DERL2
Derlin-2
Also known as: CGI-101, DERL2_HUMAN, derlin-2, F-LAN-1, F-LANa, FLANa
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9GZP9
- Gene
- DERL2
- Ensembl
- ENSG00000072849
- Chromosome
- 17
- Canonical length
- 239 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Endoplasmic reticulum
OverviewNCBI Gene
Proteins that are unfolded or misfolded in the endoplasmic reticulum (ER) must be refolded or degraded to maintain the homeostasis of the ER. DERL2 is involved in the degradation of misfolded glycoproteins in the ER (Oda et al., 2006 [PubMed 16449189]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
239 residues, UniProt reviewed canonical sequence.
>Q9GZP9|DERL2
1 MAYQSLRLEY LQIPPVSRAY TTACVLTTAA VQLELITPFQ LYFNPELIFK HFQIWRLITN
61 FLFFGPVGFN FLFNMIFLYR YCRMLEEGSF RGRTADFVFM FLFGGFLMTL FGLFVSLVFL
121 GQAFTIMLVY VWSRRNPYVR MNFFGLLNFQ APFLPWVLMG FSLLLGNSII VDLLGIAVGH
181 IYFFLEDVFP NQPGGIRILK TPSILKAIFD TPDEDPNYNP LPEERPGGFA WGEGQRLGGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DERL2 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
- 4
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 32 nTPM
- epididymis: 28 nTPM
- salivary gland: 27 nTPM
- pancreas: 26 nTPM
- liver: 25 nTPM
- thyroid gland: 23 nTPM
Single-cell type
- late primary spermatocytes: 306 nCPM
- early spermatids: 217 nCPM
- esophageal apical cells: 157 nCPM
- epididymal principal cells: 143 nCPM
- extravillous trophoblasts: 142 nCPM
- plasma cells: 127 nCPM
Immune cell
- total PBMC: 118 nTPM
- T-reg: 81 nTPM
- eosinophil: 77 nTPM
- basophil: 72 nTPM
- intermediate monocyte: 71 nTPM
- plasmacytoid DC: 69 nTPM
Brain region
- white matter: 11 nTPM
- choroid plexus: 11 nTPM
- pons: 9.7 nTPM
- medulla oblongata: 9.5 nTPM
- midbrain: 9.4 nTPM
- hypothalamus: 9 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)
- 0.33
- gnomAD pLI
- 0.96
- gnomAD missense Z
- 1.62
- DepMap mean gene effect
- -0.29
- 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
- endoplasmic reticulum unfolded protein response
- ERAD pathway
- negative regulation of retrograde protein transport, ER to cytosol
- positive regulation of cell growth
- positive regulation of cell population proliferation
- retrograde protein transport, ER to cytosol
- suckling behavior
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DERL2 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 DERL2 as an antibody target. Whether an autoantibody or antibody against DERL2 could matter depends on whether native DERL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DERL2 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 DERL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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