Scyl1 Gene Summary [Rat]

Predicted to enable ATP binding activity and protein kinase activity. Predicted to be involved in retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum. Predicted to act upstream of or within inflammatory response; neuron differentiation; and protein localization. Predicted to be located in cis-Golgi network; cytosol; and endoplasmic reticulum-Golgi intermediate compartment. Predicted to be part of COPI vesicle coat. Human ortholog(s) of this gene implicated in autosomal recessive spinocerebellar ataxia 21. Orthologous to human SCYL1 (SCY1 like pseudokinase 1). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Scyl1
Official Name
SCY1 like pseudokinase 1 [Source:RGD Symbol;Acc:1307330]
Ensembl ID
ENSRNOG00000023668
Bio databases IDs NCBI: 293684 Ensembl: ENSRNOG00000023668
Aliases SCY1 like pseudokinase 1
Synonyms 2810011O19Rik, GKLP, HT019, mdf, mfd, NKTL, NTKL, P105, SCAR21, SCY1-like 1 (S. cerevisiae), SCY1 like pseudokinase 1, TAPK, TEIF, TRAP
Species
Rat, Rattus norvegicus
OrthologiesHumanMouse

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in rat Scyl1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • kinase
  • Protein Kinases, catalytic domain
  • kinase-like domain
  • coiled-coil domain
  • protein binding
  • protein-tyrosine kinase

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • astrocytosis
  • autosomal recessive spinocerebellar ataxia type 21
  • hereditary disorder
  • psoriatic arthritis
  • motor neuron disease
  • growth failure
  • non-insulin-dependent diabetes mellitus
  • paralysis
  • SCYL1-related disorder
  • motor dysfunction
regulated by
regulates
role in cell
  • differentiation
  • number
  • size
  • degeneration
  • abnormal morphology
  • atrophy
  • switching
  • loss
  • diameter
  • development

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • perinuclear region
  • filamentous network
  • Golgi Apparatus
  • ER-to-Golgi intermediate compartment
  • cytosol
  • cis Golgi networks
  • nuclear pores
  • cis Golgi cisternae

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the rat Scyl1 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • inflammatory response
  • retrograde vesicle-mediated transport, Golgi to ER
  • spinal cord motor neuron differentiation
  • protein localization
  • neuron development

Cellular Component

Where in the cell the gene product is active
  • nucleus
  • centrosome
  • cis-Golgi network
  • cytoplasm
  • membrane
  • cytosol
  • Golgi apparatus
  • endoplasmic reticulum-Golgi intermediate compartment
  • COPI vesicle coat

Molecular Function

What the gene product does at the molecular level
  • ATP binding
  • DNA binding
  • protein tyrosine kinase activity
  • cadherin binding

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.