Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921536K21Rik |
T |
A |
11: 3,839,784 (GRCm39) |
|
probably null |
Het |
Adora3 |
T |
C |
3: 105,815,039 (GRCm39) |
V263A |
probably benign |
Het |
Adprhl1 |
C |
T |
8: 13,298,682 (GRCm39) |
V83I |
probably damaging |
Het |
Arid4a |
A |
T |
12: 71,108,363 (GRCm39) |
N56I |
possibly damaging |
Het |
Art3 |
A |
T |
5: 92,551,472 (GRCm39) |
Y277F |
probably damaging |
Het |
Atp2a1 |
A |
T |
7: 126,047,707 (GRCm39) |
|
probably null |
Het |
Banf1 |
T |
C |
19: 5,415,150 (GRCm39) |
K54E |
possibly damaging |
Het |
Bckdk |
A |
G |
7: 127,505,073 (GRCm39) |
Y151C |
probably damaging |
Het |
C1qtnf3 |
C |
A |
15: 10,958,130 (GRCm39) |
P58T |
possibly damaging |
Het |
Cadps2 |
T |
C |
6: 23,390,445 (GRCm39) |
R744G |
probably benign |
Het |
Cdc25b |
A |
G |
2: 131,031,029 (GRCm39) |
D118G |
probably damaging |
Het |
Cnot9 |
G |
A |
1: 74,566,151 (GRCm39) |
V181I |
probably damaging |
Het |
Cobl |
C |
T |
11: 12,204,488 (GRCm39) |
G738D |
probably benign |
Het |
Col18a1 |
T |
A |
10: 76,904,220 (GRCm39) |
|
probably null |
Het |
Crnkl1 |
A |
G |
2: 145,772,564 (GRCm39) |
V171A |
probably benign |
Het |
Dhx57 |
C |
T |
17: 80,580,507 (GRCm39) |
D482N |
possibly damaging |
Het |
Dpysl2 |
A |
T |
14: 67,066,425 (GRCm39) |
|
probably null |
Het |
Drd3 |
G |
T |
16: 43,582,758 (GRCm39) |
A52S |
probably benign |
Het |
Dst |
T |
C |
1: 34,220,469 (GRCm39) |
V2091A |
possibly damaging |
Het |
Evpl |
T |
C |
11: 116,112,261 (GRCm39) |
T1810A |
probably benign |
Het |
Fbxo2 |
T |
A |
4: 148,248,783 (GRCm39) |
W92R |
probably damaging |
Het |
Gas2l2 |
T |
A |
11: 83,320,103 (GRCm39) |
D51V |
possibly damaging |
Het |
Gm11232 |
A |
T |
4: 71,674,818 (GRCm39) |
V228E |
possibly damaging |
Het |
Gm14305 |
C |
T |
2: 176,412,764 (GRCm39) |
Q219* |
probably null |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Gpr39 |
G |
T |
1: 125,605,334 (GRCm39) |
M87I |
possibly damaging |
Het |
Heatr1 |
T |
C |
13: 12,432,522 (GRCm39) |
M1089T |
probably benign |
Het |
Ifi206 |
A |
T |
1: 173,308,640 (GRCm39) |
M452K |
|
Het |
Ints8 |
A |
T |
4: 11,227,190 (GRCm39) |
I561N |
probably damaging |
Het |
Itgb2 |
A |
T |
10: 77,396,946 (GRCm39) |
K660N |
probably benign |
Het |
Jun |
A |
C |
4: 94,939,081 (GRCm39) |
V143G |
probably benign |
Het |
Kalrn |
A |
G |
16: 33,851,952 (GRCm39) |
M2076T |
probably benign |
Het |
Krt10 |
G |
T |
11: 99,279,913 (GRCm39) |
S82R |
unknown |
Het |
Lipm |
T |
A |
19: 34,095,291 (GRCm39) |
H295Q |
probably damaging |
Het |
Mybpc2 |
A |
C |
7: 44,165,348 (GRCm39) |
|
probably null |
Het |
Nedd4 |
T |
C |
9: 72,584,608 (GRCm39) |
V103A |
possibly damaging |
Het |
Nol10 |
T |
C |
12: 17,398,586 (GRCm39) |
I11T |
probably damaging |
Het |
Nup210l |
A |
G |
3: 90,067,233 (GRCm39) |
S758G |
probably damaging |
Het |
Or13d1 |
T |
A |
4: 52,970,713 (GRCm39) |
C31S |
probably damaging |
Het |
Or52r1c |
T |
G |
7: 102,735,388 (GRCm39) |
I216S |
probably benign |
Het |
Or8d4 |
T |
C |
9: 40,038,661 (GRCm39) |
I199V |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 108,923,384 (GRCm39) |
H425R |
probably damaging |
Het |
Parp1 |
G |
T |
