CEND1
Cell cycle exit and neuronal differentiation protein 1
Also known as: BM88, CEND_HUMAN, FLJ90066
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N111
- Gene
- CEND1
- Ensembl
- ENSG00000184524
- Chromosome
- 11
- Canonical length
- 149 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Mitochondria
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene is a neuron-specific protein. The similar protein in pig enhances neuroblastoma cell differentiation in vitro and may be involved in neuronal differentiation in vivo. Multiple pseudogenes have been reported for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
149 residues, UniProt reviewed canonical sequence.
>Q8N111|CEND1
1 MESRGKSASS PKPDTKVPQV TTEAKVPPAA DGKAPLTKPS KKEAPAEKQQ PPAAPTTAPA
61 KKTSAKADPA LLNNHSNLKP APTVPSSPDA TPEPKGPGDG AEEDEAASGG PGGRGPWSCE
121 NFNPLLVAGG VAVAAIALIL GVAFLVRKKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CEND1 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
- 1
- Mean surface accessibility (rSASA)
- 0.69
- Highest tissue expression
- 278 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 278 nTPM
- cerebellum: 224 nTPM
- hippocampal formation: 168 nTPM
- basal ganglia: 167 nTPM
- amygdala: 147 nTPM
- midbrain: 140 nTPM
Single-cell type
- brain excitatory neurons: 70 nCPM
- other brain neurons: 58 nCPM
- brain inhibitory neurons: 53 nCPM
- retinal amacrine cells: 52 nCPM
- retinal bipolar cells: 51 nCPM
- retinal horizontal cells: 42 nCPM
Immune cell
- memory B-cell: 0.8 nTPM
- T-reg: 0.6 nTPM
- gdT-cell: 0.2 nTPM
- intermediate monocyte: 0.2 nTPM
- memory CD4 T-cell: 0.2 nTPM
- memory CD8 T-cell: 0.1 nTPM
Brain region
- cerebral cortex: 541 nTPM
- white matter: 296 nTPM
- thalamus: 282 nTPM
- pons: 276 nTPM
- medulla oblongata: 242 nTPM
- hypothalamus: 228 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CEND1.
Disease | ImmuneIEDB
Conditions an epitope on CEND1 was assayed in.
- brain glioma T cell
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)
- 1.03
- gnomAD pLI
- 0.6
- gnomAD missense Z
- -0.19
- DepMap mean gene effect
- -0.27
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adult walking behavior
- cerebellar Purkinje cell differentiation
- negative regulation of cerebellar granule cell precursor proliferation
- cerebellar granular layer maturation
- radial glia guided migration of cerebellar granule cell
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cell cycle exit/neuronal differentiation protein 1
- Cell cycle exit and neuronal differentiation protein 1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CEND1 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 CEND1 as an antibody target. Whether an autoantibody or antibody against CEND1 could matter depends on whether native CEND1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CEND1 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 CEND1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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