FRRS1L

This gene encodes a component of the outer-core of an alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor protein in the brain. The encoded protein is thought to interact with inner-core components of the receptor, and play a role in the modulation of glutamate signaling. Mutations in this gene are associated with early infantile epileptic encephalopathy 37. [provided by RefSeq, Jul 2016]

Description

Ferric chelate reductase 1 like

Tissue specificity

Tissue enhanced (brain, ovary)

Predicted location

Membrane

Protein family

Disease related genes
Human disease related genes
Mapped to neXtProt
Mapped to UniProt SWISS-PROT
Predicted membrane proteins

Chromosome

9 (109130293 - 109167249)

Ensembl ID

ENSG00000260230  (ver. 103.38)

Orthologs

Mouse Frrs1l: ENSMUSG00000045589

UniProt

Q9P0K9

neXtProt

NX_Q9P0K9

Human splice variants
Mouse splice variants

Protein structure