EXOC2 (exocyst complex component 2) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: EXOC2 (exocyst complex component 2) Homo sapiens
Analyze
Symbol: EXOC2
Name: exocyst complex component 2
RGD ID: 1348584
HGNC Page HGNC
Description: Enables protein kinase binding activity and small GTPase binding activity. Involved in regulation of entry of bacterium into host cell. Located in membrane. Part of exocyst.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: exocyst complex component Sec5; FLJ11026; NEDFACH; SEC5; SEC5-like 1; SEC5L1; Sec5p
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl6485,154 - 693,139 (-)EnsemblGRCh38hg38GRCh38
GRCh386485,154 - 693,141 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh376485,154 - 693,139 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366430,138 - 638,109 (-)NCBINCBI36hg18NCBI36
Build 346430,138 - 638,109NCBI
Celera61,712,777 - 1,920,468 (-)NCBI
Cytogenetic Map6p25.3NCBI
HuRef6356,267 - 560,885 (-)NCBIHuRef
CHM1_16486,490 - 695,247 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytosol  (TAS)
exocyst  (IBA,IDA,ISO)
Flemming body  (IEA)
membrane  (HDA)
plasma membrane  (TAS)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:9405631   PMID:9655500   PMID:11493706   PMID:11744922   PMID:12459492   PMID:12477932   PMID:12575951   PMID:12624092   PMID:12687004   PMID:12839989   PMID:14525976   PMID:14574404  
PMID:14702039   PMID:14980502   PMID:15037366   PMID:15302935   PMID:15489334   PMID:15920473   PMID:16344560   PMID:17018283   PMID:17952075   PMID:18483556   PMID:18697830   PMID:19166349  
PMID:19340012   PMID:19885391   PMID:19946888   PMID:20145037   PMID:20379614   PMID:20467437   PMID:20570966   PMID:20579884   PMID:20616560   PMID:20685960   PMID:21197618   PMID:21241894  
PMID:21516116   PMID:21700618   PMID:21873635   PMID:21988832   PMID:22534017   PMID:22658674   PMID:22761837   PMID:22885689   PMID:22939629   PMID:23027611   PMID:23064961   PMID:23470693  
PMID:23548203   PMID:23844030   PMID:24056301   PMID:25241763   PMID:25261932   PMID:25544563   PMID:25921289   PMID:26186194   PMID:26344197   PMID:26350970   PMID:26359301   PMID:26472760  
PMID:26972000   PMID:27173435   PMID:27229929   PMID:27248496   PMID:28514442   PMID:28515276   PMID:28716898   PMID:29467282   PMID:29507755   PMID:29509190   PMID:30737378   PMID:30833792  
PMID:31091453   PMID:31240132   PMID:31353912   PMID:31527615   PMID:32296183   PMID:32639540   PMID:32807901   PMID:34079125  


Genomics

Comparative Map Data
EXOC2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl6485,154 - 693,139 (-)EnsemblGRCh38hg38GRCh38
GRCh386485,154 - 693,141 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh376485,154 - 693,139 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366430,138 - 638,109 (-)NCBINCBI36hg18NCBI36
Build 346430,138 - 638,109NCBI
Celera61,712,777 - 1,920,468 (-)NCBI
Cytogenetic Map6p25.3NCBI
HuRef6356,267 - 560,885 (-)NCBIHuRef
CHM1_16486,490 - 695,247 (-)NCBICHM1_1
Exoc2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391330,972,939 - 31,162,082 (-)NCBIGRCm39mm39
GRCm39 Ensembl1330,997,902 - 31,158,076 (-)Ensembl
GRCm381330,789,516 - 30,974,096 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1330,813,919 - 30,974,093 (-)EnsemblGRCm38mm10GRCm38
MGSCv371330,905,787 - 31,065,916 (-)NCBIGRCm37mm9NCBIm37
MGSCv361330,821,383 - 30,981,512 (-)NCBImm8
Celera1331,027,688 - 31,187,698 (-)NCBICelera
Cytogenetic Map13A3.2NCBI
Exoc2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21733,506,289 - 33,698,246 (+)NCBImRatBN7.2
