Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
T |
C |
3: 36,139,564 (GRCm39) |
V388A |
probably damaging |
Het |
Acp3 |
T |
C |
9: 104,197,201 (GRCm39) |
E146G |
probably damaging |
Het |
Adap2 |
A |
T |
11: 80,066,905 (GRCm39) |
R276S |
probably damaging |
Het |
Agbl3 |
A |
T |
6: 34,816,270 (GRCm39) |
M727L |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,977,628 (GRCm39) |
|
probably benign |
Het |
Ankmy1 |
G |
T |
1: 92,813,948 (GRCm39) |
D410E |
probably damaging |
Het |
Ankra2 |
T |
C |
13: 98,402,962 (GRCm39) |
S70P |
probably damaging |
Het |
Aox4 |
T |
C |
1: 58,302,556 (GRCm39) |
|
probably null |
Het |
Arl13b |
G |
A |
16: 62,622,096 (GRCm39) |
T399I |
probably benign |
Het |
Atad2 |
A |
T |
15: 57,966,636 (GRCm39) |
D652E |
possibly damaging |
Het |
Atad2 |
T |
G |
15: 57,984,345 (GRCm39) |
M328L |
probably benign |
Het |
Ccnb1 |
T |
C |
13: 100,916,642 (GRCm39) |
|
probably null |
Het |
Ccr2 |
G |
C |
9: 123,905,976 (GRCm39) |
K85N |
possibly damaging |
Het |
Ccr2 |
A |
T |
9: 123,906,163 (GRCm39) |
T148S |
possibly damaging |
Het |
Cdc20b |
T |
C |
13: 113,192,484 (GRCm39) |
V59A |
probably benign |
Het |
Cdin1 |
C |
T |
2: 115,473,172 (GRCm39) |
R101W |
probably damaging |
Het |
Cdkl3 |
T |
C |
11: 51,923,243 (GRCm39) |
S507P |
possibly damaging |
Het |
Celf6 |
C |
A |
9: 59,510,161 (GRCm39) |
T86K |
probably benign |
Het |
Ces1g |
A |
G |
8: 94,060,317 (GRCm39) |
F101L |
probably benign |
Het |
Cimap1d |
T |
C |
10: 79,476,099 (GRCm39) |
D155G |
probably damaging |
Het |
Cntnap3 |
C |
T |
13: 65,006,492 (GRCm39) |
D107N |
probably benign |
Het |
Col15a1 |
A |
T |
4: 47,262,950 (GRCm39) |
D534V |
probably damaging |
Het |
Col27a1 |
A |
G |
4: 63,218,978 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,710,527 (GRCm39) |
T1687A |
probably benign |
Het |
Cstf3 |
A |
G |
2: 104,479,950 (GRCm39) |
I272M |
possibly damaging |
Het |
Cyp2d40 |
T |
C |
15: 82,645,418 (GRCm39) |
T150A |
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,934,483 (GRCm39) |
F1489L |
possibly damaging |
Het |
Dop1b |
A |
T |
16: 93,567,325 (GRCm39) |
T1251S |
probably benign |
Het |
Dtx2 |
G |
A |
5: 136,057,957 (GRCm39) |
G421R |
probably damaging |
Het |
Epb41l3 |
T |
A |
17: 69,554,654 (GRCm39) |
D251E |
probably benign |
Het |
Erg |
A |
C |
16: 95,161,842 (GRCm39) |
Y305* |
probably null |
Het |
Exosc4 |
G |
A |
15: 76,213,766 (GRCm39) |
A197T |
probably benign |
Het |
Fam227b |
T |
A |
2: 125,942,829 (GRCm39) |
I323L |
probably benign |
Het |
Far1 |
G |
T |
7: 113,153,503 (GRCm39) |
|
probably benign |
Het |
Fmod |
A |
G |
1: 133,968,934 (GRCm39) |
I325V |
possibly damaging |
Het |
Fshr |
C |
G |
17: 89,316,713 (GRCm39) |
S169T |
probably benign |
Het |
Gm4076 |
G |
T |
13: 85,275,345 (GRCm39) |
|
noncoding transcript |
Het |
Gm5134 |
A |
T |
10: 75,828,359 (GRCm39) |
Y313F |
probably benign |
Het |
H2-Q6 |
T |
A |
17: 35,644,179 (GRCm39) |
F54I |
probably damaging |
Het |
Hcrtr2 |
C |
A |
9: 76,161,954 (GRCm39) |
L145F |
probably damaging |
Het |
Hepacam2 |
A |
G |
6: 3,476,121 (GRCm39) |
L268P |
probably damaging |
Het |
Herc2 |
C |
A |
7: 55,834,117 (GRCm39) |
C3107* |
