Seroatlas · Human Serome Atlas

SART1

U4/U6.U5 tri-snRNP-associated protein 1

Also known as: Ara1, HAF, SNRNP110, Snu66, SNUT1_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
O43290
Gene
SART1
Ensembl
ENSG00000175467
Chromosome
11
Canonical length
800 aa
Protein class
Cancer-related genes, Plasma proteins, Predicted intracellular proteins
Subcellular location
Nuclear speckles,Golgi apparatus

OverviewNCBI Gene

This gene encodes two proteins, the SART1(800) protein expressed in the nucleus of the majority of proliferating cells, and the SART1(259) protein expressed in the cytosol of epithelial cancers. The SART1(259) protein is translated by the mechanism of -1 frameshifting during posttranscriptional regulation; its full-length sequence is not published yet. The two encoded proteins are thought to be involved in the regulation of proliferation. Both proteins have tumor-rejection antigens. The SART1(259) protein possesses tumor epitopes capable of inducing HLA-A2402-restricted cytotoxic T lymphocytes in cancer patients. This SART1(259) antigen may be useful in specific immunotherapy for cancer patients and may serve as a paradigmatic tool for the diagnosis and treatment of patients with atopy. The SART1(259) protein is found to be essential for the recruitment of the tri-snRNP to the pre-spliceosome in the spliceosome assembly pathway. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

800 residues, UniProt reviewed canonical sequence.

>O43290|SART1
     1  MGSSKKHRGE KEAAGTTAAA GTGGATEQPP RHREHKKHKH RSGGSGGSGG ERRKRSRERG
    61  GERGSGRRGA EAEARSSTHG RERSQAEPSE RRVKREKRDD GYEAAASSKT SSGDASSLSI
   121  EETNKLRAKL GLKPLEVNAI KKEAGTKEEP VTADVINPMA LRQREELREK LAAAKEKRLL
   181  NQKLGKIKTL GEDDPWLDDT AAWIERSRQL QKEKDLAEKR AKLLEEMDQE FGVSTLVEEE
   241  FGQRRQDLYS ARDLQGLTVE HAIDSFREGE TMILTLKDKG VLQEEEDVLV NVNLVDKERA
   301  EKNVELRKKK PDYLPYAEDE SVDDLAQQKP RSILSKYDEE LEGERPHSFR LEQGGTADGL
   361  RERELEEIRA KLRLQAQSLS TVGPRLASEY LTPEEMVTFK KTKRRVKKIR KKEKEVVVRA
   421  DDLLPLGDQT QDGDFGSRLR GRGRRRVSEV EEEKEPVPQP LPSDDTRVEN MDISDEEEGG
   481  APPPGSPQVL EEDEAELELQ KQLEKGRRLR QLQQLQQLRD SGEKVVEIVK KLESRQRGWE
   541  EDEDPERKGA IVFNATSEFC RTLGEIPTYG LAGNREEQEE LMDFERDEER SANGGSESDG
   601  EENIGWSTVN LDEEKQQQDF SASSTTILDE EPIVNRGLAA ALLLCQNKGL LETTVQKVAR
   661  VKAPNKSLPS AVYCIEDKMA IDDKYSRREE YRGFTQDFKE KDGYKPDVKI EYVDETGRKL
   721  TPKEAFRQLS HRFHGKGSGK MKTERRMKKL DEEALLKKMS SSDTPLGTVA LLQEKQKAQK
   781  TPYIVLSGSG KSMNANTITK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against SART1 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
39 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 39 nTPM
  • skeletal muscle: 33 nTPM
  • spleen: 28 nTPM
  • skin: 28 nTPM
  • ovary: 25 nTPM
  • endometrium: 25 nTPM

Single-cell type

  • neutrophils: 71 nCPM
  • syncytiotrophoblasts: 62 nCPM
  • erythrocyte progenitors: 53 nCPM
  • retinal pigment epithelial cells: 51 nCPM
  • early primary spermatocytes: 47 nCPM
  • cytotrophoblasts: 47 nCPM

Immune cell

  • eosinophil: 8.1 nTPM
  • T-reg: 5.4 nTPM
  • memory CD4 T-cell: 4.8 nTPM
  • memory CD8 T-cell: 4.4 nTPM
  • gdT-cell: 4.3 nTPM
  • neutrophil: 4 nTPM

Brain region

  • white matter: 23 nTPM
  • basal ganglia: 22 nTPM
  • medulla oblongata: 22 nTPM
  • cerebral cortex: 21 nTPM
  • midbrain: 21 nTPM
  • hypothalamus: 21 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about SART1.

Disease | ImmuneIEDB

Conditions an epitope on SART1 was assayed in.

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)
0.34
gnomAD pLI
0.88
gnomAD missense Z
2.3
DepMap mean gene effect
-1.11
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

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

  • SNU66/SART1 family
  • HIND motif
  • SART-1 family
  • HIND motif

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of SART1 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 SART1 as an antibody target. Whether an autoantibody or antibody against SART1 could matter depends on whether native SART1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

SART1 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 SART1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/SART1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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