Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
C |
T |
8: 124,688,791 (GRCm39) |
G495D |
probably damaging |
Het |
Acsm2 |
C |
T |
7: 119,172,468 (GRCm39) |
H104Y |
probably benign |
Het |
Adgrb3 |
G |
A |
1: 25,167,909 (GRCm39) |
T1009M |
probably damaging |
Het |
Atm |
A |
T |
9: 53,367,140 (GRCm39) |
D2491E |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,964,077 (GRCm39) |
S1706P |
probably benign |
Het |
Capn13 |
C |
T |
17: 73,674,222 (GRCm39) |
G77D |
possibly damaging |
Het |
Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
Cdhr18 |
T |
C |
14: 13,862,444 (GRCm38) |
D370G |
probably benign |
Het |
Cep135 |
A |
G |
5: 76,741,962 (GRCm39) |
K133E |
possibly damaging |
Het |
Cyp2c67 |
A |
G |
19: 39,614,585 (GRCm39) |
M314T |
possibly damaging |
Het |
Dennd5b |
T |
C |
6: 148,945,985 (GRCm39) |
D542G |
probably damaging |
Het |
Dpys |
A |
T |
15: 39,687,636 (GRCm39) |
N387K |
probably damaging |
Het |
Erc1 |
A |
T |
6: 119,720,353 (GRCm39) |
D749E |
possibly damaging |
Het |
Gucy2e |
A |
T |
11: 69,126,485 (GRCm39) |
F298L |
probably benign |
Het |
Igsf10 |
A |
G |
3: 59,239,269 (GRCm39) |
V304A |
probably benign |
Het |
Kmt2b |
A |
T |
7: 30,279,912 (GRCm39) |
C1363S |
probably damaging |
Het |
Krt87 |
A |
G |
15: 101,385,711 (GRCm39) |
Y295H |
probably damaging |
Het |
Lmo7 |
T |
C |
14: 102,138,019 (GRCm39) |
V396A |
probably damaging |
Het |
Lpl |
A |
G |
8: 69,345,311 (GRCm39) |
D105G |
probably benign |
Het |
Lrrc45 |
C |
A |
11: 120,606,297 (GRCm39) |
T135N |
probably benign |
Het |
Ltn1 |
C |
T |
16: 87,212,918 (GRCm39) |
A548T |
probably benign |
Het |
Nectin2 |
T |
G |
7: 19,451,523 (GRCm39) |
I504L |
probably benign |
Het |
Nmbr |
T |
C |
10: 14,636,187 (GRCm39) |
I52T |
probably benign |
Het |
Nop14 |
A |
T |
5: 34,807,899 (GRCm39) |
N354K |
probably benign |
Het |
Olfm1 |
A |
G |
2: 28,119,447 (GRCm39) |
I361V |
probably benign |
Het |
Or8g18 |
G |
C |
9: 39,149,547 (GRCm39) |
P58A |
probably benign |
Het |
Ovol1 |
T |
C |
19: 5,603,629 (GRCm39) |
T91A |
probably benign |
Het |
Pigz |
T |
A |
16: 31,760,808 (GRCm39) |
V3E |
possibly damaging |
Het |
Pip4k2b |
T |
C |
11: 97,635,420 (GRCm39) |
N4S |
probably benign |
Het |
Slc23a2 |
A |
T |
2: 131,904,117 (GRCm39) |
|
probably null |
Het |
Slc66a2 |
A |
G |
18: 80,334,813 (GRCm39) |
T211A |
possibly damaging |
Het |
Speg |
A |
T |
1: 75,403,739 (GRCm39) |
D2640V |
probably damaging |
Het |
Trip12 |
G |
A |
1: 84,754,071 (GRCm39) |
Q111* |
probably null |
Het |
Trub2 |
A |
G |
2: 29,672,170 (GRCm39) |
F141S |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,693,729 (GRCm39) |
|
probably null |
Het |
Zfp935 |
A |
G |
13: 62,602,355 (GRCm39) |
F282L |
probably damaging |
Het |
Zfp946 |
G |
T |
17: 22,672,560 (GRCm39) |
|
probably null |
Het |
Zkscan4 |
A |
G |
13: 21,668,044 (GRCm39) |
E165G |
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 |
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 |
|
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 |
|