probably null |
Het |
Herc4 |
T |
C |
10: 63,099,811 (GRCm39) |
V78A |
probably damaging |
Het |
Hyal5 |
T |
C |
6: 24,877,920 (GRCm39) |
W339R |
probably damaging |
Het |
Igfbp6 |
T |
A |
15: 102,056,419 (GRCm39) |
|
probably null |
Het |
Il18rap |
A |
T |
1: 40,564,218 (GRCm39) |
H112L |
probably benign |
Het |
Il1r2 |
T |
A |
1: 40,162,309 (GRCm39) |
Y317* |
probably null |
Het |
Ints8 |
C |
A |
4: 11,246,097 (GRCm39) |
V190L |
probably benign |
Het |
Ipo11 |
T |
C |
13: 107,061,595 (GRCm39) |
T22A |
probably benign |
Het |
Itgb4 |
C |
A |
11: 115,870,521 (GRCm39) |
R117S |
probably benign |
Het |
Lcorl |
C |
G |
5: 45,891,711 (GRCm39) |
G214A |
probably benign |
Het |
Lgals3bp |
T |
A |
11: 118,289,019 (GRCm39) |
|
probably null |
Het |
Lyst |
T |
A |
13: 13,791,298 (GRCm39) |
L54I |
probably damaging |
Het |
Mef2d |
T |
A |
3: 88,063,825 (GRCm39) |
I84N |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,119,913 (GRCm39) |
N261S |
probably damaging |
Het |
Mpdz |
T |
C |
4: 81,210,768 (GRCm39) |
T1693A |
probably benign |
Het |
Mss51 |
T |
A |
14: 20,534,756 (GRCm39) |
Q338L |
possibly damaging |
Het |
Mstn |
T |
A |
1: 53,103,143 (GRCm39) |
Y160N |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,226,735 (GRCm39) |
T1431A |
probably benign |
Het |
Nek9 |
A |
T |
12: 85,348,657 (GRCm39) |
M959K |
probably benign |
Het |
Or2ak6 |
G |
A |
11: 58,593,069 (GRCm39) |
V181I |
probably benign |
Het |
Or4f58 |
A |
T |
2: 111,851,777 (GRCm39) |
C141S |
probably damaging |
Het |
Or8b47 |
A |
T |
9: 38,435,801 (GRCm39) |
M258L |
probably benign |
Het |
Otog |
G |
T |
7: 45,923,256 (GRCm39) |
G1044W |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 94,123,671 (GRCm39) |
T833M |
probably damaging |
Het |
Pdcd10 |
T |
C |
3: 75,434,958 (GRCm39) |
K111R |
probably damaging |
Het |
Pde5a |
A |
G |
3: 122,542,107 (GRCm39) |
N199S |
probably damaging |
Het |
Plekhg1 |
T |
C |
10: 3,887,971 (GRCm39) |
V355A |
probably damaging |
Het |
Podn |
G |
T |
4: 107,878,791 (GRCm39) |
L359I |
probably damaging |
Het |
Psd |
T |
C |
19: 46,310,600 (GRCm39) |
E483G |
probably damaging |
Het |
Ptch2 |
T |
A |
4: 116,968,340 (GRCm39) |
L905* |
probably null |
Het |
Rxfp2 |
T |
A |
5: 149,989,880 (GRCm39) |
N420K |
probably damaging |
Het |
Scpppq1 |
C |
A |
5: 104,222,747 (GRCm39) |
G24* |
probably null |
Het |
Sde2 |
T |
A |
1: 180,689,992 (GRCm39) |
D237E |
probably benign |
Het |
Serpina1d |
A |
T |
12: 103,732,016 (GRCm39) |
L281Q |
probably damaging |
Het |
Serpina9 |
T |
C |
12: 103,967,729 (GRCm39) |
N222S |
probably benign |
Het |
Sh3bgrl2 |
A |
G |
9: 83,459,612 (GRCm39) |
K57E |
probably damaging |
Het |
Shc3 |
C |
T |
13: 51,634,264 (GRCm39) |
|
probably benign |
Het |
Sik3 |
T |
C |
9: 46,120,038 (GRCm39) |
M659T |
possibly damaging |
Het |
Slc23a2 |
A |
G |
2: 131,913,937 (GRCm39) |
L280P |
probably damaging |
Het |
Smchd1 |
G |
T |
17: 71,694,083 (GRCm39) |
Q1221K |
probably benign |
Het |
Spmip2 |
T |
A |
3: 79,313,093 (GRCm39) |
W56R |
probably damaging |
Het |
Spocd1 |
A |
G |
4: 129,849,263 (GRCm39) |
N694S |
possibly damaging |
Het |
Styxl2 |
C |
A |
1: 165,926,670 (GRCm39) |
V981L |
probably benign |
