MGARP
Protein MGARP
Also known as: C4orf49, CESP-1, HUMMR, HUMMR_HUMAN, OSAP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDB4
- Gene
- MGARP
- Ensembl
- ENSG00000137463
- Chromosome
- 4
- Canonical length
- 240 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Predicted to be involved in several processes, including axonal transport; cellular response to gonadotropin-releasing hormone; and nervous system development. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
240 residues, UniProt reviewed canonical sequence.
>Q8TDB4|MGARP
1 MYLRRAVSKT LALPLRAPPN PAPLGKDASL RRMSSNRFPG SSGSNMIYYL VVGVTVSAGG
61 YYAYKTVTSD QAKHTEHKTN LKEKTKAEIH PFQGEKENVA ETEKASSEAP EELIVEAEVV
121 DAEESPSATV VVIKEASACP GHVEAAPETT AVSAETGPEV TDAAARETTE VNPETTPEVT
181 NAALDEAVTI DNDKDTTKNE TSDEYAELEE ENSPAESESS AGDDLQEEAS VGSEAASAQGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MGARP 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
- 1
- Mean surface accessibility (rSASA)
- 0.7
- Highest tissue expression
- 215 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 215 nTPM
- retina: 108 nTPM
- ovary: 34 nTPM
- cerebellum: 16 nTPM
- pituitary gland: 12 nTPM
- adipose tissue: 9.8 nTPM
Single-cell type
- ocular epithelial cells: 409 nCPM
- müller glia: 353 nCPM
- adrenal cortex cells: 120 nCPM
- retinal horizontal cells: 100 nCPM
- granulosa cells: 78 nCPM
- retinal bipolar cells: 77 nCPM
Immune cell
- memory CD4 T-cell: 0.2 nTPM
- naive CD4 T-cell: 0.2 nTPM
- memory B-cell: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
- NK-cell: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- cerebellum: 12 nTPM
- midbrain: 3.8 nTPM
- hypothalamus: 3.7 nTPM
- medulla oblongata: 3.2 nTPM
- pons: 3.1 nTPM
- cerebral cortex: 2.7 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)
- 1.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.23
- DepMap mean gene effect
- -0.02
- 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
- anterograde axonal transport
- axon development
- axonal transport of mitochondrion
- cellular response to gonadotropin-releasing hormone
- cellular response to hypoxia
- cellular response to steroid hormone stimulus
- cerebral cortex development
- negative regulation of dendrite development
- protein targeting to mitochondrion
- regulation of mitochondrion organization
- retrograde axonal transport
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein MGARP
- Protein MGARP, N-terminal
- Mitochondria Localisation Sequence
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MGARP 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 MGARP as an antibody target. Whether an autoantibody or antibody against MGARP could matter depends on whether native MGARP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MGARP 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 MGARP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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