Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aggf1 |
C |
T |
13: 95,506,030 (GRCm39) |
E186K |
possibly damaging |
Het |
Ajm1 |
G |
T |
2: 25,467,043 (GRCm39) |
S956* |
probably null |
Het |
Anks1b |
A |
G |
10: 90,730,979 (GRCm39) |
I932V |
probably benign |
Het |
Atg2b |
A |
G |
12: 105,609,526 (GRCm39) |
Y1361H |
probably damaging |
Het |
Bcl9 |
G |
T |
3: 97,122,545 (GRCm39) |
L85M |
probably damaging |
Het |
Bcl9l |
T |
G |
9: 44,417,036 (GRCm39) |
S291R |
probably benign |
Het |
Cpa2 |
T |
A |
6: 30,550,767 (GRCm39) |
D201E |
probably benign |
Het |
Efna5 |
A |
T |
17: 62,920,384 (GRCm39) |
C164* |
probably null |
Het |
Fhip2b |
A |
T |
14: 70,823,128 (GRCm39) |
H642Q |
probably damaging |
Het |
Fhip2b |
T |
A |
14: 70,823,630 (GRCm39) |
H580L |
probably benign |
Het |
Gm6316 |
A |
G |
12: 69,967,763 (GRCm39) |
|
probably benign |
Het |
Gucy2g |
A |
G |
19: 55,229,500 (GRCm39) |
S57P |
probably damaging |
Het |
Inf2 |
C |
A |
12: 112,576,930 (GRCm39) |
A968E |
unknown |
Het |
Man2a2 |
G |
A |
7: 80,009,388 (GRCm39) |
A822V |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,398,456 (GRCm39) |
Y287C |
unknown |
Het |
Or12e9 |
T |
G |
2: 87,202,598 (GRCm39) |
S241A |
probably benign |
Het |
Or13a24 |
A |
T |
7: 140,154,554 (GRCm39) |
M163L |
probably benign |
Het |
Or14c39 |
G |
A |
7: 86,343,939 (GRCm39) |
V92M |
probably benign |
Het |
Or8u10 |
A |
G |
2: 85,915,713 (GRCm39) |
M136T |
probably damaging |
Het |
Pabpc1l |
A |
G |
2: 163,869,410 (GRCm39) |
D70G |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,187,944 (GRCm39) |
I3455F |
probably damaging |
Het |
Ppp1r17 |
C |
A |
6: 56,003,445 (GRCm39) |
S86* |
probably null |
Het |
Rasd1 |
A |
G |
11: 59,855,615 (GRCm39) |
M6T |
possibly damaging |
Het |
Rsph14 |
C |
A |
10: 74,793,466 (GRCm39) |
V345F |
probably damaging |
Het |
Slc11a2 |
T |
A |
15: 100,299,207 (GRCm39) |
Q121L |
probably benign |
Het |
Smc5 |
A |
T |
19: 23,205,536 (GRCm39) |
|
probably null |
Het |
Tanc2 |
T |
C |
11: 105,725,994 (GRCm39) |
L386P |
probably damaging |
Het |
Tmem9b |
A |
T |
7: 109,336,164 (GRCm39) |
L160Q |
probably damaging |
Het |
Trim32 |
A |
G |
4: 65,532,906 (GRCm39) |
T488A |
possibly damaging |
Het |
Tubb1 |
A |
G |
2: 174,297,462 (GRCm39) |
I24V |
probably benign |
Het |
Upf1 |
A |
T |
8: 70,788,302 (GRCm39) |
|
probably null |
Het |
Zfp263 |
T |
A |
16: 3,564,279 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Mcm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Mcm5
|
APN |
8 |
75,851,573 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00954:Mcm5
|
APN |
8 |
75,836,740 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03074:Mcm5
|
APN |
8 |
75,845,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03176:Mcm5
|
APN |
8 |
75,836,481 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03240:Mcm5
|
APN |
8 |
75,842,530 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Mcm5
|
UTSW |
8 |
75,853,864 (GRCm39) |
missense |
probably benign |
|
R0133:Mcm5
|
UTSW |
8 |
75,847,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Mcm5
|
UTSW |
8 |
75,847,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Mcm5
|
UTSW |
8 |
75,852,880 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0733:Mcm5
|
UTSW |
8 |
75,853,876 (GRCm39) |
missense |
probably benign |
0.08 |
R1217:Mcm5
|
UTSW |
8 |
75,852,919 (GRCm39) |
missense |
probably benign |
0.01 |
R1601:Mcm5
|
UTSW |
8 |
75,845,982 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1834:Mcm5
|
UTSW |
8 |
75,845,901 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1958:Mcm5
|
UTSW |
8 |
75,848,257 (GRCm39) |
missense |
probably benign |
0.34 |
R3410:Mcm5
|
UTSW |
8 |
75,848,272 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4133:Mcm5
|
UTSW |
8 |
75,842,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4441:Mcm5
|
UTSW |
8 |
75,839,172 (GRCm39) |
missense |
probably benign |
0.39 |
R5395:Mcm5
|
UTSW |
8 |
75,849,654 (GRCm39) |
missense |
probably benign |
|
R5710:Mcm5
|
UTSW |
8 |
75,847,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5714:Mcm5
|
UTSW |
8 |
75,847,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R6075:Mcm5
|
UTSW |
8 |
75,840,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R6093:Mcm5
|
UTSW |
8 |
75,836,374 (GRCm39) |
missense |
probably benign |
0.06 |
R6477:Mcm5
|
UTSW |
8 |
75,839,230 (GRCm39) |
missense |
probably benign |
0.36 |
R6848:Mcm5
|
UTSW |
8 |
75,853,918 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7098:Mcm5
|
UTSW |
8 |
75,847,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R7208:Mcm5
|
UTSW |
8 |
75,848,344 (GRCm39) |
critical splice donor site |
probably null |
|
R7278:Mcm5
|
UTSW |
8 |
75,851,487 (GRCm39) |
missense |
probably benign |
0.40 |
R7552:Mcm5
|
UTSW |
8 |
75,848,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R7701:Mcm5
|
UTSW |
8 |
75,850,551 (GRCm39) |
missense |
probably benign |
0.00 |
R9072:Mcm5
|
UTSW |
8 |
75,852,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9073:Mcm5
|
UTSW |
8 |
75,852,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9124:Mcm5
|
UTSW |
8 |
75,851,418 (GRCm39) |
splice site |
probably benign |
|
R9194:Mcm5
|
UTSW |
8 |
75,836,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R9489:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9491:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9492:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9557:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9605:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9607:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9608:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9609:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9654:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9655:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9656:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9657:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9659:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9662:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9709:Mcm5
|
UTSW |
8 |
75,842,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9730:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9731:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9732:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9773:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9774:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9785:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9786:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9788:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
R9789:Mcm5
|
UTSW |
8 |
75,844,168 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Mcm5
|
UTSW |
8 |
75,848,300 (GRCm39) |
missense |
possibly damaging |
0.52 |
|