Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap11 |
T |
C |
14: 78,750,189 (GRCm39) |
T733A |
probably benign |
Het |
Antxrl |
A |
G |
14: 33,794,999 (GRCm39) |
N476D |
possibly damaging |
Het |
Armc8 |
G |
T |
9: 99,405,301 (GRCm39) |
P268Q |
probably benign |
Het |
Asb8 |
C |
A |
15: 98,034,304 (GRCm39) |
G84C |
probably damaging |
Het |
BC035044 |
A |
T |
6: 128,862,047 (GRCm39) |
|
probably null |
Het |
Caprin1 |
A |
G |
2: 103,606,332 (GRCm39) |
F303L |
probably benign |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Ctdspl2 |
G |
A |
2: 121,837,349 (GRCm39) |
R371Q |
probably damaging |
Het |
Dctn4 |
T |
A |
18: 60,689,402 (GRCm39) |
D431E |
probably benign |
Het |
Dhx40 |
T |
C |
11: 86,688,571 (GRCm39) |
E284G |
probably benign |
Het |
Dhx9 |
A |
G |
1: 153,340,684 (GRCm39) |
V652A |
probably damaging |
Het |
Fnip2 |
G |
T |
3: 79,415,398 (GRCm39) |
N213K |
possibly damaging |
Het |
Itch |
A |
G |
2: 155,048,274 (GRCm39) |
E546G |
possibly damaging |
Het |
Map3k20 |
A |
T |
2: 72,219,838 (GRCm39) |
I257F |
probably damaging |
Het |
Mertk |
T |
C |
2: 128,613,406 (GRCm39) |
I474T |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,719,495 (GRCm39) |
V156A |
possibly damaging |
Het |
Nbea |
A |
G |
3: 55,944,702 (GRCm39) |
V554A |
probably benign |
Het |
Or10z1 |
T |
A |
1: 174,078,427 (GRCm39) |
E22V |
possibly damaging |
Het |
Or13c7c |
C |
T |
4: 43,835,582 (GRCm39) |
V303M |
possibly damaging |
Het |
Or4f57 |
A |
G |
2: 111,790,926 (GRCm39) |
V164A |
probably benign |
Het |
Pask |
A |
G |
1: 93,249,373 (GRCm39) |
Y676H |
probably benign |
Het |
Pcare |
T |
C |
17: 72,056,156 (GRCm39) |
N1174D |
probably benign |
Het |
Plpp2 |
G |
A |
10: 79,366,611 (GRCm39) |
|
probably benign |
Het |
Rab32 |
A |
G |
10: 10,426,637 (GRCm39) |
V103A |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,422,144 (GRCm39) |
E262G |
possibly damaging |
Het |
Rtn4 |
A |
G |
11: 29,658,236 (GRCm39) |
T797A |
probably benign |
Het |
Sall1 |
A |
T |
8: 89,759,072 (GRCm39) |
I344K |
probably benign |
Het |
Scnn1b |
T |
C |
7: 121,501,767 (GRCm39) |
|
probably null |
Het |
Sik3 |
G |
T |
9: 46,034,643 (GRCm39) |
|
probably benign |
Het |
Slc7a2 |
G |
T |
8: 41,358,622 (GRCm39) |
G322W |
probably damaging |
Het |
Snx29 |
A |
G |
16: 11,217,657 (GRCm39) |
M153V |
probably benign |
Het |
Stk25 |
A |
G |
1: 93,552,875 (GRCm39) |
|
probably benign |
Het |
Stk4 |
C |
T |
2: 163,942,448 (GRCm39) |
T360M |
probably benign |
Het |
Ush1c |
A |
C |
7: 45,874,965 (GRCm39) |
|
probably null |
Het |
Vmn2r8 |
C |
T |
5: 108,950,234 (GRCm39) |
M204I |
probably benign |
Het |
Zfp839 |
C |
T |
12: 110,832,744 (GRCm39) |
T554M |
probably damaging |
Het |
|
Other mutations in Mdc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01473:Mdc1
|
APN |
17 |
36,158,912 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01662:Mdc1
