Incidental Mutation 'R1868:Arfgef3'
ID |
208966 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arfgef3
|
Ensembl Gene |
ENSMUSG00000019852 |
Gene Name |
ARFGEF family member 3 |
Synonyms |
B930094H20Rik, BIG3, D10Bwg1379e |
MMRRC Submission |
039890-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.146)
|
Stock # |
R1868 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
10 |
Chromosomal Location |
18463759-18619506 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 18537135 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Lysine
at position 182
(I182K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000149210
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000019999]
[ENSMUST00000215836]
|
AlphaFold |
Q3UGY8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000019999
AA Change: I182K
PolyPhen 2
Score 0.080 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000019999 Gene: ENSMUSG00000019852 AA Change: I182K
Domain | Start | End | E-Value | Type |
Pfam:DCB
|
1 |
170 |
7.1e-15 |
PFAM |
low complexity region
|
236 |
245 |
N/A |
INTRINSIC |
low complexity region
|
276 |
295 |
N/A |
INTRINSIC |
low complexity region
|
452 |
462 |
N/A |
INTRINSIC |
Sec7
|
582 |
794 |
6e-54 |
SMART |
Blast:Sec7
|
798 |
873 |
3e-20 |
BLAST |
low complexity region
|
927 |
940 |
N/A |
INTRINSIC |
Pfam:DUF1981
|
1237 |
1312 |
1.9e-14 |
PFAM |
low complexity region
|
1641 |
1652 |
N/A |
INTRINSIC |
low complexity region
|
1710 |
1723 |
N/A |
INTRINSIC |
low complexity region
|
1838 |
1856 |
N/A |
INTRINSIC |
low complexity region
|
2088 |
2099 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000215836
AA Change: I182K
PolyPhen 2
Score 0.170 (Sensitivity: 0.92; Specificity: 0.87)
|
Meta Mutation Damage Score |
0.0788 |
Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.8%
- 10x: 95.4%
- 20x: 93.0%
|
Validation Efficiency |
97% (115/118) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased insulin granule biogenesis and insulin secretion. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130230L23Rik |
A |
T |
5: 66,157,560 (GRCm39) |
M1K |
probably null |
Het |
A630073D07Rik |
C |
T |
6: 132,603,457 (GRCm39) |
E100K |
unknown |
Het |
Abcc3 |
T |
G |
11: 94,254,889 (GRCm39) |
D638A |
probably benign |
Het |
Acadm |
T |
C |
3: 153,635,889 (GRCm39) |
I272V |
probably benign |
Het |
Adam2 |
G |
A |
14: 66,315,107 (GRCm39) |
T22I |
probably damaging |
Het |
Aldh3b1 |
G |
A |
19: 3,971,271 (GRCm39) |
|
probably benign |
Het |
Arhgef17 |
A |
G |
7: 100,528,184 (GRCm39) |
S677P |
probably benign |
Het |
Atp2b1 |
T |
C |
10: 98,832,750 (GRCm39) |
V417A |
probably damaging |
Het |
Brca1 |
T |
A |
11: 101,388,839 (GRCm39) |
H1675L |
probably benign |
Het |
Brd10 |
A |
T |
19: 29,720,998 (GRCm39) |
