Chromosome 20, the Glossary
Chromosome 20 is one of the 23 pairs of chromosomes in humans.[1]
Table of Contents
141 relations: Adenosine deaminase, Adenosine deaminase deficiency, Adenosylhomocysteinase, ADNP (gene), Alagille syndrome, Albright's hereditary osteodystrophy, APMAP, Arbitrary unit, ARFGEF2, Arterial tortuosity syndrome, Autosome, Base pair, BCAS1, BLCAP, Bone morphogenetic protein 2, BPIFA1, BPIFA2, BPIFA3, BPIFA4P, BPIFB1, BPIFB2, BPIFB3, BPIFB4, BPIFB5P, BPIFB6, BPIFB9P, C20orf27, Cathepsin A, Cell (biology), Centromere, Chromosome, Consensus CDS Project, CSRP2BP, CST9L, CSTL1, CTCFL, CTNNBL1, DBNDD2, DDX27, DEFB118, DEFB119, DEFB126, DEFB127, DEFB129, DLGAP4, DNA, DNA annotation, DNAJC5, EDEM2, Endothelin 3, ... Expand index (91 more) »
- Chromosomes (human)
Adenosine deaminase
Adenosine deaminase (also known as adenosine aminohydrolase, or ADA) is an enzyme involved in purine metabolism. Chromosome 20 and adenosine deaminase are genes on human chromosome 20.
See Chromosome 20 and Adenosine deaminase
Adenosine deaminase deficiency
Adenosine deaminase deficiency (ADA deficiency) is a metabolic disorder that causes immunodeficiency.
See Chromosome 20 and Adenosine deaminase deficiency
Adenosylhomocysteinase
Adenosylhomocysteinase (S-adenosylhomocysteine synthase, S-adenosylhomocysteine hydrolase, adenosylhomocysteine hydrolase, S-adenosylhomocysteinase, SAHase, AdoHcyase) is an enzyme that catalyzes the nicotinamide adenine dinucleotide (NAD+) dependent, reversible hydrolysis of ''S''-adenosylhomocysteine to homocysteine and adenosine. Chromosome 20 and Adenosylhomocysteinase are genes on human chromosome 20.
See Chromosome 20 and Adenosylhomocysteinase
ADNP (gene)
Activity-dependent neuroprotector homeobox is a protein that in humans is encoded by the ADNP gene. Chromosome 20 and ADNP (gene) are genes on human chromosome 20.
See Chromosome 20 and ADNP (gene)
Alagille syndrome
Alagille syndrome (ALGS) is a genetic disorder that affects primarily the liver and the heart.
See Chromosome 20 and Alagille syndrome
Albright's hereditary osteodystrophy
Albright's hereditary osteodystrophy is a form of osteodystrophy, and is classified as the phenotype of pseudohypoparathyroidism type 1A; this is a condition in which the body does not respond to parathyroid hormone.
See Chromosome 20 and Albright's hereditary osteodystrophy
APMAP
Adipocyte plasma membrane-associated protein is a protein that in humans is encoded by the APMAP gene.
Arbitrary unit
In science and technology, an arbitrary unit (abbreviated arb. unit, see below) or procedure defined unit (p.d.u.) is a relative unit of measurement to show the ratio of amount of substance, intensity, or other quantities, to a predetermined reference measurement.
See Chromosome 20 and Arbitrary unit
ARFGEF2
Brefeldin A-inhibited guanine nucleotide-exchange protein 2 is a protein that in humans is encoded by the ARFGEF2 gene. Chromosome 20 and ARFGEF2 are genes on human chromosome 20.
Arterial tortuosity syndrome
Arterial tortuosity syndrome is an extremely rare congenital connective tissue condition disorder characterized by tortuosity, elongation, stenosis, or aneurysms in major and medium-size arteries including the aorta.
See Chromosome 20 and Arterial tortuosity syndrome
Autosome
An autosome is any chromosome that is not a sex chromosome.
See Chromosome 20 and Autosome
Base pair
A base pair (bp) is a fundamental unit of double-stranded nucleic acids consisting of two nucleobases bound to each other by hydrogen bonds.
