Mus musculus Gene: Snta1
Summary
InnateDB Gene IDBG-210373.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Snta1
Gene Name syntrophin, acidic 1
Synonyms AW228934; Snt1
Species Mus musculus
Ensembl Gene ENSMUSG00000027488
Encoded Proteins
syntrophin, acidic 1
syntrophin, acidic 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000101400:
Syntrophins are cytoplasmic peripheral membrane scaffold proteins that are components of the dystrophin-associated protein complex. This gene is a member of the syntrophin gene family and encodes the most common syntrophin isoform found in cardiac tissues. The N-terminal PDZ domain of this syntrophin protein interacts with the C-terminus of the pore-forming alpha subunit (SCN5A) of the cardiac sodium channel Nav1.5. This protein also associates cardiac sodium channels with the nitric oxide synthase-PMCA4b (plasma membrane Ca-ATPase subtype 4b) complex in cardiomyocytes. This gene is a susceptibility locus for Long-QT syndrome (LQT) - an inherited disorder associated with sudden cardiac death from arrhythmia - and sudden infant death syndrome (SIDS). This protein also associates with dystrophin and dystrophin-related proteins at the neuromuscular junction and alters intracellular calcium ion levels in muscle tissue. [provided by RefSeq, Jan 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:154376313-154408099
Strand Reverse strand
Band H1
Transcripts
ENSMUST00000028991 ENSMUSP00000028991
ENSMUST00000109728 ENSMUSP00000105350
ENSMUST00000133018
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 21 experimentally validated interaction(s) in this database.
They are also associated with 67 interaction(s) predicted by orthology.
Experimentally validated
Total 21 [view]
Protein-Protein 21 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 67 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003779 actin binding
GO:0005515 protein binding
GO:0005516 calmodulin binding
GO:0017080 sodium channel regulator activity
GO:0030165 PDZ domain binding
GO:0044325 ion channel binding
GO:0050998 nitric-oxide synthase binding
GO:0051117 ATPase binding
Biological Process
GO:0002027 regulation of heart rate
GO:0003117 regulation of vasoconstriction by circulating norepinephrine
GO:0007528 neuromuscular junction development
GO:0060307 regulation of ventricular cardiac muscle cell membrane repolarization
GO:0086005 ventricular cardiac muscle cell action potential
GO:1902083 negative regulation of peptidyl-cysteine S-nitrosylation
GO:1902305 regulation of sodium ion transmembrane transport
Cellular Component
GO:0005622 intracellular
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0030054 cell junction
GO:0031594 neuromuscular junction
GO:0042383 sarcolemma
GO:0043234 protein complex
GO:0045211 postsynaptic membrane
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
KEGG
INOH
PID NCI
Signaling mediated by p38-gamma and p38-delta
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.1541
RefSeq NM_009228
OMIM
CCDS CCDS50763
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas