spectrin alpha, non-erythrocytic 1

Summary
Gene Symbol
  • SPTAN1
Organism
Homo sapiens (human)
NCBI Gene
6709
PubChem
6709
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Actin capping
  • Actin-binding
  • Alternative splicing
  • Calcium
  • Calmodulin-binding
  • Coiled coil
  • Cytoplasm
  • Cytoskeleton
  • Direct protein sequencing
  • Disease variant
  • Epilepsy
  • Hereditary spastic paraplegia
  • Intellectual disability
  • Metal-binding
  • Neuropathy
  • Phosphoprotein
  • Reference proteome
  • Repeat
  • SH3 domain
Proteins
Displaying all 2 entries
UniProt Protein Name
Q13813
  • Alpha-II spectrin
  • Fodrin alpha chain
  • Spectrin, non-erythroid alpha subunit
A0A384P5S9
Gene Ontology (GO)
Displaying all 2 entries
GO Term Evidence Code PMID
actin cytoskeleton organization
actin filament capping
GO Hierarchy
Displaying entries 1 - 5 of 14 in total
GO Term Evidence Code PMID
extracellular region
cytosol
plasma membrane
spectrin
microtubule cytoskeleton
OrthoDB (Group)
Group level
Eukaryota
Group Name
spectrin
Functional Category
  • E: Amino acid transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0080438 developmental and epileptic encephalopathy 5
DOID:0081400 autosomal dominant distal hereditary motor neuronopathy 11

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.2.1

Last updated: April 7, 2025