Incidental Mutation 'IGL02478:Exoc2'
| ID |
295070 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Exoc2
|
| Ensembl Gene |
ENSMUSG00000021357 |
| Gene Name |
exocyst complex component 2 |
| Synonyms |
2410030I24Rik, Sec5l1, Sec5, Gm29675 |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.962)
|
| Stock # |
IGL02478
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
13 |
| Chromosomal Location |
30972939-31162082 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 31111403 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Serine
at position 142
(C142S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000100010
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021785]
[ENSMUST00000102946]
|
| AlphaFold |
Q9D4H1 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000021785
AA Change: C142S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000021785
Gene: ENSMUSG00000021357
AA Change: C142S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TIG
|
8 |
92 |
3.2e-10 |
PFAM |
|
Pfam:Sec5
|
198 |
377 |
3.6e-59 |
PFAM |
|
low complexity region
|
572 |
585 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102946
AA Change: C142S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000100010
Gene: ENSMUSG00000021357
AA Change: C142S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TIG
|
8 |
92 |
2.5e-10 |
PFAM |
|
Pfam:Sec5
|
198 |
377 |
7.5e-59 |
PFAM |
|
low complexity region
|
572 |
585 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000220490
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000220532
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000221678
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000222133
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a component of the exocyst complex, a multi-protein complex essential for the polarized targeting of exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and the functions of the exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. This interaction has been shown to mediate filopodia formation in fibroblasts. This protein has been shown to interact with the Ral subfamily of GTPases and thereby mediate exocytosis by tethering vesicles to the plasma membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 56 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb1b |
C |
A |
5: 8,856,018 (GRCm39) |
A42E |
probably damaging |
Het |
| Agmo |
T |
A |
12: 37,451,985 (GRCm39) |
F247L |
probably damaging |
Het |
| Arap1 |
C |
A |
7: 101,049,332 (GRCm39) |
|
probably null |
Het |
| Arid1a |
T |
C |
4: 133,408,585 (GRCm39) |
D1974G |
unknown |
Het |
| Asxl3 |
C |
T |
18: 22,656,070 (GRCm39) |
A1360V |
possibly damaging |
Het |
| Celsr1 |
T |
A |
15: 85,825,337 (GRCm39) |
T1599S |
possibly damaging |
Het |
| Chrdl2 |
T |
C |
7: 99,670,190 (GRCm39) |
|
probably null |
Het |
| Csmd3 |
T |
C |
15: 47,701,794 (GRCm39) |
|
probably benign |
Het |
| Dis3l |
C |
T |
9: 64,222,055 (GRCm39) |
E452K |
probably benign |
Het |
| Dnajc2 |
A |
T |
5: 21,981,788 (GRCm39) |
H45Q |
probably damaging |
Het |
| Eps8 |
G |
A |
6: 137,499,840 (GRCm39) |
P213L |
probably benign |
Het |
| Erbb3 |
T |
A |
10: 128,407,227 (GRCm39) |
R978* |
probably null |
Het |
| Fam184b |
T |
C |
5: 45,695,039 (GRCm39) |
E735G |
probably damaging |
Het |
| Fancm |
T |
C |
12: 65,123,864 (GRCm39) |
V174A |
probably damaging |
Het |
| Fat4 |
T |
C |
3: 38,942,364 (GRCm39) |
L419P |
probably damaging |
Het |
| Fsip2 |
G |
T |
2: 82,814,736 (GRCm39) |
V3490L |
probably benign |
Het |
| Ftcd |
A |
T |
10: 76,417,255 (GRCm39) |
R255* |
probably null |
Het |
| Galc |
T |
C |
12: 98,179,391 (GRCm39) |
N506S |
possibly damaging |
Het |
| Gm20441 |
G |
T |
10: 75,608,644 (GRCm39) |
A26E |
probably damaging |
