NACA2
Nascent polypeptide-associated complex subunit alpha-2
Also known as: MGC71999, NACA2_HUMAN, NACAL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H009
- Gene
- NACA2
- Ensembl
- ENSG00000253506
- Chromosome
- 17
- Canonical length
- 215 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable unfolded protein binding activity. Predicted to be involved in protein targeting to membrane. Predicted to be located in nucleus. Predicted to be part of nascent polypeptide-associated complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
215 residues, UniProt reviewed canonical sequence.
>Q9H009|NACA2
1 MPGEATETVP ATEQELPQSQ AETGSGTASD SGESVPGIEE QDSTQTTTQK AWLVAAAEID
61 EEPVGKAKQS RSEKRARKAM SKLGLLQVTG VTRVTIWKSK NILFVITKLD VYKSPASDAY
121 IVFGEAKIQD LSQQAQLAAA EKFRVQGEAV GNIQENTQTP TVQEESEEEE VDETGVEVKD
181 VKLVMSQANV SRAKAVRALK NNSNDIVNAI MELTVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NACA2 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)
- 0.54
- Highest tissue expression
- 60 nTPM
Expression across tissuesHPA
Tissue
- testis: 60 nTPM
- ovary: 2 nTPM
- skin: 1.4 nTPM
- breast: 1.1 nTPM
- esophagus: 1.1 nTPM
- pancreas: 1.1 nTPM
Single-cell type
- late primary spermatocytes: 658 nCPM
- early spermatids: 371 nCPM
- late spermatids: 168 nCPM
- early primary spermatocytes: 26 nCPM
- esophageal apical cells: 14 nCPM
- papillary tip epithelial cells: 13 nCPM
Immune cell
- total PBMC: 0.8 nTPM
- intermediate monocyte: 0.7 nTPM
- non-classical monocyte: 0.7 nTPM
- memory B-cell: 0.4 nTPM
- myeloid DC: 0.4 nTPM
- naive B-cell: 0.4 nTPM
Brain region
- basal ganglia: 0.1 nTPM
- amygdala: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.82
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 0
- DepMap mean gene effect
- -0.39
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NACA2 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 NACA2 as an antibody target. Whether an autoantibody or antibody against NACA2 could matter depends on whether native NACA2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NACA2 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 NACA2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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