Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat3 |
G |
A |
17: 13,147,460 (GRCm39) |
Q186* |
probably null |
Het |
Alk |
A |
G |
17: 72,910,427 (GRCm39) |
L93P |
possibly damaging |
Het |
Ankrd24 |
C |
T |
10: 81,478,513 (GRCm39) |
|
probably benign |
Het |
Anks6 |
A |
T |
4: 47,049,212 (GRCm39) |
V231E |
probably damaging |
Het |
Ap5z1 |
C |
T |
5: 142,456,168 (GRCm39) |
S329L |
probably benign |
Het |
Asic4 |
C |
A |
1: 75,446,485 (GRCm39) |
|
probably benign |
Het |
Cemip2 |
T |
G |
19: 21,784,816 (GRCm39) |
I433S |
probably damaging |
Het |
Cers4 |
C |
A |
8: 4,568,285 (GRCm39) |
Q113K |
possibly damaging |
Het |
Ces3b |
A |
T |
8: 105,813,520 (GRCm39) |
I264F |
possibly damaging |
Het |
Cops3 |
T |
C |
11: 59,718,797 (GRCm39) |
M166V |
probably benign |
Het |
Corin |
T |
C |
5: 72,592,641 (GRCm39) |
Q184R |
probably benign |
Het |
Dnah8 |
G |
A |
17: 31,073,872 (GRCm39) |
R4514H |
probably damaging |
Het |
Drosha |
T |
A |
15: 12,912,623 (GRCm39) |
Y1080* |
probably null |
Het |
Gm53 |
T |
C |
11: 96,142,477 (GRCm39) |
|
noncoding transcript |
Het |
Hmcn1 |
A |
G |
1: 150,498,745 (GRCm39) |
S4045P |
probably benign |
Het |
Kif22 |
A |
G |
7: 126,628,668 (GRCm39) |
L480P |
probably damaging |
Het |
Lepr |
A |
T |
4: 101,648,111 (GRCm39) |
|
probably benign |
Het |
Lnpk |
A |
T |
2: 74,352,607 (GRCm39) |
S358R |
probably benign |
Het |
Lnx1 |
A |
G |
5: 74,789,027 (GRCm39) |
|
probably benign |
Het |
Lrsam1 |
T |
C |
2: 32,848,171 (GRCm39) |
E43G |
probably null |
Het |
Mug1 |
G |
A |
6: 121,861,587 (GRCm39) |
V1350I |
probably benign |
Het |
Nbea |
T |
A |
3: 55,912,450 (GRCm39) |
E1112D |
probably benign |
Het |
Nepn |
T |
A |
10: 52,276,626 (GRCm39) |
L60I |
probably damaging |
Het |
Oas1e |
T |
C |
5: 120,933,475 (GRCm39) |
E30G |
probably damaging |
Het |
Or4c122 |
A |
G |
2: 89,079,337 (GRCm39) |
F234L |
probably benign |
Het |
Or4k5 |
A |
C |
14: 50,386,026 (GRCm39) |
F102V |
possibly damaging |
Het |
Pou2f1 |
G |
C |
1: 165,722,538 (GRCm39) |
P349R |
probably damaging |
Het |
Prmt8 |
A |
T |
6: 127,688,110 (GRCm39) |
I236N |
probably damaging |
Het |
Psg23 |
C |
A |
7: 18,346,126 (GRCm39) |
V190L |
probably benign |
Het |
Psg29 |
A |
G |
7: 16,938,950 (GRCm39) |
K75E |
possibly damaging |
Het |
Ranbp17 |
GCCTGGATACTGACC |
GCC |
11: 33,169,203 (GRCm39) |
|
probably benign |
Het |
Rgs4 |
A |
G |
1: 169,571,991 (GRCm39) |
S103P |
probably damaging |
Het |
Sis |
T |
C |
3: 72,828,747 (GRCm39) |
Y1144C |
probably damaging |
Het |
Slc16a14 |
T |
C |
1: 84,907,001 (GRCm39) |
|
probably benign |
Het |
Snrnp35 |
T |
A |
5: 124,628,248 (GRCm39) |
D20E |
probably damaging |
Het |
Syce1l |
C |
A |
8: 114,369,897 (GRCm39) |
A10E |
possibly damaging |
Het |
Tdp1 |
A |
G |
12: 99,858,011 (GRCm39) |
|
probably benign |
Het |
