Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg2 |
T |
C |
6: 58,667,525 (GRCm39) |
V129A |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,992,676 (GRCm39) |
D264G |
probably damaging |
Het |
Ahnak2 |
T |
A |
12: 112,748,626 (GRCm39) |
D407V |
probably benign |
Het |
Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
Ankmy1 |
T |
C |
1: 92,809,553 (GRCm39) |
I662V |
possibly damaging |
Het |
Ano1 |
A |
G |
7: 144,201,789 (GRCm39) |
V334A |
probably damaging |
Het |
Apc |
A |
G |
18: 34,449,481 (GRCm39) |
R2092G |
probably damaging |
Het |
Atp2b4 |
G |
T |
1: 133,654,275 (GRCm39) |
Q777K |
probably benign |
Het |
Brap |
G |
A |
5: 121,801,529 (GRCm39) |
G95S |
probably damaging |
Het |
Cbfa2t2 |
G |
A |
2: 154,377,077 (GRCm39) |
A587T |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,932,477 (GRCm39) |
I1308V |
probably benign |
Het |
Ccser1 |
T |
A |
6: 61,399,936 (GRCm39) |
|
probably null |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cmtm4 |
A |
C |
8: 105,081,920 (GRCm39) |
F156V |
probably damaging |
Het |
Cntln |
G |
A |
4: 84,967,911 (GRCm39) |
R710K |
probably benign |
Het |
Csn1s1 |
A |
T |
5: 87,819,387 (GRCm39) |
T15S |
possibly damaging |
Het |
Cul9 |
T |
C |
17: 46,854,298 (GRCm39) |
T135A |
probably benign |
Het |
Cyp2d10 |
T |
A |
15: 82,288,015 (GRCm39) |
I363F |
probably damaging |
Het |
Dhx38 |
G |
T |
8: 110,289,352 (GRCm39) |
|
probably benign |
Het |
Dis3 |
A |
T |
14: 99,336,251 (GRCm39) |
I85N |
possibly damaging |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Dscaml1 |
A |
G |
9: 45,661,430 (GRCm39) |
D1776G |
probably damaging |
Het |
Erbin |
A |
G |
13: 103,966,824 (GRCm39) |
S1209P |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
Fbxo45 |
G |
T |
16: 32,057,346 (GRCm39) |
Q183K |
possibly damaging |
Het |
Frmd4b |
C |
T |
6: 97,389,448 (GRCm39) |
|
probably null |
Het |
Fzd7 |
A |
G |
1: 59,523,361 (GRCm39) |
S415G |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,229,025 (GRCm39) |
|
probably null |
Het |
Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
Gstcd |
T |
C |
3: 132,787,814 (GRCm39) |
I295V |
probably benign |
Het |
Gucy1a1 |
A |
G |
3: 82,016,592 (GRCm39) |
L132P |
possibly damaging |
Het |
Il12b |
A |
C |
11: 44,298,727 (GRCm39) |
T61P |
probably damaging |
Het |
Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
Itih3 |
A |
C |
14: 30,631,481 (GRCm39) |
|
probably null |
Het |
Kdm5b |
T |
A |
1: 134,540,952 (GRCm39) |
D681E |
probably benign |
Het |
Kif11 |
A |
G |
19: 37,390,660 (GRCm39) |
N408D |
probably benign |
Het |
Kng2 |
TATGACCATGACCATGACCATGACCATGACCATGACCAT |
TATGACCATGACCATGACCATGACCATGACCAT |
16: 22,806,703 (GRCm39) |
|
probably benign |
Het |
Kremen2 |
T |
C |
17: 23,961,691 (GRCm39) |
E272G |
possibly damaging |
Het |
Krt9 |
G |
T |
11: 100,082,321 (GRCm39) |
N201K |
probably damaging |
Het |
Lmbr1 |
G |
A |
5: 29,438,092 (GRCm39) |
P304L |
probably benign |
Het |
Lrrfip1 |
A |
G |
1: 91,043,539 (GRCm39) |
N648S |
probably benign |
Het |
Mab21l3 |
C |
A |
3: 101,722,469 (GRCm39) |
V386L |
possibly damaging |
Het |
