SAMSN1
SAM domain-containing protein SAMSN-1
Also known as: HACS1, NASH1, SAMN1_HUMAN, SASH2, SH3D6B, SLy2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NSI8
- Gene
- SAMSN1
- Ensembl
- ENSG00000155307
- Chromosome
- 21
- Canonical length
- 373 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane
OverviewNCBI Gene
SAMSN1 is a member of a novel gene family of putative adaptors and scaffold proteins containing SH3 and SAM (sterile alpha motif) domains (Claudio et al., 2001 [PubMed 11536050]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
373 residues, UniProt reviewed canonical sequence.
>Q9NSI8|SAMSN1
1 MLKRKPSNVS EKEKHQKPKR SSSFGNFDRF RNNSLSKPDD STEAHEGDPT NGSGEQSKTS
61 NNGGGLGKKM RAISWTMKKK VGKKYIKALS EEKDEEDGEN AHPYRNSDPV IGTHTEKVSL
121 KASDSMDSLY SGQSSSSGIT SCSDGTSNRD SFRLDDDGPY SGPFCGRARV HTDFTPSPYD
181 TDSLKIKKGD IIDIICKTPM GMWTGMLNNK VGNFKFIYVD VISEEEAAPK KIKANRRSNS
241 KKSKTLQEFL ERIHLQEYTS TLLLNGYETL EDLKDIKESH LIELNIENPD DRRRLLSAAE
301 NFLEEEIIQE QENEPEPLSL SSDISLNKSQ LDDCPRDSGC YISSGNSDNG KEDLESENLS
361 DMVHKIIITE PSDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SAMSN1 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)
- 0.59
- Highest tissue expression
- 182 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 182 nTPM
- appendix: 76 nTPM
- tonsil: 38 nTPM
- urinary bladder: 37 nTPM
- lymph node: 33 nTPM
- spleen: 30 nTPM
Single-cell type
- neutrophils: 14,700 nCPM
- monocytes: 2,677 nCPM
- neutrophil progenitors: 1,993 nCPM
- mast cells: 1,616 nCPM
- t-cells: 891 nCPM
- monocyte progenitors: 811 nCPM
Immune cell
- basophil: 315 nTPM
- eosinophil: 235 nTPM
- non-classical monocyte: 83 nTPM
- T-reg: 60 nTPM
- intermediate monocyte: 52 nTPM
- neutrophil: 50 nTPM
Brain region
- white matter: 17 nTPM
- medulla oblongata: 11 nTPM
- pons: 9.1 nTPM
- spinal cord: 9 nTPM
- cerebral cortex: 8.5 nTPM
- thalamus: 7.7 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)
- 1.23
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.3
- DepMap mean gene effect
- 0.07
- 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
- negative regulation of adaptive immune response
- negative regulation of B cell activation
- negative regulation of peptidyl-tyrosine phosphorylation
- regulation of intracellular signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SAMSN1 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 SAMSN1 as an antibody target. Whether an autoantibody or antibody against SAMSN1 could matter depends on whether native SAMSN1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SAMSN1 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 SAMSN1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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