Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adarb2 |
A |
G |
13: 8,751,761 (GRCm39) |
T509A |
probably benign |
Het |
Arhgap23 |
T |
C |
11: 97,337,379 (GRCm39) |
|
probably null |
Het |
Astn1 |
A |
T |
1: 158,427,889 (GRCm39) |
I687F |
possibly damaging |
Het |
Atg4d |
T |
C |
9: 21,178,217 (GRCm39) |
F112L |
probably damaging |
Het |
Bltp3b |
A |
C |
10: 89,615,846 (GRCm39) |
D163A |
probably damaging |
Het |
Cd200 |
T |
A |
16: 45,217,409 (GRCm39) |
D94V |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,194,359 (GRCm39) |
K2285R |
probably benign |
Het |
Clhc1 |
T |
A |
11: 29,521,745 (GRCm39) |
I426N |
probably damaging |
Het |
Cnnm2 |
T |
A |
19: 46,751,659 (GRCm39) |
V483E |
probably damaging |
Het |
Dennd2b |
G |
A |
7: 109,126,915 (GRCm39) |
A932V |
possibly damaging |
Het |
Dlc1 |
A |
T |
8: 37,037,436 (GRCm39) |
|
probably benign |
Het |
Fpgs |
T |
C |
2: 32,578,009 (GRCm39) |
I138V |
possibly damaging |
Het |
Gpr152 |
T |
C |
19: 4,193,506 (GRCm39) |
V349A |
probably benign |
Het |
Hk1 |
C |
A |
10: 62,122,127 (GRCm39) |
E523* |
probably null |
Het |
Ift70a1 |
C |
A |
2: 75,812,085 (GRCm39) |
|
probably benign |
Het |
Krt6a |
T |
G |
15: 101,601,229 (GRCm39) |
K241N |
probably damaging |
Het |
Meikin |
C |
T |
11: 54,289,320 (GRCm39) |
P231L |
probably damaging |
Het |
Micall1 |
G |
A |
15: 78,999,221 (GRCm39) |
|
probably benign |
Het |
Mvk |
G |
A |
5: 114,583,502 (GRCm39) |
V14I |
probably benign |
Het |
Myo6 |
C |
T |
9: 80,199,754 (GRCm39) |
S1021L |
probably damaging |
Het |
N4bp2l2 |
G |
A |
5: 150,585,401 (GRCm39) |
T193M |
probably benign |
Het |
Naip5 |
G |
T |
13: 100,367,279 (GRCm39) |
D272E |
probably damaging |
Het |
Nptn |
T |
A |
9: 58,550,922 (GRCm39) |
N316K |
probably damaging |
Het |
Pde6c |
T |
C |
19: 38,151,324 (GRCm39) |
|
probably benign |
Het |
Prg4 |
T |
A |
1: 150,327,671 (GRCm39) |
I850L |
probably damaging |
Het |
Rdm1 |
T |
G |
11: 101,526,580 (GRCm39) |
C251G |
possibly damaging |
Het |
Relch |
A |
G |
1: 105,624,324 (GRCm39) |
|
probably benign |
Het |
Rps6kl1 |
G |
A |
12: 85,186,157 (GRCm39) |
P291L |
probably benign |
Het |
Sel1l |
A |
G |
12: 91,781,387 (GRCm39) |
|
probably benign |
Het |
Serpinb1b |
T |
C |
13: 33,277,850 (GRCm39) |
F361S |
probably damaging |
Het |
Sirpb1a |
G |
A |
3: 15,475,788 (GRCm39) |
|
probably benign |
Het |
Smpd1 |
T |
G |
7: 105,205,848 (GRCm39) |
V405G |
probably damaging |
Het |
Spmip11 |
T |
C |
15: 98,486,425 (GRCm39) |
|
probably benign |
Het |
Tead3 |
T |
C |
17: 28,551,780 (GRCm39) |
T438A |
possibly damaging |
Het |
Treh |
A |
T |
9: 44,595,197 (GRCm39) |
D89V |
probably damaging |
Het |
Trim10 |
A |
T |
17: 37,188,140 (GRCm39) |
H452L |
probably benign |
Het |
Ugt2b1 |
A |
G |
5: 87,073,817 (GRCm39) |
C181R |
probably benign |
Het |
Xdh |
A |
T |
17: 74,230,101 (GRCm39) |
F277I |
possibly damaging |
Het |
Zswim4 |
T |
G |
8: 84,938,769 (GRCm39) |
T1038P |
probably damaging |
Het |
|
Other mutations in Mcm3ap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
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 |
|
|