Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
A |
G |
7: 29,273,467 (GRCm39) |
|
noncoding transcript |
Het |
Abcd3 |
A |
T |
3: 121,562,395 (GRCm39) |
|
probably null |
Het |
Adamts12 |
C |
T |
15: 11,259,108 (GRCm39) |
R551C |
probably damaging |
Het |
Adamtsl4 |
A |
G |
3: 95,585,315 (GRCm39) |
C818R |
probably damaging |
Het |
Aurka |
A |
T |
2: 172,212,326 (GRCm39) |
V17E |
probably benign |
Het |
Cdh24 |
C |
T |
14: 54,870,973 (GRCm39) |
V132I |
probably benign |
Het |
Cep57l1 |
T |
C |
10: 41,621,910 (GRCm39) |
D2G |
possibly damaging |
Het |
Cntn5 |
T |
A |
9: 9,976,400 (GRCm39) |
|
probably null |
Het |
Col10a1 |
T |
C |
10: 34,271,120 (GRCm39) |
I364T |
probably benign |
Het |
Dpp6 |
G |
A |
5: 27,254,785 (GRCm39) |
A67T |
probably benign |
Het |
Dym |
T |
A |
18: 75,376,357 (GRCm39) |
V583E |
probably damaging |
Het |
Efcab5 |
T |
G |
11: 76,994,209 (GRCm39) |
K1259N |
probably benign |
Het |
Ehbp1 |
T |
G |
11: 22,189,169 (GRCm39) |
I78L |
possibly damaging |
Het |
Epha1 |
C |
A |
6: 42,341,533 (GRCm39) |
A469S |
probably benign |
Het |
Fam135a |
T |
C |
1: 24,069,081 (GRCm39) |
D596G |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,727,029 (GRCm39) |
N530S |
probably benign |
Het |
Gm57858 |
G |
A |
3: 36,089,487 (GRCm39) |
L146F |
probably damaging |
Het |
Grhl2 |
A |
G |
15: 37,361,046 (GRCm39) |
N610S |
probably benign |
Het |
Haus6 |
T |
C |
4: 86,513,670 (GRCm39) |
I331V |
probably benign |
Het |
Ints2 |
G |
T |
11: 86,103,479 (GRCm39) |
N1192K |
possibly damaging |
Het |
Itga5 |
A |
G |
15: 103,261,662 (GRCm39) |
V445A |
probably benign |
Het |
Itga9 |
C |
A |
9: 118,636,317 (GRCm39) |
D82E |
probably damaging |
Het |
Jam2 |
G |
A |
16: 84,619,750 (GRCm39) |
|
probably benign |
Het |
Klhl32 |
T |
A |
4: 24,709,030 (GRCm39) |
I112F |
probably damaging |
Het |
Lepr |
A |
G |
4: 101,672,314 (GRCm39) |
I1113V |
probably benign |
Het |
Lrrc3b |
C |
A |
14: 15,357,888 (GRCm38) |
L239F |
probably damaging |
Het |
Lzic |
T |
A |
4: 149,572,585 (GRCm39) |
|
probably null |
Het |
Mxra8 |
T |
A |
4: 155,927,118 (GRCm39) |
F351I |
probably damaging |
Het |
Naa40 |
A |
G |
19: 7,207,347 (GRCm39) |
F126L |
probably damaging |
Het |
Nbeal1 |
C |
T |
1: 60,277,813 (GRCm39) |
S733F |
probably damaging |
Het |
Olr1 |
T |
C |
6: 129,477,044 (GRCm39) |
T74A |
probably damaging |
Het |
Or52x1 |
A |
G |
7: 104,853,232 (GRCm39) |
I106T |
probably damaging |
Het |
Or5aq7 |
A |
G |
2: 86,938,527 (GRCm39) |
F68S |
possibly damaging |
Het |
Or5h17 |
A |
C |
16: 58,820,582 (GRCm39) |
Y178S |
probably damaging |
Het |
Pgam5 |
A |
T |
5: 110,413,691 (GRCm39) |
V130D |
probably damaging |
Het |
Pop4 |
A |
G |
7: 37,965,573 (GRCm39) |
C115R |
probably damaging |
Het |
Prpf18 |
A |
T |
2: 4,629,348 (GRCm39) |
|
probably null |
Het |
Psg16 |
G |
A |
7: 16,829,031 (GRCm39) |
R205H |
possibly damaging |
Het |
Ptgr1 |
C |
A |
4: 58,981,879 (GRCm39) |
A53S |
probably benign |
Het |
Shank2 |
A |
G |
7: 143,965,008 (GRCm39) |
D1451G |
probably benign |
Het |
Slfn10-ps |
A |
G |
11: 82,920,345 (GRCm39) |
|
noncoding transcript |
Het |
Sox8 |
G |
A |
17: 25,789,330 (GRCm39) |
A56V |
probably benign |
Het |
Ssr3 |
A |
G |
3: 65,295,175 (GRCm39) |
S113P |
probably damaging |
Het |
Stx16 |
T |
C |
2: 173,938,721 (GRCm39) |
Y296H |
possibly damaging |
Het |
Tfcp2 |
A |
T |
15: 100,426,370 (GRCm39) |
N60K |
probably benign |
Het |
Thada |
T |
C |
17: 84,751,654 (GRCm39) |
T441A |
probably benign |
Het |
Trf |
G |
T |
9: 103,105,074 (GRCm39) |
|
probably benign |
Het |
Vamp2 |
T |
A |
11: 68,979,488 (GRCm39) |
|
probably benign |
Het |
Vmn2r105 |
A |
T |
17: 20,448,280 (GRCm39) |
D181E |
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,239,544 (GRCm39) |
