Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
A |
G |
5: 125,580,338 (GRCm39) |
E221G |
probably benign |
Het |
Alb |
A |
G |
5: 90,619,932 (GRCm39) |
N453S |
probably benign |
Het |
Bckdha |
C |
T |
7: 25,332,767 (GRCm39) |
V183M |
probably benign |
Het |
Brpf3 |
A |
G |
17: 29,055,674 (GRCm39) |
|
probably benign |
Het |
Ccdc163 |
T |
C |
4: 116,567,487 (GRCm39) |
|
probably null |
Het |
Ccdc178 |
A |
T |
18: 22,268,225 (GRCm39) |
C87* |
probably null |
Het |
Cfhr4 |
A |
T |
1: 139,659,312 (GRCm39) |
V739E |
probably damaging |
Het |
Clca4a |
A |
G |
3: 144,660,700 (GRCm39) |
V708A |
probably damaging |
Het |
Cyfip2 |
A |
G |
11: 46,091,512 (GRCm39) |
V1136A |
possibly damaging |
Het |
Dnah11 |
A |
C |
12: 117,874,937 (GRCm39) |
L3976R |
probably damaging |
Het |
Fam228a |
A |
T |
12: 4,782,773 (GRCm39) |
Y107N |
possibly damaging |
Het |
Iars2 |
A |
T |
1: 185,028,600 (GRCm39) |
|
probably benign |
Het |
Ifi204 |
A |
G |
1: 173,587,197 (GRCm39) |
|
probably benign |
Het |
Ifih1 |
A |
T |
2: 62,476,168 (GRCm39) |
I36N |
probably benign |
Het |
Jak1 |
C |
T |
4: 101,011,826 (GRCm39) |
G1092D |
probably damaging |
Het |
Kir3dl2 |
G |
A |
X: 135,357,097 (GRCm39) |
P122S |
probably damaging |
Het |
Nacc2 |
T |
C |
2: 25,951,678 (GRCm39) |
T386A |
probably damaging |
Het |
Nrf1 |
C |
T |
6: 30,098,477 (GRCm39) |
T135M |
probably damaging |
Het |
Or4k15 |
A |
G |
14: 50,364,214 (GRCm39) |
Y60C |
probably damaging |
Het |
Or51i2 |
G |
A |
7: 103,689,051 (GRCm39) |
G16D |
probably damaging |
Het |
Pcca |
A |
C |
14: 122,927,545 (GRCm39) |
D436A |
probably benign |
Het |
Pcdhb11 |
A |
T |
18: 37,555,174 (GRCm39) |
Q168L |
possibly damaging |
Het |
Pdgfra |
A |
G |
5: 75,340,834 (GRCm39) |
I598V |
probably benign |
Het |
Pla2g6 |
C |
T |
15: 79,171,947 (GRCm39) |
V637I |
probably damaging |
Het |
Plac1 |
A |
C |
X: 52,159,593 (GRCm39) |
V39G |
probably damaging |
Het |
Pparg |
A |
G |
6: 115,416,822 (GRCm39) |
E5G |
probably damaging |
Het |
Ppp1r9a |
A |
G |
6: 5,157,023 (GRCm39) |
D967G |
possibly damaging |
Het |
Rel |
T |
C |
11: 23,694,266 (GRCm39) |
T322A |
probably benign |
Het |
Sgk3 |
A |
G |
1: 9,947,470 (GRCm39) |
T137A |
probably benign |
Het |
Sgpp2 |
A |
G |
1: 78,367,184 (GRCm39) |
R106G |
probably benign |
Het |
Slc27a5 |
T |
A |
7: 12,724,984 (GRCm39) |
M459L |
probably benign |
Het |
Snx21 |
T |
C |
2: 164,628,140 (GRCm39) |
L52P |
probably damaging |
Het |
Srarp |
G |
A |
4: 141,160,584 (GRCm39) |
T83M |
probably benign |
Het |
Sstr2 |
A |
G |
11: 113,515,821 (GRCm39) |
R247G |
probably benign |
Het |
Tnpo3 |
G |
A |
6: 29,589,047 (GRCm39) |
S101L |
probably damaging |
Het |
Zan |
A |
G |
5: 137,387,622 (GRCm39) |
I4863T |
unknown |
Het |
|
Other mutations in Erich1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00927:Erich1
|
APN |
8 |
14,083,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01448:Erich1
|
APN |
8 |
14,128,853 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1165:Erich1
|
UTSW |
8 |
14,140,530 (GRCm39) |
unclassified |
probably benign |
|
R1541:Erich1
|
UTSW |
8 |
14,080,688 (GRCm39) |
missense |
probably damaging |
0.97 |
R1699:Erich1
|
UTSW |
8 |
14,140,259 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2094:Erich1
|
UTSW |
8 |
14,140,527 (GRCm39) |
unclassified |
probably benign |
|
R2153:Erich1
|
UTSW |
8 |
14,128,773 (GRCm39) |
missense |
probably benign |
0.08 |
R3807:Erich1
|
UTSW |
8 |
14,083,695 (GRCm39) |
missense |
probably benign |
0.11 |
R5787:Erich1
|
UTSW |
8 |
14,083,776 (GRCm39) |
splice site |
probably null |
|
R6119:Erich1
|
UTSW |
8 |
14,083,692 (GRCm39) |
missense |
probably benign |
|
R7034:Erich1
|
UTSW |
8 |
14,114,330 (GRCm39) |
missense |
probably benign |
0.02 |
R7363:Erich1
|
UTSW |
8 |
14,083,688 (GRCm39) |
missense |
probably benign |
0.05 |
R7687:Erich1
|
UTSW |
8 |
14,080,691 (GRCm39) |
missense |
probably damaging |
0.99 |
R9087:Erich1
|
UTSW |
8 |
14,083,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R9376:Erich1
|
UTSW |
8 |
14,080,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|