Homo sapiens solute carrier family 18 member A2 (SLC18A2), mRNA

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Transport and inhibition mechanism for VMAT2-mediated synaptic vesicle loading of monoamines. [Cell Res. 2024]
Transport and inhibition mechanism for VMAT2-mediated synaptic vesicle loading of monoamines.
Wang Y, Zhang P, Chao Y, Zhu Z, Yang C, Zhou Z, Li Y, Long Y, Liu Y, Li D, et al. Cell Res. 2024 Jan; 34(1):47-57. Epub 2024 Jan 2.
Transport and inhibition mechanisms of human VMAT2. [Nature. 2024]
Transport and inhibition mechanisms of human VMAT2.
Wu D, Chen Q, Yu Z, Huang B, Zhao J, Wang Y, Su J, Zhou F, Yan R, Li N, et al. Nature. 2024 Feb; 626(7998):427-434. Epub 2023 Dec 11.
Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. [Genet Med. 2023]
Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals.
Saida K, Maroofian R, Sengoku T, Mitani T, Pagnamenta AT, Marafi D, Zaki MS, O'Brien TJ, Karimiani EG, Kaiyrzhanov R, et al. Genet Med. 2023 Jan; 25(1):90-102. Epub 2022 Oct 31.

RefSeq protein product
See the reference protein sequence for synaptic vesicular amine transporter (NP_003045.2).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens solute carrier family 18 member A2 (SLC18A2), mRNA
Homo sapiens solute carrier family 18 member A2 (SLC18A2), mRNA
gi|1519312072|ref|NM_003054.6|

Nucleotide
stromal cell-derived factor 1 isoform alpha precursor [Homo sapiens]
stromal cell-derived factor 1 isoform alpha precursor [Homo sapiens]
gi|40316924|ref|NP_954637.1|

Protein

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Nucleotide