Rnor_6.0 Ensembl1734,665,872 - 34,842,266 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl1735,396,286 - 35,518,522 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01734,665,810 - 34,842,266 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01736,711,283 - 36,833,357 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.01738,560,757 - 38,736,076 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41739,951,129 - 40,125,385 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11740,115,651 - 40,128,224 (+)NCBI
Celera1733,051,147 - 33,220,181 (+)NCBICelera
Cytogenetic Map17p12NCBI
Exoc2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495546512,330,483 - 12,461,281 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495546512,327,423 - 12,457,171 (+)NCBIChiLan1.0ChiLan1.0
EXOC2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.16435,538 - 636,997 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl6435,538 - 583,027 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v06299,500 - 504,029 (-)NCBIMhudiblu_PPA_v0panPan3
EXOC2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.135859,158 - 1,084,228 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl35859,837 - 1,084,228 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha35872,080 - 1,096,582 (-)NCBI
ROS_Cfam_1.035815,341 - 1,040,700 (-)NCBI
UMICH_Zoey_3.135794,664 - 1,019,577 (-)NCBI
UNSW_CanFamBas_1.035812,292 - 1,037,209 (-)NCBI
UU_Cfam_GSD_1.0352,148,965 - 2,373,864 (-)NCBI
Exoc2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494624,772,372 - 24,963,223 (+)NCBI
SpeTri2.0NW_0049366331,657,326 - 1,848,113 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
EXOC2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl7195,081 - 341,454 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.17195,079 - 341,470 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2748,090 - 194,222 (-)NCBISscrofa10.2Sscrofa10.2susScr3
EXOC2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11771,463,836 - 71,668,429 (+)NCBI
ChlSab1.1 Ensembl1771,473,962 - 71,670,095 (+)Ensembl
Vero_WHO_p1.0NW_023666044410,819 - 613,460 (-)NCBI
Exoc2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462475623,740,248 - 23,878,386 (+)NCBI

Position Markers
RH37466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376621,443 - 621,576UniSTSGRCh37
Build 366566,443 - 566,576RGDNCBI36
Celera61,848,816 - 1,848,949RGD
Cytogenetic Map6p25.3UniSTS
HuRef6491,532 - 491,665UniSTS
GeneMap99-GB4 RH Map614.97UniSTS
RH68754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376625,599 - 625,828UniSTSGRCh37
Build 366570,599 - 570,828RGDNCBI36
Celera61,852,972 - 1,853,201RGD
Cytogenetic Map6p25.3UniSTS
HuRef6495,689 - 495,918UniSTS
GeneMap99-GB4 RH Map614.97UniSTS
AL035370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376621,947 - 622,096UniSTSGRCh37
Build 366566,947 - 567,096RGDNCBI36
Celera61,849,320 - 1,849,469RGD
Cytogenetic Map6p25.3UniSTS
HuRef6492,036 - 492,185UniSTS
RH45976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376582,284 - 582,428UniSTSGRCh37
Build 366527,284 - 527,428RGDNCBI36
Celera61,810,019 - 1,810,163RGD
Cytogenetic Map6p25.3UniSTS
HuRef6452,971 - 453,115UniSTS
GeneMap99-GB4 RH Map612.13UniSTS
SEC5_1861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376485,147 - 486,019UniSTSGRCh37
Build 366430,147 - 431,019RGDNCBI36
Celera61,712,786 - 1,713,658RGD
HuRef6356,276 - 357,148UniSTS
RH68454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376510,843 - 511,001UniSTSGRCh37
Build 366455,843 - 456,001RGDNCBI36
Celera61,738,492 - 1,738,650RGD
Cytogenetic Map6p25.3UniSTS
HuRef6381,936 - 382,094UniSTS
GeneMap99-GB4 RH Map610.05UniSTS
STS-AA019205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376485,152 - 485,376UniSTSGRCh37
Build 366430,152 - 430,376RGDNCBI36
Celera61,712,791 - 1,713,015RGD
Cytogenetic Map6p25.3UniSTS