Y340N |
probably damaging |
Het |
Wasf2 |
C |
A |
4: 132,923,170 (GRCm39) |
D493E |
unknown |
Het |
Wdfy4 |
T |
C |
14: 32,769,213 (GRCm39) |
D2084G |
possibly damaging |
Het |
Zfp229 |
T |
A |
17: 21,965,354 (GRCm39) |
I528N |
probably damaging |
Het |
Zfp703 |
T |
A |
8: 27,468,879 (GRCm39) |
V181E |
possibly damaging |
Het |
|
Other mutations in Arfgef3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:Arfgef3
|
APN |
10 |
18,536,352 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00835:Arfgef3
|
APN |
10 |
18,537,106 (GRCm39) |
missense |
probably benign |
|
IGL00961:Arfgef3
|
APN |
10 |
18,486,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01400:Arfgef3
|
APN |
10 |
18,528,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01501:Arfgef3
|
APN |
10 |
18,476,308 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01595:Arfgef3
|
APN |
10 |
18,470,660 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01695:Arfgef3
|
APN |
10 |
18,479,167 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Arfgef3
|
APN |
10 |
18,619,363 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02348:Arfgef3
|
APN |
10 |
18,467,095 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02371:Arfgef3
|
APN |
10 |
18,522,287 (GRCm39) |
missense |
probably benign |
|
IGL02400:Arfgef3
|
APN |
10 |
18,522,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02630:Arfgef3
|
APN |
10 |
18,537,140 (GRCm39) |
splice site |
probably benign |
|
IGL02815:Arfgef3
|
APN |
10 |
18,528,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03178:Arfgef3
|
APN |
10 |
18,488,973 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03182:Arfgef3
|
APN |
10 |
18,476,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Arfgef3
|
APN |
10 |
18,467,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Arfgef3
|
APN |
10 |
18,540,660 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03410:Arfgef3
|
APN |
10 |
18,476,238 (GRCm39) |
missense |
probably damaging |
1.00 |
Bow-wow
|
UTSW |
10 |
18,522,478 (GRCm39) |
nonsense |
probably null |
|
R0098:Arfgef3
|
UTSW |
10 |
18,465,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Arfgef3
|
UTSW |
10 |
18,465,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0141:Arfgef3
|
UTSW |
10 |
18,473,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Arfgef3
|
UTSW |
10 |
18,523,663 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0164:Arfgef3
|
UTSW |
10 |
18,523,663 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0241:Arfgef3
|
UTSW |
10 |
18,474,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Arfgef3
|
UTSW |
10 |
18,468,029 (GRCm39) |
missense |
probably damaging |
0.98 |
R0352:Arfgef3
|
UTSW |
10 |
18,537,135 (GRCm39) |
missense |
probably benign |
0.17 |
R0415:Arfgef3
|
UTSW |
10 |
18,488,875 (GRCm39) |
splice site |
probably benign |
|
R0417:Arfgef3
|
UTSW |
10 |
18,479,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Arfgef3
|
UTSW |
10 |
18,553,563 (GRCm39) |
splice site |
probably benign |
|
R0507:Arfgef3
|
UTSW |
10 |
18,467,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Arfgef3
|
UTSW |
10 |
18,475,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0582:Arfgef3
|
UTSW |
10 |
18,487,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Arfgef3
|
UTSW |
10 |
18,473,179 (GRCm39) |
missense |
probably benign |
0.31 |
R0826:Arfgef3
|
UTSW |
10 |
18,465,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R0919:Arfgef3
|
UTSW |
10 |
18,465,483 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0980:Arfgef3
|
UTSW |
10 |
18,467,866 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1027:Arfgef3
|
UTSW |
10 |
18,467,123 (GRCm39) |
missense |
probably benign |
0.02 |
R1140:Arfgef3
|
