RBM38
RNA-binding protein 38
Also known as: dJ800J21.2, HSRNASEB, RBM38_HUMAN, RNPC1, seb4B, SEB4D
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H0Z9
- Gene
- RBM38
- Ensembl
- ENSG00000132819
- Chromosome
- 20
- Canonical length
- 239 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables mRNA 3'-UTR binding activity. Involved in several processes, including DNA damage response, signal transduction by p53 class mediator; negative regulation of cell population proliferation; and regulation of gene expression. Located in cytosol and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
239 residues, UniProt reviewed canonical sequence.
>Q9H0Z9|RBM38
1 MLLQPAPCAP SAGFPRPLAA PGAMHGSQKD TTFTKIFVGG LPYHTTDASL RKYFEGFGDI
61 EEAVVITDRQ TGKSRGYGFV TMADRAAAER ACKDPNPIID GRKANVNLAY LGAKPRSLQT
121 GFAIGVQQLH PTLIQRTYGL TPHYIYPPAI VQPSVVIPAA PVPSLSSPYI EYTPASPAYA
181 QYPPATYDQY PYAASPATAA SFVGYSYPAA VPQALSAAAP AGTTFVQYQA PQLQPDRMQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RBM38 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
- 261 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 261 nTPM
- bone marrow: 252 nTPM
- colon: 86 nTPM
- lymph node: 65 nTPM
- heart muscle: 64 nTPM
- spleen: 58 nTPM
Single-cell type
- erythrocytes: 427 nCPM
- platelets: 331 nCPM
- megakaryocytes: 235 nCPM
- pdcs: 139 nCPM
- fallopian tube ciliated cells: 117 nCPM
- nk-cells: 90 nCPM
Immune cell
- T-reg: 15 nTPM
- naive B-cell: 11 nTPM
- naive CD8 T-cell: 10 nTPM
- memory B-cell: 10 nTPM
- naive CD4 T-cell: 10 nTPM
- gdT-cell: 9.5 nTPM
Brain region
- choroid plexus: 46 nTPM
- cerebellum: 40 nTPM
- midbrain: 34 nTPM
- thalamus: 31 nTPM
- white matter: 30 nTPM
- basal ganglia: 29 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)
- 0.56
- gnomAD pLI
- 0.72
- gnomAD missense Z
- 1.03
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
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
- 3'-UTR-mediated mRNA stabilization
- cell differentiation
- DNA damage response, signal transduction by p53 class mediator
- mRNA processing
- negative regulation of cell population proliferation
- regulation of cell cycle
- regulation of myotube differentiation
- regulation of RNA splicing
- RNA splicing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RBM38 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 RBM38 as an antibody target. Whether an autoantibody or antibody against RBM38 could matter depends on whether native RBM38 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RBM38 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 RBM38 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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