Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agrn |
A |
C |
4: 156,255,029 (GRCm39) |
|
probably benign |
Het |
Antkmt |
A |
G |
17: 26,010,418 (GRCm39) |
Y104H |
probably damaging |
Het |
Arid4a |
A |
G |
12: 71,119,367 (GRCm39) |
K651E |
probably damaging |
Het |
Atpaf2 |
A |
T |
11: 60,300,410 (GRCm39) |
|
probably null |
Het |
Cd209g |
A |
T |
8: 4,185,622 (GRCm39) |
T19S |
probably benign |
Het |
Cxcr4 |
A |
G |
1: 128,516,792 (GRCm39) |
W290R |
probably damaging |
Het |
D930020B18Rik |
T |
C |
10: 121,521,489 (GRCm39) |
L491P |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,458,843 (GRCm39) |
D3765G |
probably damaging |
Het |
Dpy19l4 |
T |
G |
4: 11,290,411 (GRCm39) |
M327L |
probably benign |
Het |
Eya3 |
G |
A |
4: 132,431,709 (GRCm39) |
G314D |
probably damaging |
Het |
Fmo1 |
G |
A |
1: 162,657,632 (GRCm39) |
T503I |
probably benign |
Het |
Galnt3 |
A |
G |
2: 65,925,628 (GRCm39) |
S370P |
probably damaging |
Het |
Gm5431 |
A |
T |
11: 48,786,241 (GRCm39) |
S45T |
probably benign |
Het |
Gnai3 |
A |
G |
3: 108,023,073 (GRCm39) |
|
probably benign |
Het |
Gpat2 |
A |
G |
2: 127,276,381 (GRCm39) |
E637G |
probably damaging |
Het |
Gpr84 |
T |
C |
15: 103,217,834 (GRCm39) |
Y81C |
probably damaging |
Het |
Hnmt |
A |
T |
2: 23,893,896 (GRCm39) |
Y199* |
probably null |
Het |
Homer1 |
G |
T |
13: 93,483,156 (GRCm39) |
R81L |
probably damaging |
Het |
Hspa4 |
A |
T |
11: 53,171,544 (GRCm39) |
|
probably null |
Het |
Marchf6 |
A |
G |
15: 31,475,909 (GRCm39) |
I649T |
probably benign |
Het |
Mcm8 |
A |
G |
2: 132,659,094 (GRCm39) |
N26S |
probably benign |
Het |
Mgat5 |
T |
C |
1: 127,315,204 (GRCm39) |
L310P |
probably damaging |
Het |
Pah |
T |
C |
10: 87,414,755 (GRCm39) |
L369P |
probably benign |
Het |
Parp4 |
A |
C |
14: 56,853,917 (GRCm39) |
K844N |
possibly damaging |
Het |
Tlr5 |
A |
G |
1: 182,801,394 (GRCm39) |
T233A |
probably benign |
Het |
Tsnaxip1 |
A |
G |
8: 106,568,055 (GRCm39) |
T274A |
probably benign |
Het |
Wdr48 |
A |
G |
9: 119,734,456 (GRCm39) |
Y125C |
probably damaging |
Het |
|
Other mutations in Cd177 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Cd177
|
APN |
7 |
24,459,176 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL00673:Cd177
|
APN |
7 |
24,451,442 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00913:Cd177
|
APN |
7 |
24,455,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01445:Cd177
|
APN |
7 |
24,451,496 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02021:Cd177
|
APN |
7 |
24,444,631 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02134:Cd177
|
APN |
7 |
24,451,777 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02532:Cd177
|
APN |
7 |
24,444,674 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02821:Cd177
|
APN |
7 |
24,443,819 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02821:Cd177
|
APN |
7 |
24,443,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02888:Cd177
|
APN |
7 |
24,457,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R0506:Cd177
|
UTSW |
7 |
24,457,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Cd177
|
UTSW |
7 |
24,451,738 (GRCm39) |
missense |
probably benign |
0.00 |
R0631:Cd177
|
UTSW |
7 |
24,456,111 (GRCm39) |
missense |
probably benign |
0.03 |
R0713:Cd177
|
UTSW |
7 |
24,443,855 (GRCm39) |
missense |
probably benign |
0.25 |
R1595:Cd177
|
UTSW |
7 |
24,444,389 (GRCm39) |
missense |
probably benign |
|
R1659:Cd177
|
UTSW |
7 |
24,445,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Cd177
|
UTSW |
7 |
24,455,661 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2260:Cd177
|
UTSW |
7 |
24,455,661 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2379:Cd177
|
UTSW |
7 |
24,457,468 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2763:Cd177
|
UTSW |
