SARNP
SAP domain-containing ribonucleoprotein
Also known as: CIP29, Hcc-1, SARNP_HUMAN, THO1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P82979
- Gene
- SARNP
- Ensembl
- ENSG00000205323
- Chromosome
- 12
- Canonical length
- 210 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
This gene encodes a protein that is upregulated in response to various cytokines. The encoded protein may play a role in cell cycle progression. A translocation between this gene and the myeloid/lymphoid leukemia gene, resulting in expression of a chimeric protein, has been associated with acute myelomonocytic leukemia. Pseudogenes exist on chromosomes 7 and 8. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]
Canonical amino-acid sequenceUniProt
210 residues, UniProt reviewed canonical sequence.
>P82979|SARNP
1 MATETVELHK LKLAELKQEC LARGLETKGI KQDLIHRLQA YLEEHAEEEA NEEDVLGDET
61 EEEETKPIEL PVKEEEPPEK TVDVAAEKKV VKITSEIPQT ERMQKRAERF NVPVSLESKK
121 AARAARFGIS SVPTKGLSSD NKPMVNLDKL KERAQRFGLN VSSISRKSED DEKLKKRKER
181 FGIVTSSAGT GTTEDTEAKK RKRAERFGIALocalizationUniProt · AlphaFold · HPA
Whether an antibody against SARNP 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
- 100 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 100 nTPM
- bone marrow: 84 nTPM
- heart muscle: 83 nTPM
- choroid plexus: 81 nTPM
- tonsil: 79 nTPM
- tongue: 78 nTPM
Single-cell type
- choroid plexus epithelial cells: 75 nCPM
- oligodendrocytes: 60 nCPM
- microglia: 57 nCPM
- late spermatids: 54 nCPM
- oligodendrocyte progenitor cells: 47 nCPM
- ependymal cells: 47 nCPM
Immune cell
- basophil: 247 nTPM
- eosinophil: 219 nTPM
- T-reg: 171 nTPM
- intermediate monocyte: 156 nTPM
- total PBMC: 154 nTPM
- myeloid DC: 154 nTPM
Brain region
- hypothalamus: 37 nTPM
- cerebral cortex: 35 nTPM
- midbrain: 29 nTPM
- cerebellum: 28 nTPM
- white matter: 26 nTPM
- pons: 26 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)
- 0.19
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.18
- DepMap mean gene effect
- -0.43
- DepMap dependency class
- selective
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
Biological processes
- mRNA export from nucleus
- negative regulation of transcription by RNA polymerase II
- poly(A)+ mRNA export from nucleus
- regulation of translation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SAP domain
- SAP domain superfamily
- SAP domain
- SAP domain-containing ribonucleoprotein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SARNP 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 SARNP as an antibody target. Whether an autoantibody or antibody against SARNP could matter depends on whether native SARNP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SARNP 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 SARNP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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