp1 |
G |
A |
14: 121,460,138 (GRCm39) |
|
probably benign |
Het |
Fat2 |
G |
T |
11: 55,202,622 (GRCm39) |
P151T |
probably damaging |
Het |
Fbxl17 |
A |
T |
17: 63,778,419 (GRCm39) |
M497K |
probably damaging |
Het |
Foxn4 |
T |
C |
5: 114,396,776 (GRCm39) |
T236A |
probably damaging |
Het |
Gm525 |
C |
T |
11: 88,979,374 (GRCm39) |
|
probably benign |
Het |
Golga4 |
C |
A |
9: 118,386,448 (GRCm39) |
T1190K |
possibly damaging |
Het |
H2-T23 |
T |
A |
17: 36,341,855 (GRCm39) |
M248L |
probably benign |
Het |
Homez |
T |
C |
14: 55,094,778 (GRCm39) |
E310G |
probably benign |
Het |
Hydin |
A |
G |
8: 111,233,138 (GRCm39) |
I1746V |
probably benign |
Het |
Igkv1-35 |
T |
A |
6: 69,988,641 (GRCm39) |
H6L |
probably benign |
Het |
Kcnt2 |
T |
C |
1: 140,356,622 (GRCm39) |
S354P |
probably damaging |
Het |
Khdc4 |
A |
G |
3: 88,596,599 (GRCm39) |
T127A |
probably damaging |
Het |
Klra4 |
G |
T |
6: 130,040,141 (GRCm39) |
Q44K |
probably benign |
Het |
L3mbtl3 |
A |
G |
10: 26,220,119 (GRCm39) |
|
probably benign |
Het |
Lamb1 |
C |
T |
12: 31,337,528 (GRCm39) |
R372C |
probably damaging |
Het |
Magea14 |
A |
T |
X: 51,057,968 (GRCm39) |
Y239* |
probably null |
Het |
Map3k9 |
A |
G |
12: 81,790,698 (GRCm39) |
I285T |
probably damaging |
Het |
Or4a47 |
T |
A |
2: 89,665,858 (GRCm39) |
I144L |
probably benign |
Het |
Or6c6 |
A |
G |
10: 129,186,552 (GRCm39) |
N40S |
possibly damaging |
Het |
Pcdhb16 |
A |
T |
18: 37,611,271 (GRCm39) |
Q77L |
possibly damaging |
Het |
Proser3 |
A |
G |
7: 30,239,796 (GRCm39) |
V436A |
probably benign |
Het |
Relch |
A |
G |
1: 105,653,524 (GRCm39) |
N834S |
probably benign |
Het |
Resf1 |
T |
A |
6: 149,230,741 (GRCm39) |
C1262* |
probably null |
Het |
Sec24b |
C |
T |
3: 129,795,953 (GRCm39) |
|
probably null |
Het |
Slc2a2 |
A |
G |
3: 28,775,898 (GRCm39) |
Q336R |
probably benign |
Het |
Sowahb |
T |
C |
5: 93,191,261 (GRCm39) |
D486G |
possibly damaging |
Het |
Spidr |
T |
C |
16: 15,958,724 (GRCm39) |
K13E |
probably damaging |
Het |
Tiam2 |
T |
A |
17: 3,489,977 (GRCm39) |
M786K |
probably benign |
Het |
Tktl2 |
T |
A |
8: 66,964,808 (GRCm39) |
V122E |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,451,172 (GRCm39) |
I729M |
possibly damaging |
Het |
Zbbx |
T |
C |
3: 74,989,153 (GRCm39) |
T317A |
possibly damaging |
Het |
Zfp976 |
A |
G |
7: 42,262,938 (GRCm39) |
C300R |
probably damaging |
Het |
|
Other mutations in Pramel20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02118:Pramel20
|
APN |
4 |
143,297,726 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02533:Pramel20
|
APN |
4 |
143,297,572 (GRCm39) |
utr 5 prime |
probably benign |
|
R0352:Pramel20
|
UTSW |
4 |
143,297,878 (GRCm39) |
splice site |
probably benign |
|
R1600:Pramel20
|
UTSW |
4 |
143,298,537 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4005:Pramel20
|
UTSW |
4 |
143,298,839 (GRCm39) |
missense |
probably benign |
0.00 |
R4477:Pramel20
|
UTSW |
4 |
143,297,732 (GRCm39) |
missense |
probably benign |
0.21 |
R4639:Pramel20
|
UTSW |
4 |
143,298,467 (GRCm39) |
missense |
probably benign |
0.22 |
R4791:Pramel20
|
UTSW |
4 |
143,297,559 (GRCm39) |
start gained |
probably benign |
|
R5118:Pramel20
|
UTSW |
4 |
143,297,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5353:Pramel20
|
UTSW |
4 |
143,297,807 (GRCm39) |
missense |
probably benign |
0.00 |
R5861:Pramel20
|
UTSW |
4 |
143,297,810 (GRCm39) |
missense |
probably benign |
|
R6163:Pramel20
|
UTSW |
4 |
143,298,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R6286:Pramel20
|
UTSW |
4 |
143,297,796 (GRCm39) |
missense |
probably benign |
|
R6958:Pramel20
|
UTSW |
4 |
143,297,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Pramel20
|
UTSW |
4 |
143,298,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R7625:Pramel20
|
UTSW |
4 |
143,298,821 (GRCm39) |
missense |
probably benign |
0.00 |
R8189:Pramel20
|
UTSW |
4 |
143,298,530 (GRCm39) |
missense |
probably benign |
|
R8190:Pramel20
|
UTSW |
4 |
143,298,530 (GRCm39) |
missense |
probably benign |
|
R8192:Pramel20
|
UTSW |
4 |
143,298,530 (GRCm39) |
missense |
probably benign |
|
R8219:Pramel20
|
UTSW |
4 |
143,298,530 (GRCm39) |
missense |
probably benign |
|
R8221:Pramel20
|
UTSW |
4 |
143,298,530 (GRCm39) |
missense |
probably benign |
|
R8223:Pramel20
|
UTSW |
4 |
143,298,530 (GRCm39) |
missense |
probably benign |
|
R8226:Pramel20
|
UTSW |
4 |
143,298,530 (GRCm39) |
missense |
probably benign |
|
R9005:Pramel20
|
UTSW |
4 |
143,298,425 (GRCm39) |
missense |
probably benign |
0.11 |
R9150:Pramel20
|
UTSW |
4 |
143,298,531 (GRCm39) |
missense |
probably benign |
|
R9295:Pramel20
|
UTSW |
4 |
143,298,704 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9307:Pramel20
|
UTSW |
4 |
143,299,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R9691:Pramel20
|
UTSW |
4 |
143,299,328 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Pramel20
|
UTSW |
4 |
143,298,822 (GRCm39) |
missense |
probably benign |
0.00 |
|