PPAN-P2RY11 Gene Summary [Human]

This locus represents naturally occurring read-through transcription between the adjacent PPAN and P2RY11 genes. Alternative splicing results in two transcript variants, one of which encodes a fusion protein that shares sequence identity with each individual gene product. This transcript is found to be ubiquitously expressed and is up-regulated by agents inducing granulocytic differentiation. However, its functional significance in vivo remains unclear. [provided by RefSeq, Nov 2010]

Details

Type
Protein Coding
Official Symbol
PPAN-P2RY11
Official Name
PPAN-P2RY11 readthrough [Source:HGNC Symbol;Acc:HGNC:33526]
Ensembl ID
ENSG00000243207
Bio databases IDs NCBI: 692312 Ensembl: ENSG00000243207
Aliases PPAN-P2RY11 readthrough
Synonyms BXDC3, P2RY11, P2Y11, PPAN, PPAN-P2RY11 readthrough, SSF1
Species
Human, Homo sapiens

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 human PPAN-P2RY11 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • 7 transmembrane receptor (rhodopsin family)
  • Brix domain
  • seven-transmembrane G protein-coupled receptor superfamily
  • The Brix domain is found in a number of eukaryotic proteins

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • narcolepsy with cataplexy
regulated by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Unknown

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.