CD34
Hematopoietic progenitor cell antigen CD34
Also known as: CD34_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P28906
- Gene
- CD34
- Ensembl
- ENSG00000174059
- Chromosome
- 1
- Canonical length
- 385 aa
- Protein class
- CD markers, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cell Junctions
OverviewNCBI Gene
The protein encoded by this gene may play a role in the attachment of stem cells to the bone marrow extracellular matrix or to stromal cells. This single-pass membrane protein is highly glycosylated and phosphorylated by protein kinase C. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
Canonical amino-acid sequenceUniProt
385 residues, UniProt reviewed canonical sequence.
>P28906|CD34
1 MLVRRGARAG PRMPRGWTAL CLLSLLPSGF MSLDNNGTAT PELPTQGTFS NVSTNVSYQE
61 TTTPSTLGST SLHPVSQHGN EATTNITETT VKFTSTSVIT SVYGNTNSSV QSQTSVISTV
121 FTTPANVSTP ETTLKPSLSP GNVSDLSTTS TSLATSPTKP YTSSSPILSD IKAEIKCSGI
181 REVKLTQGIC LEQNKTSSCA EFKKDRGEGL ARVLCGEEQA DADAGAQVCS LLLAQSEVRP
241 QCLLLVLANR TEISSKLQLM KKHQSDLKKL GILDFTEQDV ASHQSYSQKT LIALVTSGAL
301 LAVLGITGYF LMNRRSWSPT GERLGEDPYY TENGGGQGYS SGPGTSPEAQ GKASVNRGAQ
361 ENGTGQATSR NGHSARQHVV ADTELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CD34 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)
- 0.59
- Highest tissue expression
- 206 nTPM
Expression across tissuesHPA
Tissue
- placenta: 206 nTPM
- adipose tissue: 193 nTPM
- heart muscle: 147 nTPM
- breast: 118 nTPM
- fallopian tube: 93 nTPM
- cervix: 90 nTPM
Single-cell type
- vascular endothelial cells: 311 nCPM
- fibro-adipogenic progenitors: 168 nCPM
- leydig cells: 165 nCPM
- peritubular myoid cells: 137 nCPM
- fibroblasts: 133 nCPM
- mesothelial cells: 114 nCPM
Immune cell
- basophil: 0.2 nTPM
- neutrophil: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- total PBMC: 0.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- thalamus: 33 nTPM
- pons: 28 nTPM
- medulla oblongata: 25 nTPM
- midbrain: 25 nTPM
- amygdala: 24 nTPM
- cerebral cortex: 23 nTPM
ReferencesPubMed · IEDB
Publications for CD34 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
4 publications
- Immunophenotyping of dermal spindle cell tumors: diagnostic value of monocyte marker Ki-M1p and histogenetic considerations.
1997 · Am J Surg Pathol · RCR 1.6 · 34 citations - CD34 expression as a novel marker of transformed mesangial cells in biopsied glomerular diseases.
1999 · J Pathol · RCR 0.5 · 17 citations - Erythroblastic islands in the bone marrow of patients with immune-related pancytopenia.
2014 · PLoS One · RCR 0.5 · 14 citations - Anti-CD34+ Fabs generated against hematopoietic stem cells in HIV-derived combinatorial immunoglobulin library suggest antigen-selected autoantibodies.
1998 · Mol Immunol · RCR 0.2 · 6 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 1.02
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.77
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
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
- cell motility
- cell-cell adhesion
- cell-matrix adhesion
- endothelial cell proliferation
- endothelium development
- glomerular endothelium development
- glomerular filtration
- hematopoietic stem cell proliferation
- hemopoiesis
- leukocyte migration
- mesangial cell-matrix adhesion
- negative regulation of gene expression
- negative regulation of interleukin-2 production
- paracrine signaling
- positive regulation of angiogenesis
- positive regulation of gene expression
- positive regulation of granulocyte colony-stimulating factor production
- positive regulation of odontogenesis
- positive regulation of vasculogenesis
- signal transduction
- stem cell proliferation
- tissue homeostasis
- transdifferentiation
- vascular wound healing
- extracellular exosome assembly
- metanephric glomerular mesangial cell differentiation
Molecular functions
- carbohydrate binding
- RNA polymerase II-specific DNA-binding transcription factor binding
- sulfate binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- CD34/Podocalyxin
- CD34/Podocalyxin family
- CD34 antigen
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CD34 as an antibody target. Whether an autoantibody or antibody against CD34 could matter depends on whether native CD34 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CD34 is annotated at the cell surface, where native CD34 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 CD34 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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