Pseudogene in the species Homo sapiens
| glutamate receptor, ionotropic, N-methyl D-aspartate-like 1B |
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| Identifiers |
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| Symbol | GRINL1B |
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| NCBI gene | 84534 |
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| HGNC | 15712 |
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| OMIM | 608311 |
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| UniProt | Q9BZD3 |
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| Other data |
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| Locus | Chr. 4 q12 |
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| Search for |
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| Structures | Swiss-model |
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| Domains | InterPro |
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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. S2CID 6923047.
External links
- GRINL1B+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
Ion channel, cell surface receptor: ligand-gated ion channels
| Cys-loop receptors | | 5-HT/serotonin | |
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| GABA | - GABAA
- α1
- α2
- α3
- α4
- α5
- α6
- β1
- β2
- β3
- γ1
- γ2
- γ3
- δ
- ε
- π
- θ
- GABAA-ρ
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| Glycine | |
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| Nicotinic acetylcholine | - pentamers: (α3)2(β4)3
- (α4)2(β2)3
- (α7)5
- (α1)2(β4)3 - Ganglion type
- (α1)2β1δε - Muscle type
|
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| Zinc | |
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|
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| Ionotropic glutamates | | Ligand-gated only | |
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| Voltage- and ligand-gated | |
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| ‘Orphan’ | |
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|
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| ATP-gated channels | |
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