GRIA1 wt Allele

Preferred Label : GRIA1 wt Allele;

NCIt synonyms : HBGR1; HBGR2; MRT76; GLUR1; Glutamate Ionotropic Receptor AMPA Type Subunit 1 wt Allele; AMPA Receptor Subunit GluA1 Gene; GLUH1; GLURA; GLUA1; MRD67; Glutamate Receptor, Ionotropic, AMPA 1 Gene;

NCIt definition : Human GRIA1 wild-type allele is located in the vicinity of 5q33.2 and is approximately 324 kb in length. This allele, which encodes glutamate receptor 1 protein, plays a role in glutamate-gated cation transport. Mutations in the gene are associated with autosomal recessive intellectual developmental disorder 76 and autosomal dominant intellectual developmental disorder 67.;

GenBank Accession Number : NM_000827;

Détails

Origin ID

C207250;

OMIM relation
- Glutamate receptor, ionotropic, ampa 1 [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 5q33.2 [NCIt concept]
gene_is_element_in_pathway
- Amyotrophic Lateral Sclerosis Pathway [NCIt concept]
- Huntington's Disease Pathway [NCIt concept]
- Long-Term Depression Pathway [NCIt concept]
- Neuroactive Ligand-Receptor Signaling Pathway [NCIt concept]
gene_plays_role_in_process
- Ion Transport Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Neuronal Transmission [NCIt concept]
- Receptor Signaling [NCIt concept]
- Transmembrane Transport [NCIt concept]
- Transport Process [NCIt concept]

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