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  2. Snta1 - syntrophin, acidic 1 Gene

Snta1 - syntrophin, acidic 1 Gene

Mus musculus

Also known as Snt1

Gene ID: 20648 | Gene type: protein coding

About Snta1

Summary

Enables transmembrane transporter binding activity. Acts upstream of or within neuromuscular junction development and regulation of vasoconstriction by circulating norepinephrine. Located in postsynaptic membrane and sarcolemma. Human ortholog(s) of this gene implicated in long QT syndrome; long QT syndrome 12; and sudden infant death syndrome. Orthologous to human SNTA1 (syntrophin alpha 1). [provided by Alliance of Genome Resources, Apr 2022]

Snta1 Products(1)

mRNA Protein Name
NM_009228.2 NP_033254.2 alpha-1-syntrophin
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
9214383 MGI
enables transmembrane transporter binding IPI
IPI: Inferred from physical interaction
18591664 MGI
Biological Process GO Annotation Evidence Reference Source
acts upstream of or within neuromuscular junction development IMP
IMP: Inferred from mutant phenotype
10995443 MGI
acts upstream of or within regulation of vasoconstriction by circulating norepinephrine IMP
IMP: Inferred from mutant phenotype
12600881 MGI
Cellular Component GO Annotation Evidence Reference Source
located in postsynaptic membrane IDA
IDA: Inferred from direct assay
10995443 MGI
located in sarcolemma IDA
IDA: Inferred from direct assay
11115849 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

alpha-1-syntrophin

59 kDa dystrophin-associated protein A1 acidic component 1

alpha1-syntrophin

syntrophin-1

Orthologs Information

Species Symbol Source ID
Homo sapiens Snta1 NCBI NCBI:6640