1: 180,416,963 (GRCm39) |
R582S |
possibly damaging |
Het |
Piwil1 |
A |
T |
5: 128,816,527 (GRCm39) |
R36S |
probably benign |
Het |
Pjvk |
T |
C |
2: 76,487,877 (GRCm39) |
|
probably null |
Het |
Plekha6 |
G |
T |
1: 133,097,760 (GRCm39) |
E31D |
possibly damaging |
Het |
Polr1b |
C |
A |
2: 128,967,464 (GRCm39) |
F952L |
probably damaging |
Het |
Prm3 |
CTCTTCTTCTTCTTC |
CTCTTCTTCTTC |
16: 10,608,565 (GRCm39) |
|
probably benign |
Het |
Psmc6 |
T |
A |
14: 45,581,107 (GRCm39) |
I301N |
probably damaging |
Het |
Rfpl4 |
C |
A |
7: 5,118,543 (GRCm39) |
S9I |
probably benign |
Het |
Rnf14 |
G |
T |
18: 38,442,629 (GRCm39) |
C310F |
probably damaging |
Het |
Rnf17 |
T |
A |
14: 56,715,144 (GRCm39) |
F845L |
probably benign |
Het |
Robo2 |
T |
C |
16: 73,758,777 (GRCm39) |
I665V |
probably benign |
Het |
Rtl1 |
T |
A |
12: 109,559,619 (GRCm39) |
H740L |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,765,897 (GRCm39) |
S1280P |
probably benign |
Het |
Slc12a8 |
G |
A |
16: 33,371,335 (GRCm39) |
R126H |
probably damaging |
Het |
Slc9a1 |
T |
C |
4: 133,139,276 (GRCm39) |
F165L |
probably damaging |
Het |
Snx19 |
T |
C |
9: 30,340,221 (GRCm39) |
I453T |
probably damaging |
Het |
Spag17 |
T |
C |
3: 99,987,434 (GRCm39) |
Y1575H |
probably damaging |
Het |
Spef2 |
T |
C |
15: 9,704,567 (GRCm39) |
I415M |
probably damaging |
Het |
Ssx2ip |
T |
G |
3: 146,138,885 (GRCm39) |
I459S |
probably damaging |
Het |
Stfa1 |
A |
G |
16: 36,097,363 (GRCm39) |
|
probably null |
Het |
Tmem156 |
A |
T |
5: 65,237,517 (GRCm39) |
S48T |
probably damaging |
Het |
Tmx3 |
T |
A |
18: 90,545,918 (GRCm39) |
|
probably null |
Het |
Unc93a |
A |
T |
17: 13,328,639 (GRCm39) |
F405I |
possibly damaging |
Het |
Vmn1r209 |
T |
A |
13: 22,990,664 (GRCm39) |
I9F |
possibly damaging |
Het |
Vmn2r93 |
A |
G |
17: 18,533,482 (GRCm39) |
D462G |
probably damaging |
Het |
Wdr90 |
T |
A |
17: 26,080,465 (GRCm39) |
|
probably benign |
Het |
Zfp551 |
T |
C |
7: 12,152,535 (GRCm39) |
D66G |
probably damaging |
Het |
Znrf4 |
A |
C |
17: 56,819,247 (GRCm39) |
V20G |
possibly damaging |
Het |
Zscan4d |
T |
C |
7: 10,896,770 (GRCm39) |
E200G |
probably benign |
Het |
Zup1 |
A |
T |
10: 33,797,698 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Arfgef1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00766:Arfgef1
|
APN |
1 |
10,270,012 (GRCm39) |
missense |
probably benign |
|
IGL00919:Arfgef1
|
APN |
1 |
10,243,462 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01022:Arfgef1
|
APN |
1 |
10,244,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01155:Arfgef1
|
APN |
1 |
10,269,207 (GRCm39) |
splice site |
probably benign |
|
IGL01288:Arfgef1
|
APN |
1 |
10,283,436 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01397:Arfgef1
|
APN |
1 |
10,229,796 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01433:Arfgef1
|
APN |
1 |
10,223,657 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01653:Arfgef1
|
APN |
1 |
10,230,133 (GRCm39) |
nonsense |
probably null |
|
IGL01669:Arfgef1
|
APN |
1 |
10,229,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01795:Arfgef1
|
APN |
1 |
10,217,753 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01860:Arfgef1
