Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr2 |
C |
A |
9: 121,738,040 (GRCm39) |
S138R |
probably damaging |
Het |
Alpk3 |
C |
A |
7: 80,742,501 (GRCm39) |
P773T |
probably benign |
Het |
Aspscr1 |
T |
C |
11: 120,580,048 (GRCm39) |
S196P |
probably benign |
Het |
AU040320 |
A |
T |
4: 126,762,484 (GRCm39) |
|
probably null |
Het |
BC002059 |
T |
C |
17: 17,193,932 (GRCm39) |
|
noncoding transcript |
Het |
Cep112 |
A |
G |
11: 108,643,408 (GRCm39) |
N799S |
possibly damaging |
Het |
Cilp |
A |
G |
9: 65,181,927 (GRCm39) |
|
probably benign |
Het |
Cpn2 |
T |
C |
16: 30,079,392 (GRCm39) |
E103G |
probably benign |
Het |
Cpt1b |
G |
A |
15: 89,304,283 (GRCm39) |
|
probably benign |
Het |
Epor |
T |
A |
9: 21,870,785 (GRCm39) |
D365V |
probably damaging |
Het |
H2bc21 |
T |
A |
3: 96,128,750 (GRCm39) |
I90N |
possibly damaging |
Het |
Hip1r |
T |
C |
5: 124,139,306 (GRCm39) |
Y900H |
probably damaging |
Het |
Hoxc9 |
A |
T |
15: 102,892,540 (GRCm39) |
N251I |
probably damaging |
Het |
Hpd |
C |
T |
5: 123,315,587 (GRCm39) |
|
probably null |
Het |
Lrrc34 |
T |
A |
3: 30,688,711 (GRCm39) |
I197L |
probably benign |
Het |
Msi2 |
A |
G |
11: 88,607,373 (GRCm39) |
V78A |
probably damaging |
Het |
Myh4 |
A |
G |
11: 67,141,594 (GRCm39) |
I818V |
probably benign |
Het |
Nol4 |
T |
C |
18: 22,956,629 (GRCm39) |
|
probably null |
Het |
Plekha5 |
A |
G |
6: 140,496,582 (GRCm39) |
N362S |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,945,054 (GRCm39) |
|
probably benign |
Het |
Rc3h2 |
A |
T |
2: 37,289,831 (GRCm39) |
|
probably null |
Het |
Sgsm3 |
A |
G |
15: 80,890,946 (GRCm39) |
N136D |
probably benign |
Het |
Slco1a5 |
A |
G |
6: 142,181,976 (GRCm39) |
C583R |
probably damaging |
Het |
Surf1 |
A |
G |
2: 26,806,295 (GRCm39) |
W13R |
probably damaging |
Het |
Tesk2 |
T |
C |
4: 116,658,954 (GRCm39) |
W276R |
possibly damaging |
Het |
Tmem8b |
A |
G |
4: 43,673,892 (GRCm39) |
|
probably benign |
Het |
Togaram2 |
T |
G |
17: 72,023,304 (GRCm39) |
|
probably benign |
Het |
Ttll11 |
A |
G |
2: 35,869,546 (GRCm39) |
S31P |
unknown |
Het |
Ttll8 |
A |
G |
15: 88,820,336 (GRCm39) |
|
probably benign |
Het |
Tub |
A |
G |
7: 108,626,240 (GRCm39) |
K259E |
probably damaging |
Het |
Ube2o |
T |
C |
11: 116,439,683 (GRCm39) |
I162M |
probably benign |
Het |
Vamp8 |
C |
T |
6: 72,365,326 (GRCm39) |
M1I |
probably null |
Het |
Zfp503 |
C |
A |
14: 22,036,032 (GRCm39) |
G295* |
probably null |
Het |
|
Other mutations in Arfgef2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00942:Arfgef2
|
APN |
2 |
166,727,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01323:Arfgef2
|
APN |
2 |
166,713,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01415:Arfgef2
|
APN |
2 |
166,709,275 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01638:Arfgef2
|
APN |
2 |
166,715,865 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02618:Arfgef2
|
APN |
2 |
166,695,233 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02899:Arfgef2
|
APN |
2 |
166,710,971 (GRCm39) |
splice site |
probably benign |
|
IGL03012:Arfgef2
|
APN |
2 |
166,710,808 (GRCm39) |
splice site |
probably benign |
|
IGL03063:Arfgef2
|
APN |
2 |
166,701,702 (GRCm39) |
splice site |
probably benign |
|
migrainous
|
UTSW |
2 |
166,676,383 (GRCm39) |
frame shift |
probably null |
|
Scotomata
|
UTSW |
2 |
166,693,199 (GRCm39) |
critical splice donor site |
probably null |
|