7 |
24,457,462 (GRCm39) |
missense |
probably benign |
0.05 |
R2929:Cd177
|
UTSW |
7 |
24,453,704 (GRCm39) |
nonsense |
probably null |
|
R3815:Cd177
|
UTSW |
7 |
24,453,817 (GRCm39) |
missense |
probably benign |
0.00 |
R3818:Cd177
|
UTSW |
7 |
24,453,817 (GRCm39) |
missense |
probably benign |
0.00 |
R3919:Cd177
|
UTSW |
7 |
24,443,858 (GRCm39) |
missense |
probably benign |
0.15 |
R4300:Cd177
|
UTSW |
7 |
24,449,845 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4494:Cd177
|
UTSW |
7 |
24,451,428 (GRCm39) |
missense |
probably benign |
0.06 |
R4781:Cd177
|
UTSW |
7 |
24,450,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4819:Cd177
|
UTSW |
7 |
24,451,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R5062:Cd177
|
UTSW |
7 |
24,443,741 (GRCm39) |
missense |
probably benign |
0.03 |
R5186:Cd177
|
UTSW |
7 |
24,444,348 (GRCm39) |
missense |
probably benign |
0.31 |
R5285:Cd177
|
UTSW |
7 |
24,445,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5415:Cd177
|
UTSW |
7 |
24,451,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R5577:Cd177
|
UTSW |
7 |
24,444,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R5637:Cd177
|
UTSW |
7 |
24,455,748 (GRCm39) |
missense |
probably benign |
0.01 |
R5673:Cd177
|
UTSW |
7 |
24,449,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5731:Cd177
|
UTSW |
7 |
24,443,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Cd177
|
UTSW |
7 |
24,451,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5840:Cd177
|
UTSW |
7 |
24,457,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R5870:Cd177
|
UTSW |
7 |
24,455,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5872:Cd177
|
UTSW |
7 |
24,451,688 (GRCm39) |
missense |
probably null |
1.00 |
R6148:Cd177
|
UTSW |
7 |
24,443,698 (GRCm39) |
nonsense |
probably null |
|
R6505:Cd177
|
UTSW |
7 |
24,443,671 (GRCm39) |
missense |
probably benign |
0.00 |
R6897:Cd177
|
UTSW |
7 |
24,444,499 (GRCm39) |
missense |
probably benign |
0.31 |
R7023:Cd177
|
UTSW |
7 |
24,459,187 (GRCm39) |
missense |
probably benign |
0.44 |
R7088:Cd177
|
UTSW |
7 |
24,444,558 (GRCm39) |
nonsense |
probably null |
|
R7188:Cd177
|
UTSW |
7 |
24,456,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R7366:Cd177
|
UTSW |
7 |
24,456,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R7744:Cd177
|
UTSW |
7 |
24,449,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R8008:Cd177
|
UTSW |
7 |
24,451,774 (GRCm39) |
missense |
not run |
|
R8029:Cd177
|
UTSW |
7 |
24,455,594 (GRCm39) |
nonsense |
probably null |
|
R8030:Cd177
|
UTSW |
7 |
24,455,594 (GRCm39) |
nonsense |
probably null |
|
R8032:Cd177
|
UTSW |
7 |
24,455,594 (GRCm39) |
nonsense |
probably null |
|
R8094:Cd177
|
UTSW |
7 |
24,443,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R8121:Cd177
|
UTSW |
7 |
24,459,067 (GRCm39) |
missense |
probably benign |
|
R8192:Cd177
|
UTSW |
7 |
24,453,727 (GRCm39) |
missense |
probably benign |
0.00 |
R8314:Cd177
|
UTSW |
7 |
24,450,013 (GRCm39) |
missense |
probably benign |
0.15 |
R8682:Cd177
|
UTSW |
7 |
24,459,438 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8730:Cd177
|
UTSW |
7 |
24,457,501 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9185:Cd177
|
UTSW |
7 |
24,443,668 (GRCm39) |
missense |
probably benign |
0.00 |
R9217:Cd177
|
UTSW |
7 |
24,445,550 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9335:Cd177
|
UTSW |
7 |
24,443,711 (GRCm39) |
missense |
probably benign |
0.04 |
R9595:Cd177
|
UTSW |
7 |
24,451,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R9796:Cd177
|
UTSW |
7 |
24,459,169 (GRCm39) |
missense |
probably benign |
|
Z1176:Cd177
|
UTSW |
7 |
24,445,596 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Cd177
|
UTSW |
7 |
24,459,681 (GRCm39) |
missense |
probably damaging |
1.00 |
|