Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts7 |
C |
A |
9: 90,073,857 (GRCm39) |
|
probably null |
Het |
Adcy4 |
T |
C |
14: 56,015,848 (GRCm39) |
T414A |
possibly damaging |
Het |
Bop1 |
A |
G |
15: 76,338,188 (GRCm39) |
F561L |
probably damaging |
Het |
Ccdc18 |
T |
C |
5: 108,309,401 (GRCm39) |
V332A |
probably benign |
Het |
Cep290 |
A |
G |
10: 100,365,918 (GRCm39) |
T1042A |
probably damaging |
Het |
Cnot8 |
G |
T |
11: 58,008,331 (GRCm39) |
V266L |
probably benign |
Het |
Cxxc4 |
C |
T |
3: 133,946,277 (GRCm39) |
S286F |
possibly damaging |
Het |
Cyp2d12 |
A |
T |
15: 82,443,248 (GRCm39) |
I386L |
probably benign |
Het |
Dgka |
A |
T |
10: 128,568,884 (GRCm39) |
I227N |
probably damaging |
Het |
Eif2d |
T |
C |
1: 131,092,404 (GRCm39) |
V354A |
probably benign |
Het |
Fgr |
T |
A |
4: 132,722,380 (GRCm39) |
|
probably null |
Het |
Idnk |
A |
G |
13: 58,308,055 (GRCm39) |
|
probably null |
Het |
Kmt2e |
T |
C |
5: 23,702,543 (GRCm39) |
S952P |
probably damaging |
Het |
Kng1 |
A |
G |
16: 22,896,124 (GRCm39) |
H343R |
probably benign |
Het |
Lgals8 |
G |
A |
13: 12,469,682 (GRCm39) |
|
probably benign |
Het |
Lrit3 |
T |
A |
3: 129,582,883 (GRCm39) |
Q368L |
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,273,592 (GRCm39) |
T24S |
probably benign |
Het |
Map3k4 |
G |
A |
17: 12,479,456 (GRCm39) |
Q704* |
probably null |
Het |
Mettl25 |
A |
G |
10: 105,662,053 (GRCm39) |
F306L |
probably benign |
Het |
Mos |
A |
C |
4: 3,871,585 (GRCm39) |
V77G |
probably damaging |
Het |
Muc4 |
C |
T |
16: 32,596,177 (GRCm39) |
R3130C |
possibly damaging |
Het |
Naxd |
T |
C |
8: 11,552,757 (GRCm39) |
V59A |
probably damaging |
Het |
Nup107 |
A |
G |
10: 117,593,179 (GRCm39) |
V833A |
probably benign |
Het |
Or1p4-ps1 |
C |
T |
11: 74,208,370 (GRCm39) |
S173L |
unknown |
Het |
Or5m10b |
T |
C |
2: 85,699,271 (GRCm39) |
F112L |
probably benign |
Het |
Pcnx2 |
C |
T |
8: 126,577,021 (GRCm39) |
|
probably null |
Het |
Pde10a |
T |
A |
17: 9,188,424 (GRCm39) |
I908N |
probably damaging |
Het |
Plcb1 |
A |
G |
2: 135,228,075 (GRCm39) |
K1058R |
probably benign |
Het |
Rad17 |
A |
T |
13: 100,759,383 (GRCm39) |
F548Y |
probably damaging |
Het |
Rad54b |
T |
G |
4: 11,569,859 (GRCm39) |
S58R |
possibly damaging |
Het |
Rbm20 |
G |
A |
19: 53,839,696 (GRCm39) |
G895D |
probably damaging |
Het |
Rgs22 |
T |
C |
15: 36,104,036 (GRCm39) |
|
probably null |
Het |
Rhobtb3 |
A |
G |
13: 76,058,785 (GRCm39) |
S338P |
probably benign |
Het |
Ruvbl2 |
A |
G |
7: 45,074,373 (GRCm39) |
|
probably null |
Het |
Slc16a12 |
A |
G |
19: 34,650,007 (GRCm39) |
F343L |
probably benign |
Het |
Slc22a28 |
A |
G |
19: 8,041,875 (GRCm39) |
L444P |
possibly damaging |
Het |
Slc44a4 |
A |
T |
17: 35,147,044 (GRCm39) |
Q358L |
probably null |
Het |
Sowaha |
A |
G |
11: 53,369,225 (GRCm39) |
F504L |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,125,789 (GRCm39) |
L6035P |
probably damaging |
Het |
Thbs2 |
A |
T |
17: 14,910,029 (GRCm39) |
M190K |
possibly damaging |
Het |
Tmem171 |
A |
G |
13: 98,824,950 (GRCm39) |
F227L |
possibly damaging |
Het |
Trp53 |
A |
G |
11: 69,479,307 (GRCm39) |
K162E |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,724,732 (GRCm39) |
K2098* |
probably null |
Het |
Usp30 |
T |
C |
5: 114,241,821 (GRCm39) |
S88P |
probably benign |
Het |
Zfp276 |
C |
A |
8: 123,981,643 (GRCm39) |
D63E |
probably benign |
Het |
|
Other mutations in Mcm3ap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Mcm3ap
|
APN |
10 |
76,307,011 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00742:Mcm3ap
|
APN |
10 |
76,328,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00898:Mcm3ap
|
APN |
10 |
76,306,159 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00984:Mcm3ap
|
APN |
10 |
