Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
T |
14: 32,382,131 (GRCm39) |
I1278N |
possibly damaging |
Het |
Adcy5 |
T |
A |
16: 35,087,585 (GRCm39) |
L482Q |
probably damaging |
Het |
Adora2a |
A |
G |
10: 75,162,145 (GRCm39) |
I95V |
probably damaging |
Het |
Anapc1 |
A |
C |
2: 128,457,350 (GRCm39) |
C1887G |
probably damaging |
Het |
Capn11 |
G |
T |
17: 45,949,622 (GRCm39) |
S448* |
probably null |
Het |
Capn7 |
C |
T |
14: 31,058,642 (GRCm39) |
|
probably benign |
Het |
Cep55 |
T |
A |
19: 38,048,539 (GRCm39) |
V65D |
possibly damaging |
Het |
Col5a1 |
A |
G |
2: 27,818,096 (GRCm39) |
K107R |
unknown |
Het |
Dbh |
T |
A |
2: 27,055,622 (GRCm39) |
I32N |
possibly damaging |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Dzip3 |
A |
T |
16: 48,802,489 (GRCm39) |
N13K |
probably benign |
Het |
Emilin1 |
A |
G |
5: 31,074,422 (GRCm39) |
N221S |
probably benign |
Het |
Ext2 |
A |
G |
2: 93,570,002 (GRCm39) |
F470L |
probably damaging |
Het |
Filip1 |
T |
A |
9: 79,760,916 (GRCm39) |
Q206L |
probably damaging |
Het |
Garin1b |
T |
A |
6: 29,323,809 (GRCm39) |
L178H |
probably damaging |
Het |
Gpr63 |
G |
T |
4: 25,007,320 (GRCm39) |
A15S |
probably benign |
Het |
Grhl3 |
T |
C |
4: 135,276,551 (GRCm39) |
|
probably null |
Het |
Hspa5 |
C |
T |
2: 34,663,204 (GRCm39) |
P127L |
probably damaging |
Het |
Ift172 |
G |
T |
5: 31,433,238 (GRCm39) |
Y193* |
probably null |
Het |
Ints1 |
A |
C |
5: 139,744,226 (GRCm39) |
L1512* |
probably null |
Het |
Kat2b |
A |
G |
17: 53,970,597 (GRCm39) |
Q661R |
probably benign |
Het |
Kat6a |
A |
G |
8: 23,428,554 (GRCm39) |
N1303S |
possibly damaging |
Het |
L3mbtl4 |
G |
T |
17: 68,768,561 (GRCm39) |
R223L |
probably benign |
Het |
Maml2 |
T |
C |
9: 13,532,177 (GRCm39) |
|
probably benign |
Het |
Mixl1 |
A |
G |
1: 180,524,183 (GRCm39) |
|
probably null |
Het |
Mocs1 |
T |
C |
17: 49,759,887 (GRCm39) |
|
probably null |
Het |
Ms4a15 |
T |
G |
19: 10,962,236 (GRCm39) |
N36T |
probably damaging |
Het |
Msr1 |
G |
A |
8: 40,095,657 (GRCm39) |
T2I |
possibly damaging |
Het |
Nlgn1 |
A |
C |
3: 25,490,199 (GRCm39) |
Y509* |
probably null |
Het |
Nsmce1 |
C |
A |
7: 125,090,606 (GRCm39) |
G4C |
probably benign |
Het |
Or4c113 |
A |
T |
2: 88,885,490 (GRCm39) |
F93L |
probably damaging |
Het |
Or51v15-ps1 |
A |
G |
7: 103,278,918 (GRCm39) |
V83A |
probably damaging |
Het |
Pan3 |
G |
A |
5: 147,483,175 (GRCm39) |
G452D |
probably damaging |
Het |
Pcyox1 |
G |
T |
6: 86,365,891 (GRCm39) |
P441H |
probably damaging |
Het |
Phf12 |
T |
C |
11: 77,904,099 (GRCm39) |
V273A |
probably damaging |
Het |
Plcd4 |
A |
G |
1: 74,591,148 (GRCm39) |
E181G |
possibly damaging |
Het |
Ptgfr |
A |
T |
3: 151,541,178 (GRCm39) |
I110N |
possibly damaging |
Het |
Rab40c |
A |
C |
17: 26,138,458 (GRCm39) |
V8G |
probably damaging |
Het |
Rasal3 |
T |
A |
17: 32,615,458 (GRCm39) |
Y460F |
probably damaging |
Het |
Rhbdf2 |
A |
G |
11: 116,494,477 (GRCm39) |
|
probably null |
Het |
Ryr2 |
T |
A |
13: 11,839,286 (GRCm39) |
N496Y |
possibly damaging |
Het |
Sacs |
A |
T |
14: 61,450,451 (GRCm39) |
I4166F |
probably damaging |
Het |
Sh2d3c |
T |
C |
2: 32,611,172 (GRCm39) |
M1T |
probably null |
Het |
Smarca2 |
C |
T |
19: 26,646,555 (GRCm39) |
S651L |
possibly damaging |
Het |
Sned1 |
A |
T |
1: 93,213,540 (GRCm39) |
R1204S |
possibly damaging |
Het |
Spata31d1b |
T |
C |
13: 59,860,249 (GRCm39) |
Y41H |
probably damaging |
Het |
Stab2 |
C |
T |
10: 86,694,016 (GRCm39) |
C2075Y |
probably damaging |
Het |
Tcte1 |
A |
T |
17: 45,844,294 (GRCm39) |
Q90L |
possibly damaging |
Het |
Tll2 |
C |
T |
19: 41,074,679 (GRCm39) |
G945S |
probably damaging |
Het |
Tmbim7 |
A |
T |
5: 3,720,112 (GRCm39) |
T116S |
probably benign |
Het |
Tnfrsf19 |
A |
T |
14: 61,242,667 (GRCm39) |
C72* |
probably null |
Het |
Usp17le |
T |
A |
7: 104,417,640 (GRCm39) |
T501S |
probably benign |
Het |
Wnt5b |
T |
A |
6: 119,425,217 (GRCm39) |
|
probably benign |
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 |
R2414:Arfgef2
|
UTSW |
2 |
166,687,424 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|
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 |
|