shimmering
|
UTSW |
2 |
166,668,848 (GRCm39) |
missense |
probably benign |
|
R0102:Arfgef2
|
UTSW |
2 |
166,687,385 (GRCm39) |
missense |
probably benign |
0.00 |
R0102:Arfgef2
|
UTSW |
2 |
166,687,385 (GRCm39) |
missense |
probably benign |
0.00 |
R0116:Arfgef2
|
UTSW |
2 |
166,715,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:Arfgef2
|
UTSW |
2 |
166,677,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0130:Arfgef2
|
UTSW |
2 |
166,677,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Arfgef2
|
UTSW |
2 |
166,709,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Arfgef2
|
UTSW |
2 |
166,702,320 (GRCm39) |
critical splice donor site |
probably null |
|
R0945:Arfgef2
|
UTSW |
2 |
166,668,889 (GRCm39) |
unclassified |
probably benign |
|
R1226:Arfgef2
|
UTSW |
2 |
166,669,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Arfgef2
|
UTSW |
2 |
166,701,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Arfgef2
|
UTSW |
2 |
166,706,632 (GRCm39) |
missense |
probably damaging |
0.98 |
R1696:Arfgef2
|
UTSW |
2 |
166,703,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Arfgef2
|
UTSW |
2 |
166,708,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Arfgef2
|
UTSW |
2 |
166,705,523 (GRCm39) |
missense |
probably benign |
0.28 |
R1936:Arfgef2
|
UTSW |
2 |
166,705,523 (GRCm39) |
missense |
probably benign |
0.28 |
R1939:Arfgef2
|
UTSW |
2 |
166,715,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Arfgef2
|
UTSW |
2 |
166,707,679 (GRCm39) |
missense |
probably benign |
0.00 |
R2279:Arfgef2
|
UTSW |
2 |
166,707,679 (GRCm39) |
missense |
probably benign |
0.00 |
R2349:Arfgef2
|
UTSW |
2 |
166,693,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2359:Arfgef2
|
UTSW |
2 |
166,702,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R2519:Arfgef2
|
UTSW |
2 |
166,723,164 (GRCm39) |
missense |
probably benign |
0.03 |
R2938:Arfgef2
|
UTSW |
2 |
166,736,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3696:Arfgef2
|
UTSW |
2 |
166,695,220 (GRCm39) |
nonsense |
probably null |
|
R4022:Arfgef2
|
UTSW |
2 |
166,715,865 (GRCm39) |
missense |
probably benign |
0.01 |
R4227:Arfgef2
|
UTSW |
2 |
166,709,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4293:Arfgef2
|
UTSW |
2 |
166,732,211 (GRCm39) |
missense |
probably benign |
|
R4455:Arfgef2
|
UTSW |
2 |
166,736,635 (GRCm39) |
missense |
probably benign |
0.43 |
R4499:Arfgef2
|
UTSW |
2 |
166,727,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R4570:Arfgef2
|
UTSW |
2 |
166,698,458 (GRCm39) |
missense |
probably damaging |
0.99 |
R4888:Arfgef2
|
UTSW |
2 |
166,677,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Arfgef2
|
UTSW |
2 |
166,708,876 (GRCm39) |
missense |
probably benign |
|
R5032:Arfgef2
|
UTSW |
2 |
166,720,464 (GRCm39) |
missense |
probably benign |
|
R5191:Arfgef2
|
UTSW |
2 |
166,718,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R5200:Arfgef2
|
UTSW |
2 |
166,702,604 (GRCm39) |
missense |
probably benign |
0.00 |
R5318:Arfgef2
|
UTSW |
2 |
166,715,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R5378:Arfgef2
|
UTSW |
2 |
166,715,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5537:Arfgef2
|
UTSW |
2 |
166,698,513 (GRCm39) |
splice site |
probably null |
|
R5866:Arfgef2
|
UTSW |
2 |
166,678,177 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5878:Arfgef2
|
UTSW |
2 |
166,712,137 (GRCm39) |
missense |
probably benign |
