CD164
Sialomucin core protein 24
Also known as: DFNA66, MGC-24, MUC-24, MUC24_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q04900
- Gene
- CD164
- Ensembl
- ENSG00000135535
- Chromosome
- 6
- Canonical length
- 197 aa
- Protein class
- CD markers, Disease related genes, Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins
- Secretome location
- Intracellular and membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a transmembrane sialomucin and cell adhesion molecule that regulates the proliferation, adhesion and migration of hematopoietic progenitor cells. The encoded protein also interacts with the C-X-C chemokine receptor type 4 and may regulate muscle development. Elevated expression of this gene has been observed in human patients with Sezary syndrome, a type of blood cancer, and a mutation in this gene may be associated with impaired hearing. [provided by RefSeq, Oct 2016]
Canonical amino-acid sequenceUniProt
197 residues, UniProt reviewed canonical sequence.
>Q04900|CD164
1 MSRLSRSLLW AATCLGVLCV LSADKNTTQH PNVTTLAPIS NVTSAPVTSL PLVTTPAPET
61 CEGRNSCVSC FNVSVVNTTC FWIECKDESY CSHNSTVSDC QVGNTTDFCS VSTATPVPTA
121 NSTAKPTVQP SPSTTSKTVT TSGTTNNTVT PTSQPVRKST FDAASFIGGI VLVLGVQAVI
181 FFLYKFCKSK ERNYHTLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CD164 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)
- 0.58
- Highest tissue expression
- 337 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 337 nTPM
- salivary gland: 286 nTPM
- kidney: 278 nTPM
- small intestine: 262 nTPM
- stomach: 258 nTPM
- rectum: 254 nTPM
Single-cell type
- syncytiotrophoblasts: 886 nCPM
- parietal cells: 732 nCPM
- kupffer cells: 537 nCPM
- extravillous trophoblasts: 537 nCPM
- neutrophil progenitors: 535 nCPM
- retinal pigment epithelial cells: 529 nCPM
Immune cell
- total PBMC: 413 nTPM
- basophil: 350 nTPM
- NK-cell: 256 nTPM
- plasmacytoid DC: 214 nTPM
- intermediate monocyte: 199 nTPM
- non-classical monocyte: 199 nTPM
Brain region
- white matter: 104 nTPM
- choroid plexus: 100 nTPM
- medulla oblongata: 94 nTPM
- hypothalamus: 77 nTPM
- cerebellum: 75 nTPM
- midbrain: 73 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CD164.
Disease | AllUniProt
Conditions CD164 is implicated in, by any mechanism.
- Deafness, autosomal dominant, 66 (DFNA66) MIM:616969
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)
- 0.61
- gnomAD pLI
- 0.49
- gnomAD missense Z
- -0.26
- DepMap mean gene effect
- 0
- 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
- cell adhesion
- hemopoiesis
- heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules
- immune response
- muscle organ development
- negative regulation of cell adhesion
- signal transduction
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CD164 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 CD164 as an antibody target. Whether an autoantibody or antibody against CD164 could matter depends on whether native CD164 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CD164 is annotated at the cell surface, where native CD164 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 CD164 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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