CIDEB
Lipid transferase CIDEB
Also known as: CIDEB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UHD4
- Gene
- CIDEB
- Ensembl
- ENSG00000136305
- Chromosome
- 14
- Canonical length
- 219 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Vesicles
OverviewNCBI Gene
Enables identical protein binding activity. Involved in lipid droplet fusion and positive regulation of apoptotic process. Acts upstream of or within apoptotic process. Located in cytosol and perinuclear region of cytoplasm. Is active in lipid droplet. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
219 residues, UniProt reviewed canonical sequence.
>Q9UHD4|CIDEB
1 MEYLSALNPS DLLRSVSNIS SEFGRRVWTS APPPQRPFRV CDHKRTIRKG LTAATRQELL
61 AKALETLLLN GVLTLVLEED GTAVDSEDFF QLLEDDTCLM VLQSGQSWSP TRSGVLSYGL
121 GRERPKHSKD IARFTFDVYK QNPRDLFGSL NVKATFYGLY SMSCDFQGLG PKKVLRELLR
181 WTSTLLQGLG HMLLGISSTL RHAVEGAEQW QQKGRLHSYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CIDEB 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)
- 0.46
- Highest tissue expression
- 448 nTPM
Expression across tissuesHPA
Tissue
- liver: 448 nTPM
- duodenum: 176 nTPM
- small intestine: 143 nTPM
- spleen: 101 nTPM
- adrenal gland: 43 nTPM
- esophagus: 39 nTPM
Single-cell type
- ependymal cells: 4.7 nCPM
- enterocytes: 3.9 nCPM
- microglia: 3.5 nCPM
- hepatocytes: 3.1 nCPM
- innate lymphoid cells: 2.2 nCPM
- papillary tip epithelial cells: 1.8 nCPM
Immune cell
- NK-cell: 8.6 nTPM
- eosinophil: 7.9 nTPM
- myeloid DC: 7.6 nTPM
- classical monocyte: 7.1 nTPM
- neutrophil: 4.9 nTPM
- gdT-cell: 4.6 nTPM
Brain region
- hypothalamus: 5.2 nTPM
- cerebellum: 3.4 nTPM
- choroid plexus: 3.4 nTPM
- midbrain: 3.2 nTPM
- thalamus: 3 nTPM
- medulla oblongata: 2.8 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)
- 1.92
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.12
- DepMap mean gene effect
- -0.13
- 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
- apoptotic process
- COPII-coated vesicle cargo loading
- execution phase of apoptosis
- intrinsic apoptotic signaling pathway in response to DNA damage
- lipid droplet fusion
- lipid storage
- positive regulation of apoptotic process
- regulation of triglyceride metabolic process
- response to nutrient levels
- very-low-density lipoprotein particle assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CIDEB 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 CIDEB as an antibody target. Whether an autoantibody or antibody against CIDEB could matter depends on whether native CIDEB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CIDEB 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 CIDEB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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