Target intelligence / Profile preview

Spectrin alpha chain, non-erythrocytic 1 (SPTAN1)

Target
SPTAN1
Molecular classification
Cytoskeletal protein, Scaffold protein, Actin-binding protein, Other
01

Overview

Spectrin alpha chain, non-erythrocytic 1 (SPTAN1) encodes the ubiquitous alpha-II spectrin protein, a cytoskeletal scaffolding protein, that forms heterodimers with beta-spectrins and is essential for plasma membrane stability, actin network organization, and subcellular architecture in non-erythroid cells[1][4][5][6]. SPTAN1 plays roles in cell adhesion, cell shape, cell cycle control, apoptosis, and DNA repair and is implicated in multiple cellular pathways, including cytoskeletal remodeling, signal transduction, and protein trafficking[1][3][4][5][6]. Mutations cause early infantile epileptic encephalopathy and various neurodevelopmental disorders; SPTAN1 and its proteolytic breakdown products are candidate biomarkers for neuronal injury, including traumatic brain injury, and are upregulated in diseases such as Guillain–Barré syndrome and congenital heart disease[3][4][5][6]. SPTAN1’s role in cancer includes effects on apoptosis, cell detachment, and metastasis, and altered expression is linked with both tumor suppression and promotion depending on context[1]. There are currently no approved drugs directly targeting SPTAN1.

Other names
Spectrin alpha chain, non-erythrocytic 1SPTAN1NEASSPTA2Alpha-II spectrinFodrin alpha chainSpectrin, non-erythroid alpha subunitalpha-fodrinDEE5DEVEPEIEE5HMN11HMND11SPG91epididymis secretory sperm binding proteinfodrin alpha chainspectrin, non-erythroid alpha chainspectrin, non-erythroid alpha subunitalpha-II spectrin
02

Biological functions

Actin cytoskeleton organizationCell adhesionCell cycle regulationDNA repairApoptosisIntercellular communicationCell proliferationCell shape maintenanceCell migrationProtein trafficking
03

Disease associations

Neurodevelopmental diseaseEpileptic encephalopathyNeuromuscular diseaseHereditary spastic paraplegiaCancerCardiovascular disease (notably congenital heart disease)Peripheral neuropathy (e.g., Guillain–Barré syndrome biomarker)
04

Safety considerations

Loss-of-function mutations cause neurodevelopmental syndromes (early infantile epileptic encephalopathy, intellectual disability, motor neuropathy)Role in tumor progression and metastasis may influence therapeutic responses and cancer prognosis
05

Biomarkers

Spectrin breakdown products (traumatic brain injury, brain necrosis, apoptosis)Alpha II-spectrin protein levels (Guillain–Barré syndrome, congenital heart disease)

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