human chromosome 16

GPTKB entity

Statements (72)
Predicate Object
gptkbp:instance_of gptkb:physicist
gptkbp:bfsLayer 4
gptkbp:bfsParent gptkb:CYBA
gptkb:FANCF
gptkbp:associated_with various genetic disorders
gptkbp:contains the gene for the protein dystrophin-associated glycoprotein complex
the gene for the enzyme phenylalanine hydroxylase
the gene for the protein apolipoprotein E
the gene for the protein collagen type IV
the gene for the protein dystrophin
the gene for the protein glutamate receptor
the gene for the protein insulin receptor
the gene for the protein interleukin-6
the gene for the protein myelin basic protein
the gene for the protein myeloperoxidase
the gene for the protein neurofibromin
the gene for the protein tumor necrosis factor-alpha
gptkbp:descendant both parents
gptkbp:genetic_diversity approximately 1,000
gptkbp:has multiple single nucleotide polymorphisms (SN Ps)
https://www.w3.org/2000/01/rdf-schema#label human chromosome 16
gptkbp:is_analyzed_in genome-wide association studies (GWAS)
gptkbp:is_associated_with gptkb:psychologist
mental health disorders
cardiovascular diseases
chronic inflammation
developmental disorders
cognitive disorders
gptkbp:is_characterized_by gene duplications
high gene density
high recombination rates
repetitive sequences
structural variations
gptkbp:is_involved_in cell signaling pathways
cellular differentiation
neurodevelopmental processes
the immune response
the regulation of metabolism
the regulation of gene expression
chromosomal rearrangements
the development of the nervous system
the development of various tissues
the immune system regulation
the regulation of cell growth
the response to environmental stress
gptkbp:is_linked_to metabolic disorders
autoimmune diseases
chronic diseases
obesity
schizophrenia
aging processes
fertility issues
endocrine disorders
autism spectrum disorders
metabolic syndromes
various hereditary conditions
gptkbp:is_part_of the study of human evolution
the human genome
the 23 pairs of chromosomes in humans
the genetic basis of human traits
the human genetic architecture
gptkbp:is_studied_in cancer research
genetic research
its evolutionary significance
its implications in genetic testing
its implications in personalized medicine
its role in gene therapy
its role in genetic counseling
its role in hereditary diseases
its role in population genetics
gptkbp:length 90 million base pairs
gptkbp:location located on the 16th chromosome of the human genome