Tmem212 |
T |
C |
3: 27,940,594 (GRCm39) |
|
probably null |
Het |
Tomm20l |
C |
T |
12: 71,158,516 (GRCm39) |
A58V |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,568,471 (GRCm39) |
C27474F |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,804,552 (GRCm39) |
V240A |
probably benign |
Het |
Vars1 |
A |
G |
17: 35,218,310 (GRCm39) |
V48A |
probably benign |
Het |
Vmn2r1 |
T |
C |
3: 63,994,185 (GRCm39) |
|
probably null |
Het |
Washc2 |
A |
G |
6: 116,224,933 (GRCm39) |
|
probably benign |
Het |
Zfp943 |
A |
G |
17: 22,211,403 (GRCm39) |
D163G |
possibly damaging |
Het |
|
Other mutations in Zmym5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01933:Zmym5
|
APN |
14 |
57,041,617 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02028:Zmym5
|
APN |
14 |
57,041,617 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02535:Zmym5
|
APN |
14 |
57,035,123 (GRCm39) |
critical splice donor site |
probably null |
|
cerveza
|
UTSW |
14 |
57,031,918 (GRCm39) |
nonsense |
probably null |
|
Yeast
|
UTSW |
14 |
57,049,618 (GRCm39) |
unclassified |
probably benign |
|
R0391:Zmym5
|
UTSW |
14 |
57,041,908 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1692:Zmym5
|
UTSW |
14 |
57,041,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R1939:Zmym5
|
UTSW |
14 |
57,036,577 (GRCm39) |
missense |
probably damaging |
0.98 |
R1997:Zmym5
|
UTSW |
14 |
57,035,210 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4027:Zmym5
|
UTSW |
14 |
57,035,268 (GRCm39) |
missense |
probably benign |
0.18 |
R4345:Zmym5
|
UTSW |
14 |
57,034,083 (GRCm39) |
missense |
probably benign |
0.00 |
R4622:Zmym5
|
UTSW |
14 |
57,049,693 (GRCm39) |
unclassified |
probably benign |
|
R4686:Zmym5
|
UTSW |
14 |
57,049,618 (GRCm39) |
unclassified |
probably benign |
|
R5092:Zmym5
|
UTSW |
14 |
57,034,236 (GRCm39) |
missense |
probably benign |
0.27 |
R5344:Zmym5
|
UTSW |
14 |
57,031,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R6356:Zmym5
|
UTSW |
14 |
57,031,622 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7074:Zmym5
|
UTSW |
14 |
57,042,255 (GRCm39) |
missense |
probably benign |
|
R7358:Zmym5
|
UTSW |
14 |
57,031,597 (GRCm39) |
nonsense |
probably null |
|
R7657:Zmym5
|
UTSW |
14 |
57,041,653 (GRCm39) |
missense |
probably benign |
0.01 |
R7811:Zmym5
|
UTSW |
14 |
57,036,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R8013:Zmym5
|
UTSW |
14 |
57,031,883 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8014:Zmym5
|
UTSW |
14 |
57,031,883 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8174:Zmym5
|
UTSW |
14 |
57,031,918 (GRCm39) |
nonsense |
probably null |
|
R9260:Zmym5
|
UTSW |
14 |
57,041,641 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zmym5
|
UTSW |
14 |
57,035,277 (GRCm39) |
missense |
probably benign |
0.01 |
|