See Chromosome 20 and Base pair
BCAS1
Breast carcinoma-amplified sequence 1 is a protein that in humans is encoded by the BCAS1 gene. Chromosome 20 and BCAS1 are genes on human chromosome 20.
BLCAP
Bladder cancer-associated protein is a protein that in humans is encoded by the BLCAP gene. Chromosome 20 and BLCAP are genes on human chromosome 20.
Bone morphogenetic protein 2
Bone morphogenetic protein 2 or BMP-2 belongs to the TGF-β superfamily of proteins. Chromosome 20 and Bone morphogenetic protein 2 are genes on human chromosome 20.
See Chromosome 20 and Bone morphogenetic protein 2
BPIFA1
BPI fold containing family A, member 1 (BPIFA1), also known as Palate, lung, and nasal epithelium clone (PLUNC), is a protein that in humans is encoded by the BPIFA1 gene. Chromosome 20 and BPIFA1 are genes on human chromosome 20.
BPIFA2
BPI fold containing family A, member 2 (BPIFA2), also known as Parotid Secretory Protein (PSP), is a protein that in humans is encoded by the BPIFA2 gene. Chromosome 20 and BPIFA2 are genes on human chromosome 20.
BPIFA3
BPI fold containing family A, member 3 (BPIFA3) is a protein that in humans is encoded by the BPIFA3 gene. Chromosome 20 and BPIFA3 are genes on human chromosome 20.
BPIFA4P
BPI fold containing family A, member 4 (BPIFA4) is a non-human protein encoded by the Bpifa4 gene in mammals such as monkey, cat, and cow but does not appear in rodents and humans. Chromosome 20 and BPIFA4P are genes on human chromosome 20.
BPIFB1
BPI fold-containing family B member 1 (BPIFB1) is a protein that in humans is encoded by the BPIFB1 gene. Chromosome 20 and BPIFB1 are genes on human chromosome 20.
BPIFB2
BPI fold-containing family B, member 2, (BPIFB2) also known as bactericidal/permeability-increasing protein-like 1, (BPI-like 1) is a protein that in humans is encoded by the BPIFB2 gene. Chromosome 20 and BPIFB2 are genes on human chromosome 20.
BPIFB3
BPI fold containing family B, member 3 (BPIFB3) is a protein that in humans is encoded by the BPIFB3 gene. Chromosome 20 and BPIFB3 are genes on human chromosome 20.
BPIFB4
BPI fold containing family B, member 4 (BPIFB4) is a protein that in humans is encoded by the BPIFB4 gene. Chromosome 20 and BPIFB4 are genes on human chromosome 20.
BPIFB5P
BPI fold containing family B, member 5 is a non-human protein encoded by the Bpifb5 gene, also known as Lplunc5. The BPIFB5 protein and Bpifb5 gene have been characterized in mammals such as rodents (mouse, rat) and even-toed ungulates (pig, cow) but are apparently lacking in primates and other vertebrates such as birds, reptiles, and amphibians. Chromosome 20 and BPIFB5P are genes on human chromosome 20.
BPIFB6
BPI fold containing family B, member 6 (BPIFB6), also known as bactericidal/permeability-increasing protein-like 3 (BPIL3), is a protein that in humans is encoded by the BPIFB6 gene, also known as BPIL3 and LPLUNC6. Chromosome 20 and BPIFB6 are genes on human chromosome 20.
BPIFB9P
Vomeromodulin is a non-human protein also known as BPI fold containing family B, member 9 (BPIFB9) in the rat encoded by the Bpifb9/RYF3 gene, and as BPI fold containing family B, member 9A (BPIFB9A) encoded by the Bpifb9a gene in the mouse. Chromosome 20 and BPIFB9P are genes on human chromosome 20.
C20orf27
UPF0687 protein C20orf27 is a protein that in humans is encoded by the C20orf27 gene. Chromosome 20 and C20orf27 are genes on human chromosome 20.
See Chromosome 20 and C20orf27
Cathepsin A
Cathepsin A is an enzyme that is classified both as a cathepsin and a carboxypeptidase. Chromosome 20 and cathepsin A are genes on human chromosome 20.
See Chromosome 20 and Cathepsin A
Cell (biology)
The cell is the basic structural and functional unit of all forms of life.
See Chromosome 20 and Cell (biology)
Centromere
The centromere links a pair of sister chromatids together during cell division.