76,335,400 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01591:Mcm3ap
|
APN |
10 |
76,306,639 (GRCm39) |
missense |
probably benign |
|
IGL01882:Mcm3ap
|
APN |
10 |
76,319,018 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01973:Mcm3ap
|
APN |
10 |
76,306,951 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02253:Mcm3ap
|
APN |
10 |
76,305,899 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02304:Mcm3ap
|
APN |
10 |
76,320,572 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02340:Mcm3ap
|
APN |
10 |
76,332,386 (GRCm39) |
nonsense |
probably null |
|
IGL02487:Mcm3ap
|
APN |
10 |
76,343,389 (GRCm39) |
unclassified |
probably benign |
|
IGL02488:Mcm3ap
|
APN |
10 |
76,335,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02640:Mcm3ap
|
APN |
10 |
76,342,255 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02714:Mcm3ap
|
APN |
10 |
76,346,867 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02748:Mcm3ap
|
APN |
10 |
76,337,082 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02894:Mcm3ap
|
APN |
10 |
76,313,601 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02903:Mcm3ap
|
APN |
10 |
76,307,092 (GRCm39) |
splice site |
probably benign |
|
IGL02955:Mcm3ap
|
APN |
10 |
76,343,300 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02989:Mcm3ap
|
APN |
10 |
76,306,894 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03003:Mcm3ap
|
APN |
10 |
76,340,531 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03081:Mcm3ap
|
APN |
10 |
76,306,150 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03218:Mcm3ap
|
APN |
10 |
76,318,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Mcm3ap
|
APN |
10 |
76,320,483 (GRCm39) |
splice site |
probably benign |
|
Bane
|
UTSW |
10 |
76,319,060 (GRCm39) |
missense |
probably damaging |
1.00 |
Doom
|
UTSW |
10 |
76,337,148 (GRCm39) |
missense |
probably benign |
|
woeful
|
UTSW |
10 |
76,316,849 (GRCm39) |
missense |
probably benign |
0.44 |
PIT4377001:Mcm3ap
|
UTSW |
10 |
76,338,596 (GRCm39) |
missense |
possibly damaging |
0.78 |
PIT4791001:Mcm3ap
|
UTSW |
10 |
76,342,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R0105:Mcm3ap
|
UTSW |
10 |
76,335,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:Mcm3ap
|
UTSW |
10 |
76,316,849 (GRCm39) |
missense |
probably benign |
0.44 |
R0423:Mcm3ap
|
UTSW |
10 |
76,338,539 (GRCm39) |
missense |
probably benign |
0.00 |
R0692:Mcm3ap
|
UTSW |
10 |
76,319,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1402:Mcm3ap
|
UTSW |
10 |
76,313,748 (GRCm39) |
unclassified |
probably benign |
|
R1441:Mcm3ap
|
UTSW |
10 |
76,307,000 (GRCm39) |
missense |
probably benign |
|
R1512:Mcm3ap
|
UTSW |
10 |
76,306,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Mcm3ap
|
UTSW |
10 |
76,340,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1569:Mcm3ap
|
UTSW |
10 |
76,319,022 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1590:Mcm3ap
|
UTSW |
10 |
76,332,375 (GRCm39) |
missense |
probably benign |
0.36 |
R1597:Mcm3ap
|
UTSW |
10 |
76,319,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R1743:Mcm3ap
|
UTSW |
10 |
76,320,508 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1773:Mcm3ap
|
UTSW |
10 |
76,306,994 (GRCm39) |
missense |
probably benign |
|
R1922:Mcm3ap
|
UTSW |
10 |
76,343,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Mcm3ap
|
UTSW |
10 |
76,305,902 (GRCm39) |
missense |
probably benign |
0.43 |
R2097:Mcm3ap
|
UTSW |
10 |
76,348,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R2436:Mcm3ap
|
UTSW |
10 |
76,325,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R3684:Mcm3ap
|
UTSW |
10 |
76,325,260 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3690:Mcm3ap
|
UTSW |
10 |
76,318,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R3881:Mcm3ap
