Seroatlas · Human Serome Atlas

DLK2

Protein delta homolog 2

Also known as: DLK2_HUMAN, EGFL9, MGC2487

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q6UY11
Gene
DLK2
Ensembl
ENSG00000171462
Chromosome
6
Canonical length
383 aa
Protein class
Predicted membrane proteins
Subcellular location
Nucleoplasm,Nucleoli,Vesicles

OverviewNCBI Gene

Predicted to enable Notch binding activity. Involved in negative regulation of Notch signaling pathway. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

383 residues, UniProt reviewed canonical sequence.

>Q6UY11|DLK2
     1  MPSGCRCLHL VCLLCILGAP GQPVRADDCS SHCDLAHGCC APDGSCRCDP GWEGLHCERC
    61  VRMPGCQHGT CHQPWQCICH SGWAGKFCDK DEHICTTQSP CQNGGQCMYD GGGEYHCVCL
   121  PGFHGRDCER KAGPCEQAGS PCRNGGQCQD DQGFALNFTC RCLVGFVGAR CEVNVDDCLM
   181  RPCANGATCL DGINRFSCLC PEGFAGRFCT INLDDCASRP CQRGARCRDR VHDFDCLCPS
   241  GYGGKTCELV LPVPDPPTTV DTPLGPTSAV VVPATGPAPH SAGAGLLRIS VKEVVRRQEA
   301  GLGEPSLVAL VVFGALTAAL VLATVLLTLR AWRRGVCPPG PCCYPAPHYA PACQDQECQV
   361  SMLPAGLPLP RDLPPEPGKT TAL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against DLK2 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)
0.5
Highest tissue expression
12 nTPM

Expression across tissuesHPA

Tissue

  • prostate: 12 nTPM
  • skin: 12 nTPM
  • esophagus: 12 nTPM
  • cerebellum: 10 nTPM
  • basal ganglia: 8.4 nTPM
  • salivary gland: 7.6 nTPM

Single-cell type

  • breast myoepithelial cells: 80 nCPM
  • epididymal basal cells: 70 nCPM
  • basal prostatic cells: 51 nCPM
  • respiratory basal cells: 42 nCPM
  • esophageal basal cells: 35 nCPM
  • salivary basal cells: 34 nCPM

Immune cell

  • MAIT T-cell: 0.8 nTPM
  • NK-cell: 0.7 nTPM
  • memory CD4 T-cell: 0.5 nTPM
  • memory CD8 T-cell: 0.5 nTPM
  • plasmacytoid DC: 0.5 nTPM
  • basophil: 0.3 nTPM

Brain region

  • cerebellum: 14 nTPM
  • cerebral cortex: 9.8 nTPM
  • basal ganglia: 8.7 nTPM
  • hypothalamus: 8.1 nTPM
  • hippocampal formation: 7.2 nTPM
  • amygdala: 6.8 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)
0.46
gnomAD pLI
0.78
gnomAD missense Z
1.93
DepMap mean gene effect
-0.07
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads DLK2 as an antibody target. Whether an autoantibody or antibody against DLK2 could matter depends on whether native DLK2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

DLK2 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 DLK2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/DLK2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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