Het |
Tecta |
T |
C |
9: 42,263,359 (GRCm39) |
D1409G |
probably damaging |
Het |
Tmem131 |
A |
T |
1: 36,880,754 (GRCm39) |
V172D |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,964,237 (GRCm39) |
M1244T |
possibly damaging |
Het |
Ugcg |
G |
C |
4: 59,217,036 (GRCm39) |
V187L |
possibly damaging |
Het |
Usp17le |
T |
C |
7: 104,417,708 (GRCm39) |
N478S |
probably benign |
Het |
Usp36 |
A |
G |
11: 118,164,397 (GRCm39) |
V205A |
probably damaging |
Het |
Vmn1r25 |
T |
A |
6: 57,955,494 (GRCm39) |
Q265L |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,615,077 (GRCm39) |
H1176L |
probably benign |
Het |
Zfyve28 |
C |
T |
5: 34,389,550 (GRCm39) |
D217N |
possibly damaging |
Het |
Zranb3 |
A |
C |
1: 127,882,817 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Mcm9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00660:Mcm9
|
APN |
10 |
53,499,069 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00904:Mcm9
|
APN |
10 |
53,499,017 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00943:Mcm9
|
APN |
10 |
53,424,685 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01019:Mcm9
|
APN |
10 |
53,506,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02452:Mcm9
|
APN |
10 |
53,417,653 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02481:Mcm9
|
APN |
10 |
53,502,033 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Mcm9
|
APN |
10 |
53,501,922 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03300:Mcm9
|
APN |
10 |
53,487,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R0021:Mcm9
|
UTSW |
10 |
53,413,997 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0117:Mcm9
|
UTSW |
10 |
53,413,832 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0137:Mcm9
|
UTSW |
10 |
53,439,526 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0420:Mcm9
|
UTSW |
10 |
53,424,623 (GRCm39) |
missense |
probably benign |
0.10 |
R0543:Mcm9
|
UTSW |
10 |
53,417,694 (GRCm39) |
missense |
probably damaging |
0.97 |
R0947:Mcm9
|
UTSW |
10 |
53,413,597 (GRCm39) |
small deletion |
probably benign |
|
R0975:Mcm9
|
UTSW |
10 |
53,414,742 (GRCm39) |
nonsense |
probably null |
|
R1573:Mcm9
|
UTSW |
10 |
53,424,752 (GRCm39) |
missense |
probably damaging |
0.97 |
R1726:Mcm9
|
UTSW |
10 |
53,413,977 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1839:Mcm9
|
UTSW |
10 |
53,417,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R2050:Mcm9
|
UTSW |
10 |
53,488,921 (GRCm39) |
critical splice donor site |
probably null |
|
R2113:Mcm9
|
UTSW |
10 |
53,491,943 (GRCm39) |
splice site |
probably null |
|
R2172:Mcm9
|
UTSW |
10 |
53,424,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R3417:Mcm9
|
UTSW |
10 |
53,413,503 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3755:Mcm9
|
UTSW |
10 |
53,502,048 (GRCm39) |
missense |
probably benign |
0.08 |
R3787:Mcm9
|
UTSW |
10 |
53,492,076 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3789:Mcm9
|
UTSW |
10 |
53,492,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:Mcm9
|
UTSW |
10 |
53,439,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Mcm9
|
UTSW |
10 |
53,423,668 (GRCm39) |
missense |
probably benign |
0.22 |