HuRef6356,281 - 356,505UniSTS
GeneMap99-GB4 RH Map62.87UniSTS
NCBI RH Map615.4UniSTS
D6S962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376101,352,491 - 101,352,617UniSTSGRCh37
Build 366101,459,212 - 101,459,338RGDNCBI36
Celera6101,996,673 - 101,996,807RGD
Cytogenetic Map6p25.3UniSTS
HuRef698,794,831 - 98,794,977UniSTS
HuRef6536,483 - 536,582UniSTS
deCODE Assembly Map6105.06UniSTS
SHGC-35174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376486,449 - 486,550UniSTSGRCh37
Build 366431,449 - 431,550RGDNCBI36
Celera61,714,088 - 1,714,189RGD
Cytogenetic Map6p25.3UniSTS
HuRef6357,578 - 357,679UniSTS
GeneMap99-GB4 RH Map614.07UniSTS
GeneMap99-GB4 RH Map68.57UniSTS
Whitehead-RH Map632.3UniSTS
GeneMap99-G3 RH Map677.0UniSTS
SHGC-64315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376485,159 - 485,356UniSTSGRCh37
Build 366430,159 - 430,356RGDNCBI36
Celera61,712,798 - 1,712,995RGD
Cytogenetic Map6p25.3UniSTS
HuRef6356,288 - 356,485UniSTS
ha3001  
Human AssemblyChrPosition (strand)SourceJBrowse
HuRef6548,748 - 548,969UniSTS
HuRef320,005,238 - 20,005,382UniSTS
HuRef5163,496,742 - 163,497,034UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:827
Count of miRNA genes:595
Interacting mature miRNAs:642
Transcripts:ENST00000230449, ENST00000443083, ENST00000448181, ENST00000475028
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1925 1426 1252 242 1193 129 3623 998 2416 288 1356 1582 130 1 1089 2095 6 2
Low 514 1561 474 382 755 336 734 1198 1318 131 104 31 45 115 693
Below cutoff 4 3 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_047166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_073064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AJ414403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ420556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL031770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL357054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL512308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC080542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA228027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000230449   ⟹   ENSP00000230449
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl6485,154 - 693,139 (-)Ensembl
RefSeq Acc Id: ENST00000443083   ⟹   ENSP00000406400
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl6629,835 - 693,111 (-)Ensembl
RefSeq Acc Id: ENST00000475028
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl6679,143 - 693,108 (-)Ensembl
RefSeq Acc Id: NM_018303   ⟹   NP_060773
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386485,154 - 693,139 (-)NCBI
GRCh376485,138 - 693,141 (-)NCBI
Build 366430,138 - 638,109 (-)NCBI Archive
HuRef6356,267 - 560,885 (-)NCBI
CHM1_16486,490 - 695,247 (-)NCBI
Sequence:
RefSeq Acc Id: NR_073064
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386485,154 - 693,139 (-)NCBI
GRCh376485,138 - 693,141 (-)NCBI
HuRef6356,267 - 560,885 (-)NCBI
CHM1_16486,490 - 695,247 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011018   ⟹   XP_016866507
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386485,158 - 693,113 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011019   ⟹   XP_016866508
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386486,097 - 692,530 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011020   ⟹   XP_016866509
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386485,158 - 693,121 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011021   ⟹   XP_016866510
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386485,158 - 647,927 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011022   ⟹   XP_016866511