|
APN |
1 |
10,224,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02137:Arfgef1
|
APN |
1 |
10,283,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02365:Arfgef1
|
APN |
1 |
10,270,108 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02519:Arfgef1
|
APN |
1 |
10,279,893 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02542:Arfgef1
|
APN |
1 |
10,243,067 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02604:Arfgef1
|
APN |
1 |
10,251,275 (GRCm39) |
splice site |
probably benign |
|
IGL02743:Arfgef1
|
APN |
1 |
10,270,054 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03225:Arfgef1
|
APN |
1 |
10,224,543 (GRCm39) |
missense |
probably damaging |
1.00 |
Collected
|
UTSW |
1 |
10,251,163 (GRCm39) |
missense |
probably damaging |
1.00 |
uncle_joe
|
UTSW |
1 |
10,231,060 (GRCm39) |
missense |
probably damaging |
1.00 |
G1Funyon:Arfgef1
|
UTSW |
1 |
10,250,058 (GRCm39) |
missense |
probably damaging |
1.00 |
I2288:Arfgef1
|
UTSW |
1 |
10,243,478 (GRCm39) |
missense |
probably damaging |
1.00 |
I2289:Arfgef1
|
UTSW |
1 |
10,243,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Arfgef1
|
UTSW |
1 |
10,269,067 (GRCm39) |
critical splice donor site |
probably null |
|
R0491:Arfgef1
|
UTSW |
1 |
10,250,212 (GRCm39) |
splice site |
probably benign |
|
R0636:Arfgef1
|
UTSW |
1 |
10,270,076 (GRCm39) |
missense |
probably benign |
|
R1006:Arfgef1
|
UTSW |
1 |
10,210,706 (GRCm39) |
missense |
probably benign |
0.00 |
R1212:Arfgef1
|
UTSW |
1 |
10,286,784 (GRCm39) |
missense |
probably benign |
0.05 |
R1233:Arfgef1
|
UTSW |
1 |
10,254,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R1346:Arfgef1
|
UTSW |
1 |
10,229,958 (GRCm39) |
missense |
probably benign |
0.41 |
R1416:Arfgef1
|
UTSW |
1 |
10,243,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R1477:Arfgef1
|
UTSW |
1 |
10,259,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R1581:Arfgef1
|
UTSW |
1 |
10,270,103 (GRCm39) |
missense |
probably benign |
0.02 |
R1587:Arfgef1
|
UTSW |
1 |
10,230,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R1602:Arfgef1
|
UTSW |
1 |
10,275,115 (GRCm39) |
missense |
probably benign |
0.01 |
R1745:Arfgef1
|
UTSW |
1 |
10,243,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R1831:Arfgef1
|
UTSW |
1 |
10,275,115 (GRCm39) |
missense |
probably benign |
0.01 |
R1832:Arfgef1
|
UTSW |
1 |
10,275,115 (GRCm39) |
missense |
probably benign |
0.01 |
R1833:Arfgef1
|
UTSW |
1 |
10,275,115 (GRCm39) |
missense |
probably benign |
0.01 |
R1918:Arfgef1
|
UTSW |
1 |
10,270,103 (GRCm39) |
missense |
probably benign |
0.02 |
R1919:Arfgef1
|
UTSW |
1 |
10,270,103 (GRCm39) |
missense |
probably benign |
0.02 |
R2059:Arfgef1
|
UTSW |
1 |
10,258,977 (GRCm39) |
splice site |
probably null |
|
R2146:Arfgef1
|
UTSW |
1 |
10,270,103 (GRCm39) |
missense |
probably benign |
0.02 |
R2148:Arfgef1
|
UTSW |
1 |
10,270,103 (GRCm39) |
missense |
probably benign |
0.02 |
R2149:Arfgef1
|
UTSW |
1 |
10,270,103 (GRCm39) |
missense |
probably benign |
0.02 |
R2150:Arfgef1
|
UTSW |
1 |
10,270,103 (GRCm39) |
missense |
probably benign |
0.02 |
R2373:Arfgef1
|
UTSW |
1 |
