SMTNL1
Smoothelin-like protein 1
Also known as: CHASM, SMTL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A8MU46
- Gene
- SMTNL1
- Ensembl
- ENSG00000214872
- Chromosome
- 11
- Canonical length
- 494 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene is involved in the contraction of both striated and smooth muscle. During pregnancy, the encoded protein interacts with progesterone receptor to attenuate the expression of contractile and metabolic proteins. [provided by RefSeq, Jul 2016]
Canonical amino-acid sequenceUniProt
494 residues, UniProt reviewed canonical sequence.
>A8MU46|SMTNL1
1 MEQKEGKLSE DGTTVSPAAD NPEMSGGGAP AEETKGTAGK AINEGPPTES GKQEKAPAED
61 GMSAELQGEA NGLDEVKVES QREAGGKEDA EAELKKEDGE KEETTVGSQE MTGRKEETKS
121 EPKEAEEKES TLASEKQKAE EKEAKPESGQ KADANDRDKP EPKATVEEED AKTASQEETG
181 QRKECSTEPK EKATDEEAKA ESQKAVVEDE AKAEPKEPDG KEEAKHGAKE EADAKEEAED
241 AEEAEPGSPS EEQEQDVEKE PEGGAGVIPS SPEEWPESPT GEGHNLSTDG LGPDCVASGQ
301 TSPSASESSP SDVPQSPPES PSSGEKKEKA PERRVSAPAR PRGPRAQNRK AIVDKFGGAA
361 SGPTALFRNT KAAGAAIGGV KNMLLEWCRA MTKKYEHVDI QNFSSSWSSG MAFCALIHKF
421 FPDAFDYAEL DPAKRRHNFT LAFSTAEKLA DCAQLLDVDD MVRLAVPDSK CVYTYIQELY
481 RSLVQKGLVK TKKKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SMTNL1 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)
- 0.62
- Highest tissue expression
- 652 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 652 nTPM
- tongue: 175 nTPM
- esophagus: 8 nTPM
- salivary gland: 5.8 nTPM
- bone marrow: 2.1 nTPM
- prostate: 1.4 nTPM
Single-cell type
- myonuclei: 109 nCPM
- epicardial cells: 11 nCPM
- thymic myoid cells: 5.4 nCPM
- hematopoietic stem cells: 4.9 nCPM
- retinal amacrine cells: 4.9 nCPM
- mesothelial cells: 4.5 nCPM
Immune cell
- neutrophil: 1 nTPM
- eosinophil: 0.7 nTPM
- basophil: 0.6 nTPM
- naive CD4 T-cell: 0.5 nTPM
- gdT-cell: 0.4 nTPM
- MAIT T-cell: 0.4 nTPM
Brain region
- medulla oblongata: 8.8 nTPM
- spinal cord: 6 nTPM
- thalamus: 5.5 nTPM
- midbrain: 5.1 nTPM
- amygdala: 4.7 nTPM
- cerebral cortex: 4.4 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)
- 1.33
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.43
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
- muscle organ morphogenesis
- negative regulation of DNA-templated transcription
- positive regulation of vasoconstriction
- response to activity
- response to xenobiotic stimulus
- vasoconstriction
Molecular functions
- calmodulin binding
- disordered domain specific binding
- protein phosphatase 1 binding
- tropomyosin binding
- CH domain binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SMTNL1 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 SMTNL1 as an antibody target. Whether an autoantibody or antibody against SMTNL1 could matter depends on whether native SMTNL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SMTNL1 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 SMTNL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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