See Chromosome 20 and Centromere
Chromosome
A chromosome is a package of DNA with part or all of the genetic material of an organism.
See Chromosome 20 and Chromosome
Consensus CDS Project
The Consensus Coding Sequence (CCDS) Project is a collaborative effort to maintain a dataset of protein-coding regions that are identically annotated on the human and mouse reference genome assemblies.
See Chromosome 20 and Consensus CDS Project
CSRP2BP
CSRP2 binding protein is a protein that in humans is encoded by the CSRP2BP gene. Chromosome 20 and CSRP2BP are genes on human chromosome 20.
CST9L
Cystatin-9-like is a protein that in humans is encoded by the CST9L gene. Chromosome 20 and CST9L are genes on human chromosome 20.
CSTL1
Cystatin-like 1 is a protein that in humans is encoded by the CSTL1 gene. Chromosome 20 and CSTL1 are genes on human chromosome 20.
CTCFL
Transcriptional repressor CTCFL also known as BORIS (Brother of Regulator of Imprinted Sites) is a protein that in humans is encoded by the CTCFL gene.
CTNNBL1
Beta-catenin-like protein 1 is a protein that in humans is encoded by the CTNNBL1 gene. Chromosome 20 and CTNNBL1 are genes on human chromosome 20.
DBNDD2
Dysbindin domain-containing protein 2 is a protein that in humans is encoded by the DBNDD2 gene. Chromosome 20 and DBNDD2 are genes on human chromosome 20.
DDX27
DEAD (Asp-Glu-Ala-Asp) box polypeptide 27, also known as DDX27, is a human gene. Chromosome 20 and DDX27 are genes on human chromosome 20.
DEFB118
Beta-defensin 118 is a protein that in humans is encoded by the DEFB118 gene. Chromosome 20 and DEFB118 are genes on human chromosome 20.
DEFB119
Beta-defensin 119 is a protein that in humans is encoded by the DEFB119 gene. Chromosome 20 and DEFB119 are genes on human chromosome 20.
DEFB126
Beta-defensin 126 is a protein that in humans is encoded by the DEFB126 gene. Chromosome 20 and DEFB126 are genes on human chromosome 20.
DEFB127
Beta-defensin 127 is a protein that in humans is encoded by the DEFB127 gene. Chromosome 20 and DEFB127 are genes on human chromosome 20.
DEFB129
Beta-defensin 129 is a protein that in humans is encoded by the DEFB129 gene. Chromosome 20 and DEFB129 are genes on human chromosome 20.
DLGAP4
Disks large-associated protein 4 (DAP-4) also known as SAP90/PSD-95-associated protein 4 (SAPAP-4) is a protein that in humans is encoded by the DLGAP4 gene. Chromosome 20 and DLGAP4 are genes on human chromosome 20.
DNA
Deoxyribonucleic acid (DNA) is a polymer composed of two polynucleotide chains that coil around each other to form a double helix.
DNA annotation
In molecular biology and genetics, DNA annotation or genome annotation is the process of describing the structure and function of the components of a genome, by analyzing and interpreting them in order to extract their biological significance and understand the biological processes in which they participate.
See Chromosome 20 and DNA annotation
DNAJC5
DnaJ homolog subfamily C member 5, also known as cysteine string protein or CSP is a protein, that in humans encoded by the DNAJC5 gene. Chromosome 20 and DNAJC5 are genes on human chromosome 20.
EDEM2
ER degradation-enhancing alpha-mannosidase-like 2 is an enzyme that in humans is encoded by the EDEM2 gene. Chromosome 20 and EDEM2 are genes on human chromosome 20.
Endothelin 3
Endothelin-3 is a protein that in humans is encoded by the EDN3 gene. Chromosome 20 and Endothelin 3 are genes on human chromosome 20.
See Chromosome 20 and Endothelin 3
Ensembl genome database project
Ensembl genome database project is a scientific project at the European Bioinformatics Institute, which provides a centralized resource for geneticists, molecular biologists and other researchers studying the genomes of our own species and other vertebrates and model organisms.
