EXOC3L2
Exocyst complex component 3-like protein 2
Also known as: EX3L2_HUMAN
Protein identityUniProt · HPA
- UniProt accession
- Q2M3D2
- Gene
- EXOC3L2
- Canonical length
- 802 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
No narrative summary is available for EXOC3L2 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
802 residues, UniProt reviewed canonical sequence.
>Q2M3D2|EXOC3L2
1 MPILKNLGVS DPKVPRAGTL PLRSSRNPFE EVSGLEEEEA GELGSLPNGT SCRRRATLEK
61 LAGLAPFRLG WAPGRRAGSP GDGQPRSFLG RVLVPGIRRS SADFGLLARL HGTRAHGDEE
121 AAGEAARRLA FLRLGRGSKP QRASLAERVV PAGEAAPEPP PKVPEPPKMK EPLSVLEILS
181 LIQQRELARA DEHILELEAE ELAPSRGGAP GPPKAEGAGG GRRARDVALL YEALQRELWA
241 LVRETLAGPG PGACAGAGAV AQLGQVLVQE EAADGRRGPG AARKLRARWA EAVARAARER
301 LEAAAPGAPG GLAGQLEALR ARLLEDMAVV RGRLAPAYPA GLGAFGVYLR GYHGALAEWL
361 GASARRRLPL ADRYALLHWH NQVYPREVLG LVDMAALENG ELGPLLSPGT LRGLEDECVT
421 DVKAQTRAAL LRVLQEDEEH WGSLEDQPSS LAQDVCELLE EHTERAPRIS QEFGERMAHC
481 CLGGLAEFLQ SFQQRVERFH ENPAVREMLP DTYISKTIAL VNCGPPLRAL AERLARVGPP
541 ESEPAREASA SALDHVTRLC HRVVANLLFQ ELQPHFNKLM RRKWLSSPEA LDGIVGTLGA
601 QALALRRMQD EPYQALVAEL HRRALVEYVR PLLRGRLRCS SARTRSRVAG RLREDAAQLQ
661 RLFRRLESQA SWLDAVVPHL AEVMQLEDTP SIQVEVGVLV RDYPDIRQKH VAALLDIRGL
721 RNTAARQEIL AVARDLELSE EGALSPPRDR AFFADIPVPR PSFCLSLPLF LGRLPLSRLA
781 RPSLACLPRP RPPSLARPRA QRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EXOC3L2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.41
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- kidney: 21 nTPM
- thyroid gland: 18 nTPM
- adrenal gland: 9 nTPM
- spleen: 8.7 nTPM
- pituitary gland: 5.4 nTPM
- prostate: 5.3 nTPM
Single-cell type
- megakaryocytes: 80 nCPM
- vascular endothelial cells: 60 nCPM
- oocytes: 46 nCPM
- platelets: 33 nCPM
- megakaryocyte progenitors: 27 nCPM
- undifferentiated spermatogonia: 17 nCPM
Immune cell
- basophil: 0.3 nTPM
- neutrophil: 0.3 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- choroid plexus: 4.8 nTPM
- medulla oblongata: 3 nTPM
- basal ganglia: 2.7 nTPM
- white matter: 2.7 nTPM
- midbrain: 2.6 nTPM
- pons: 2.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about EXOC3L2.
Disease | AllUniProt
Conditions EXOC3L2 is implicated in, by any mechanism.
- Brain malformation renal syndrome (BMRS) MIM:620943
Disease | GeneticClinVar
3 pathogenic / likely-pathogenic of 138 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Meckel-Gruber syndrome
- Brain malformation renal syndrome
- Meckel-like syndrome
- EXOC3L2-related brain malformations and/or renal disease
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.43
- gnomAD pLI
- 0.76
- gnomAD missense Z
- 0.66
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads EXOC3L2 as an antibody target. Whether an autoantibody or antibody against EXOC3L2 could matter depends on whether native EXOC3L2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EXOC3L2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label EXOC3L2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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