EPDR1
Mammalian ependymin-related protein 1
Also known as: EPDR, EPDR1_HUMAN, MERP-1, MERP1, UCC1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UM22
- Gene
- EPDR1
- Ensembl
- ENSG00000086289
- Chromosome
- 7
- Canonical length
- 224 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted in other tissues
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene is a type II transmembrane protein that is similar to two families of cell adhesion molecules, the protocadherins and ependymins. This protein may play a role in calcium-dependent cell adhesion. This protein is glycosylated, and the orthologous mouse protein is localized to the lysosome. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 8. [provided by RefSeq, Aug 2011]
Canonical amino-acid sequenceUniProt
224 residues, UniProt reviewed canonical sequence.
>Q9UM22|EPDR1
1 MPGRAPLRTV PGALGAWLLG GLWAWTLCGL CSLGAVGAPR PCQAPQQWEG RQVMYQQSSG
61 RNSRALLSYD GLNQRVRVLD ERKALIPCKR LFEYILLYKD GVMFQIDQAT KQCSKMTLTQ
121 PWDPLDIPQN STFEDQYSIG GPQEQITVQE WSDRKSARSY ETWIGIYTVK DCYPVQETFT
181 INYSVILSTR FFDIQLGIKD PSVFTPPSTC QMAQLEKMSE DCSWLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EPDR1 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 114 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 114 nTPM
- cerebellum: 76 nTPM
- tongue: 67 nTPM
- hypothalamus: 58 nTPM
- cerebral cortex: 53 nTPM
- blood vessel: 50 nTPM
Single-cell type
- epididymal clear cells: 106 nCPM
- other brain neurons: 92 nCPM
- peritubular myoid cells: 84 nCPM
- alveolar cells type 2: 80 nCPM
- brain excitatory neurons: 69 nCPM
- epididymal efferent duct ciliated cells: 64 nCPM
Immune cell
- plasmacytoid DC: 2.2 nTPM
- NK-cell: 0.8 nTPM
- gdT-cell: 0.6 nTPM
- memory CD8 T-cell: 0.6 nTPM
- naive CD8 T-cell: 0.4 nTPM
- myeloid DC: 0.3 nTPM
Brain region
- pons: 176 nTPM
- cerebral cortex: 173 nTPM
- hypothalamus: 146 nTPM
- medulla oblongata: 121 nTPM
- spinal cord: 112 nTPM
- midbrain: 111 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)
- 1.05
- gnomAD pLI
- 0.02
- gnomAD missense Z
- -0.41
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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
- Ependymin
- Ependymin, conserved site
- Ependymin
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EPDR1 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 EPDR1 as an antibody target. Whether an autoantibody or antibody against EPDR1 could matter depends on whether native EPDR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EPDR1 is annotated as secreted, so native EPDR1 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label EPDR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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