See Chromosome 20 and Ensembl genome database project
ENTPD6
Ectonucleoside triphosphate diphosphohydrolase 6 is an enzyme that in humans is encoded by the ENTPD6 gene. Chromosome 20 and ENTPD6 are genes on human chromosome 20.
Enzyme
Enzymes are proteins that act as biological catalysts by accelerating chemical reactions.
ESF1
ESF1 homolog is a protein that in humans is encoded by the ESF1 gene. Chromosome 20 and ESF1 are genes on human chromosome 20.
FAM210B
FAM210B is a gene that which in Homo sapiens encodes the protein FAM210B. Chromosome 20 and FAM210B are genes on human chromosome 20.
FASTKD5
FAST kinase domain-containing protein 5 (FASTKD5) is a protein that in humans is encoded by the FASTKD5 gene on chromosome 20. Chromosome 20 and FASTKD5 are genes on human chromosome 20.
FITM2
Fat storage-inducing transmembrane protein 2 is a protein that in humans is encoded by the FITM2 gene. Chromosome 20 and FITM2 are genes on human chromosome 20.
G banding
G-banding, G banding or Giemsa banding is a technique used in cytogenetics to produce a visible karyotype by staining condensed chromosomes.
See Chromosome 20 and G banding
Galactosialidosis
Galactosialidosis, also known as neuraminidase deficiency with beta-galactosidase deficiency, is a genetic lysosomal storage disease.
See Chromosome 20 and Galactosialidosis
GC-content
In molecular biology and genetics, GC-content (or guanine-cytosine content) is the percentage of nitrogenous bases in a DNA or RNA molecule that are either guanine (G) or cytosine (C).
See Chromosome 20 and GC-content
Gdnf-inducible zinc finger protein 1
GDNF-inducible zinc finger protein 1 is a protein in humans that is encoded by the GZF1 gene. Chromosome 20 and Gdnf-inducible zinc finger protein 1 are genes on human chromosome 20.
See Chromosome 20 and Gdnf-inducible zinc finger protein 1
Gene
In biology, the word gene has two meanings.
Gene prediction
In computational biology, gene prediction or gene finding refers to the process of identifying the regions of genomic DNA that encode genes.
See Chromosome 20 and Gene prediction
Glutathione synthetase
Glutathione synthetase (GSS) is the second enzyme in the glutathione (GSH) biosynthesis pathway. Chromosome 20 and glutathione synthetase are genes on human chromosome 20.
See Chromosome 20 and Glutathione synthetase
GMEB2
Glucocorticoid modulatory element-binding protein 2 is a protein that in humans is encoded by the GMEB2 gene. Chromosome 20 and GMEB2 are genes on human chromosome 20.
Gs alpha subunit
The Gs alpha subunit (Gαs, Gsα) is a subunit of the heterotrimeric G protein Gs that stimulates the cAMP-dependent pathway by activating adenylyl cyclase. Chromosome 20 and Gs alpha subunit are genes on human chromosome 20.
See Chromosome 20 and Gs alpha subunit
Heat shock protein family a (hsp70) member 12b
Heat shock protein family A (Hsp70) member 12B is a protein that in humans is encoded by the HSPA12B gene. Chromosome 20 and Heat shock protein family a (hsp70) member 12b are genes on human chromosome 20.
See Chromosome 20 and Heat shock protein family a (hsp70) member 12b
HUGO Gene Nomenclature Committee
The HUGO Gene Nomenclature Committee (HGNC) is a committee of the Human Genome Organisation (HUGO) that sets the standards for human gene nomenclature.
See Chromosome 20 and HUGO Gene Nomenclature Committee
Human
Humans (Homo sapiens, meaning "thinking man") or modern humans are the most common and widespread species of primate, and the last surviving species of the genus Homo.
Human genome
The human genome is a complete set of nucleic acid sequences for humans, encoded as DNA within the 23 chromosome pairs in cell nuclei and in a small DNA molecule found within individual mitochondria. Chromosome 20 and human genome are chromosomes (human).
See Chromosome 20 and Human genome
ITPA
Inosine triphosphate pyrophosphatase is an enzyme that in humans is encoded by the ITPA gene, by the rdgB gene in bacteria E.coli and the HAM1 gene in yeast S. cerevisiae; the protein is also encoded by some RNA viruses of the Potyviridae family. Chromosome 20 and ITPA are genes on human chromosome 20.
