Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 78,903,668 (GRCm39) |
D216G |
probably benign |
Het |
Abcg5 |
A |
T |
17: 84,965,956 (GRCm39) |
I640K |
possibly damaging |
Het |
Acadvl |
T |
C |
11: 69,905,168 (GRCm39) |
K128R |
probably benign |
Het |
Angptl7 |
T |
A |
4: 148,581,018 (GRCm39) |
N259I |
probably damaging |
Het |
Ankrd35 |
A |
G |
3: 96,586,997 (GRCm39) |
K104R |
possibly damaging |
Het |
Antxr1 |
T |
C |
6: 87,165,198 (GRCm39) |
N413S |
probably damaging |
Het |
Atf6b |
T |
G |
17: 34,872,949 (GRCm39) |
S622A |
probably damaging |
Het |
Atp5pd |
T |
A |
11: 115,306,851 (GRCm39) |
Y115F |
possibly damaging |
Het |
Axin2 |
T |
C |
11: 108,822,369 (GRCm39) |
L307P |
probably damaging |
Het |
B4galnt4 |
C |
T |
7: 140,644,564 (GRCm39) |
T153M |
possibly damaging |
Het |
Brd8 |
A |
G |
18: 34,740,231 (GRCm39) |
V604A |
probably benign |
Het |
Ccser2 |
T |
C |
14: 36,618,240 (GRCm39) |
Y765C |
probably damaging |
Het |
Cdh26 |
A |
G |
2: 178,110,006 (GRCm39) |
D433G |
probably damaging |
Het |
Cep85l |
T |
G |
10: 53,175,420 (GRCm39) |
|
probably null |
Het |
Ciao3 |
A |
G |
17: 25,996,395 (GRCm39) |
T135A |
probably benign |
Het |
Col23a1 |
T |
A |
11: 51,461,014 (GRCm39) |
|
probably null |
Het |
Col7a1 |
A |
G |
9: 108,804,452 (GRCm39) |
D2261G |
unknown |
Het |
Comp |
C |
A |
8: 70,833,936 (GRCm39) |
N650K |
probably damaging |
Het |
Copb1 |
A |
G |
7: 113,834,202 (GRCm39) |
M476T |
possibly damaging |
Het |
Dapk1 |
T |
A |
13: 60,897,009 (GRCm39) |
S743T |
probably damaging |
Het |
Ddx39a |
A |
G |
8: 84,451,105 (GRCm39) |
|
probably null |
Het |
Dgkb |
A |
G |
12: 38,186,580 (GRCm39) |
H243R |
probably damaging |
Het |
Dsg1c |
T |
G |
18: 20,416,171 (GRCm39) |
Y691D |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,117,535 (GRCm39) |
S933N |
probably benign |
Het |
Ece1 |
T |
C |
4: 137,641,133 (GRCm39) |
S19P |
probably benign |
Het |
Edem1 |
G |
A |
6: 108,829,524 (GRCm39) |
E548K |
probably damaging |
Het |
Eif4a3l2 |
C |
T |
6: 116,528,468 (GRCm39) |
T115I |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,402,839 (GRCm39) |
V174A |
possibly damaging |
Het |
Fyco1 |
A |
T |
9: 123,658,453 (GRCm39) |
N574K |
probably benign |
Het |
Glb1l2 |
T |
A |
9: 26,676,980 (GRCm39) |
M551L |
probably benign |
Het |
Gm7694 |
G |
T |
1: 170,130,284 (GRCm39) |
P38Q |
probably damaging |
Het |
Grip1 |
A |
G |
10: 119,814,440 (GRCm39) |
T324A |
probably benign |
Het |
Htr3b |
A |
G |
9: 48,857,849 (GRCm39) |
V131A |
possibly damaging |
Het |
Igfbp1 |
T |
C |
11: 7,148,106 (GRCm39) |
C50R |
probably damaging |
Het |
Il5ra |
A |
G |
6: 106,692,611 (GRCm39) |
I378T |
possibly damaging |
Het |
Ints11 |
T |
C |
4: 155,972,687 (GRCm39) |
L504P |
possibly damaging |
Het |
Iqca1 |
A |
T |
1: 89,987,330 (GRCm39) |
I74N |
|
Het |
Kbtbd12 |
C |
T |
6: 88,595,663 (GRCm39) |
A56T |
probably damaging |
Het |
Kcnq5 |
T |
C |
1: 21,549,620 (GRCm39) |
N369S |
possibly damaging |
Het |
Kmt5b |
A |
G |
19: 3,865,381 (GRCm39) |
D815G |
probably benign |
Het |
Lnpk |
T |
C |
2: 74,352,599 (GRCm39) |
Q361R |
probably benign |
Het |
Mep1b |
T |
C |
18: 21,222,442 (GRCm39) |
I277T |
possibly damaging |
Het |
Naip6 |
G |
A |
13: 100,437,851 (GRCm39) |
T385I |
probably benign |
Het |
Npepl1 |
A |
T |
2: 173,953,002 (GRCm39) |
I95F |
probably benign |
Het |
Nxpe4 |
T |
C |
9: 48,304,020 (GRCm39) |
F36L |
probably benign |
Het |
Optn |
C |
A |
2: 5,045,013 (GRCm39) |
C243F |
probably damaging |
Het |
Or10al7 |
A |
T |
17: 38,365,903 (GRCm39) |
C185S |
probably damaging |
Het |
Or1e33 |
C |
T |
11: 73,738,735 (GRCm39) |
C72Y |