UTSW |
10 |
18,473,096 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1491:Arfgef3
|
UTSW |
10 |
18,522,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Arfgef3
|
UTSW |
10 |
18,506,627 (GRCm39) |
missense |
probably damaging |
0.96 |
R1529:Arfgef3
|
UTSW |
10 |
18,488,970 (GRCm39) |
nonsense |
probably null |
|
R1564:Arfgef3
|
UTSW |
10 |
18,467,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Arfgef3
|
UTSW |
10 |
18,500,896 (GRCm39) |
missense |
probably null |
0.15 |
R1868:Arfgef3
|
UTSW |
10 |
18,537,135 (GRCm39) |
missense |
probably benign |
0.17 |
R1876:Arfgef3
|
UTSW |
10 |
18,473,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Arfgef3
|
UTSW |
10 |
18,528,511 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2211:Arfgef3
|
UTSW |
10 |
18,467,993 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2316:Arfgef3
|
UTSW |
10 |
18,492,701 (GRCm39) |
missense |
probably benign |
0.19 |
R2393:Arfgef3
|
UTSW |
10 |
18,473,535 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2407:Arfgef3
|
UTSW |
10 |
18,553,614 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3076:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R3077:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R3963:Arfgef3
|
UTSW |
10 |
18,468,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R4201:Arfgef3
|
UTSW |
10 |
18,495,530 (GRCm39) |
missense |
probably benign |
0.01 |
R4241:Arfgef3
|
UTSW |
10 |
18,500,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4244:Arfgef3
|
UTSW |
10 |
18,506,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R4395:Arfgef3
|
UTSW |
10 |
18,473,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4455:Arfgef3
|
UTSW |
10 |
18,483,423 (GRCm39) |
missense |
probably benign |
0.18 |
R4480:Arfgef3
|
UTSW |
10 |
18,476,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R4499:Arfgef3
|
UTSW |
10 |
18,484,091 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4589:Arfgef3
|
UTSW |
10 |
18,521,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4635:Arfgef3
|
UTSW |
10 |
18,510,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Arfgef3
|
UTSW |
10 |
18,529,995 (GRCm39) |
missense |
probably benign |
|
R4801:Arfgef3
|
UTSW |
10 |
18,467,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Arfgef3
|
UTSW |
10 |
18,467,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4807:Arfgef3
|
UTSW |
10 |
18,522,385 (GRCm39) |
missense |
probably benign |
|
R4828:Arfgef3
|
UTSW |
10 |
18,528,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R4861:Arfgef3
|
UTSW |
10 |
18,483,479 (GRCm39) |
missense |
probably benign |
0.01 |
R4861:Arfgef3
|
UTSW |
10 |
18,483,479 (GRCm39) |
missense |
probably benign |
0.01 |
R4917:Arfgef3
|
UTSW |
10 |
18,492,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R4918:Arfgef3
|
UTSW |
10 |
18,492,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R4922:Arfgef3
|
UTSW |
10 |
18,467,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R4937:Arfgef3
|
UTSW |
10 |
18,465,454 (GRCm39) |
missense |
probably damaging |
0.98 |
R5290:Arfgef3
|
UTSW |
10 |
18,476,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R5410:Arfgef3
|
UTSW |
10 |
18,486,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R5807:Arfgef3
|
UTSW |
10 |
18,523,546 (GRCm39) |
splice site |
probably null |
|
R5832:Arfgef3
|
UTSW |
10 |
18,506,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Arfgef3
|
UTSW |
10 |
18,483,413 (GRCm39) |
nonsense |
probably null |
|
R6272:Arfgef3
|
UTSW |
10 |
18,522,711 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Arfgef3
|
UTSW |
10 |
18,528,589 (GRCm39) |
missense |
probably damaging |
0.97 |
R6397:Arfgef3
|
UTSW |
10 |
18,483,413 (GRCm39) |
nonsense |
probably null |
