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VAT1L vesicle amine transport 1 like [ Homo sapiens (human) ]

Gene ID: 57687, updated on 1-Jun-2020

Summary

Official Symbol
VAT1Lprovided by HGNC
Official Full Name
vesicle amine transport 1 likeprovided by HGNC
Primary source
HGNC:HGNC:29315
See related
Ensembl:ENSG00000171724
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in adrenal (RPKM 44.1), brain (RPKM 16.6) and 3 other tissues See more
Orthologs

Genomic context

See VAT1L in Genome Data Viewer
Location:
16q23.1
Exon count:
9
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 16 NC_000016.10 (77788564..77980107)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (77822483..78014001)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2131 Neighboring gene Sharpr-MPRA regulatory region 41 Neighboring gene uncharacterized LOC107984878 Neighboring gene nudix hydrolase 7 Neighboring gene peptidylprolyl isomerase A pseudogene 50 Neighboring gene uncharacterized LOC105371351 Neighboring gene C-type lectin domain family 3 member A Neighboring gene keratin 8 pseudogene 22

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Phenotypes

NHGRI GWAS Catalog

Description
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
NHGRI GWA Catalog
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
NHGRI GWA Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • KIAA1576

Gene Ontology Provided by GOA

Function Evidence Code Pubs
oxidoreductase activity IEA
Inferred from Electronic Annotation
more info
 
protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
zinc ion binding IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
oxidation-reduction process IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
synaptic vesicle membrane protein VAT-1 homolog-like
Names
vesicle amine transport protein 1 homolog (T. californica)-like
vesicle amine transport protein 1 homolog-like (T. californica)

NCBI Reference Sequences (RefSeq)

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_020927.3NP_065978.1  synaptic vesicle membrane protein VAT-1 homolog-like

    See identical proteins and their annotated locations for NP_065978.1

    Status: VALIDATED

    Source sequence(s)
    AA609348, AC010650, AK290153, BC033537, HY132852
    Consensus CDS
    CCDS32492.1
    UniProtKB/Swiss-Prot
    Q9HCJ6
    UniProtKB/TrEMBL
    A8K288
    Related
    ENSP00000303129.2, ENST00000302536.3
    Conserved Domains (1) summary
    cd08275
    Location:43380
    MDR3; Medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p13 Primary Assembly

    Range
    77788564..77980107
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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