probably damaging |
Het |
Paqr7 |
T |
C |
4: 134,234,821 (GRCm39) |
V226A |
probably benign |
Het |
Pcdh12 |
T |
A |
18: 38,415,212 (GRCm39) |
I638F |
probably damaging |
Het |
Pfas |
T |
C |
11: 68,883,119 (GRCm39) |
T722A |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,270,981 (GRCm39) |
I3191F |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,706,944 (GRCm39) |
H531L |
probably benign |
Het |
Pom121l2 |
A |
G |
13: 22,166,544 (GRCm39) |
T272A |
probably benign |
Het |
Pparg |
T |
C |
6: 115,450,102 (GRCm39) |
V367A |
possibly damaging |
Het |
Psen2 |
A |
T |
1: 180,068,356 (GRCm39) |
M99K |
probably damaging |
Het |
Ranbp10 |
T |
C |
8: 106,499,179 (GRCm39) |
T536A |
probably benign |
Het |
Rbfox2 |
G |
T |
15: 76,983,654 (GRCm39) |
P284T |
probably damaging |
Het |
Rbmyf9 |
C |
T |
Y: 3,776,675 (GRCm39) |
T104I |
possibly damaging |
Het |
Rere |
G |
A |
4: 150,701,796 (GRCm39) |
R25H |
probably damaging |
Het |
Rhpn1 |
T |
A |
15: 75,581,115 (GRCm39) |
L119Q |
probably null |
Het |
Rlig1 |
C |
A |
10: 100,413,110 (GRCm39) |
V178F |
probably benign |
Het |
Rreb1 |
A |
G |
13: 38,125,677 (GRCm39) |
T1328A |
probably benign |
Het |
Septin11 |
A |
T |
5: 93,309,007 (GRCm39) |
|
probably null |
Het |
Skida1 |
T |
A |
2: 18,052,549 (GRCm39) |
Q201L |
probably benign |
Het |
Sptan1 |
T |
A |
2: 29,910,055 (GRCm39) |
I1805N |
probably damaging |
Het |
Stard13 |
T |
A |
5: 150,970,435 (GRCm39) |
Q853L |
possibly damaging |
Het |
Susd1 |
T |
A |
4: 59,365,916 (GRCm39) |
|
probably null |
Het |
Szt2 |
T |
A |
4: 118,245,061 (GRCm39) |
Q1158H |
possibly damaging |
Het |
Tbcc |
A |
C |
17: 47,202,046 (GRCm39) |
D144A |
probably benign |
Het |
Tsn |
A |
G |
1: 118,232,437 (GRCm39) |
I146T |
probably benign |
Het |
Umad1 |
A |
T |
6: 8,427,121 (GRCm39) |
T99S |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,805,777 (GRCm39) |
E3261V |
probably damaging |
Het |
Vcan |
C |
A |
13: 89,851,439 (GRCm39) |
E1174* |
probably null |
Het |
Vmn2r100 |
C |
A |
17: 19,751,415 (GRCm39) |
|
probably null |
Het |
Vmn2r65 |
A |
G |
7: 84,595,919 (GRCm39) |
I255T |
probably damaging |
Het |
Vps35l |
T |
C |
7: 118,342,855 (GRCm39) |
S47P |
probably benign |
Het |
Wdr70 |
A |
G |
15: 8,006,612 (GRCm39) |
L313P |
possibly damaging |
Het |
Ythdf2 |
C |
A |
4: 131,932,089 (GRCm39) |
R357L |
probably damaging |
Het |
Zfp523 |
T |
C |
17: 28,420,267 (GRCm39) |
C262R |
probably damaging |
Het |
Zfp553 |
T |
C |
7: 126,835,936 (GRCm39) |
V497A |
probably benign |
Het |
Zhx1 |
A |
G |
15: 57,916,662 (GRCm39) |
L528S |
probably benign |
Het |
|
Other mutations in Arhgap26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00706:Arhgap26
|
APN |
18 |
39,419,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01116:Arhgap26
|
APN |
18 |
39,244,856 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01409:Arhgap26
|
APN |
18 |
39,243,504 (GRCm39) |
splice site |
probably benign |
|
IGL02316:Arhgap26
|
APN |
18 |
38,775,599 (GRCm39) |
exon |
noncoding transcript |
|
IGL02418:Arhgap26
|
APN |
18 |
39,490,620 (GRCm39) |
intron |
probably benign |
|
IGL02588:Arhgap26
|
APN |
18 |
38,734,670 (GRCm39) |
unclassified |
probably benign |
|
IGL03241:Arhgap26
|
APN |
18 |
39,362,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Arhgap26
|
UTSW |
18 |
38,750,726 (GRCm39) |
missense |
unknown |
|
R0244:Arhgap26
|
UTSW |
18 |
39,496,184 (GRCm39) |
missense |
probably benign |
0.05 |
R0347:Arhgap26
|
UTSW |
18 |
38,750,797 (GRCm39) |
missense |
unknown |
|
R1533:Arhgap26
|
UTSW |
18 |
39,504,130 (GRCm39) |
missense |
probably benign |
0.16 |
R1606:Arhgap26
|
UTSW |
