Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt2 |
T |
A |
7: 27,328,824 (GRCm39) |
I182N |
probably damaging |
Het |
Alpk3 |
A |
G |
7: 80,728,255 (GRCm39) |
T462A |
probably benign |
Het |
Amz1 |
A |
G |
5: 140,738,014 (GRCm39) |
R425G |
probably damaging |
Het |
Aoc2 |
A |
G |
11: 101,217,201 (GRCm39) |
E428G |
probably damaging |
Het |
Car4 |
C |
T |
11: 84,856,593 (GRCm39) |
P294S |
probably damaging |
Het |
Chchd6 |
A |
T |
6: 89,396,762 (GRCm39) |
H216Q |
probably damaging |
Het |
Chl1 |
A |
G |
6: 103,675,086 (GRCm39) |
Y591C |
probably damaging |
Het |
Cln8 |
T |
C |
8: 14,945,178 (GRCm39) |
L164S |
probably damaging |
Het |
Dscaml1 |
T |
C |
9: 45,581,474 (GRCm39) |
I431T |
possibly damaging |
Het |
Fam234b |
T |
C |
6: 135,208,659 (GRCm39) |
L524P |
probably damaging |
Het |
Fmo1 |
T |
C |
1: 162,660,559 (GRCm39) |
N410S |
probably benign |
Het |
Ftsj3 |
G |
A |
11: 106,143,972 (GRCm39) |
R251* |
probably null |
Het |
Greb1l |
A |
T |
18: 10,515,200 (GRCm39) |
D555V |
probably damaging |
Het |
Hcar1 |
G |
T |
5: 124,017,135 (GRCm39) |
H185Q |
probably damaging |
Het |
Kcnj12 |
G |
A |
11: 60,960,319 (GRCm39) |
V206I |
probably benign |
Het |
Lamc3 |
G |
A |
2: 31,808,469 (GRCm39) |
G742S |
probably damaging |
Het |
Lipg |
T |
C |
18: 75,093,946 (GRCm39) |
|
probably null |
Het |
Ltbp2 |
A |
G |
12: 84,839,729 (GRCm39) |
|
probably null |
Het |
Myh6 |
T |
A |
14: 55,194,612 (GRCm39) |
D719V |
possibly damaging |
Het |
Myo9b |
A |
G |
8: 71,743,689 (GRCm39) |
N250S |
probably damaging |
Het |
Nherf1 |
A |
G |
11: 115,070,858 (GRCm39) |
E270G |
probably benign |
Het |
Notch2 |
G |
A |
3: 98,054,652 (GRCm39) |
W2438* |
probably null |
Het |
Nphp1 |
G |
A |
2: 127,621,987 (GRCm39) |
Q47* |
probably null |
Het |
Nptx2 |
T |
C |
5: 144,493,056 (GRCm39) |
L381P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 90,171,402 (GRCm39) |
N911S |
possibly damaging |
Het |
Or10j2 |
A |
T |
1: 173,097,972 (GRCm39) |
I77F |
probably benign |
Het |
Or5d46 |
T |
C |
2: 88,169,906 (GRCm39) |
|
probably benign |
Het |
P4ha1 |
T |
A |
10: 59,188,023 (GRCm39) |
F260Y |
probably benign |
Het |
Pitpnm2 |
T |
C |
5: 124,268,676 (GRCm39) |
D504G |
probably damaging |
Het |
Prss54 |
A |
G |
8: 96,292,237 (GRCm39) |
V114A |
probably benign |
Het |
Ptprc |
G |
A |
1: 137,998,957 (GRCm39) |
T1031M |
probably damaging |
Het |
Rtf2 |
T |
C |
2: 172,310,511 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,777,349 (GRCm39) |
|
probably benign |
Het |
Slc14a2 |
C |
T |
18: 78,206,341 (GRCm39) |
E492K |
probably damaging |
Het |
Stab1 |
G |
T |
14: 30,862,367 (GRCm39) |
N2322K |
probably damaging |
Het |
Thsd7b |
A |
G |
1: 130,087,369 (GRCm39) |
N1162S |
probably benign |
Het |
Tmprss11b |
T |
C |
5: 86,810,090 (GRCm39) |
I297V |
probably benign |
Het |
Tnn |
T |
C |
1: 159,972,775 (GRCm39) |
N276D |
probably benign |
Het |
Trhde |
A |
T |
10: 114,428,118 (GRCm39) |
|
probably benign |
Het |
Vmn1r115 |
T |
A |
7: 20,578,453 (GRCm39) |
H153L |
possibly damaging |
Het |
Vmn1r203 |
T |
A |
13: 22,708,997 (GRCm39) |
C259* |
probably null |
Het |
Xpot |
T |
A |
10: 121,451,109 (GRCm39) |
E97V |
probably damaging |
Het |
Zbtb2 |
T |
C |
10: 4,318,712 (GRCm39) |
D438G |
probably damaging |
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 |
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 |
R6947:Mcm3ap
|
UTSW |
10 |
76,351,500 (GRCm39) |
missense |
probably benign |
0.09 |
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 |
|
|