GRINL1B

glutamate receptor, ionotropic, N-methyl D-aspartate-like 1B
Identifiers
Symbol	GRINL1B
Entrez	84534
HUGO	15712
OMIM	608311
UniProt	Q9BZD3
Other data
Locus	Chr. 4 q12

Glutamate receptor, ionotropic, N-methyl D-aspartate-like 1B, also known as GRINL1B, is a human gene.^[1] The protein encoded by this gene is a subunit of the NMDA receptor.

References

↑ Mohan Raj BK, Roginski RS, Finkernagel SW, Sciorra LJ (2001). "Assignment of GRINL1B, a glutamate receptor-like processed gene, to human chromosome 4q12 by in situ hybridization". Cytogenet. Cell Genet. 95 (3-4): 238–9. doi:10.1159/000059353. PMID 12063407.

External links

GRINL1B protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)

Ion channel, cell surface receptor: ligand-gated ion channels

Cys-loop receptors

5-HT/serotonin	5-HT₃ A B C D E

GABA	GABA_A α₁ α₂ α₃ α₄ α₅ α₆ β₁ β₂ β₃ γ₁ γ₂ γ₃ δ ε π θ GABA_A-ρ ρ₁ ρ₂ ρ₃

Glycine	α₁ α₂ α₃ α₄ β

Nicotinic acetylcholine	monomers: α1 α2 α3 α4 α5 α6 α7 α9 α10 β1 β2 β3 β4 δ ε pentamers: (α3)₂(β4)₃ (α4)₂(β2)₃ (α7)₅ (α1)₂(β4)₃ - Ganglion type (α1)₂β1δε - Muscle type

Zinc	Zinc-activated

Ionotropic glutamates

Ligand-gated only	AMPA (1 2 3 4) Kainate 1 2 3 4 5

Voltage- and ligand-gated	NMDA 1 2A 2B 2C 2D 3A 3B L1A L1B

‘Orphan’	GluD δ₁ δ₂

ATP-gated channels

Purinergic receptors	P2X 1 2 3 4 5 6 7

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