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stn-1 Syntrophin-1 [ Caenorhabditis elegans ]

Gene ID: 266844, updated on 9-Dec-2024

Summary

Official Symbol
stn-1
Official Full Name
Syntrophin-1
Primary source
WormBase:WBGene00006062
Locus tag
CELE_F30A10.8
See related
AllianceGenome:WB:WBGene00006062
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Caenorhabditis elegans (strain: Bristol N2)
Lineage
Eukaryota; Metazoa; Ecdysozoa; Nematoda; Chromadorea; Rhabditida; Rhabditina; Rhabditomorpha; Rhabditoidea; Rhabditidae; Peloderinae; Caenorhabditis
Summary
Enables acetylcholine transmembrane transporter activity and calcium channel regulator activity. Involved in several processes, including acetylcholine transport; muscle cell cellular homeostasis; and sarcomere organization. Part of dystrophin-associated glycoprotein complex. Is expressed in body wall musculature; enteric muscle; nervous system; and reproductive system. Used to study Duchenne muscular dystrophy. Human ortholog(s) of this gene implicated in long QT syndrome; long QT syndrome 12; and sudden infant death syndrome. Orthologous to several human genes including SNTB2 (syntrophin beta 2). [provided by Alliance of Genome Resources, Dec 2024]
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Genomic context

See stn-1 in Genome Data Viewer
Location:
chromosome: I
Exon count:
6
Sequence:
Chromosome: I; NC_003279.8 (9501268..9505173)

Chromosome I - NC_003279.8Genomic Context describing neighboring genes Neighboring gene phosphatidylinositol-3-phosphatase Neighboring gene Kinase Neighboring gene ncRNA Neighboring gene PIN domain-containing protein Neighboring gene Ubiquitin carboxyl-terminal hydrolase usp-48 Neighboring gene miscRNA Neighboring gene Tudor domain-containing protein

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by WormBase

Function Evidence Code Pubs
enables acetylcholine transmembrane transporter activity IMP
Inferred from Mutant Phenotype
more info
PubMed 
enables calcium channel regulator activity IMP
Inferred from Mutant Phenotype
more info
PubMed 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
enables structural molecule activity IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
 
located_in cytoskeleton IEA
Inferred from Electronic Annotation
more info
 
part_of dystrophin-associated glycoprotein complex IBA
Inferred from Biological aspect of Ancestor
more info
 
part_of dystrophin-associated glycoprotein complex IMP
Inferred from Mutant Phenotype
more info
PubMed 
part_of dystrophin-associated glycoprotein complex IPI
Inferred from Physical Interaction
more info
PubMed 
located_in membrane IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
Syntrophin-1
NP_492521.1
  • Confirmed by transcript evidence

NCBI Reference Sequences (RefSeq)

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Genome Annotation

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference assembly

Genomic

  1. NC_003279.8 Reference assembly

    Range
    9501268..9505173
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_060120.7NP_492521.1  Syntrophin-1 [Caenorhabditis elegans]

    See identical proteins and their annotated locations for NP_492521.1

    Status: REVIEWED

    UniProtKB/Swiss-Prot
    Q93646, Q9XVP8
    Conserved Domains (4) summary
    smart00233
    Location:228334
    PH; Pleckstrin homology domain
    cd00992
    Location:44125
    PDZ_signaling; PDZ domain found in a variety of Eumetazoan signaling molecules, often in tandem arrangements. May be responsible for specific protein-protein interactions, as most PDZ domains bind C-terminal polypeptides, and binding to internal (non-C-terminal) ...
    pfam00169
    Location:228334
    PH; PH domain
    cl17171
    Location:152208
    PH-like; Pleckstrin homology-like domain