Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
A |
G |
8: 73,208,959 (GRCm39) |
E363G |
probably benign |
Het |
Abca3 |
A |
G |
17: 24,596,693 (GRCm39) |
Y382C |
probably damaging |
Het |
Abca5 |
A |
G |
11: 110,183,000 (GRCm39) |
I1019T |
probably benign |
Het |
Acox3 |
A |
T |
5: 35,762,568 (GRCm39) |
S481C |
probably damaging |
Het |
Ankrd7 |
T |
A |
6: 18,870,030 (GRCm39) |
M261K |
probably benign |
Het |
Aqr |
A |
C |
2: 113,967,485 (GRCm39) |
M510R |
probably damaging |
Het |
Arpc1a |
A |
T |
5: 145,029,369 (GRCm39) |
T56S |
probably benign |
Het |
Asap2 |
A |
T |
12: 21,162,084 (GRCm39) |
T14S |
probably damaging |
Het |
Aspg |
A |
G |
12: 112,087,408 (GRCm39) |
E288G |
probably benign |
Het |
Atp2c2 |
A |
G |
8: 120,482,841 (GRCm39) |
N901S |
probably benign |
Het |
Cabcoco1 |
A |
G |
10: 68,267,092 (GRCm39) |
L205P |
probably damaging |
Het |
Cant1 |
A |
G |
11: 118,302,263 (GRCm39) |
L18P |
probably damaging |
Het |
Cdca2 |
G |
A |
14: 67,914,425 (GRCm39) |
P945S |
probably damaging |
Het |
Cfap74 |
A |
G |
4: 155,513,753 (GRCm39) |
K522E |
possibly damaging |
Het |
Chek1 |
C |
A |
9: 36,635,279 (GRCm39) |
V35F |
probably damaging |
Het |
Cpa6 |
A |
T |
1: 10,407,547 (GRCm39) |
M330K |
probably damaging |
Het |
Creb3l4 |
G |
T |
3: 90,145,792 (GRCm39) |
N246K |
probably damaging |
Het |
Cyp2c55 |
T |
A |
19: 39,022,819 (GRCm39) |
V319D |
probably damaging |
Het |
Dapk1 |
T |
A |
13: 60,877,317 (GRCm39) |
S519T |
probably benign |
Het |
Dis3l |
T |
A |
9: 64,214,545 (GRCm39) |
N981I |
probably benign |
Het |
Dock4 |
T |
A |
12: 40,870,661 (GRCm39) |
V1467E |
probably damaging |
Het |
Dock4 |
ACCTGCTCTGCC |
ACCTGCTCTGCCTGCTCTGCC |
12: 40,894,547 (GRCm39) |
|
probably benign |
Het |
Dok5 |
G |
A |
2: 170,642,816 (GRCm39) |
G38D |
probably damaging |
Het |
Ercc6l2 |
T |
C |
13: 64,013,821 (GRCm39) |
S631P |
probably damaging |
Het |
Fat4 |
A |
T |
3: 38,941,688 (GRCm39) |
S194C |
probably damaging |
Het |
Fcsk |
T |
A |
8: 111,615,704 (GRCm39) |
T542S |
probably benign |
Het |
Garem2 |
T |
C |
5: 30,313,297 (GRCm39) |
S54P |
probably damaging |
Het |
Gdf10 |
T |
C |
14: 33,656,346 (GRCm39) |
I436T |
probably damaging |
Het |
Gfod1 |
T |
C |
13: 43,456,946 (GRCm39) |
T10A |
possibly damaging |
Het |
Gucy1a1 |
A |
G |
3: 82,018,458 (GRCm39) |
|
probably null |
Het |
Heatr5b |
G |
T |
17: 79,138,873 (GRCm39) |
Q90K |
probably benign |
Het |
Ikzf3 |
T |
A |
11: 98,376,475 (GRCm39) |
K211* |
probably null |
Het |
Itgam |
A |
C |
7: 127,684,749 (GRCm39) |
D373A |
probably damaging |
Het |
Itpripl2 |
A |
G |
7: 118,089,107 (GRCm39) |
F484S |
probably damaging |
Het |
Kat6b |
A |
T |
14: 21,718,735 (GRCm39) |
H1138L |
probably benign |
Het |
Kif16b |
T |
C |
2: 142,532,500 (GRCm39) |
K1213R |
probably damaging |
Het |
Klra3 |
G |
C |
6: 130,310,107 (GRCm39) |
R138G |
probably benign |
Het |
Mmp25 |
T |
A |
17: 23,850,048 (GRCm39) |
Y504F |
probably damaging |
Het |
Mtf2 |
A |
G |
5: 108,228,797 (GRCm39) |
K38E |
possibly damaging |
Het |
Myh14 |
A |
C |
7: 44,301,853 (GRCm39) |
|
probably null |
Het |
Nedd4l |
T |
A |
18: 65,343,401 (GRCm39) |
H820Q |
probably damaging |
Het |
Nfkb1 |
T |
C |
3: 135,307,240 (GRCm39) |
T562A |
probably benign |
Het |
Or8b49 |
G |
T |
