Erlin2 Gene Summary [Rat]

Predicted to enable cholesterol binding activity and ubiquitin protein ligase binding activity. Predicted to be involved in ERAD pathway; SREBP signaling pathway; and negative regulation of lipid biosynthetic process. Predicted to be located in several cellular components, including cytosol; endoplasmic reticulum; and membrane raft. Predicted to be part of protein-containing complex. Predicted to be active in endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 18. Orthologous to human ERLIN2 (ER lipid raft associated 2). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Erlin2
Official Name
ER lipid raft associated 2 [Source:RGD Symbol;Acc:1309010]
Ensembl ID
ENSRNOG00000013763
Bio databases IDs NCBI: 290823 Ensembl: ENSRNOG00000013763
Aliases ER lipid raft associated 2
Synonyms BC036333, C87251, C8orf2, ER lipid raft associated 2, NET32, RGD1309010, SPFH2, SPG18, SPG18A, SPG18B
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 Erlin2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • ubiquitin protein ligase binding
  • SPFH_like
  • prohibitin homologues
  • protein binding
  • SPFH domain / Band 7 family

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • autosomal recessive spastic paraplegia type 18
  • hereditary spastic paraplegia
  • spastic paraplegia
  • autosomal dominant spastic paraplegia type 18A
  • neonatal late-onset sepsis
  • breast cancer
  • autosomal recessive nonsyndromic mental retardation
  • autosomal dominant hereditary spastic paraplegia
regulated by
regulates
role in cell
  • degradation in
  • ubiquitination in

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
  • pH resistant lipid raft fraction
  • detergent resistant lipid raft fraction
  • cellular membrane
  • Plasma Membrane
  • Endoplasmic Reticulum
  • cytosol
  • endoplasmic reticulum membrane
  • microsomal membrane
  • membrane rafts

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the rat Erlin2 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • negative regulation of fatty acid biosynthetic process
  • SREBP-mediated signaling pathway
  • regulation of cholesterol biosynthetic process
  • negative regulation of cholesterol biosynthetic process
  • cholesterol metabolic process

Cellular Component

Where in the cell the gene product is active
  • endoplasmic reticulum membrane
  • membrane raft
  • cytosol
  • endoplasmic reticulum
  • macromolecular complex
  • plasma membrane

Molecular Function

What the gene product does at the molecular level
  • ubiquitin protein ligase binding
  • protein binding
  • cholesterol 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.