0.41 |
R5972:Arfgef2
|
UTSW |
2 |
166,733,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6147:Arfgef2
|
UTSW |
2 |
166,713,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Arfgef2
|
UTSW |
2 |
166,715,508 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6323:Arfgef2
|
UTSW |
2 |
166,676,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R6338:Arfgef2
|
UTSW |
2 |
166,687,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R6538:Arfgef2
|
UTSW |
2 |
166,735,541 (GRCm39) |
splice site |
probably null |
|
R6726:Arfgef2
|
UTSW |
2 |
166,735,540 (GRCm39) |
critical splice donor site |
probably null |
|
R7047:Arfgef2
|
UTSW |
2 |
166,693,865 (GRCm39) |
splice site |
probably null |
|
R7086:Arfgef2
|
UTSW |
2 |
166,718,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R7108:Arfgef2
|
UTSW |
2 |
166,715,528 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7155:Arfgef2
|
UTSW |
2 |
166,707,733 (GRCm39) |
missense |
probably benign |
0.19 |
R7159:Arfgef2
|
UTSW |
2 |
166,668,848 (GRCm39) |
missense |
probably benign |
|
R7482:Arfgef2
|
UTSW |
2 |
166,693,199 (GRCm39) |
critical splice donor site |
probably null |
|
R7598:Arfgef2
|
UTSW |
2 |
166,698,444 (GRCm39) |
missense |
probably benign |
|
R7869:Arfgef2
|
UTSW |
2 |
166,715,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R8003:Arfgef2
|
UTSW |
2 |
166,695,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R8092:Arfgef2
|
UTSW |
2 |
166,701,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8093:Arfgef2
|
UTSW |
2 |
166,736,577 (GRCm39) |
missense |
probably benign |
0.02 |
R8110:Arfgef2
|
UTSW |
2 |
166,720,464 (GRCm39) |
missense |
probably benign |
0.01 |
R8130:Arfgef2
|
UTSW |
2 |
166,678,170 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8153:Arfgef2
|
UTSW |
2 |
166,676,383 (GRCm39) |
frame shift |
probably null |
|
R8156:Arfgef2
|
UTSW |
2 |
166,676,383 (GRCm39) |
frame shift |
probably null |
|
R8411:Arfgef2
|
UTSW |
2 |
166,715,903 (GRCm39) |
missense |
probably benign |
0.15 |
R8418:Arfgef2
|
UTSW |
2 |
166,698,468 (GRCm39) |
missense |
probably benign |
0.19 |
R8738:Arfgef2
|
UTSW |
2 |
166,708,867 (GRCm39) |
missense |
probably benign |
0.00 |
R8826:Arfgef2
|
UTSW |
2 |
166,677,386 (GRCm39) |
intron |
probably benign |
|
R8967:Arfgef2
|
UTSW |
2 |
166,677,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R8971:Arfgef2
|
UTSW |
2 |
166,701,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8972:Arfgef2
|
UTSW |
2 |
166,709,253 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9010:Arfgef2
|
UTSW |
2 |
166,701,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R9077:Arfgef2
|
UTSW |
2 |
166,706,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R9249:Arfgef2
|
UTSW |
2 |
166,733,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R9306:Arfgef2
|
UTSW |
2 |
166,723,188 (GRCm39) |
missense |
probably benign |
0.02 |
R9394:Arfgef2
|
UTSW |
2 |
166,676,469 (GRCm39) |
missense |
probably benign |
0.13 |
R9776:Arfgef2
|
UTSW |
2 |
166,713,447 (GRCm39) |
missense |
probably damaging |
1.00 |
X0040:Arfgef2
|
UTSW |
2 |
166,701,803 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Arfgef2
|
UTSW |
2 |
166,733,761 (GRCm39) |
missense |
probably benign |
0.32 |
Z1088:Arfgef2
|
UTSW |
2 |
166,735,515 (GRCm39) |
missense |
possibly damaging |
0.78 |
Z1176:Arfgef2
|
UTSW |
2 |
166,736,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|