Het |
| Gm21969 |
T |
G |
4: 139,367,999 (GRCm39) |
|
probably null |
Het |
| Ifitm3 |
T |
A |
7: 140,589,787 (GRCm39) |
M89L |
possibly damaging |
Het |
| Ift25 |
T |
A |
4: 107,132,449 (GRCm39) |
S79T |
probably benign |
Het |
| Inmt |
T |
C |
6: 55,150,355 (GRCm39) |
E94G |
probably damaging |
Het |
| Insrr |
G |
A |
3: 87,716,719 (GRCm39) |
G649D |
probably benign |
Het |
| Ivd |
T |
C |
2: 118,692,572 (GRCm39) |
L24P |
probably benign |
Het |
| Kcnc1 |
A |
G |
7: 46,084,593 (GRCm39) |
N506D |
probably benign |
Het |
| Krt39 |
T |
A |
11: 99,411,723 (GRCm39) |
D121V |
probably benign |
Het |
| Lcp1 |
A |
G |
14: 75,461,536 (GRCm39) |
I510V |
probably benign |
Het |
| Mkx |
C |
T |
18: 7,002,418 (GRCm39) |
V43M |
probably damaging |
Het |
| Mmp2 |
A |
G |
8: 93,579,235 (GRCm39) |
N108S |
possibly damaging |
Het |
| Mob1b |
T |
C |
5: 88,903,947 (GRCm39) |
|
probably benign |
Het |
| Morc3 |
A |
G |
16: 93,661,844 (GRCm39) |
|
probably benign |
Het |
| Myh13 |
T |
G |
11: 67,260,204 (GRCm39) |
S1881A |
probably benign |
Het |
| Nalcn |
T |
C |
14: 123,558,717 (GRCm39) |
E843G |
probably benign |
Het |
| Ngef |
A |
G |
1: 87,408,301 (GRCm39) |
|
probably benign |
Het |
| Or14c40 |
T |
A |
7: 86,313,344 (GRCm39) |
I158N |
probably damaging |
Het |
| Osm |
A |
G |
11: 4,189,507 (GRCm39) |
Y97C |
probably damaging |
Het |
| Pclo |
T |
A |
5: 14,816,792 (GRCm39) |
L4556Q |
unknown |
Het |
| Pcyox1l |
T |
C |
18: 61,830,780 (GRCm39) |
D364G |
probably benign |
Het |
| Plekha6 |
T |
A |
1: 133,211,031 (GRCm39) |
V467E |
probably benign |
Het |
| Qrsl1 |
A |
T |
10: 43,758,158 (GRCm39) |
S312T |
probably damaging |
Het |
| Ripk1 |
T |
A |
13: 34,194,572 (GRCm39) |
L70Q |
probably damaging |
Het |
| Rnaseh1 |
A |
T |
12: 28,705,662 (GRCm39) |
Y162F |
probably damaging |
Het |
| Ror2 |
T |
A |
13: 53,275,703 (GRCm39) |
T195S |
probably damaging |
Het |
| Sh3bp2 |
T |
C |
5: 34,709,006 (GRCm39) |
L33P |
probably damaging |
Het |
| Skil |
T |
A |
3: 31,151,968 (GRCm39) |
C163* |
probably null |
Het |
| Slc25a37 |
A |
T |
14: 69,486,883 (GRCm39) |
N133K |
probably benign |
Het |
| Slitrk3 |
A |
C |
3: 72,958,046 (GRCm39) |
V242G |
probably damaging |
Het |
| Sra1 |
A |
G |
18: 36,801,845 (GRCm39) |
S82P |
probably benign |
Het |
| Synj2 |
A |
G |
17: 6,088,199 (GRCm39) |
N1417D |
probably benign |
Het |
| Tas2r122 |
A |
G |
6: 132,688,578 (GRCm39) |
V105A |
possibly damaging |
Het |
| Tasor2 |
T |
C |
13: 3,624,661 (GRCm39) |
E1763G |
probably benign |
Het |
| Ttc21b |
T |
C |
2: 66,018,624 (GRCm39) |
N1261S |
probably benign |
Het |
| Vmn2r69 |
A |
G |
7: 85,055,889 (GRCm39) |
S750P |
probably damaging |
Het |
| Wdr95 |
A |
G |
5: 149,519,786 (GRCm39) |
T568A |
probably benign |
Het |
| Zfp319 |
T |
A |
8: 96,055,721 (GRCm39) |
I161F |
possibly damaging |
Het |
|
| Other mutations in Exoc2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00095:Exoc2
|
APN |
13 |
31,004,609 (GRCm39) |
missense |
probably benign |
0.17 |
|
IGL01839:Exoc2
|
APN |
13 |
31,090,782 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02092:Exoc2
|
APN |
13 |
31,059,260 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL02245:Exoc2
|
APN |
13 |
31,090,842 (GRCm39) |
missense |
probably benign |
0.10 |
|
IGL02267:Exoc2
|
APN |
13 |
30,999,304 (GRCm39) |
missense |
probably benign |
|
|
IGL02500:Exoc2
|
APN |
13 |
31,095,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03081:Exoc2
|
APN |
13 |
31,084,885 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL03112:Exoc2
|
APN |
13 |
31,090,570 (GRCm39) |
splice site |
probably benign |
|
|
IGL03409:Exoc2
|
APN |
13 |
31,124,720 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R0284:Exoc2
|
UTSW |
13 |
31,061,608 (GRCm39) |