9: 38,505,707 (GRCm39) |
L63F |
probably damaging |
Het |
Pds5a |
A |
T |
5: 65,807,841 (GRCm39) |
V464E |
probably damaging |
Het |
Peak1 |
C |
T |
9: 56,114,496 (GRCm39) |
V452M |
probably damaging |
Het |
Phf2 |
T |
C |
13: 48,973,549 (GRCm39) |
Y372C |
unknown |
Het |
Poc1a |
T |
A |
9: 106,162,773 (GRCm39) |
|
probably null |
Het |
Prss33 |
C |
T |
17: 24,053,817 (GRCm39) |
V87M |
probably damaging |
Het |
Psmc2 |
C |
G |
5: 22,008,127 (GRCm39) |
L344V |
possibly damaging |
Het |
Ptpn12 |
C |
A |
5: 21,207,466 (GRCm39) |
Q297H |
probably damaging |
Het |
Rabgap1 |
T |
C |
2: 37,365,453 (GRCm39) |
V242A |
probably damaging |
Het |
Rad1 |
C |
A |
15: 10,486,721 (GRCm39) |
H39Q |
possibly damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,986 (GRCm39) |
H636R |
probably benign |
Het |
Samd9l |
C |
T |
6: 3,372,945 (GRCm39) |
D1439N |
possibly damaging |
Het |
Sbno1 |
A |
T |
5: 124,516,574 (GRCm39) |
D1266E |
probably benign |
Het |
Sidt2 |
T |
C |
9: 45,856,638 (GRCm39) |
D477G |
probably damaging |
Het |
Slc22a13 |
T |
C |
9: 119,037,753 (GRCm39) |
K125R |
probably benign |
Het |
Slc6a1 |
G |
T |
6: 114,284,731 (GRCm39) |
G263V |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,139,402 (GRCm39) |
Y771H |
probably damaging |
Het |
Smg1 |
A |
T |
7: 117,757,299 (GRCm39) |
|
probably benign |
Het |
Spinkl |
A |
T |
18: 44,302,194 (GRCm39) |
N32K |
probably benign |
Het |
Stxbp1 |
T |
A |
2: 32,692,868 (GRCm39) |
I383F |
probably damaging |
Het |
Taf3 |
C |
T |
2: 9,956,377 (GRCm39) |
E597K |
possibly damaging |
Het |
Tln2 |
T |
C |
9: 67,209,842 (GRCm39) |
T432A |
probably damaging |
Het |
Tmco6 |
T |
C |
18: 36,874,740 (GRCm39) |
V409A |
probably benign |
Het |
Tstd2 |
T |
C |
4: 46,129,235 (GRCm39) |
T198A |
probably damaging |
Het |
Vmn1r230 |
T |
A |
17: 21,067,063 (GRCm39) |
M84K |
probably damaging |
Het |
Vmn1r45 |
T |
A |
6: 89,910,965 (GRCm39) |
S2C |
possibly damaging |
Het |
Vmn2r25 |
T |
A |
6: 123,816,805 (GRCm39) |
T259S |
probably benign |
Het |
Vmn2r70 |
A |
G |
7: 85,212,923 (GRCm39) |
S495P |
possibly damaging |
Het |
Vmn2r97 |
A |
T |
17: 19,167,584 (GRCm39) |
R613* |
probably null |
Het |
Yme1l1 |
T |
C |
2: 23,052,520 (GRCm39) |
L58P |
probably damaging |
Het |
Zan |
G |
A |
5: 137,412,511 (GRCm39) |
|
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,466,801 (GRCm39) |
T2320A |
possibly damaging |
Het |
Zfp407 |
T |
C |
18: 84,227,774 (GRCm39) |
D1945G |
possibly damaging |
Het |
|
Other mutations in Dhx38 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00508:Dhx38
|
APN |
8 |
110,283,566 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL00821:Dhx38
|
APN |
8 |
110,282,286 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00910:Dhx38
|
APN |
8 |
110,285,666 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01011:Dhx38
|
APN |
8 |
110,289,323 (GRCm39) |
missense |
probably benign |
|
IGL01401:Dhx38
|
APN |
8 |
110,278,746 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02133:Dhx38
|
APN |
8 |
110,284,873 (GRCm39) |
nonsense |
probably null |
|
IGL02529:Dhx38
|
APN |
8 |
110,285,645 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02652:Dhx38
|
APN |
8 |
110,282,761 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03241:Dhx38
|
