DMAC2
Distal membrane-arm assembly complex protein 2
Also known as: ATP5SL, DMAC2_HUMAN, FLJ10241
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NW81
- Gene
- DMAC2
- Ensembl
- ENSG00000105341
- Chromosome
- 19
- Canonical length
- 257 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
257 residues, UniProt reviewed canonical sequence.
>Q9NW81|DMAC2
1 MAAPWASLRL VAPMWNGRIR GIHRLGAAVA PEGNQKKKRT ILQFLTNYFY DVEALRDYLL
61 QREMYKVHEK NRSYTWLEKQ HGPYGAGAFF ILKQGGAVKF RDKEWIRPDK YGHFSQEFWN
121 FCEVPVEAVD AGDCDINYEG LDNLLRLKEL QSLSLQRCCH VDDWCLSRLY PLADSLQELS
181 LAGCPRISER GLACLHHLQN LRRLDISDLP AVSNPGLTQI LVEEMLPNCE VVGVDWAEGL
241 KSGPEEQPRD TASPVPALocalizationUniProt · AlphaFold · HPA
Whether an antibody against DMAC2 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 105 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 105 nTPM
- tongue: 75 nTPM
- skeletal muscle: 64 nTPM
- kidney: 44 nTPM
- duodenum: 42 nTPM
- small intestine: 40 nTPM
Single-cell type
- enterocytes: 95 nCPM
- extravillous trophoblasts: 81 nCPM
- esophageal basal cells: 78 nCPM
- migrating cytotrophoblasts: 67 nCPM
- esophageal suprabasal cells: 58 nCPM
- hofbauer cells: 57 nCPM
Immune cell
- myeloid DC: 40 nTPM
- classical monocyte: 28 nTPM
- plasmacytoid DC: 27 nTPM
- intermediate monocyte: 26 nTPM
- eosinophil: 24 nTPM
- total PBMC: 23 nTPM
Brain region
- thalamus: 29 nTPM
- midbrain: 29 nTPM
- medulla oblongata: 29 nTPM
- pons: 28 nTPM
- hypothalamus: 27 nTPM
- cerebellum: 27 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)
- 1.37
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- mitochondrial respiratory chain complex I assembly
- SCF-dependent proteasomal ubiquitin-dependent protein catabolic process
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DMAC2 as an antibody target. Whether an autoantibody or antibody against DMAC2 could matter depends on whether native DMAC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DMAC2 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 DMAC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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