10,244,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Arfgef1
|
UTSW |
1 |
10,223,879 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3863:Arfgef1
|
UTSW |
1 |
10,212,811 (GRCm39) |
frame shift |
probably null |
|
R3916:Arfgef1
|
UTSW |
1 |
10,259,668 (GRCm39) |
missense |
probably benign |
0.01 |
R3948:Arfgef1
|
UTSW |
1 |
10,212,811 (GRCm39) |
frame shift |
probably null |
|
R3949:Arfgef1
|
UTSW |
1 |
10,212,811 (GRCm39) |
frame shift |
probably null |
|
R3977:Arfgef1
|
UTSW |
1 |
10,279,859 (GRCm39) |
missense |
probably benign |
0.01 |
R3978:Arfgef1
|
UTSW |
1 |
10,279,859 (GRCm39) |
missense |
probably benign |
0.01 |
R3979:Arfgef1
|
UTSW |
1 |
10,279,859 (GRCm39) |
missense |
probably benign |
0.01 |
R4086:Arfgef1
|
UTSW |
1 |
10,233,984 (GRCm39) |
missense |
probably benign |
0.06 |
R4175:Arfgef1
|
UTSW |
1 |
10,229,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R4257:Arfgef1
|
UTSW |
1 |
10,229,771 (GRCm39) |
intron |
probably benign |
|
R4572:Arfgef1
|
UTSW |
1 |
10,283,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Arfgef1
|
UTSW |
1 |
10,243,487 (GRCm39) |
missense |
probably damaging |
0.98 |
R4678:Arfgef1
|
UTSW |
1 |
10,212,891 (GRCm39) |
missense |
probably benign |
0.03 |
R4737:Arfgef1
|
UTSW |
1 |
10,259,836 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4779:Arfgef1
|
UTSW |
1 |
10,223,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4818:Arfgef1
|
UTSW |
1 |
10,286,772 (GRCm39) |
missense |
probably benign |
|
R4898:Arfgef1
|
UTSW |
1 |
10,229,798 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4979:Arfgef1
|
UTSW |
1 |
10,283,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R5039:Arfgef1
|
UTSW |
1 |
10,269,961 (GRCm39) |
missense |
probably benign |
0.37 |
R5194:Arfgef1
|
UTSW |
1 |
10,275,132 (GRCm39) |
missense |
probably benign |
0.09 |
R5428:Arfgef1
|
UTSW |
1 |
10,231,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R5533:Arfgef1
|
UTSW |
1 |
10,269,952 (GRCm39) |
critical splice donor site |
probably null |
|
R5547:Arfgef1
|
UTSW |
1 |
10,231,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R5562:Arfgef1
|
UTSW |
1 |
10,214,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Arfgef1
|
UTSW |
1 |
10,259,085 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5697:Arfgef1
|
UTSW |
1 |
10,231,063 (GRCm39) |
missense |
probably benign |
0.03 |
R5704:Arfgef1
|
UTSW |
1 |
10,229,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R5722:Arfgef1
|
UTSW |
1 |
10,209,109 (GRCm39) |
missense |
probably benign |
0.04 |
R5793:Arfgef1
|
UTSW |
1 |
10,279,753 (GRCm39) |
missense |
probably benign |
0.01 |
R5835:Arfgef1
|
UTSW |
1 |
10,230,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R5870:Arfgef1
|
UTSW |
1 |
10,251,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R5990:Arfgef1
|
UTSW |
1 |
10,243,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R6290:Arfgef1
|
UTSW |
1 |
10,259,036 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6460:Arfgef1
|
UTSW |
1 |
10,283,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R6613:Arfgef1
|
UTSW |
1 |
10,264,621 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6802:Arfgef1
|
