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Gene : FRRS1L Homo sapiens

Name  ? ferric chelate reductase 1 like Cytological Location  9q31.3
Brief Description  ferric chelate reductase 1 like
Description  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]
  • synonyms:
  • uc004bdv.4,
  • ferric-chelate reductase 1-like,
  • NM_014334,
  • AF155065,
  • C9orf4,
  • OTTHUMG00000020468,
  • C9orf4,
  • HGNC:1362,
  • CG-6,
  • FRRS1L,
  • CG-6,
  • EIEE37,
  • CG6,
  • chromosome 9 open reading frame 4
  • identifiers:
  • 23732,
  • ENSG00000260230,
  • FRRS1L

Genome feature

Region: gene ? Length: 36957  
Location: 9:109130293-109167249 reverse strand Cyto location: 9q31.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

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Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3753 SN Ps

5 Cross References

17 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results