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386486,097 - 693,141 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011023   ⟹   XP_016866512
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386486,097 - 693,141 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011024   ⟹   XP_016866513
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386486,097 - 693,113 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011025   ⟹   XP_016866514
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386507,893 - 693,141 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011026   ⟹   XP_016866515
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386534,551 - 693,141 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_060773   ⟸   NM_018303
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866509   ⟸   XM_017011020
- Peptide Label: isoform X1
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866507   ⟸   XM_017011018
- Peptide Label: isoform X1
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866510   ⟸   XM_017011021
- Peptide Label: isoform X1
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866511   ⟸   XM_017011022
- Peptide Label: isoform X1
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866512   ⟸   XM_017011023
- Peptide Label: isoform X1
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866513   ⟸   XM_017011024
- Peptide Label: isoform X1
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866508   ⟸   XM_017011019
- Peptide Label: isoform X1
- UniProtKB: Q96KP1 (UniProtKB/Swiss-Prot),   A0A024QZT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016866514   ⟸   XM_017011025
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016866515   ⟸   XM_017011026
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000230449   ⟸   ENST00000230449
RefSeq Acc Id: ENSP00000406400   ⟸   ENST00000443083
Protein Domains
IPT/TIG   Sec5

Promoters
RGD ID:6804209
Promoter ID:HG_KWN:52076
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000039627,   OTTHUMT00000039628,   UC003MTE.1
Position:
Human AssemblyChrPosition (strand)Source
Build 366637,654 - 638,154 (-)MPROMDB
RGD ID:6871862
Promoter ID:EPDNEW_H9095
Type:initiation region
Name:EXOC2_1
Description:exocyst complex component 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386693,109 - 693,169EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6p25.3(chr6:163083-1951351)x3 copy number gain See cases [RCV000050603] Chr6:163083..1951351 [GRCh38]
Chr6:163083..1951585 [GRCh37]
Chr6:108083..1896584 [NCBI36]
Chr6:6p25.3
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:163083-6062800)x1 copy number loss See cases [RCV000050686] Chr6:163083..6062800 [GRCh38]
Chr6:163083..6063033 [GRCh37]
Chr6:108083..6008032 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3(chr6:163083-918985)x1 copy number loss See cases [RCV000050372] Chr6:163083..918985 [GRCh38]
Chr6:163083..919234 [GRCh37]
Chr6:108083..864234 [NCBI36]
Chr6:6p25.3
pathogenic|uncertain significance|conflicting data from submitters
GRCh38/hg38 6p25.3-23(chr6:389423-13474956)x3 copy number gain See cases [RCV000051896] Chr6:389423..13474956 [GRCh38]
Chr6:389423..13475188 [GRCh37]
Chr6:334423..13583167 [NCBI36]
Chr6:6p25.3-23
pathogenic
GRCh38/hg38 6p25.3-22.3(chr6:106431-18360595)x3 copy number gain See cases [RCV000051869] Chr6:106431..18360595 [GRCh38]
Chr6:106431..18360826 [GRCh37]
Chr6:51431..18468805 [NCBI36]
Chr6:6p25.3-22.3
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:144957-5239181)x3 copy number gain See cases [RCV000051870] Chr6:144957..5239181 [GRCh38]
Chr6:144957..5239414 [GRCh37]
Chr6:89957..5184413 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:107682-4978781)x1 copy number loss See cases [RCV000052159] Chr6:107682..4978781 [GRCh38]