S743T |
probably damaging |
Het |
Btd |
G |
T |
14: 31,389,266 (GRCm39) |
G329V |
probably benign |
Het |
Capsl |
T |
A |
15: 9,461,916 (GRCm39) |
L104* |
probably null |
Het |
Cbx1 |
T |
C |
11: 96,693,554 (GRCm39) |
S107P |
probably benign |
Het |
Cd207 |
G |
T |
6: 83,648,683 (GRCm39) |
Y326* |
probably null |
Het |
Cenpp |
T |
C |
13: 49,794,759 (GRCm39) |
D136G |
probably damaging |
Het |
Chsy3 |
A |
G |
18: 59,309,560 (GRCm39) |
|
probably null |
Het |
Cntrl |
T |
A |
2: 35,019,827 (GRCm39) |
H551Q |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,310,858 (GRCm39) |
|
probably benign |
Het |
Cybrd1 |
T |
A |
2: 70,967,978 (GRCm39) |
F183Y |
possibly damaging |
Het |
D5Ertd579e |
G |
A |
5: 36,773,771 (GRCm39) |
S208L |
probably damaging |
Het |
Dlg2 |
A |
T |
7: 92,036,160 (GRCm39) |
K719* |
probably null |
Het |
Dppa1 |
A |
T |
11: 46,516,393 (GRCm39) |
|
probably null |
Het |
Dse |
A |
G |
10: 34,029,284 (GRCm39) |
V602A |
possibly damaging |
Het |
Elapor2 |
T |
A |
5: 9,529,251 (GRCm39) |
I1028K |
probably damaging |
Het |
Elmo1 |
C |
T |
13: 20,773,823 (GRCm39) |
A611V |
possibly damaging |
Het |
Ets2 |
T |
C |
16: 95,516,118 (GRCm39) |
S233P |
probably benign |
Het |
Fchsd2 |
G |
A |
7: 100,899,645 (GRCm39) |
|
probably benign |
Het |
Fhip2a |
T |
C |
19: 57,374,737 (GRCm39) |
I704T |
possibly damaging |
Het |
Fkbp4 |
T |
C |
6: 128,409,453 (GRCm39) |
R402G |
probably benign |
Het |
G2e3 |
T |
A |
12: 51,400,412 (GRCm39) |
D21E |
probably benign |
Het |
Gask1a |
A |
G |
9: 121,794,493 (GRCm39) |
T216A |
possibly damaging |
Het |
Gck |
A |
T |
11: 5,852,165 (GRCm39) |
N391K |
probably damaging |
Het |
Gm11077 |
T |
A |
6: 140,675,017 (GRCm39) |
I3N |
unknown |
Het |
Gm6793 |
T |
C |
8: 112,741,088 (GRCm39) |
M185V |
probably benign |
Het |
Gucy2d |
T |
A |
7: 98,103,268 (GRCm39) |
L504H |
probably damaging |
Het |
Hat1 |
T |
A |
2: 71,251,627 (GRCm39) |
Y225* |
probably null |
Het |
Iars2 |
A |
T |
1: 185,050,765 (GRCm39) |
D441E |
probably benign |
Het |
Ido2 |
C |
A |
8: 25,043,776 (GRCm39) |
M92I |
possibly damaging |
Het |
Ifne |
T |
C |
4: 88,797,908 (GRCm39) |
E170G |
probably damaging |
Het |
Ints8 |
C |
A |
4: 11,241,684 (GRCm39) |
C253F |
probably damaging |
Het |
Intu |
G |
T |
3: 40,618,765 (GRCm39) |
G257V |
probably damaging |
Het |
Jakmip3 |
A |
G |
7: 138,609,316 (GRCm39) |
K140R |
probably benign |
Het |
Kcnip3 |
T |
C |
2: 127,301,263 (GRCm39) |
E237G |
probably damaging |
Het |
Ksr2 |
A |
C |
5: 117,643,594 (GRCm39) |
E121A |
probably benign |
Het |
Lars1 |
T |
A |
18: 42,347,902 (GRCm39) |
I974F |
probably benign |
Het |
Lce1b |
A |
G |
3: 92,563,318 (GRCm39) |
S72P |
unknown |
Het |
Lhfpl4 |
T |
A |
6: 113,153,394 (GRCm39) |
D125V |
probably benign |
