ITM2C
Integral membrane protein 2C
Also known as: BRI3, BRICD2C, E25, hRPC.1050_D_4, ITM2C_HUMAN, ITM3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NQX7
- Gene
- ITM2C
- Ensembl
- ENSG00000135916
- Chromosome
- 2
- Canonical length
- 267 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Enables amyloid-beta binding activity. Involved in negative regulation of neuron projection development and neuron differentiation. Located in several cellular components, including Golgi apparatus; lysosome; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
267 residues, UniProt reviewed canonical sequence.
>Q9NQX7|ITM2C
1 MVKISFQPAV AGIKGDKADK ASASAPAPAS ATEILLTPAR EEQPPQHRSK RGGSVGGVCY
61 LSMGMVVLLM GLVFASVYIY RYFFLAQLAR DNFFRCGVLY EDSLSSQVRT QMELEEDVKI
121 YLDENYERIN VPVPQFGGGD PADIIHDFQR GLTAYHDISL DKCYVIELNT TIVLPPRNFW
181 ELLMNVKRGT YLPQTYIIQE EMVVTEHVSD KEALGSFIYH LCNGKDTYRL RRRATRRRIN
241 KRGAKNCNAI RHFENTFVVE TLICGVVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ITM2C 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.41
- Highest tissue expression
- 1,021 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 1,021 nTPM
- cerebral cortex: 948 nTPM
- amygdala: 836 nTPM
- midbrain: 716 nTPM
- hypothalamus: 681 nTPM
- colon: 663 nTPM
Single-cell type
- colonocytes: 2,243 nCPM
- goblet cells: 864 nCPM
- pdcs: 836 nCPM
- enteric transient amplifying cells: 791 nCPM
- plasma cells: 657 nCPM
- enteric stem cells: 635 nCPM
Immune cell
- plasmacytoid DC: 2,468 nTPM
- eosinophil: 292 nTPM
- memory B-cell: 186 nTPM
- naive B-cell: 95 nTPM
- basophil: 77 nTPM
- myeloid DC: 69 nTPM
Brain region
- thalamus: 1,335 nTPM
- hypothalamus: 1,313 nTPM
- midbrain: 1,077 nTPM
- medulla oblongata: 1,013 nTPM
- spinal cord: 976 nTPM
- basal ganglia: 929 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)
- 0.5
- gnomAD pLI
- 0.7
- gnomAD missense Z
- 0.38
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of amyloid precursor protein biosynthetic process
- negative regulation of neuron projection development
- neuron differentiation
- positive regulation of extrinsic apoptotic signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ITM2C 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 ITM2C as an antibody target. Whether an autoantibody or antibody against ITM2C could matter depends on whether native ITM2C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ITM2C is annotated at the cell surface, where native ITM2C is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ITM2C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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