JAG1
Jagged1 (JAG1) is one of five cell surface proteins (ligands) that interact with four receptors in the mammalian Notch signaling pathway. Chromosome 20 and JAG1 are genes on human chromosome 20.
JPH2
Junctophilin 2, also known as JPH2, is a protein which in humans is encoded by the JPH2 gene. Chromosome 20 and JPH2 are genes on human chromosome 20.
Karyotype
A karyotype is the general appearance of the complete set of chromosomes in the cells of a species or in an individual organism, mainly including their sizes, numbers, and shapes.
See Chromosome 20 and Karyotype
Kiaa1755
KIAA1755 is a protein that in humans is encoded by the KIAA1755 gene. Chromosome 20 and Kiaa1755 are genes on human chromosome 20.
See Chromosome 20 and Kiaa1755
KIZ (gene)
Kizuna centrosomal protein is a protein that in humans is encoded by the KIZ gene. Chromosome 20 and KIZ (gene) are genes on human chromosome 20.
See Chromosome 20 and KIZ (gene)
Kua-UEV
Ubiquitin-conjugating enzyme E2 variant 1, also known as Kua-UEV, is a human gene. Chromosome 20 and Kua-UEV are genes on human chromosome 20.
L3MBTL
Lethal(3)malignant brain tumor-like protein is a protein that in humans is encoded by the L3MBTL gene. Chromosome 20 and L3MBTL are genes on human chromosome 20.
LIME1
Lck-interacting transmembrane adapter 1 is a protein that in humans is encoded by the LIME1 gene.
Locus (genetics)
In genetics, a locus (loci) is a specific, fixed position on a chromosome where a particular gene or genetic marker is located.
See Chromosome 20 and Locus (genetics)
LZTS3
Leucine zipper, putative tumor suppressor family member 3 is a protein in humans that is encoded by the LZTS3 gene. Chromosome 20 and LZTS3 are genes on human chromosome 20.
Major prion protein
The major prion protein (PrP) is encoded in the human body by the PRNP gene also known as CD230 (cluster of differentiation 230). Chromosome 20 and major prion protein are genes on human chromosome 20.
See Chromosome 20 and Major prion protein
Maturity-onset diabetes of the young
Maturity-onset diabetes of the young (MODY) refers to any of several hereditary forms of diabetes mellitus caused by mutations in an autosomal dominant gene disrupting insulin production.
See Chromosome 20 and Maturity-onset diabetes of the young
MicroRNA 499a
MicroRNA 499a is a non-coding RNA that in humans is encoded by the MIR499A gene. Chromosome 20 and MicroRNA 499a are genes on human chromosome 20.
See Chromosome 20 and MicroRNA 499a
MIR124-3
MicroRNA 124-3 is a protein that in humans is encoded by the MIR124-3 gene. Chromosome 20 and MIR124-3 are genes on human chromosome 20.
See Chromosome 20 and MIR124-3
Mitosis
Mitosis is a part of the cell cycle in which replicated chromosomes are separated into two new nuclei.
MROH8
MROH8 is a protein in humans that is encoded by the MROH8 gene. Chromosome 20 and MROH8 are genes on human chromosome 20.
NAPB
Beta-soluble NSF attachment protein is a SNAP protein involved in vesicular trafficking and exocytosis which is encoded by the NAPB gene humans is. Chromosome 20 and NAPB are genes on human chromosome 20.
National Center for Biotechnology Information
The National Center for Biotechnology Information (NCBI) is part of the United States National Library of Medicine (NLM), a branch of the National Institutes of Health (NIH).
See Chromosome 20 and National Center for Biotechnology Information
NDUFAF5
NADH:ubiquinone oxidoreductase complex assembly factor 5, also known as Arginine-hydroxylase NDUFAF5, or Putative methyltransferase NDUFAF5, is a protein that in humans is encoded by the NDUFAF5 gene. Chromosome 20 and NDUFAF5 are genes on human chromosome 20.
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis is the general name for a family of at least eight genetically separate neurodegenerative lysosomal storage diseases that result from excessive accumulation of lipopigments (lipofuscin) in the body's tissues.