|
APN |
17 |
36,163,397 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01931:Mdc1
|
APN |
17 |
36,159,123 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02542:Mdc1
|
APN |
17 |
36,164,048 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02823:Mdc1
|
APN |
17 |
36,163,815 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03411:Mdc1
|
APN |
17 |
36,164,018 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02799:Mdc1
|
UTSW |
17 |
36,157,083 (GRCm39) |
missense |
possibly damaging |
0.86 |
PIT4362001:Mdc1
|
UTSW |
17 |
36,155,361 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0054:Mdc1
|
UTSW |
17 |
36,159,925 (GRCm39) |
missense |
probably benign |
0.00 |
R0129:Mdc1
|
UTSW |
17 |
36,165,337 (GRCm39) |
missense |
probably benign |
0.04 |
R0131:Mdc1
|
UTSW |
17 |
36,163,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R0131:Mdc1
|
UTSW |
17 |
36,163,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R0132:Mdc1
|
UTSW |
17 |
36,163,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R1406:Mdc1
|
UTSW |
17 |
36,164,424 (GRCm39) |
missense |
probably benign |
0.10 |
R1597:Mdc1
|
UTSW |
17 |
36,156,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Mdc1
|
UTSW |
17 |
36,158,718 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1888:Mdc1
|
UTSW |
17 |
36,165,117 (GRCm39) |
missense |
probably benign |
0.03 |
R1888:Mdc1
|
UTSW |
17 |
36,165,117 (GRCm39) |
missense |
probably benign |
0.03 |
R1912:Mdc1
|
UTSW |
17 |
36,161,703 (GRCm39) |
missense |
probably benign |
0.19 |
R1912:Mdc1
|
UTSW |
17 |
36,155,430 (GRCm39) |
missense |
probably benign |
0.00 |
R1977:Mdc1
|
UTSW |
17 |
36,161,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2121:Mdc1
|
UTSW |
17 |
36,158,835 (GRCm39) |
missense |
probably benign |
0.03 |
R2122:Mdc1
|
UTSW |
17 |
36,158,835 (GRCm39) |
missense |
probably benign |
0.03 |
R2357:Mdc1
|
UTSW |
17 |
36,158,337 (GRCm39) |
missense |
probably benign |
0.00 |
R2842:Mdc1
|
UTSW |
17 |
36,159,686 (GRCm39) |
missense |
probably benign |
0.01 |
R2851:Mdc1
|
UTSW |
17 |
36,159,902 (GRCm39) |
missense |
probably benign |
0.04 |
R2852:Mdc1
|
UTSW |
17 |
36,159,902 (GRCm39) |
missense |
probably benign |
0.04 |
R2964:Mdc1
|
UTSW |
17 |
36,164,529 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2996:Mdc1
|
UTSW |
17 |
36,158,785 (GRCm39) |
unclassified |
probably benign |
|
R3752:Mdc1
|
UTSW |
17 |
36,156,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Mdc1
|
UTSW |
17 |
36,159,716 (GRCm39) |
missense |
probably benign |
0.00 |
R4641:Mdc1
|
UTSW |
17 |
36,168,361 (GRCm39) |
missense |
probably benign |
0.09 |
R4706:Mdc1
|
UTSW |
17 |
36,163,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R4809:Mdc1
|
UTSW |
17 |
36,159,993 (GRCm39) |
critical splice donor site |
probably null |
|
