Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
C |
T |
12: 72,953,008 (GRCm39) |
E242K |
possibly damaging |
Het |
A930011G23Rik |
A |
G |
5: 99,370,263 (GRCm39) |
M499T |
possibly damaging |
Het |
Abcb8 |
G |
A |
5: 24,605,779 (GRCm39) |
V196M |
possibly damaging |
Het |
Ahnak |
T |
C |
19: 8,988,331 (GRCm39) |
M3205T |
possibly damaging |
Het |
Ankrd1 |
A |
G |
19: 36,092,433 (GRCm39) |
Y265H |
probably damaging |
Het |
Apeh |
A |
G |
9: 107,965,024 (GRCm39) |
S446P |
probably benign |
Het |
Apip |
C |
A |
2: 102,922,226 (GRCm39) |
Y197* |
probably null |
Het |
Arid4b |
T |
C |
13: 14,362,062 (GRCm39) |
V929A |
probably damaging |
Het |
Asah2 |
T |
A |
19: 32,030,306 (GRCm39) |
D122V |
probably benign |
Het |
B2m |
A |
T |
2: 121,982,128 (GRCm39) |
D116V |
possibly damaging |
Het |
Bhmt-ps1 |
A |
G |
4: 26,369,184 (GRCm39) |
|
noncoding transcript |
Het |
Cacna1g |
T |
A |
11: 94,334,899 (GRCm39) |
I803F |
probably damaging |
Het |
Ccdc43 |
A |
T |
11: 102,581,111 (GRCm39) |
V113E |
probably damaging |
Het |
Cenpj |
A |
T |
14: 56,772,238 (GRCm39) |
Y388* |
probably null |
Het |
Chd3 |
G |
A |
11: 69,245,034 (GRCm39) |
|
probably benign |
Het |
Chil3 |
C |
T |
3: 106,071,524 (GRCm39) |
D47N |
possibly damaging |
Het |
Colgalt2 |
A |
G |
1: 152,375,710 (GRCm39) |
T361A |
possibly damaging |
Het |
Cops3 |
C |
A |
11: 59,726,193 (GRCm39) |
|
probably benign |
Het |
Crb2 |
G |
T |
2: 37,673,326 (GRCm39) |
G74V |
probably damaging |
Het |
Cspg4b |
G |
T |
13: 113,464,196 (GRCm39) |
G1453C |
probably damaging |
Het |
Cyp20a1 |
A |
T |
1: 60,405,878 (GRCm39) |
Y224F |
probably damaging |
Het |
Diaph3 |
A |
G |
14: 87,378,602 (GRCm39) |
|
probably benign |
Het |
Dnah3 |
A |
T |
7: 119,550,904 (GRCm39) |
Y3127* |
probably null |
Het |
Eef1akmt3 |
A |
C |
10: 126,877,224 (GRCm39) |
S14A |
possibly damaging |
Het |
Ehf |
C |
A |
2: 103,097,202 (GRCm39) |
R250L |
probably damaging |
Het |
Eps8l1 |
G |
A |
7: 4,463,915 (GRCm39) |
R13Q |
possibly damaging |
Het |
Frem2 |
A |
C |
3: 53,563,736 (GRCm39) |
V257G |
possibly damaging |
Het |
Gc |
T |
C |
5: 89,587,448 (GRCm39) |
T259A |
probably benign |
Het |
Gm4952 |
A |
T |
19: 12,604,376 (GRCm39) |
N263Y |
probably benign |
Het |
Gpcpd1 |
T |
A |
2: 132,388,794 (GRCm39) |
H326L |
probably damaging |
Het |
Helz |
T |
C |
11: 107,510,994 (GRCm39) |
F617L |
probably damaging |
Het |
Hoxb4 |
T |
C |
11: 96,209,662 (GRCm39) |
Y23H |
probably damaging |
Het |
Hsf4 |
T |
A |
8: 105,999,330 (GRCm39) |
|
probably null |
Het |
Ift56 |
A |
T |
6: 38,368,475 (GRCm39) |
Y174F |
probably damaging |
Het |
Ighv1-81 |
T |
C |
12: 115,883,924 (GRCm39) |
D109G |
probably damaging |
Het |
Irx4 |
T |
C |
13: 73,417,032 (GRCm39) |
V476A |
probably benign |
Het |
Katnb1 |
T |
A |
8: 95,823,922 (GRCm39) |
|
probably null |
Het |
L3mbtl1 |
A |
G |
2: 162,807,692 (GRCm39) |
Y490C |
probably damaging |
Het |
Lemd2 |
A |
G |
17: 27,412,806 (GRCm39) |
|
probably null |
Het |
Lrrc38 |