See Chromosome 20 and Neuronal ceroid lipofuscinosis
Neuronatin
Neuronatin is a protein that in humans is encoded by the NNAT gene involved in mammalian brain development. Chromosome 20 and Neuronatin are genes on human chromosome 20.
See Chromosome 20 and Neuronatin
NOL5A
Nucleolar protein 56 is a protein that in humans is encoded by the NOP56 gene. Chromosome 20 and NOL5A are genes on human chromosome 20.
Non-coding RNA
A non-coding RNA (ncRNA) is a functional RNA molecule that is not translated into a protein.
See Chromosome 20 and Non-coding RNA
NRSN2
Neurensin-2 is a protein that in humans is encoded by the NRSN2 gene. Chromosome 20 and NRSN2 are genes on human chromosome 20.
Osteoclast stimulatory transmembrane protein
Osteoclast stimulatory transmembrane protein is a protein that in humans is encoded by the OCSTAMP gene. Chromosome 20 and Osteoclast stimulatory transmembrane protein are genes on human chromosome 20.
See Chromosome 20 and Osteoclast stimulatory transmembrane protein
OTOR
Otoraplin is a protein that in humans is encoded by the OTOR gene. Chromosome 20 and OTOR are genes on human chromosome 20.
Oxytocin/neurophysin i prepropeptide
Oxytocin/neurophysin I prepropeptide is a protein that in humans is encoded by the OXT gene. Chromosome 20 and Oxytocin/neurophysin i prepropeptide are genes on human chromosome 20.
See Chromosome 20 and Oxytocin/neurophysin i prepropeptide
PANK2 (gene)
Pantothenate kinase 2, mitochondrial is an enzyme that in humans is encoded by the PANK2 gene. Chromosome 20 and PANK2 (gene) are genes on human chromosome 20.
See Chromosome 20 and PANK2 (gene)
Pantothenate kinase-associated neurodegeneration
Pantothenate kinase-associated neurodegeneration (PKAN), formerly called Hallervorden–Spatz syndrome, is a genetic degenerative disease of the brain that can lead to parkinsonism, dystonia, dementia, and ultimately death.
See Chromosome 20 and Pantothenate kinase-associated neurodegeneration
PKIG
cAMP-dependent protein kinase inhibitor gamma is a protein that in humans is encoded by the PKIG gene. Chromosome 20 and PKIG are genes on human chromosome 20.
PLAGL2
Zinc finger protein PLAGL2 is a protein that in humans is encoded by the PLAGL2 gene. Chromosome 20 and PLAGL2 are genes on human chromosome 20.
POLR3F
DNA-directed RNA polymerase III subunit RPC6 is an enzyme that in humans is encoded by the POLR3F gene. Chromosome 20 and POLR3F are genes on human chromosome 20.
PRIC285
Peroxisomal proliferator-activated receptor A interacting complex 285, also known as PRIC285, is a human gene. Chromosome 20 and PRIC285 are genes on human chromosome 20.
Protein
Proteins are large biomolecules and macromolecules that comprise one or more long chains of amino acid residues.
Pseudogene
Pseudogenes are nonfunctional segments of DNA that resemble functional genes.
See Chromosome 20 and Pseudogene
PXMP4
Peroxisomal membrane protein 4 is a protein that in humans is encoded by the PXMP4 gene. Chromosome 20 and PXMP4 are genes on human chromosome 20.
R3HDML
R3H domain containing-like is a protein in humans that is encoded by the R3HDML gene. Chromosome 20 and R3HDML are genes on human chromosome 20.
SALL4
Sal-like protein 4 (SALL4) is a transcription factor encoded by a member of the Spalt-like (SALL) gene family, SALL4. Chromosome 20 and SALL4 are genes on human chromosome 20.
SERINC3
Serine incorporator 3 is a protein that in humans is encoded by the SERINC3 gene. Chromosome 20 and SERINC3 are genes on human chromosome 20.
SHLD1
SHLD1 or shieldin complex subunit 1 is a gene on chromosome 20. Chromosome 20 and SHLD1 are genes on human chromosome 20.
SLC17A9
Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene. Chromosome 20 and SLC17A9 are genes on human chromosome 20.