splice site |
probably benign |
|
|
R0452:Exoc2
|
UTSW |
13 |
31,070,310 (GRCm39) |
splice site |
probably benign |
|
|
R0826:Exoc2
|
UTSW |
13 |
31,040,780 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1251:Exoc2
|
UTSW |
13 |
31,070,259 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1367:Exoc2
|
UTSW |
13 |
31,066,256 (GRCm39) |
nonsense |
probably null |
|
|
R1501:Exoc2
|
UTSW |
13 |
31,119,485 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1593:Exoc2
|
UTSW |
13 |
31,040,744 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R1839:Exoc2
|
UTSW |
13 |
31,090,480 (GRCm39) |
splice site |
probably benign |
|
|
R1872:Exoc2
|
UTSW |
13 |
31,006,644 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2064:Exoc2
|
UTSW |
13 |
31,119,544 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2070:Exoc2
|
UTSW |
13 |
30,999,353 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2227:Exoc2
|
UTSW |
13 |
31,048,867 (GRCm39) |
missense |
probably benign |
|
|
R2507:Exoc2
|
UTSW |
13 |
31,066,348 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R3965:Exoc2
|
UTSW |
13 |
31,061,565 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4601:Exoc2
|
UTSW |
13 |
31,066,251 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4914:Exoc2
|
UTSW |
13 |
31,060,796 (GRCm39) |
missense |
probably benign |
0.21 |
|
R5299:Exoc2
|
UTSW |
13 |
31,055,901 (GRCm39) |
splice site |
probably null |
|
|
R5410:Exoc2
|
UTSW |
13 |
31,048,839 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5461:Exoc2
|
UTSW |
13 |
31,109,738 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5956:Exoc2
|
UTSW |
13 |
31,004,606 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6056:Exoc2
|
UTSW |
13 |
31,084,812 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6107:Exoc2
|
UTSW |
13 |
31,060,780 (GRCm39) |
missense |
probably benign |
|
|
R6548:Exoc2
|
UTSW |
13 |
31,010,047 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6692:Exoc2
|
UTSW |
13 |
31,119,490 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6969:Exoc2
|
UTSW |
13 |
31,095,161 (GRCm39) |
missense |
probably benign |
|
|
R7386:Exoc2
|
UTSW |
13 |
31,090,646 (GRCm39) |
splice site |
probably null |
|
|
R7461:Exoc2
|
UTSW |
13 |
31,066,255 (GRCm39) |
missense |
probably benign |
0.32 |
|
R7467:Exoc2
|
UTSW |
13 |
31,109,716 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7473:Exoc2
|
UTSW |
13 |
31,006,613 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7613:Exoc2
|
UTSW |
13 |
31,066,255 (GRCm39) |
missense |
probably benign |
0.32 |
|
R7767:Exoc2
|
UTSW |
13 |
31,060,752 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7793:Exoc2
|
UTSW |
13 |
31,095,161 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7795:Exoc2
|
UTSW |
13 |
31,060,756 (GRCm39) |
nonsense |
probably null |
|
|
R7993:Exoc2
|
UTSW |
13 |
31,090,713 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8085:Exoc2
|
UTSW |
13 |
31,124,686 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8330:Exoc2
|
UTSW |
13 |
31,061,556 (GRCm39) |
missense |
probably benign |
|
|
R8716:Exoc2
|
UTSW |
13 |
31,095,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8735:Exoc2
|
UTSW |
13 |
31,090,822 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8922:Exoc2
|
UTSW |
13 |
31,055,838 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9237:Exoc2
|
UTSW |
13 |
31,048,858 (GRCm39) |
missense |
probably benign |
|
|
R9243:Exoc2
|
UTSW |
13 |
31,109,778 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9365:Exoc2
|
UTSW |
13 |
31,040,697 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9731:Exoc2
|
UTSW |
13 |
31,061,233 (GRCm39) |
missense |
probably benign |
0.06 |
|
| Posted On |
2015-04-16 |
Incidental Mutation