APN |
8 |
110,289,288 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03378:Dhx38
|
APN |
8 |
110,285,722 (GRCm39) |
splice site |
probably null |
|
R0358:Dhx38
|
UTSW |
8 |
110,279,094 (GRCm39) |
missense |
probably benign |
0.13 |
R0375:Dhx38
|
UTSW |
8 |
110,281,813 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0437:Dhx38
|
UTSW |
8 |
110,285,261 (GRCm39) |
splice site |
probably benign |
|
R0481:Dhx38
|
UTSW |
8 |
110,282,848 (GRCm39) |
splice site |
probably benign |
|
R0492:Dhx38
|
UTSW |
8 |
110,288,576 (GRCm39) |
splice site |
probably benign |
|
R0528:Dhx38
|
UTSW |
8 |
110,289,293 (GRCm39) |
missense |
probably benign |
0.00 |
R0607:Dhx38
|
UTSW |
8 |
110,285,575 (GRCm39) |
missense |
probably benign |
0.07 |
R1638:Dhx38
|
UTSW |
8 |
110,280,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Dhx38
|
UTSW |
8 |
110,283,501 (GRCm39) |
splice site |
probably benign |
|
R2056:Dhx38
|
UTSW |
8 |
110,289,352 (GRCm39) |
unclassified |
probably benign |
|
R2096:Dhx38
|
UTSW |
8 |
110,280,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Dhx38
|
UTSW |
8 |
110,287,306 (GRCm39) |
missense |
probably benign |
0.00 |
R2382:Dhx38
|
UTSW |
8 |
110,282,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R4367:Dhx38
|
UTSW |
8 |
110,279,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4368:Dhx38
|
UTSW |
8 |
110,279,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4369:Dhx38
|
UTSW |
8 |
110,279,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Dhx38
|
UTSW |
8 |
110,283,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Dhx38
|
UTSW |
8 |
110,282,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R5668:Dhx38
|
UTSW |
8 |
110,280,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R5777:Dhx38
|
UTSW |
8 |
110,283,534 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5784:Dhx38
|
UTSW |
8 |
110,286,245 (GRCm39) |
nonsense |
probably null |
|
R6799:Dhx38
|
UTSW |
8 |
110,279,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Dhx38
|
UTSW |
8 |
110,286,231 (GRCm39) |
missense |
probably benign |
0.15 |
R6932:Dhx38
|
UTSW |
8 |
110,279,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R7042:Dhx38
|
UTSW |
8 |
110,283,617 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7248:Dhx38
|
UTSW |
8 |
110,285,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7394:Dhx38
|
UTSW |
8 |
110,283,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Dhx38
|
UTSW |
8 |
110,287,221 (GRCm39) |
missense |
probably benign |
0.00 |
R7569:Dhx38
|
UTSW |
8 |
110,287,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R8003:Dhx38
|
UTSW |
8 |
110,282,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R8071:Dhx38
|
UTSW |
8 |
110,285,333 (GRCm39) |
missense |
probably benign |
0.10 |
R8537:Dhx38
|
UTSW |
8 |
110,280,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R8852:Dhx38
|
UTSW |
8 |
110,289,361 (GRCm39) |
nonsense |
probably null |
|
R8860:Dhx38
|
UTSW |
8 |
110,289,361 (GRCm39) |
nonsense |
probably null |
|
R8937:Dhx38
|
UTSW |
8 |
110,283,098 (GRCm39) |
missense |
probably damaging |
0.96 |
R9099:Dhx38
|
UTSW |
8 |
110,282,783 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dhx38
|
UTSW |
8 |
110,282,717 (GRCm39) |
missense |
probably benign |
0.00 |
|