Chr6:107682..4979015 [GRCh37]
Chr6:52682..4924014 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:162883-5979198)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052160]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052160]|See cases [RCV000052160] Chr6:162883..5979198 [GRCh38]
Chr6:162883..5979431 [GRCh37]
Chr6:107883..5924430 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:163083-5875402)x1 copy number loss See cases [RCV000052161] Chr6:163083..5875402 [GRCh38]
Chr6:163083..5875635 [GRCh37]
Chr6:108083..5820634 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.2(chr6:163083-2724611)x1 copy number loss See cases [RCV000052162] Chr6:163083..2724611 [GRCh38]
Chr6:163083..2724845 [GRCh37]
Chr6:108083..2669844 [NCBI36]
Chr6:6p25.3-25.2
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:164633-6284237)x1 copy number loss See cases [RCV000052163] Chr6:164633..6284237 [GRCh38]
Chr6:164633..6284470 [GRCh37]
Chr6:109633..6229469 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:164633-5823601)x1 copy number loss See cases [RCV000052164] Chr6:164633..5823601 [GRCh38]
Chr6:164633..5823834 [GRCh37]
Chr6:109633..5768833 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-24.3(chr6:165675-9036034)x1 copy number loss See cases [RCV000052165] Chr6:165675..9036034 [GRCh38]
Chr6:165675..9036267 [GRCh37]
Chr6:110675..8981266 [NCBI36]
Chr6:6p25.3-24.3
pathogenic
GRCh38/hg38 6p25.3(chr6:163083-588213)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053318]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053318]|See cases [RCV000053318] Chr6:163083..588213 [GRCh38]
Chr6:163083..588213 [GRCh37]
Chr6:108083..533213 [NCBI36]
Chr6:6p25.3
uncertain significance
NM_018303.5(EXOC2):c.2381-509A>G single nucleotide variant Lung cancer [RCV000096928] Chr6:500209 [GRCh38]
Chr6:500209 [GRCh37]
Chr6:6p25.3
uncertain significance
NM_018303.5(EXOC2):c.1667+125G>A single nucleotide variant Lung cancer [RCV000096988] Chr6:564420 [GRCh38]
Chr6:564420 [GRCh37]
Chr6:6p25.3
uncertain significance
NM_018303.6(EXOC2):c.1241G>A (p.Arg414His) single nucleotide variant Malignant tumor of prostate [RCV000149250] Chr6:576834 [GRCh38]
Chr6:576834 [GRCh37]
Chr6:6p25.3
uncertain significance
GRCh38/hg38 6p25.3(chr6:490850-700078)x3 copy number gain See cases [RCV000134311] Chr6:490850..700078 [GRCh38]
Chr6:490850..700078 [GRCh37]
Chr6:435850..645078 [NCBI36]
Chr6:6p25.3
benign
GRCh38/hg38 6p25.3-24.1(chr6:164360-13339881)x3 copy number gain See cases [RCV000134022] Chr6:164360..13339881 [GRCh38]
Chr6:164360..13340113 [GRCh37]
Chr6:109360..13448092 [NCBI36]
Chr6:6p25.3-24.1
pathogenic
GRCh38/hg38 6p25.3(chr6:163083-1365190)x1 copy number loss See cases [RCV000135669] Chr6:163083..1365190 [GRCh38]
Chr6:163083..1365425 [GRCh37]
Chr6:108083..1310424 [NCBI36]
Chr6:6p25.3
uncertain significance
GRCh38/hg38 6p25.3(chr6:163083-2029531)x3 copy number gain See cases [RCV000135617] Chr6:163083..2029531 [GRCh38]
Chr6:163083..2029765 [GRCh37]
Chr6:108083..1974764 [NCBI36]
Chr6:6p25.3
pathogenic|uncertain significance
GRCh38/hg38 6p25.3-24.3(chr6:163083-9525496)x3 copy number gain See cases [RCV000136567] Chr6:163083..9525496 [GRCh38]
Chr6:163083..9525729 [GRCh37]
Chr6:108083..9633715 [NCBI36]
Chr6:6p25.3-24.3
pathogenic
GRCh38/hg38 6p25.3(chr6:265806-588274)x3 copy number gain See cases [RCV000135986] Chr6:265806..588274 [GRCh38]
Chr6:265806..588274 [GRCh37]
Chr6:210806..533274 [NCBI36]
Chr6:6p25.3
benign
GRCh38/hg38 6p25.3-25.1(chr6:152634-5315679)x1 copy number loss See cases [RCV000137496] Chr6:152634..5315679 [GRCh38]
Chr6:152634..5315912 [GRCh37]