Mamdc4 |
T |
C |
2: 25,454,180 (GRCm39) |
Q1149R |
probably benign |
Het |
Mast1 |
A |
G |
8: 85,646,995 (GRCm39) |
F677L |
possibly damaging |
Het |
Mcoln3 |
A |
G |
3: 145,833,979 (GRCm39) |
D173G |
probably benign |
Het |
Mmrn1 |
C |
T |
6: 60,921,789 (GRCm39) |
T82I |
probably benign |
Het |
Mtcl2 |
C |
T |
2: 156,864,747 (GRCm39) |
G1154S |
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,345,772 (GRCm39) |
T203A |
probably benign |
Het |
Myo9b |
T |
C |
8: 71,812,334 (GRCm39) |
I2035T |
possibly damaging |
Het |
Ndst3 |
T |
C |
3: 123,465,534 (GRCm39) |
N146S |
probably damaging |
Het |
Neu4 |
A |
G |
1: 93,950,172 (GRCm39) |
T21A |
possibly damaging |
Het |
Nos1ap |
G |
A |
1: 170,155,215 (GRCm39) |
L267F |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,591 (GRCm39) |
K240N |
probably damaging |
Het |
Or3a4 |
A |
T |
11: 73,944,819 (GRCm39) |
Y255* |
probably null |
Het |
Or4p8 |
A |
G |
2: 88,727,105 (GRCm39) |
F279L |
probably damaging |
Het |
Phc1 |
T |
C |
6: 122,310,299 (GRCm39) |
N136S |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,545,469 (GRCm39) |
T1862A |
probably benign |
Het |
Psd2 |
A |
G |
18: 36,139,744 (GRCm39) |
D596G |
possibly damaging |
Het |
Psmc3 |
T |
C |
2: 90,888,433 (GRCm39) |
F315L |
probably benign |
Het |
Rerg |
G |
A |
6: 137,034,878 (GRCm39) |
T42I |
probably benign |
Het |
Rif1 |
T |
A |
2: 51,983,588 (GRCm39) |
M577K |
probably damaging |
Het |
Sap30 |
T |
C |
8: 57,940,282 (GRCm39) |
|
probably null |
Het |
Scn2b |
T |
C |
9: 45,036,815 (GRCm39) |
Y108H |
probably damaging |
Het |
Senp2 |
C |
T |
16: 21,832,949 (GRCm39) |
T79I |
probably damaging |
Het |
Serpinb2 |
T |
C |
1: 107,451,543 (GRCm39) |
V232A |
probably damaging |
Het |
Sgpp2 |
T |
A |
1: 78,393,588 (GRCm39) |
L197Q |
probably damaging |
Het |
Slc27a4 |
T |
C |
2: 29,700,953 (GRCm39) |
W320R |
probably damaging |
Het |
Spmip4 |
T |
C |
6: 50,550,725 (GRCm39) |
R575G |
possibly damaging |
Het |
Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
Thbs4 |
T |
A |
13: 92,927,387 (GRCm39) |
D34V |
probably benign |
Het |
Tlcd4 |
T |
G |
3: 121,001,070 (GRCm39) |
I188L |
probably benign |
Het |
Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
Tmod2 |
T |
C |
9: 75,484,524 (GRCm39) |
E248G |
probably benign |
Het |
Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
Ttn |
T |
C |
2: 76,615,882 (GRCm39) |
D8360G |
possibly damaging |
Het |
Unc80 |
A |
G |
1: 66,679,711 (GRCm39) |
E2094G |
possibly damaging |
Het |
Vmn2r18 |
A |
T |
5: 151,508,160 (GRCm39) |
D321E |
probably damaging |
Het |
|
Other mutations in Arhgap18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01609:Arhgap18
|
APN |
10 |
26,756,744 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02393:Arhgap18
|
APN |
10 |
26,753,179 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03368:Arhgap18
|
APN |
10 |
26,648,689 (GRCm39) |
missense |
possibly damaging |
0.60 |
Half_pint
|
UTSW |
10 |
26,648,694 (GRCm39) |
critical splice donor site |
probably null |
|
R0698:Arhgap18
|
UTSW |
10 |
26,788,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Arhgap18
