Mus musculus Gene: Syn1 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Gene | IDBG-135538.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | Syn1 | ||||||||||||||||||||||
Gene Name | synapsin I | ||||||||||||||||||||||
Synonyms | Syn-1 | ||||||||||||||||||||||
Species | Mus musculus | ||||||||||||||||||||||
Ensembl Gene | ENSMUSG00000037217 | ||||||||||||||||||||||
Encoded Proteins |
synapsin I
synapsin I
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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 ENSG00000008056:
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||
Genomic Location | Chromosome X:20860511-20921004 | ||||||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||||||
Band | A1.3 | ||||||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 14 experimentally validated interaction(s) in this database.
They are also associated with 20 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||||||
Species
Homo sapiens
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Gene ID
Gene Order
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Pathway Predictions based on Human Orthology Data | |||||||||||||||||||||||
NETPATH | |||||||||||||||||||||||
REACTOME |
Dopamine Neurotransmitter Release Cycle pathway
Serotonin Neurotransmitter Release Cycle pathway
Neuronal System pathway
Transmission across Chemical Synapses pathway
Neurotransmitter Release Cycle pathway
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KEGG | |||||||||||||||||||||||
INOH | |||||||||||||||||||||||
PID NCI | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | O88935 | ||||||||||||||||||||||
TrEMBL | W8QPF2 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 20964 | ||||||||||||||||||||||
UniGene | Mm.439844 | ||||||||||||||||||||||
RefSeq | NM_001110780 NM_013680 | ||||||||||||||||||||||
OMIM | |||||||||||||||||||||||
CCDS | CCDS53017 CCDS53018 | ||||||||||||||||||||||
HPRD | |||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
MGI ID | MGI:98460 | ||||||||||||||||||||||
MGI Symbol | Syn1 | ||||||||||||||||||||||
EMBL | AF085809 BC022954 KJ174470 L32025 | ||||||||||||||||||||||
GenPept | AAA79963 AAD09833 AAH22954 AHL39032 | ||||||||||||||||||||||
RNA Seq Atlas | 20964 | ||||||||||||||||||||||