Chr6:97634..5260911 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.2(chr6:163083-3459607)x1 copy number loss See cases [RCV000138184] Chr6:163083..3459607 [GRCh38]
Chr6:163083..3459841 [GRCh37]
Chr6:108083..3404840 [NCBI36]
Chr6:6p25.3-25.2
pathogenic
GRCh38/hg38 6p25.3-22.3(chr6:152634-15732163)x3 copy number gain See cases [RCV000138121] Chr6:152634..15732163 [GRCh38]
Chr6:152634..15732394 [GRCh37]
Chr6:97634..15840373 [NCBI36]
Chr6:6p25.3-22.3
likely benign
GRCh38/hg38 6p25.3-25.1(chr6:152634-6027547)x3 copy number gain See cases [RCV000138716] Chr6:152634..6027547 [GRCh38]
Chr6:152634..6027780 [GRCh37]
Chr6:97634..5972779 [NCBI36]
Chr6:6p25.3-25.1
likely pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:152634-6027547)x1 copy number loss See cases [RCV000138717] Chr6:152634..6027547 [GRCh38]
Chr6:152634..6027780 [GRCh37]
Chr6:97634..5972779 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-22.3(chr6:155807-17058414)x3 copy number gain See cases [RCV000140307] Chr6:155807..17058414 [GRCh38]
Chr6:155807..17058645 [GRCh37]
Chr6:100807..17166624 [NCBI36]
Chr6:6p25.3-22.3
pathogenic
GRCh38/hg38 6p25.3(chr6:170426-1621983)x1 copy number loss See cases [RCV000140309] Chr6:170426..1621983 [GRCh38]
Chr6:170426..1622218 [GRCh37]
Chr6:115426..1567217 [NCBI36]
Chr6:6p25.3
pathogenic
GRCh38/hg38 6p25.3-24.2(chr6:156974-11550817)x3 copy number gain See cases [RCV000142295] Chr6:156974..11550817 [GRCh38]
Chr6:156974..11551050 [GRCh37]
Chr6:101974..11659036 [NCBI36]
Chr6:6p25.3-24.2
likely pathogenic
GRCh38/hg38 6p25.3-24.3(chr6:156974-7122759)x1 copy number loss See cases [RCV000142299] Chr6:156974..7122759 [GRCh38]
Chr6:156974..7122992 [GRCh37]
Chr6:101974..7067991 [NCBI36]
Chr6:6p25.3-24.3
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:156974-4907692)x1 copy number loss See cases [RCV000142304] Chr6:156974..4907692 [GRCh38]
Chr6:156974..4907926 [GRCh37]
Chr6:101974..4852925 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:152634-6289804)x1 copy number loss See cases [RCV000142916] Chr6:152634..6289804 [GRCh38]
Chr6:152634..6290037 [GRCh37]
Chr6:97634..6235036 [NCBI36]
Chr6:6p25.3-25.1
pathogenic
GRCh38/hg38 6p25.3-25.1(chr6:156974-4946857)x3 copy number gain See cases [RCV000143375] Chr6:156974..4946857 [GRCh38]
Chr6:156974..4947091 [GRCh37]
Chr6:101974..4892090 [NCBI36]
Chr6:6p25.3-25.1
uncertain significance
GRCh38/hg38 6p25.3-23(chr6:152634-14417003)x3 copy number gain See cases [RCV000143334] Chr6:152634..14417003 [GRCh38]
Chr6:152634..14417234 [GRCh37]
Chr6:97634..14525213 [NCBI36]
Chr6:6p25.3-23
pathogenic
GRCh38/hg38 6p25.3-24.1(chr6:156974-13081201)x3 copy number gain See cases [RCV000143698] Chr6:156974..13081201 [GRCh38]
Chr6:156974..13081433 [GRCh37]
Chr6:101974..13189419 [NCBI36]
Chr6:6p25.3-24.1
likely pathogenic
GRCh38/hg38 6p25.3-23(chr6:156974-13855925)x1 copy number loss See cases [RCV000143782] Chr6:156974..13855925 [GRCh38]
Chr6:156974..13856156 [GRCh37]
Chr6:101974..13964135 [NCBI36]
Chr6:6p25.3-23
pathogenic
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3 copy number gain See cases [RCV000143497] Chr6:156974..46789291 [GRCh38]
Chr6:156974..46757028 [GRCh37]
Chr6:101974..46864987 [NCBI36]
Chr6:6p25.3-12.3
pathogenic
GRCh38/hg38 6p25.3(chr6:163083-918985)x1 copy number loss See cases [RCV000148109] Chr6:163083..918985 [GRCh38]
Chr6:163083..919234 [GRCh37]
Chr6:108083..864234 [NCBI36]
Chr6:6p25.3
pathogenic
GRCh37/hg19 6p25.3-25.2(chr6:255350-3189972)x3 copy number gain Brachydactyly type E1 [RCV000234962] Chr6:255350..3189972 [GRCh37]
Chr6:6p25.3-25.2
pathogenic
GRCh37/hg19 6p25.3-24.1(chr6:204009-11608587)x1 copy number loss See cases [RCV000240433] Chr6:204009..11608587 [GRCh37]
Chr6:6p25.3-24.1
pathogenic
GRCh37/hg19 6p25.3(chr6:180959-2180143)x1 copy number loss See cases [RCV000240471] Chr6:180959..2180143 [GRCh37]
Chr6:6p25.3
pathogenic
GRCh37/hg19 6p25.3-25.1(chr6:204009-6447311)x1 copy number loss See cases [RCV000240475] Chr6:204009..6447311 [GRCh37]
Chr6:6p25.3-25.1
pathogenic
GRCh37/hg19 6p25.3-22.3(chr6:168775-24023234)x3 copy number gain See cases [RCV000240460] Chr6:168775..24023234 [GRCh37]
Chr6:6p25.3-22.3
pathogenic
GRCh37/hg19 6p25.3-22.3(chr6:302272-18375047)x3 copy number gain See cases [RCV000446145] Chr6:302272..18375047 [GRCh37]
Chr6:6p25.3-22.3
pathogenic
GRCh37/hg19 6p25.3(chr6:525487-780702)x3 copy number gain See cases [RCV000447050] Chr6:525487..780702 [GRCh37]
Chr6:6p25.3
uncertain significance
GRCh37/hg19 6p25.3-24.3(chr6:156974-8349511)x3 copy number gain See cases [RCV000445742] Chr6:156974..8349511 [GRCh37]
Chr6:6p25.3-24.3
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-25.2(chr6:383951-4183288)x1 copy number loss See cases [RCV000510370] Chr6:383951..4183288 [GRCh37]
Chr6:6p25.3-25.2
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3(chr6:195229-2117379)x1 copy number loss See cases [RCV000510359] Chr6:195229..2117379 [GRCh37]
Chr6:6p25.3
pathogenic
GRCh37/hg19 6p25.3(chr6:156974-2030623)x1 copy number loss See cases [RCV000511982] Chr6:156974..2030623 [GRCh37]
Chr6:6p25.3
pathogenic
GRCh37/hg19 6p25.3-25.1(chr6:156974-6417749)x1 copy number loss See cases [RCV000511093] Chr6:156974..6417749 [GRCh37]
Chr6:6p25.3-25.1
pathogenic
GRCh37/hg19 6p25.3-25.2(chr6:156974-3398920)x1 copy number loss not provided [RCV000682627] Chr6:156974..3398920 [GRCh37]
Chr6:6p25.3-25.2
pathogenic
GRCh37/hg19 6p25.3(chr6:514917-1136513)x3 copy number gain not provided [RCV000682631] Chr6:514917..1136513 [GRCh37]
Chr6:6p25.3
likely benign
GRCh37/hg19 6p25.3-23(chr6:156974-13502033)x3 copy number gain not provided [RCV000682628] Chr6:156974..13502033 [GRCh37]
Chr6:6p25.3-23
pathogenic
GRCh37/hg19 6p25.3-22.3(chr6:156974-21955964)x3 copy number gain not provided [RCV000682629] Chr6:156974..21955964 [GRCh37]
Chr6:6p25.3-22.3
pathogenic
GRCh37/hg19 6p25.3(chr6:462405-866857)x3 copy number gain not provided [RCV000682630] Chr6:462405..866857 [GRCh37]
Chr6:6p25.3
likely benign
Single allele duplication not provided [RCV000677944] Chr6:168775..24023234 [GRCh37]
Chr6:6p25.3-22.3
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3(chr6:108666-1505511)x1 copy number loss not provided [RCV000745402] Chr6:108666..1505511 [GRCh37]
Chr6:6p25.3
pathogenic
GRCh37/hg19 6p25.3(chr6:464093-861929)x3 copy number gain not provided [RCV000745415] Chr6:464093..861929 [GRCh37]
Chr6:6p25.3
benign
GRCh37/hg19 6p25.3(chr6:595257-596160)x1 copy number loss not provided [RCV000745416] Chr6:595257..596160 [GRCh37]
Chr6:6p25.3
benign
GRCh37/hg19 6p25.3(chr6:595257-598095)x1 copy number loss not provided [RCV000745417] Chr6:595257..598095 [GRCh37]
Chr6:6p25.3
benign
GRCh37/hg19 6p25.3(chr6:595763-602414)x1 copy number loss not provided [RCV000745418] Chr6:595763..602414 [GRCh37]
Chr6:6p25.3
benign
GRCh37/hg19 6p25.3(chr6:595998-602414)x1 copy number loss not provided [RCV000745419] Chr6:595998..602414 [GRCh37]
Chr6:6p25.3
benign
GRCh37/hg19 6p25.3(chr6:666535-672798)x0 copy number loss not provided [RCV000745420] Chr6:666535..672798 [GRCh37]
Chr6:6p25.3
benign
NM_018303.6(EXOC2):c.2409G>T (p.Leu803=) single nucleotide variant not provided [RCV000972421] Chr6:499672 [GRCh38]
Chr6:499672 [GRCh37]
Chr6:6p25.3
benign
NM_018303.6(EXOC2):c.1554C>T (p.Arg518=) single nucleotide variant not provided [RCV000901385] Chr6:564658 [GRCh38]
Chr6:564658 [GRCh37]
Chr6:6p25.3
benign
NM_018303.6(EXOC2):c.1759G>A (p.Val587Ile) single nucleotide variant not provided [RCV000884562] Chr6:564063 [GRCh38]
Chr6:564063 [GRCh37]