R4358:Mcm9
|
UTSW |
10 |
53,413,749 (GRCm39) |
missense |
probably benign |
0.03 |
R4660:Mcm9
|
UTSW |
10 |
53,424,623 (GRCm39) |
missense |
probably benign |
0.10 |
R4662:Mcm9
|
UTSW |
10 |
53,424,623 (GRCm39) |
missense |
probably benign |
0.10 |
R5082:Mcm9
|
UTSW |
10 |
53,414,156 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5130:Mcm9
|
UTSW |
10 |
53,506,495 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5193:Mcm9
|
UTSW |
10 |
53,492,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R5238:Mcm9
|
UTSW |
10 |
53,506,093 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5317:Mcm9
|
UTSW |
10 |
53,414,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Mcm9
|
UTSW |
10 |
53,414,788 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5524:Mcm9
|
UTSW |
10 |
53,424,786 (GRCm39) |
nonsense |
probably null |
|
R5593:Mcm9
|
UTSW |
10 |
53,414,393 (GRCm39) |
missense |
probably damaging |
0.99 |
R5748:Mcm9
|
UTSW |
10 |
53,501,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Mcm9
|
UTSW |
10 |
53,492,073 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6299:Mcm9
|
UTSW |
10 |
53,413,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R6344:Mcm9
|
UTSW |
10 |
53,414,033 (GRCm39) |
missense |
probably benign |
0.03 |
R6502:Mcm9
|
UTSW |
10 |
53,488,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R6621:Mcm9
|
UTSW |
10 |
53,439,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R6883:Mcm9
|
UTSW |
10 |
53,492,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R6932:Mcm9
|
UTSW |
10 |
53,496,299 (GRCm39) |
missense |
probably benign |
0.06 |
R6963:Mcm9
|
UTSW |
10 |
53,424,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R7094:Mcm9
|
UTSW |
10 |
53,496,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R7114:Mcm9
|
UTSW |
10 |
53,414,669 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7200:Mcm9
|
UTSW |
10 |
53,492,019 (GRCm39) |
missense |
|
|
R7593:Mcm9
|
UTSW |
10 |
53,506,088 (GRCm39) |
missense |
probably benign |
0.04 |
R7671:Mcm9
|
UTSW |
10 |
53,413,665 (GRCm39) |
missense |
probably benign |
0.01 |
R7697:Mcm9
|
UTSW |
10 |
53,491,990 (GRCm39) |
missense |
|
|
R7997:Mcm9
|
UTSW |
10 |
53,473,502 (GRCm39) |
start gained |
probably benign |
|
R8136:Mcm9
|
UTSW |
10 |
53,487,439 (GRCm39) |
makesense |
probably null |
|
R8137:Mcm9
|
UTSW |
10 |
53,499,076 (GRCm39) |
missense |
|
|
R8494:Mcm9
|
UTSW |
10 |
53,501,856 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8526:Mcm9
|
UTSW |
10 |
53,506,221 (GRCm39) |
unclassified |
probably benign |
|
R8558:Mcm9
|
UTSW |
10 |
53,492,068 (GRCm39) |
missense |
probably benign |
0.07 |
R8703:Mcm9
|
UTSW |
10 |
53,506,073 (GRCm39) |
missense |
probably damaging |
0.96 |
R8836:Mcm9
|
UTSW |
10 |
53,502,130 (GRCm39) |
missense |
|
|
R8994:Mcm9
|
UTSW |
10 |
53,424,620 (GRCm39) |
missense |
probably benign |
0.31 |
R9150:Mcm9
|
UTSW |
10 |
53,502,110 (GRCm39) |
missense |
|
|
R9564:Mcm9
|
UTSW |
10 |
53,506,104 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Mcm9
|
UTSW |
10 |
53,505,884 (GRCm39) |
frame shift |
probably null |
|
Z1176:Mcm9
|
UTSW |
10 |
53,413,603 (GRCm39) |
missense |
unknown |
|
|