A |
T |
4: 143,096,438 (GRCm39) |
T250S |
probably damaging |
Het |
Map3k8 |
A |
T |
18: 4,349,215 (GRCm39) |
Y34* |
probably null |
Het |
Mgst1 |
T |
A |
6: 138,130,507 (GRCm39) |
F79I |
probably benign |
Het |
Midn |
T |
C |
10: 79,991,189 (GRCm39) |
S357P |
probably benign |
Het |
Mmp3 |
T |
A |
9: 7,447,640 (GRCm39) |
D208E |
probably benign |
Het |
Mrps26 |
A |
G |
2: 130,406,862 (GRCm39) |
E163G |
probably damaging |
Het |
Mycbpap |
A |
T |
11: 94,393,983 (GRCm39) |
M371K |
probably benign |
Het |
Mynn |
A |
C |
3: 30,661,191 (GRCm39) |
N91T |
probably damaging |
Het |
Nek11 |
A |
G |
9: 105,177,265 (GRCm39) |
L292P |
probably damaging |
Het |
Nid1 |
A |
T |
13: 13,684,596 (GRCm39) |
R1228W |
probably damaging |
Het |
Nphs2 |
T |
C |
1: 156,148,499 (GRCm39) |
Y121H |
probably damaging |
Het |
Or1f19 |
T |
G |
16: 3,410,299 (GRCm39) |
L13R |
probably damaging |
Het |
Or4p7 |
G |
A |
2: 88,222,284 (GRCm39) |
R231H |
probably benign |
Het |
Or5ac22 |
C |
A |
16: 59,135,236 (GRCm39) |
C178F |
probably damaging |
Het |
Or5ap2 |
T |
A |
2: 85,680,237 (GRCm39) |
I147N |
probably benign |
Het |
Or5d38 |
A |
C |
2: 87,954,684 (GRCm39) |
I215S |
probably benign |
Het |
Or7e176 |
T |
C |
9: 20,171,313 (GRCm39) |
I59T |
probably damaging |
Het |
Or9q2 |
T |
C |
19: 13,772,915 (GRCm39) |
H20R |
probably benign |
Het |
P2rx7 |
C |
T |
5: 122,808,542 (GRCm39) |
T308M |
probably damaging |
Het |
Prdx6 |
C |
T |
1: 161,069,263 (GRCm39) |
|
probably benign |
Het |
Rad54b |
T |
A |
4: 11,615,579 (GRCm39) |
D862E |
probably damaging |
Het |
Ripor1 |
A |
G |
8: 106,343,814 (GRCm39) |
Y344C |
probably damaging |
Het |
Rnf112 |
T |
C |
11: 61,344,291 (GRCm39) |
M43V |
probably benign |
Het |
Rp1l1 |
A |
G |
14: 64,269,655 (GRCm39) |
N1747S |
probably benign |
Het |
Rps27 |
A |
G |
3: 90,120,306 (GRCm39) |
V22A |
probably damaging |
Het |
Spaca1 |
A |
G |
4: 34,044,236 (GRCm39) |
V86A |
possibly damaging |
Het |
Spdef |
A |
G |
17: 27,937,136 (GRCm39) |
Y156H |
probably damaging |
Het |
Specc1 |
A |
C |
11: 62,009,784 (GRCm39) |
E433D |
possibly damaging |
Het |
Srpra |
T |
A |
9: 35,126,326 (GRCm39) |
F506L |
probably benign |
Het |
Stxbp5 |
A |
G |
10: 9,636,610 (GRCm39) |
|
probably benign |
Het |
Syne1 |
C |
T |
10: 5,002,777 (GRCm39) |
R8046Q |
probably damaging |
Het |
Tbx5 |
T |
A |
5: 120,021,090 (GRCm39) |
S365R |
probably benign |
Het |
Terb1 |
G |
T |
8: 105,174,580 (GRCm39) |
P698Q |
probably benign |
Het |
Tmbim7 |
T |
A |
5: 3,711,948 (GRCm39) |
Y27* |
probably null |
Het |
Tmem106c |
C |
A |
15: 97,862,909 (GRCm39) |
A60E |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,720,609 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,562,714 (GRCm39) |
I28747V |
possibly damaging |
Het |
Unc13a |
C |
T |
8: 72,083,148 (GRCm39) |
|
probably null |
Het |
Wdr81 |
T |
C |
11: 75,342,750 (GRCm39) |
D839G |
probably benign |
Het |
Wfdc15a |
G |
C |
2: 164,041,725 (GRCm39) |
Q33E |
probably benign |
Het |