SLC2A4RG
SLC2A4 regulator is a protein that in humans is encoded by the SLC2A4RG gene. Chromosome 20 and SLC2A4RG are genes on human chromosome 20.
See Chromosome 20 and SLC2A4RG
SLX4IP
SLX4 interacting protein is a protein that in humans is encoded by the SLX4IP gene. Chromosome 20 and SLX4IP are genes on human chromosome 20.
SPATA2
Spermatogenesis-associated protein 2 is a protein that in humans is encoded by the SPATA2 gene. Chromosome 20 and SPATA2 are genes on human chromosome 20.
SPEF1
Sperm flagellar protein 1 is a protein that in humans is encoded by the SPEF1 gene. Chromosome 20 and SPEF1 are genes on human chromosome 20.
SRXN1
Sulfiredoxin-1 is a protein that in humans is encoded by the SRXN1 gene. Chromosome 20 and SRXN1 are genes on human chromosome 20.
STAU1
Double-stranded RNA-binding protein Staufen homolog 1 is a protein that in humans is encoded by the STAU1 gene. Chromosome 20 and STAU1 are genes on human chromosome 20.
STK35L1
STK35L1 is a protein that in humans is encoded by the STK35 (serine/threonine kinase 35) gene. Chromosome 20 and STK35L1 are genes on human chromosome 20.
SUN domain-containing protein 5
SUN domain-containing protein 5, formerly known as sperm-associated antigen 4-like protein (SPAGL4), is a protein that in humans is encoded by the SUN5 gene. Chromosome 20 and SUN domain-containing protein 5 are genes on human chromosome 20.
See Chromosome 20 and SUN domain-containing protein 5
Syntaphilin
Syntaphilin is a protein that in humans is encoded by the SNPH gene. Chromosome 20 and Syntaphilin are genes on human chromosome 20.
See Chromosome 20 and Syntaphilin
TASP1
Threonine aspartase 1 is an enzyme that in humans is encoded by the TASP1 gene. Chromosome 20 and TASP1 are genes on human chromosome 20.
Tissue transglutaminase
Tissue transglutaminase (abbreviated as tTG or TG2) is a 78-kDa, calcium-dependent enzyme of the protein-glutamine γ-glutamyltransferases family (or simply transglutaminase family). Chromosome 20 and Tissue transglutaminase are genes on human chromosome 20.
See Chromosome 20 and Tissue transglutaminase
TMEPAI
Transmembrane prostate androgen-induced protein is a protein that in humans is encoded by the PMEPA1 gene. Chromosome 20 and TMEPAI are genes on human chromosome 20.
Transmissible spongiform encephalopathy
Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, are a group of progressive, incurable, and fatal conditions that are associated with prions and affect the brain and nervous system of many animals, including humans, cattle, and sheep.
See Chromosome 20 and Transmissible spongiform encephalopathy
TTPAL
Tocopherol (alpha) transfer protein-like is a protein that in humans is encoded by the TTPAL gene. Chromosome 20 and TTPAL are genes on human chromosome 20.
UCKL1
Uridine-cytidine kinase-like 1 is an enzyme that in humans is encoded by the UCKL1 gene. Chromosome 20 and UCKL1 are genes on human chromosome 20.
UCSC Genome Browser
The UCSC Genome Browser is an online and downloadable genome browser hosted by the University of California, Santa Cruz (UCSC).
See Chromosome 20 and UCSC Genome Browser
UniProt
UniProt is a freely accessible database of protein sequence and functional information, many entries being derived from genome sequencing projects.
UQCC
Ubiquinol-cytochrome c reductase complex chaperone CBP3 homolog is an enzyme that in humans is encoded by the UQCC gene. Chromosome 20 and UQCC are genes on human chromosome 20.
VAPB
Vesicle-associated membrane protein-associated protein B/C is a protein that in humans is encoded by the VAPB gene. Chromosome 20 and VAPB are genes on human chromosome 20.
Waardenburg syndrome
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin.
See Chromosome 20 and Waardenburg syndrome
YTHDF1
YTH domain family, member 1 is a protein that in humans is encoded by the YTHDF1 gene. Chromosome 20 and YTHDF1 are genes on human chromosome 20.
ZFP64
Zinc finger protein 64 homolog, isoforms 1 and 2 is a protein that in humans is encoded by the ZFP64 gene. Chromosome 20 and ZFP64 are genes on human chromosome 20.
