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- Table of Contents
Facts about Chromaffin granule amine transporter.
Human | |
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Gene Name: | SLC18A1 |
Uniprot: | P54219 |
Entrez: | 6570 |
Belongs to: |
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major facilitator superfamily |
CGAT; SLC18A1; solute carrier family 18 (vesicular monoamine), member 1; VAT1; VMAT1
Mass (kDA):
56.257 kDA
Human | |
---|---|
Location: | 8p21.3 |
Sequence: | 8; NC_000008.11 (20144855..20183206, complement) |
Highly expressed in chromaffin cells of the adrenal medulla (at protein level). Detected in peripheral sympathetic ganglia (at protein level). Found in some paracrine cells in stomach and duodenum (at protein level).
[Isoform 1]: Cytoplasmic vesicle membrane; Multi-pass membrane protein. Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane; Multi-pass membrane protein.; [Isoform 2]: Endoplasmic reticulum membrane; Multi-pass membrane protein.
This Boster Bio will provide you with a brief history of Steven Boster, His current research, and upcoming projects. You will also find out about His books. This bio is an invaluable resource for anyone who is interested in advancing our knowledge about the SLC18A1 marker. You'll be able to use this genetic marker in your own research after reading this Boster bio: Best Uses of The SLC18A1Marker.
Steven Boster, a lifelong researcher and historian, compiled many public records that provide information about his past as well as present. You can find Steve Boster's current home address and previous addresses, as well as cell phone numbers and emails, as well as known relatives. To find out more about Steve Boster's life, you can search his public records by state and age. Here are some highlights about Steve Boster.
Don "Steve" Boster grew up in Joliet on July 22, 1924. He died from COVID-19, June 26, 2022. Boster was born to James and Evelyn Meier. He served in the U.S. Army for a time, and was a member of Concordia Hall in Staunton, VA. Boster is survived by his mother Frances, his sisters Kimberly and Tammy, and his son Jonathan and grandson Cory.
His recent discovery of the SLC18A1 gene marked the beginning of his research on the disease. This gene codes the vesicular monamine transporter (VMAT1) protein, which carries neurochemicals throughout your body. This protein is often misfunctioned, which can lead to a variety mental disorders. Several amino acid variants in VMAT1 cause various disorders and mutations at this site are a major part of his current research.
PMID: 8643547 by Erickson J.D., et al. Distinct pharmacological properties and distribution in neurons and endocrine cells of two isoforms of the human vesicular monoamine transporter.
PMID: 16326835 by Essand M., et al. Identification and characterization of a novel splicing variant of vesicular monoamine transporter 1.