Zfp456 |
T |
C |
13: 67,515,065 (GRCm39) |
R214G |
probably benign |
Het |
Zfp457 |
T |
A |
13: 67,442,164 (GRCm39) |
Y137F |
probably damaging |
Het |
|
Other mutations in Arhgef11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00898:Arhgef11
|
APN |
3 |
87,636,810 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00900:Arhgef11
|
APN |
3 |
87,590,867 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01291:Arhgef11
|
APN |
3 |
87,640,481 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01475:Arhgef11
|
APN |
3 |
87,634,433 (GRCm39) |
splice site |
probably benign |
|
IGL01599:Arhgef11
|
APN |
3 |
87,644,353 (GRCm39) |
missense |
probably benign |
|
IGL02251:Arhgef11
|
APN |
3 |
87,590,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02651:Arhgef11
|
APN |
3 |
87,606,171 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02884:Arhgef11
|
APN |
3 |
87,635,313 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02900:Arhgef11
|
APN |
3 |
87,640,467 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03017:Arhgef11
|
APN |
3 |
87,624,367 (GRCm39) |
nonsense |
probably null |
|
ANU05:Arhgef11
|
UTSW |
3 |
87,640,481 (GRCm39) |
missense |
probably benign |
0.00 |
R0049:Arhgef11
|
UTSW |
3 |
87,636,500 (GRCm39) |
splice site |
probably null |
|
R0049:Arhgef11
|
UTSW |
3 |
87,636,500 (GRCm39) |
splice site |
probably null |
|
R0129:Arhgef11
|
UTSW |
3 |
87,635,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R0486:Arhgef11
|
UTSW |
3 |
87,596,159 (GRCm39) |
splice site |
probably null |
|
R0698:Arhgef11
|
UTSW |
3 |
87,640,766 (GRCm39) |
missense |
probably benign |
0.24 |
R0701:Arhgef11
|
UTSW |
3 |
87,640,766 (GRCm39) |
missense |
probably benign |
0.24 |
R0849:Arhgef11
|
UTSW |
3 |
87,643,203 (GRCm39) |
missense |
probably benign |
0.24 |
R1055:Arhgef11
|
UTSW |
3 |
87,624,425 (GRCm39) |
missense |
probably benign |
0.19 |
R1256:Arhgef11
|
UTSW |
3 |
87,634,442 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1401:Arhgef11
|
UTSW |
3 |
87,640,776 (GRCm39) |
nonsense |
probably null |
|
R1543:Arhgef11
|
UTSW |
3 |
87,620,324 (GRCm39) |
missense |
probably benign |
0.10 |
R1547:Arhgef11
|
UTSW |
3 |
87,602,709 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1564:Arhgef11
|
UTSW |
3 |
87,609,817 (GRCm39) |
missense |
probably benign |
|
R1675:Arhgef11
|
UTSW |
3 |
87,638,518 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2082:Arhgef11
|
UTSW |
3 |
87,633,303 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2293:Arhgef11
|
UTSW |
3 |
87,635,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Arhgef11
|
UTSW |
3 |
87,605,306 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5130:Arhgef11
|
UTSW |
3 |
87,633,321 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5151:Arhgef11
|
UTSW |
3 |
87,642,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R5157:Arhgef11
|
UTSW |
3 |
87,635,817 (GRCm39) |
splice site |
probably null |
|
R5203:Arhgef11
|
UTSW |
3 |