R4833:Mdc1
|
UTSW |
17 |
36,161,286 (GRCm39) |
missense |
probably benign |
0.20 |
R5032:Mdc1
|
UTSW |
17 |
36,161,481 (GRCm39) |
missense |
probably benign |
0.00 |
R5047:Mdc1
|
UTSW |
17 |
36,158,736 (GRCm39) |
missense |
probably benign |
0.00 |
R5086:Mdc1
|
UTSW |
17 |
36,159,522 (GRCm39) |
missense |
probably benign |
0.00 |
R5172:Mdc1
|
UTSW |
17 |
36,163,982 (GRCm39) |
missense |
probably benign |
0.00 |
R5254:Mdc1
|
UTSW |
17 |
36,158,814 (GRCm39) |
missense |
probably benign |
0.00 |
R5473:Mdc1
|
UTSW |
17 |
36,158,952 (GRCm39) |
missense |
probably benign |
0.01 |
R5550:Mdc1
|
UTSW |
17 |
36,156,776 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5561:Mdc1
|
UTSW |
17 |
36,159,438 (GRCm39) |
missense |
probably benign |
0.00 |
R5888:Mdc1
|
UTSW |
17 |
36,158,712 (GRCm39) |
missense |
probably benign |
0.01 |
R6020:Mdc1
|
UTSW |
17 |
36,168,464 (GRCm39) |
missense |
probably benign |
0.01 |
R6020:Mdc1
|
UTSW |
17 |
36,159,525 (GRCm39) |
missense |
probably benign |
0.04 |
R6219:Mdc1
|
UTSW |
17 |
36,161,566 (GRCm39) |
missense |
probably benign |
0.10 |
R7053:Mdc1
|
UTSW |
17 |
36,157,218 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Mdc1
|
UTSW |
17 |
36,164,960 (GRCm39) |
missense |
probably benign |
0.18 |
R7077:Mdc1
|
UTSW |
17 |
36,156,839 (GRCm39) |
missense |
probably damaging |
0.97 |
R7424:Mdc1
|
UTSW |
17 |
36,164,201 (GRCm39) |
missense |
probably benign |
0.04 |
R7443:Mdc1
|
UTSW |
17 |
36,161,712 (GRCm39) |
missense |
probably damaging |
0.98 |
R7467:Mdc1
|
UTSW |
17 |
36,155,448 (GRCm39) |
missense |
probably benign |
0.29 |
R7549:Mdc1
|
UTSW |
17 |
36,159,749 (GRCm39) |
missense |
probably null |
0.04 |
R7655:Mdc1
|
UTSW |
17 |
36,161,773 (GRCm39) |
missense |
probably benign |
0.01 |
R7656:Mdc1
|
UTSW |
17 |
36,161,773 (GRCm39) |
missense |
probably benign |
0.01 |
R7960:Mdc1
|
UTSW |
17 |
36,161,570 (GRCm39) |
nonsense |
probably null |
|
R8350:Mdc1
|
UTSW |
17 |
36,159,191 (GRCm39) |
missense |
probably benign |
0.00 |
R8450:Mdc1
|
UTSW |
17 |
36,159,191 (GRCm39) |
missense |
probably benign |
0.00 |
R8688:Mdc1
|
UTSW |
17 |
36,161,383 (GRCm39) |
missense |
probably benign |
0.10 |
R8726:Mdc1
|
UTSW |
17 |
36,158,475 (GRCm39) |
missense |
probably benign |
0.04 |
R8919:Mdc1
|
UTSW |
17 |
36,158,843 (GRCm39) |
missense |
probably benign |
0.00 |
R8961:Mdc1
|
UTSW |
17 |
36,159,407 (GRCm39) |
missense |
probably benign |
0.10 |
R9324:Mdc1
|
UTSW |
17 |
36,164,258 (GRCm39) |
missense |
probably benign |
0.10 |
R9363:Mdc1
|
UTSW |
17 |
36,162,019 (GRCm39) |
missense |
probably benign |
0.00 |
R9385:Mdc1
|
UTSW |
17 |
36,161,396 (GRCm39) |
missense |
probably benign |
0.00 |
RF025:Mdc1
|
UTSW |
17 |
36,165,299 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0022:Mdc1
|
UTSW |
17 |
36,161,829 (GRCm39) |
missense |
probably benign |
0.01 |
|