ZGPAT
Zinc finger CCCH-type with G patch domain-containing protein is a protein that in humans is encoded by the ZGPAT gene. Chromosome 20 and ZGPAT are genes on human chromosome 20.
ZHX3
Zinc fingers and homeoboxes protein 3 is a protein that in humans is encoded by the ZHX3 gene. Chromosome 20 and ZHX3 are genes on human chromosome 20.
Zinc finger protein 334
Zinc finger protein 334 is a protein that in humans is encoded by the ZNF334 gene.
See Chromosome 20 and Zinc finger protein 334
Zinc finger protein 343
Zinc finger protein 343 is a protein that in humans is encoded by the ZNF343 gene. Chromosome 20 and Zinc finger protein 343 are genes on human chromosome 20.
See Chromosome 20 and Zinc finger protein 343
Zinc finger swim-type containing 3
Zinc finger SWIM-type containing 3 is a protein that in humans is encoded by the ZSWIM3 gene. Chromosome 20 and Zinc finger swim-type containing 3 are genes on human chromosome 20.
See Chromosome 20 and Zinc finger swim-type containing 3
ZMYND8
Protein kinase C-binding protein 1 is an enzyme that in humans is encoded by the ZMYND8 gene. Chromosome 20 and ZMYND8 are genes on human chromosome 20.
ZNF133
Zinc finger protein 133 is a protein that in humans is encoded by the ZNF133 gene. Chromosome 20 and ZNF133 are genes on human chromosome 20.
See also
Chromosomes (human)
- Chromosome 1
- Chromosome 10
- Chromosome 11
- Chromosome 12
- Chromosome 13
- Chromosome 14
- Chromosome 15
- Chromosome 16
- Chromosome 17
- Chromosome 18
- Chromosome 19
- Chromosome 2
- Chromosome 20
- Chromosome 21
- Chromosome 22
- Chromosome 3
- Chromosome 4
- Chromosome 5
- Chromosome 6
- Chromosome 7
- Chromosome 8
- Chromosome 9
- Human genome
- Lists of human genes
- RCCX
- X chromosome
- Y chromosome
References
[1] https://en.wikipedia.org/wiki/Chromosome_20
Also known as Chromosome 20 (human), Chromosomes, human, pair 20, Human Chromosome 20.
, Ensembl genome database project, ENTPD6, Enzyme, ESF1, FAM210B, FASTKD5, FITM2, G banding, Galactosialidosis, GC-content, Gdnf-inducible zinc finger protein 1, Gene, Gene prediction, Glutathione synthetase, GMEB2, Gs alpha subunit, Heat shock protein family a (hsp70) member 12b, HUGO Gene Nomenclature Committee, Human, Human genome, ITPA, JAG1, JPH2, Karyotype, Kiaa1755, KIZ (gene), Kua-UEV, L3MBTL, LIME1, Locus (genetics), LZTS3, Major prion protein, Maturity-onset diabetes of the young, MicroRNA 499a, MIR124-3, Mitosis, MROH8, NAPB, National Center for Biotechnology Information, NDUFAF5, Neuronal ceroid lipofuscinosis, Neuronatin, NOL5A, Non-coding RNA, NRSN2, Osteoclast stimulatory transmembrane protein, OTOR, Oxytocin/neurophysin i prepropeptide, PANK2 (gene), Pantothenate kinase-associated neurodegeneration, PKIG, PLAGL2, POLR3F, PRIC285, Protein, Pseudogene, PXMP4, R3HDML, SALL4, SERINC3, SHLD1, SLC17A9, SLC2A4RG, SLX4IP, SPATA2, SPEF1, SRXN1, STAU1, STK35L1, SUN domain-containing protein 5, Syntaphilin, TASP1, Tissue transglutaminase, TMEPAI, Transmissible spongiform encephalopathy, TTPAL, UCKL1, UCSC Genome Browser, UniProt, UQCC, VAPB, Waardenburg syndrome, YTHDF1, ZFP64, ZGPAT, ZHX3, Zinc finger protein 334, Zinc finger protein 343, Zinc finger swim-type containing 3, ZMYND8, ZNF133.