|
UTSW |
10 |
76,342,280 (GRCm39) |
missense |
probably benign |
0.21 |
R4296:Mcm3ap
|
UTSW |
10 |
76,343,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Mcm3ap
|
UTSW |
10 |
76,306,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Mcm3ap
|
UTSW |
10 |
76,324,300 (GRCm39) |
missense |
probably benign |
0.00 |
R4882:Mcm3ap
|
UTSW |
10 |
76,320,495 (GRCm39) |
nonsense |
probably null |
|
R4907:Mcm3ap
|
UTSW |
10 |
76,329,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R5108:Mcm3ap
|
UTSW |
10 |
76,338,536 (GRCm39) |
missense |
probably benign |
0.04 |
R5279:Mcm3ap
|
UTSW |
10 |
76,343,373 (GRCm39) |
missense |
probably damaging |
0.96 |
R5316:Mcm3ap
|
UTSW |
10 |
76,306,760 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5402:Mcm3ap
|
UTSW |
10 |
76,319,148 (GRCm39) |
missense |
probably benign |
0.04 |
R5459:Mcm3ap
|
UTSW |
10 |
76,332,316 (GRCm39) |
nonsense |
probably null |
|
R5473:Mcm3ap
|
UTSW |
10 |
76,338,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R5570:Mcm3ap
|
UTSW |
10 |
76,316,930 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5931:Mcm3ap
|
UTSW |
10 |
76,307,000 (GRCm39) |
missense |
probably benign |
|
R5939:Mcm3ap
|
UTSW |
10 |
76,344,195 (GRCm39) |
missense |
probably benign |
0.00 |
R5950:Mcm3ap
|
UTSW |
10 |
76,324,253 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5998:Mcm3ap
|
UTSW |
10 |
76,316,976 (GRCm39) |
critical splice donor site |
probably null |
|
R6122:Mcm3ap
|
UTSW |
10 |
76,342,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Mcm3ap
|
UTSW |
10 |
76,336,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R6226:Mcm3ap
|
UTSW |
10 |
76,351,540 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6293:Mcm3ap
|
UTSW |
10 |
76,307,312 (GRCm39) |
nonsense |
probably null |
|
R6669:Mcm3ap
|
UTSW |
10 |
76,343,171 (GRCm39) |
missense |
probably damaging |
0.98 |
R6715:Mcm3ap
|
UTSW |
10 |
76,325,366 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6759:Mcm3ap
|
UTSW |
10 |
76,337,148 (GRCm39) |
missense |
probably benign |
|
R6864:Mcm3ap
|
UTSW |
10 |
76,343,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R6870:Mcm3ap
|
UTSW |
10 |
76,306,049 (GRCm39) |
missense |
probably benign |
0.00 |
R6935:Mcm3ap
|
UTSW |
10 |
76,340,087 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7212:Mcm3ap
|
UTSW |
10 |
76,337,145 (GRCm39) |
missense |
probably benign |
0.01 |
R7403:Mcm3ap
|
UTSW |
10 |
76,318,657 (GRCm39) |
critical splice donor site |
probably null |
|
R7470:Mcm3ap
|
UTSW |
10 |
76,344,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7561:Mcm3ap
|
UTSW |
10 |
76,328,712 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7610:Mcm3ap
|
UTSW |
10 |
76,332,554 (GRCm39) |
splice site |
probably null |
|
R7620:Mcm3ap
|
UTSW |
10 |
76,306,267 (GRCm39) |
missense |
probably benign |
0.00 |
R7898:Mcm3ap
|
UTSW |
10 |
76,342,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R8266:Mcm3ap
|
UTSW |
10 |
76,312,414 (GRCm39) |
nonsense |
probably null |
|
R8355:Mcm3ap
|
UTSW |
10 |
76,329,335 (GRCm39) |
missense |
probably benign |
0.32 |
R8367:Mcm3ap
|
UTSW |
10 |
76,313,693 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8867:Mcm3ap
|
UTSW |
10 |
76,306,538 (GRCm39) |
missense |
probably benign |
0.31 |
R9282:Mcm3ap
|
UTSW |
10 |
76,342,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Mcm3ap
|
UTSW |
10 |
76,318,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Mcm3ap
|
UTSW |
10 |
76,306,358 (GRCm39) |
missense |
probably benign |
0.04 |
R9554:Mcm3ap
|
UTSW |
10 |
76,332,310 (GRCm39) |
missense |
probably damaging |
0.97 |
R9706:Mcm3ap
|
UTSW |
10 |
76,312,352 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Mcm3ap
|
UTSW |
10 |
76,318,619 (GRCm39) |
nonsense |
probably null |
|
|