18 |
39,429,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Arhgap26
|
UTSW |
18 |
39,439,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R2182:Arhgap26
|
UTSW |
18 |
39,490,862 (GRCm39) |
intron |
probably benign |
|
R2291:Arhgap26
|
UTSW |
18 |
39,490,751 (GRCm39) |
intron |
probably benign |
|
R3611:Arhgap26
|
UTSW |
18 |
39,066,972 (GRCm39) |
missense |
probably benign |
|
R3700:Arhgap26
|
UTSW |
18 |
39,253,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R3887:Arhgap26
|
UTSW |
18 |
39,363,019 (GRCm39) |
critical splice donor site |
probably null |
|
R4621:Arhgap26
|
UTSW |
18 |
39,032,894 (GRCm39) |
intron |
probably benign |
|
R4877:Arhgap26
|
UTSW |
18 |
39,429,982 (GRCm39) |
splice site |
probably null |
|
R4910:Arhgap26
|
UTSW |
18 |
39,126,690 (GRCm39) |
splice site |
probably benign |
|
R4911:Arhgap26
|
UTSW |
18 |
39,126,690 (GRCm39) |
splice site |
probably benign |
|
R4954:Arhgap26
|
UTSW |
18 |
39,376,694 (GRCm39) |
missense |
probably benign |
0.00 |
R4967:Arhgap26
|
UTSW |
18 |
39,379,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R5221:Arhgap26
|
UTSW |
18 |
39,243,525 (GRCm39) |
nonsense |
probably null |
|
R5232:Arhgap26
|
UTSW |
18 |
39,126,529 (GRCm39) |
start codon destroyed |
probably null |
0.97 |
R5297:Arhgap26
|
UTSW |
18 |
39,254,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Arhgap26
|
UTSW |
18 |
38,775,509 (GRCm39) |
exon |
noncoding transcript |
|
R5570:Arhgap26
|
UTSW |
18 |
39,232,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R5692:Arhgap26
|
UTSW |
18 |
39,254,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R5752:Arhgap26
|
UTSW |
18 |
39,419,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Arhgap26
|
UTSW |
18 |
39,283,145 (GRCm39) |
missense |
probably damaging |
0.96 |
R6131:Arhgap26
|
UTSW |
18 |
39,419,638 (GRCm39) |
nonsense |
probably null |
|
R6251:Arhgap26
|
UTSW |
18 |
39,490,880 (GRCm39) |
missense |
probably null |
|
R6481:Arhgap26
|
UTSW |
18 |
39,283,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R6622:Arhgap26
|
UTSW |
18 |
39,032,916 (GRCm39) |
intron |
probably benign |
|
R6799:Arhgap26
|
UTSW |
18 |
39,232,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6878:Arhgap26
|
UTSW |
18 |
39,360,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Arhgap26
|
UTSW |
18 |
39,232,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Arhgap26
|
UTSW |
18 |
39,439,907 (GRCm39) |
critical splice donor site |
probably null |
|
R7936:Arhgap26
|
UTSW |
18 |
39,338,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Arhgap26
|
UTSW |
18 |
39,362,980 (GRCm39) |
missense |
|
|
R8206:Arhgap26
|
UTSW |
18 |
39,439,803 (GRCm39) |
nonsense |
probably null |
|
R8356:Arhgap26
|
UTSW |
18 |
39,244,901 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8456:Arhgap26
|
UTSW |
18 |
39,244,901 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8987:Arhgap26
|
UTSW |
18 |
39,490,652 (GRCm39) |
missense |
|
|
R9025:Arhgap26
|
UTSW |
18 |
39,379,898 (GRCm39) |
missense |
|
|
R9149:Arhgap26
|
UTSW |
18 |
39,244,917 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9172:Arhgap26
|
UTSW |
18 |
39,378,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R9191:Arhgap26
|
UTSW |
18 |
39,439,893 (GRCm39) |
missense |
|
|
R9576:Arhgap26
|
UTSW |
18 |
39,253,207 (GRCm39) |
nonsense |
probably null |
|
X0013:Arhgap26
|
UTSW |
18 |
39,504,165 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Arhgap26
|
UTSW |
18 |
39,283,158 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Arhgap26
|
UTSW |
18 |
39,490,724 (GRCm39) |
splice site |
probably benign |
|
|