|
R6495:Arfgef3
|
UTSW |
10 |
18,486,950 (GRCm39) |
critical splice donor site |
probably null |
|
R6707:Arfgef3
|
UTSW |
10 |
18,496,903 (GRCm39) |
missense |
probably benign |
0.11 |
R6814:Arfgef3
|
UTSW |
10 |
18,470,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Arfgef3
|
UTSW |
10 |
18,540,637 (GRCm39) |
critical splice donor site |
probably null |
|
R6870:Arfgef3
|
UTSW |
10 |
18,522,478 (GRCm39) |
nonsense |
probably null |
|
R6941:Arfgef3
|
UTSW |
10 |
18,501,203 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7094:Arfgef3
|
UTSW |
10 |
18,522,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Arfgef3
|
UTSW |
10 |
18,475,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Arfgef3
|
UTSW |
10 |
18,522,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Arfgef3
|
UTSW |
10 |
18,501,139 (GRCm39) |
missense |
probably benign |
0.00 |
R7249:Arfgef3
|
UTSW |
10 |
18,506,583 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7318:Arfgef3
|
UTSW |
10 |
18,506,211 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7391:Arfgef3
|
UTSW |
10 |
18,522,007 (GRCm39) |
missense |
probably benign |
0.05 |
R7527:Arfgef3
|
UTSW |
10 |
18,522,377 (GRCm39) |
missense |
probably benign |
|
R7618:Arfgef3
|
UTSW |
10 |
18,522,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Arfgef3
|
UTSW |
10 |
18,470,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R7851:Arfgef3
|
UTSW |
10 |
18,468,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R8112:Arfgef3
|
UTSW |
10 |
18,528,379 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8133:Arfgef3
|
UTSW |
10 |
18,486,951 (GRCm39) |
critical splice donor site |
probably null |
|
R8242:Arfgef3
|
UTSW |
10 |
18,505,824 (GRCm39) |
missense |
probably benign |
0.25 |
R8369:Arfgef3
|
UTSW |
10 |
18,465,477 (GRCm39) |
missense |
probably benign |
0.34 |
R8396:Arfgef3
|
UTSW |
10 |
18,528,280 (GRCm39) |
critical splice donor site |
probably null |
|
R8553:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Arfgef3
|
UTSW |
10 |
18,522,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R8821:Arfgef3
|
UTSW |
10 |
18,528,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8831:Arfgef3
|
UTSW |
10 |
18,528,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8918:Arfgef3
|
UTSW |
10 |
18,511,453 (GRCm39) |
missense |
probably benign |
0.01 |
R8929:Arfgef3
|
UTSW |
10 |
18,479,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Arfgef3
|
UTSW |
10 |
18,522,476 (GRCm39) |
missense |
probably benign |
0.32 |
R9077:Arfgef3
|
UTSW |
10 |
18,500,899 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9258:Arfgef3
|
UTSW |
10 |
18,465,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Arfgef3
|
UTSW |
10 |
18,475,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R9358:Arfgef3
|
UTSW |
10 |
18,492,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Arfgef3
|
UTSW |
10 |
18,505,877 (GRCm39) |
missense |
probably benign |
0.35 |
R9389:Arfgef3
|
UTSW |
10 |
18,479,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Arfgef3
|
UTSW |
10 |
18,522,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9713:Arfgef3
|
UTSW |
10 |
18,528,556 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Arfgef3
|
UTSW |
10 |
18,528,374 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Arfgef3
|
UTSW |
10 |
18,510,600 (GRCm39) |
missense |
probably benign |
0.26 |
Z1176:Arfgef3
|
UTSW |
10 |
18,484,106 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Arfgef3
|
UTSW |
10 |
18,467,185 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arfgef3
|
UTSW |
10 |
18,503,376 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arfgef3
|
UTSW |
10 |
18,483,524 (GRCm39) |
missense |
probably damaging |
1.00 |
|