Kalpana Kalpana (Editor)

Chromosome 16 (human)

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Length (bp)
  
90,338,345 bp

Type
  
Autosome

RefSeq
  
NC_000016

No. of genes
  
1,920 2,256

Centromere position
  
Metacentric

GenBank
  
CM000678

Chromosome 16 (human)

Chromosome 16 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 16 spans about 90 million base pairs (the building material of DNA) and represents just under 3% of the total DNA in cells.

Contents

Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to genome annotation their predictions of the number of genes on each chromosome varies. In January 2017, two estimates differed by 18%, with one estimate giving 1,920 genes, and the other estimate giving 2,256 genes.

In February 2010, a new cause of obesity due to a microdeletion on chromosome 16 was announced. It may explain about 1% of obesity cases. Research showed that this microdeletion is relatively common in obese people but lacking in most non-obese people.

Associated genes

  • ACSM2B: encoding enzyme Acyl-coenzyme A synthetase ACSM2B, mitochondrial
  • ACSM3: encoding enzyme Acyl-coenzyme A synthetase ACSM3, mitochondrial 2
  • ARL6IP1: encoding protein ADP-ribosylation factor-like protein 6-interacting protein 1
  • ARMC5
  • ADHD1: Attention deficit-hyperactivity disorder, susceptibility to, 1
  • BMIQ5: Body mass index quantitative trait locus 5
  • C16orf13/JFP2: encoding protein Chromosome 16 open reading frame 13
  • C16orf62: encoding protein Chromosome 16 open reading frame 62
  • C16orf95
  • C16orf96
  • CHDS1: Coronary heart disease, susceptibility to, 1
  • DEL16p13.3, RSTSS: Chromosome 16p13.3 deletion syndrome (Rubinstein-Taybi deletion syndrome)
  • DUP16p13.3, C16DUPq13.3: Chromosome 16p13.3 duplication syndrome
  • HBHR, ATR1: Alpha-thalassemia/mental retardation syndrome, type 1
  • IBD8: Inflammatory bowel disease 8
  • IHPS2: Pyloric stenosis, infantile hypertrophic, 2
  • MC1R: melanocortin 1 receptor
  • MCOPCT1: Microphthalmia with cataract 1
  • PKDTS: Polycystic kidney disease, infantile severe, with tuberous sclerosis
  • RPS15A: encoding protein 40S ribosomal protein S15a
  • Diseases and disorders

  • Trisomy 16
  • Familial Mediterranean fever (FMF)
  • Thalassemia
  • Autosomal dominant polycystic kidney disease (PKD-1)
  • Asperger syndrome
  • Schizophrenia
  • Attention deficit hyperactivity disorder (ADHD)
  • Synesthesia
  • Associated traits

  • Red hair
  • References

    Chromosome 16 (human) Wikipedia