Het |
Luc7l |
G |
A |
17: 26,499,030 (GRCm39) |
|
probably benign |
Het |
Mei1 |
T |
C |
15: 82,009,154 (GRCm39) |
L833P |
probably damaging |
Het |
Mier2 |
A |
G |
10: 79,384,664 (GRCm39) |
V150A |
probably damaging |
Het |
Muc4 |
C |
T |
16: 32,576,715 (GRCm39) |
R2072C |
unknown |
Het |
Myh3 |
A |
G |
11: 66,975,852 (GRCm39) |
K295E |
probably benign |
Het |
Ndufaf5 |
A |
G |
2: 140,023,509 (GRCm39) |
I115V |
probably benign |
Het |
Neb |
T |
C |
2: 52,216,756 (GRCm39) |
K140E |
probably damaging |
Het |
Niban1 |
A |
G |
1: 151,517,302 (GRCm39) |
S104G |
possibly damaging |
Het |
Npas2 |
A |
G |
1: 39,339,759 (GRCm39) |
D103G |
probably benign |
Het |
Ntrk3 |
A |
T |
7: 77,842,352 (GRCm39) |
H825Q |
possibly damaging |
Het |
Nup62 |
T |
A |
7: 44,478,472 (GRCm39) |
S162R |
possibly damaging |
Het |
Or4c108 |
T |
C |
2: 88,804,128 (GRCm39) |
T36A |
possibly damaging |
Het |
Or5g23 |
T |
A |
2: 85,438,409 (GRCm39) |
I282F |
probably damaging |
Het |
Or5t7 |
G |
A |
2: 86,507,629 (GRCm39) |
T16I |
possibly damaging |
Het |
Or8c8 |
A |
G |
9: 38,164,986 (GRCm39) |
E91G |
probably damaging |
Het |
Orc4 |
A |
G |
2: 48,800,305 (GRCm39) |
M281T |
probably benign |
Het |
Osbpl5 |
C |
A |
7: 143,269,510 (GRCm39) |
R22L |
probably damaging |
Het |
Otos |
A |
G |
1: 92,572,185 (GRCm39) |
F47S |
probably damaging |
Het |
Parp11 |
A |
G |
6: 127,447,740 (GRCm39) |
T25A |
probably damaging |
Het |
Pcdhb9 |
A |
C |
18: 37,535,137 (GRCm39) |
D377A |
probably damaging |
Het |
Pdgfra |
C |
T |
5: 75,331,534 (GRCm39) |
S348L |
probably benign |
Het |
Pdlim5 |
C |
A |
3: 142,012,060 (GRCm39) |
|
probably null |
Het |
Peg12 |
T |
C |
7: 62,113,416 (GRCm39) |
H227R |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,152,415 (GRCm39) |
E2559G |
probably damaging |
Het |
Pnisr |
C |
T |
4: 21,874,086 (GRCm39) |
|
probably benign |
Het |
Ppa2 |
A |
T |
3: 133,053,858 (GRCm39) |
I183F |
probably damaging |
Het |
Pramel48 |
T |
A |
5: 95,630,758 (GRCm39) |
Y212N |
probably benign |
Het |
Prl2a1 |
T |
C |
13: 27,988,923 (GRCm39) |
L16P |
probably damaging |
Het |
Rai14 |
C |
A |
15: 10,633,314 (GRCm39) |
Q25H |
probably damaging |
Het |
Rapgef6 |
TG |
TGG |
11: 54,437,223 (GRCm39) |
|
probably null |
Het |
Rbm34 |
C |
A |
8: 127,697,631 (GRCm39) |
A27S |
probably benign |
Het |
Rchy1 |
T |
C |
5: 92,099,762 (GRCm39) |
D192G |
probably damaging |
Het |
Rexo1 |
T |
C |
10: 80,378,754 (GRCm39) |
D1094G |
probably damaging |
Het |
Rtl1 |
T |
A |
12: 109,556,970 (GRCm39) |
D1623V |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,746,586 (GRCm39) |
E1989K |
probably benign |
Het |
Sema6c |
A |
G |
3: 95,078,124 (GRCm39) |
E500G |
probably damaging |
Het |
Slc13a1 |
T |
A |
6: 24,117,999 (GRCm39) |
Y246F |
probably damaging |