UTSW |
1 |
10,259,677 (GRCm39) |
missense |
probably benign |
0.35 |
R6967:Arfgef1
|
UTSW |
1 |
10,223,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R6967:Arfgef1
|
UTSW |
1 |
10,223,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Arfgef1
|
UTSW |
1 |
10,223,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R6968:Arfgef1
|
UTSW |
1 |
10,223,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R6969:Arfgef1
|
UTSW |
1 |
10,223,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R6969:Arfgef1
|
UTSW |
1 |
10,223,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Arfgef1
|
UTSW |
1 |
10,223,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R6970:Arfgef1
|
UTSW |
1 |
10,223,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R7092:Arfgef1
|
UTSW |
1 |
10,223,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R7251:Arfgef1
|
UTSW |
1 |
10,269,200 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7334:Arfgef1
|
UTSW |
1 |
10,254,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Arfgef1
|
UTSW |
1 |
10,251,122 (GRCm39) |
missense |
probably benign |
0.00 |
R7631:Arfgef1
|
UTSW |
1 |
10,302,694 (GRCm39) |
missense |
probably benign |
0.00 |
R7699:Arfgef1
|
UTSW |
1 |
10,264,636 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7700:Arfgef1
|
UTSW |
1 |
10,264,636 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7968:Arfgef1
|
UTSW |
1 |
10,243,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R8195:Arfgef1
|
UTSW |
1 |
10,243,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R8292:Arfgef1
|
UTSW |
1 |
10,227,194 (GRCm39) |
missense |
probably benign |
0.06 |
R8301:Arfgef1
|
UTSW |
1 |
10,250,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8341:Arfgef1
|
UTSW |
1 |
10,224,553 (GRCm39) |
missense |
probably benign |
0.37 |
R8410:Arfgef1
|
UTSW |
1 |
10,229,867 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8411:Arfgef1
|
UTSW |
1 |
10,286,759 (GRCm39) |
missense |
probably benign |
0.01 |
R8793:Arfgef1
|
UTSW |
1 |
10,212,832 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8903:Arfgef1
|
UTSW |
1 |
10,211,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Arfgef1
|
UTSW |
1 |
10,270,062 (GRCm39) |
missense |
probably benign |
0.25 |
R9036:Arfgef1
|
UTSW |
1 |
10,259,055 (GRCm39) |
missense |
probably benign |
0.01 |
R9185:Arfgef1
|
UTSW |
1 |
10,215,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R9252:Arfgef1
|
UTSW |
1 |
10,243,122 (GRCm39) |
nonsense |
probably null |
|
R9333:Arfgef1
|
UTSW |
1 |
10,222,037 (GRCm39) |
nonsense |
probably null |
|
R9335:Arfgef1
|
UTSW |
1 |
10,228,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:Arfgef1
|
UTSW |
1 |
10,283,419 (GRCm39) |
missense |
probably benign |
0.03 |
R9355:Arfgef1
|
UTSW |
1 |
10,270,000 (GRCm39) |
missense |
probably benign |
0.00 |
R9564:Arfgef1
|
UTSW |
1 |
10,217,758 (GRCm39) |
missense |
probably benign |
0.00 |
R9600:Arfgef1
|
UTSW |
1 |
10,233,977 (GRCm39) |
missense |
probably benign |
0.01 |
R9789:Arfgef1
|
UTSW |
1 |
10,243,427 (GRCm39) |
missense |
probably damaging |
1.00 |
V1662:Arfgef1
|
UTSW |
1 |
10,243,478 (GRCm39) |
missense |
probably damaging |
1.00 |
|