SH3GL3
Endophilin-A3
Also known as: CNSA3, EEN-B2, HsT19371, SH3D2C, SH3G3_HUMAN, SH3P13
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99963
- Gene
- SH3GL3
- Ensembl
- ENSG00000140600
- Chromosome
- 15
- Canonical length
- 347 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Enables identical protein binding activity. Predicted to be involved in central nervous system development and signal transduction. Predicted to be located in acrosomal vesicle and early endosome membrane. Predicted to be part of early endosome. Predicted to be active in several cellular components, including glutamatergic synapse; postsynaptic density, intracellular component; and postsynaptic endosome. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
347 residues, UniProt reviewed canonical sequence.
>Q99963|SH3GL3
1 MSVAGLKKQF HKASQLFSEK ISGAEGTKLD DEFLDMERKI DVTNKVVAEI LSKTTEYLQP
61 NPAYRAKLGM LNTVSKIRGQ VKTTGYPQTE GLLGDCMLKY GKELGEDSTF GNALIEVGES
121 MKLMAEVKDS LDINVKQTFI DPLQLLQDKD LKEIGHHLKK LEGRRLDYDY KKKRVGKIPD
181 EEVRQAVEKF EESKELAERS MFNFLENDVE QVSQLAVFIE AALDYHRQST EILQELQSKL
241 QMRISAASSV PRREYKPRPV KRSSSELNGV STTSVVKTTG SNIPMDQPCC RGLYDFEPEN
301 QGELGFKEGD IITLTNQIDE NWYEGMIHGE SGFFPINYVE VIVPLPQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SH3GL3 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 57 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 57 nTPM
- midbrain: 42 nTPM
- hippocampal formation: 40 nTPM
- amygdala: 32 nTPM
- hypothalamus: 29 nTPM
- cerebral cortex: 28 nTPM
Single-cell type
- late spermatids: 2,396 nCPM
- oligodendrocytes: 1,311 nCPM
- early spermatids: 804 nCPM
- retinal horizontal cells: 539 nCPM
- loop of henle epithelial cells: 328 nCPM
- brain inhibitory neurons: 285 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 127 nTPM
- basal ganglia: 82 nTPM
- cerebral cortex: 76 nTPM
- midbrain: 70 nTPM
- pons: 66 nTPM
- hypothalamus: 66 nTPM
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)
- 0.8
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.21
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
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
- central nervous system development
- endocytosis
- negative regulation of clathrin-dependent endocytosis
- positive regulation of neuron differentiation
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SH3GL3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SH3GL3 as an antibody target. Whether an autoantibody or antibody against SH3GL3 could matter depends on whether native SH3GL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SH3GL3 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 SH3GL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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