87,642,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5329:Arhgef11
|
UTSW |
3 |
87,587,059 (GRCm39) |
intron |
probably benign |
|
R5615:Arhgef11
|
UTSW |
3 |
87,629,792 (GRCm39) |
critical splice donor site |
probably null |
|
R5646:Arhgef11
|
UTSW |
3 |
87,591,793 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6125:Arhgef11
|
UTSW |
3 |
87,636,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Arhgef11
|
UTSW |
3 |
87,635,385 (GRCm39) |
missense |
probably benign |
|
R6543:Arhgef11
|
UTSW |
3 |
87,640,715 (GRCm39) |
missense |
probably benign |
0.09 |
R6801:Arhgef11
|
UTSW |
3 |
87,643,159 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6939:Arhgef11
|
UTSW |
3 |
87,594,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R7008:Arhgef11
|
UTSW |
3 |
87,636,525 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7155:Arhgef11
|
UTSW |
3 |
87,616,879 (GRCm39) |
nonsense |
probably null |
|
R7169:Arhgef11
|
UTSW |
3 |
87,634,755 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7325:Arhgef11
|
UTSW |
3 |
87,620,599 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7392:Arhgef11
|
UTSW |
3 |
87,624,482 (GRCm39) |
critical splice donor site |
probably null |
|
R7683:Arhgef11
|
UTSW |
3 |
87,629,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R7875:Arhgef11
|
UTSW |
3 |
87,591,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R7912:Arhgef11
|
UTSW |
3 |
87,640,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R7980:Arhgef11
|
UTSW |
3 |
87,605,297 (GRCm39) |
missense |
probably benign |
0.01 |
R8028:Arhgef11
|
UTSW |
3 |
87,642,859 (GRCm39) |
missense |
probably benign |
|
R8081:Arhgef11
|
UTSW |
3 |
87,632,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Arhgef11
|
UTSW |
3 |
87,643,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8207:Arhgef11
|
UTSW |
3 |
87,606,082 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8290:Arhgef11
|
UTSW |
3 |
87,633,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R8443:Arhgef11
|
UTSW |
3 |
87,620,406 (GRCm39) |
missense |
probably benign |
0.17 |
R8543:Arhgef11
|
UTSW |
3 |
87,589,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R8808:Arhgef11
|
UTSW |
3 |
87,593,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R8969:Arhgef11
|
UTSW |
3 |
87,632,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Arhgef11
|
UTSW |
3 |
87,635,321 (GRCm39) |
missense |
probably benign |
|
R8983:Arhgef11
|
UTSW |
3 |
87,640,508 (GRCm39) |
missense |
|
|
R8987:Arhgef11
|
UTSW |
3 |
87,637,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R9168:Arhgef11
|
UTSW |
3 |
87,633,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Arhgef11
|
UTSW |
3 |
87,640,484 (GRCm39) |
missense |
probably benign |
|
R9741:Arhgef11
|
UTSW |
3 |
87,595,156 (GRCm39) |
missense |
probably benign |
0.03 |
X0011:Arhgef11
|
UTSW |
3 |
87,629,713 (GRCm39) |
missense |
probably benign |
|
Z1176:Arhgef11
|
UTSW |
3 |
87,642,769 (GRCm39) |
missense |
not run |
|
|