Chr6:6p25.3
benign
NM_018303.6(EXOC2):c.-43-18555A>G single nucleotide variant not provided [RCV000946909] Chr6:656416 [GRCh38]
Chr6:656416 [GRCh37]
Chr6:6p25.3
benign
NM_018303.6(EXOC2):c.-43-18678G>T single nucleotide variant not provided [RCV000975098] Chr6:656539 [GRCh38]
Chr6:656539 [GRCh37]
Chr6:6p25.3
benign
GRCh37/hg19 6p25.3-22.3(chr6:156974-23221621)x3 copy number gain not provided [RCV000848108] Chr6:156974..23221621 [GRCh37]
Chr6:6p25.3-22.3
pathogenic
GRCh37/hg19 6p25.3(chr6:156974-2208360)x1 copy number loss not provided [RCV001005754] Chr6:156974..2208360 [GRCh37]
Chr6:6p25.3
pathogenic
GRCh37/hg19 6p25.3(chr6:614445-859115)x3 copy number gain not provided [RCV001005756] Chr6:614445..859115 [GRCh37]
Chr6:6p25.3
likely benign
NM_018303.6(EXOC2):c.-43-18820C>T single nucleotide variant not provided [RCV000907829] Chr6:656681 [GRCh38]
Chr6:656681 [GRCh37]
Chr6:6p25.3
benign
NM_018303.6(EXOC2):c.999A>G (p.Glu333=) single nucleotide variant not provided [RCV000956357] Chr6:598095 [GRCh38]
Chr6:598095 [GRCh37]
Chr6:6p25.3
benign
GRCh37/hg19 6p25.3(chr6:378555-687754)x3 copy number gain not provided [RCV001005755] Chr6:378555..687754 [GRCh37]
Chr6:6p25.3
likely benign
GRCh37/hg19 6p25.3(chr6:152849-1888703)x1 copy number loss See cases [RCV001263042] Chr6:152849..1888703 [GRCh37]
Chr6:6p25.3
pathogenic
GRCh37/hg19 6p25.3-25.2(chr6:302183-3290583)x3 copy number gain not provided [RCV001259379] Chr6:302183..3290583 [GRCh37]
Chr6:6p25.3-25.2
pathogenic
NM_018303.6(EXOC2):c.1309C>T (p.Arg437Ter) AND NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES single nucleotide variant NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA [RCV001387535] Chr6:576766 [GRCh38]
Chr6:576766 [GRCh37]
Chr6:6p25.3
pathogenic
NM_018303.6(EXOC2):c.389G>A (p.Arg130His) AND NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES single nucleotide variant NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA [RCV001387536] Chr6:629868 [GRCh38]
Chr6:629868 [GRCh37]
Chr6:6p25.3
pathogenic
NM_018303.6(EXOC2):c.1739T>C (p.Leu580Ser) AND NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES single nucleotide variant NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA [RCV001387537] Chr6:564083 [GRCh38]
Chr6:564083 [GRCh37]
Chr6:6p25.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24968 AgrOrtholog
COSMIC EXOC2 COSMIC
Ensembl Genes ENSG00000112685 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000230449 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000406400 UniProtKB/TrEMBL
Ensembl Transcript ENST00000230449 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000443083 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000112685 GTEx
HGNC ID HGNC:24968 ENTREZGENE
Human Proteome Map EXOC2 Human Proteome Map
InterPro EXOC2/Sec5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EXOC2/Sec5_N_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_E-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IPT_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55770 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 55770 ENTREZGENE
OMIM 615329 OMIM
  619306 OMIM
PANTHER PTHR13043 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Sec5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TIG UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134862170 PharmGKB
Superfamily-SCOP SSF81296 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024QZT2 ENTREZGENE, UniProtKB/TrEMBL
  EXOC2_HUMAN UniProtKB/Swiss-Prot
  Q2MDF5_HUMAN UniProtKB/TrEMBL
  Q96KP1 ENTREZGENE
UniProt Secondary B2RBE6 UniProtKB/Swiss-Prot
  Q5JPC8 UniProtKB/Swiss-Prot
  Q96AN6 UniProtKB/Swiss-Prot
  Q9NUZ8 UniProtKB/Swiss-Prot
  Q9UJM7 UniProtKB/Swiss-Prot