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Protein Coding Gene : Stx3 syntaxin 3
Primary Identifier  MGI:103077 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  20908
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable SNAP receptor activity; SNARE binding activity; and arachidonic acid binding activity. Involved in exocytic insertion of neurotransmitter receptor to postsynaptic membrane; modulation of chemical synaptic transmission; and vesicle-mediated transport in synapse. Acts upstream of or within exocytosis and long-term synaptic potentiation. Located in several cellular components, including cytoplasmic vesicle; photoreceptor inner segment; and photoreceptor outer segment. Part of SNARE complex. Is active in Schaffer collateral - CA1 synapse; glutamatergic synapse; and postsynapse. Is expressed in several structures, including alimentary system; central nervous system; eye; genitourinary system; and respiratory system. Human ortholog(s) of this gene implicated in congenital diarrhea. Orthologous to human STX3 (syntaxin 3).
  • synonyms:
  • AV006285,
  • MGI:2147735,
  • syntaxin 3A,
  • Syn-3,
  • MGI:2147464,
  • syntaxin 3,
  • syntaxin 3B,
  • Stx3,
  • AA960228,
  • expressed sequence AW536415,
  • expressed sequence AV006285,
  • MGI:2147666,
  • MGD-MRK-23941,
  • AW536415,
  • expressed sequence AA960228
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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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