NOL12
Nucleolar protein 12
Also known as: MGC3731, NOL12_HUMAN, Nop25, RRP17
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UGY1
- Gene
- NOL12
- Ensembl
- ENSG00000273899
- Chromosome
- 22
- Canonical length
- 213 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Mitotic chromosome,Vesicles
OverviewNCBI Gene
Enables identical protein binding activity. Predicted to be located in cytoplasm and nucleus. Predicted to be active in nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
213 residues, UniProt reviewed canonical sequence.
>Q9UGY1|NOL12
1 MGRNKKKKRD GDDRRPRLVL SFDEEKRREY LTGFHKRKVE RKKAAIEEIK QRLKEEQRKL
61 REERHQEYLK MLAEREEALE EADELDRLVT AKTESVQYDH PNHTVTVTTI SDLDLSGARL
121 LGLTPPEGGA GDRSEEEASS TEKPTKALPR KSRDPLLSQR ISSLTASLHA HSRKKVKRKH
181 PRRAQDSKKP PRAPRTSKAQ RRRLTGKARH SGELocalizationUniProt · AlphaFold · HPA
Whether an antibody against NOL12 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)
- 0.6
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 33 nTPM
- cerebellum: 32 nTPM
- adrenal gland: 28 nTPM
- bone marrow: 27 nTPM
- spleen: 25 nTPM
- spinal cord: 24 nTPM
Single-cell type
- early spermatids: 50 nCPM
- late primary spermatocytes: 36 nCPM
- colonocytes: 17 nCPM
- enterocytes: 16 nCPM
- brain excitatory neurons: 15 nCPM
- late spermatids: 15 nCPM
Immune cell
- basophil: 57 nTPM
- neutrophil: 54 nTPM
- non-classical monocyte: 34 nTPM
- intermediate monocyte: 29 nTPM
- eosinophil: 27 nTPM
- classical monocyte: 25 nTPM
Brain region
- white matter: 17 nTPM
- basal ganglia: 17 nTPM
- medulla oblongata: 16 nTPM
- hypothalamus: 16 nTPM
- cerebral cortex: 16 nTPM
- cerebellum: 16 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)
- 1.13
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.26
- DepMap mean gene effect
- -0.71
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Nucleolar protein 12
- Nucleolar protein 12 (25kDa)
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NOL12 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 NOL12 as an antibody target. Whether an autoantibody or antibody against NOL12 could matter depends on whether native NOL12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NOL12 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 NOL12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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