Het |
Slc39a9 |
C |
T |
12: 80,726,297 (GRCm39) |
L249F |
probably damaging |
Het |
Slc6a21 |
C |
T |
7: 44,937,252 (GRCm39) |
P261S |
probably benign |
Het |
Slco2b1 |
C |
T |
7: 99,335,243 (GRCm39) |
C179Y |
probably damaging |
Het |
Sox6 |
T |
C |
7: 115,258,773 (GRCm39) |
N252S |
possibly damaging |
Het |
Spr-ps1 |
C |
T |
6: 85,132,885 (GRCm39) |
|
noncoding transcript |
Het |
Sptbn1 |
C |
A |
11: 30,064,781 (GRCm39) |
R1906L |
possibly damaging |
Het |
Stac2 |
T |
C |
11: 97,943,771 (GRCm39) |
D13G |
probably benign |
Het |
Stat5a |
G |
T |
11: 100,764,955 (GRCm39) |
R226L |
probably damaging |
Het |
Suz12 |
A |
G |
11: 79,904,425 (GRCm39) |
|
probably null |
Het |
Tas2r144 |
C |
A |
6: 42,192,936 (GRCm39) |
H225Q |
probably benign |
Het |
Tdo2 |
T |
A |
3: 81,867,853 (GRCm39) |
M331L |
probably benign |
Het |
Tesk1 |
T |
C |
4: 43,447,201 (GRCm39) |
W530R |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,112,172 (GRCm39) |
N245S |
probably benign |
Het |
Tnfrsf11a |
G |
T |
1: 105,772,431 (GRCm39) |
A573S |
probably damaging |
Het |
Tpbpb |
A |
T |
13: 61,050,344 (GRCm39) |
|
probably benign |
Het |
Trim24 |
T |
A |
6: 37,928,447 (GRCm39) |
S590T |
probably damaging |
Het |
Ttll3 |
G |
T |
6: 113,369,725 (GRCm39) |
A90S |
possibly damaging |
Het |
Ubr5 |
A |
T |
15: 38,042,090 (GRCm39) |
S169T |
probably benign |
Het |
Usp28 |
T |
C |
9: 48,928,007 (GRCm39) |
V363A |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,838,990 (GRCm39) |
S2185P |
probably benign |
Het |
Vmn1r211 |
T |
C |
13: 23,035,779 (GRCm39) |
H296R |
probably benign |
Het |
Vmn2r3 |
G |
A |
3: 64,166,537 (GRCm39) |
P865S |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,414,415 (GRCm39) |
T426A |
probably benign |
Het |
Wdr37 |
G |
T |
13: 8,886,887 (GRCm39) |
T300K |
probably damaging |
Het |
Wrap53 |
A |
T |
11: 69,452,990 (GRCm39) |
V439E |
probably null |
Het |
Wrn |
A |
G |
8: 33,747,249 (GRCm39) |
S868P |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,477,774 (GRCm39) |
E3463G |
probably damaging |
Het |
Zfp189 |
T |
A |
4: 49,529,283 (GRCm39) |
C129S |
possibly damaging |
Het |
Zfp442 |
T |
C |
2: 150,250,100 (GRCm39) |
K544E |
probably damaging |
Het |
Zfp939 |
T |
A |
7: 39,122,728 (GRCm39) |
|
noncoding transcript |
Het |
Zfyve26 |
T |
C |
12: 79,308,573 (GRCm39) |
H228R |
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 |
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 |
R4929:Arfgef3
|
UTSW |
10 |
18,506,599 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|
Predicted Primers |
PCR Primer
(F):5'- ACCAAAAGTCTCCAAATGGGG -3'
(R):5'- AGTTTGGAGATGGGCACACTC -3'
Sequencing Primer
(F):5'- GGGGATGTAAAATGCTAATTCCCCC -3'
(R):5'- CATTGTCTAACAGTCGGG -3'
|
Posted On |
2014-06-30 |