|
UTSW |
10 |
26,792,436 (GRCm39) |
missense |
probably benign |
0.29 |
R1532:Arhgap18
|
UTSW |
10 |
26,736,718 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1768:Arhgap18
|
UTSW |
10 |
26,763,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Arhgap18
|
UTSW |
10 |
26,763,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Arhgap18
|
UTSW |
10 |
26,736,732 (GRCm39) |
unclassified |
probably benign |
|
R1867:Arhgap18
|
UTSW |
10 |
26,722,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R2020:Arhgap18
|
UTSW |
10 |
26,730,900 (GRCm39) |
missense |
probably benign |
|
R2049:Arhgap18
|
UTSW |
10 |
26,725,938 (GRCm39) |
missense |
probably benign |
0.00 |
R2058:Arhgap18
|
UTSW |
10 |
26,730,904 (GRCm39) |
missense |
probably benign |
0.03 |
R2986:Arhgap18
|
UTSW |
10 |
26,730,903 (GRCm39) |
missense |
probably benign |
0.00 |
R3027:Arhgap18
|
UTSW |
10 |
26,722,092 (GRCm39) |
missense |
probably benign |
|
R5103:Arhgap18
|
UTSW |
10 |
26,745,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Arhgap18
|
UTSW |
10 |
26,788,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R5532:Arhgap18
|
UTSW |
10 |
26,722,104 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5710:Arhgap18
|
UTSW |
10 |
26,736,729 (GRCm39) |
splice site |
probably null |
|
R6019:Arhgap18
|
UTSW |
10 |
26,736,646 (GRCm39) |
missense |
probably damaging |
0.98 |
R6190:Arhgap18
|
UTSW |
10 |
26,722,031 (GRCm39) |
start codon destroyed |
probably null |
0.22 |
R6346:Arhgap18
|
UTSW |
10 |
26,722,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6438:Arhgap18
|
UTSW |
10 |
26,648,694 (GRCm39) |
critical splice donor site |
probably null |
|
R6572:Arhgap18
|
UTSW |
10 |
26,722,412 (GRCm39) |
splice site |
probably null |
|
R6799:Arhgap18
|
UTSW |
10 |
26,725,917 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6844:Arhgap18
|
UTSW |
10 |
26,648,682 (GRCm39) |
missense |
probably benign |
0.04 |
R7051:Arhgap18
|
UTSW |
10 |
26,725,917 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7084:Arhgap18
|
UTSW |
10 |
26,748,734 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7727:Arhgap18
|
UTSW |
10 |
26,746,007 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8046:Arhgap18
|
UTSW |
10 |
26,763,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R8252:Arhgap18
|
UTSW |
10 |
26,730,932 (GRCm39) |
missense |
probably benign |
0.00 |
R8392:Arhgap18
|
UTSW |
10 |
26,721,936 (GRCm39) |
missense |
probably benign |
0.38 |
R8485:Arhgap18
|
UTSW |
10 |
26,722,104 (GRCm39) |
missense |
probably benign |
0.05 |
R9132:Arhgap18
|
UTSW |
10 |
26,730,886 (GRCm39) |
missense |
probably benign |
|
R9159:Arhgap18
|
UTSW |
10 |
26,730,886 (GRCm39) |
missense |
probably benign |
|
R9245:Arhgap18
|
UTSW |
10 |
26,722,107 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9375:Arhgap18
|
UTSW |
10 |
26,648,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R9597:Arhgap18
|
UTSW |
10 |
26,788,655 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Arhgap18
|
UTSW |
10 |
26,726,000 (GRCm39) |
splice site |
probably null |
|
|