Faster access than browser!
123 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, BPIFB1, BPIFB4, 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, Ensembl genome database project, ENTPD6, Enzyme, ESF1, Euchromatin, FASTKD5, Fatal insomnia, FITM2, G banding, ..., Galactosialidosis, GC-content, Gdnf-inducible zinc finger protein 1, Gene, Gene prediction, Glutathione synthetase, GMEB2, Gs alpha subunit, HUGO Gene Nomenclature Committee, Human, Human genome, ITPA, JAG1, JPH2, Karyotype, KIZ (gene), Kua-UEV, LIME1, Locus (genetics), LZTS3, Maturity onset diabetes of the young, Mitosis, MROH8, NAPB, National Center for Biotechnology Information, Neuronal ceroid lipofuscinosis, NOL5A, Non-coding RNA, NRSN2, OTOR, PANK2 (gene), Pantothenate kinase-associated neurodegeneration, PKIG, PLAGL2, POLR3F, PRIC285, PRNP, Protein, Pseudogene, PXMP4, R3HDML, Reference genome, RTFDC1, SALL4, SERINC3, SLC2A4RG, SLX4IP, SPATA2, SPEF1, SRXN1, STAU1, STK35L1, SUN domain-containing protein 5, 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. Expand index (73 more) »
Adenosine deaminase
Adenosine deaminase (also known as adenosine aminohydrolase, or ADA) is an enzyme involved in purine metabolism.
New!!: Chromosome 20 and Adenosine deaminase · See more »
Adenosine deaminase deficiency
Adenosine deaminase deficiency (also called ADA deficiency or ADA-SCID) is an autosomal recessive metabolic disorder that causes immunodeficiency.
New!!: Chromosome 20 and Adenosine deaminase deficiency · See more »
Adenosylhomocysteinase
Adenosylhomocysteinase (S-adenosylhomocysteine synthase, S-adenosylhomocysteine hydrolase, adenosylhomocysteine hydrolase, S-adenosylhomocysteinase, SAHase, AdoHcyase) is an enzyme that converts S-adenosylhomocysteine to homocysteine and adenosine.
New!!: Chromosome 20 and Adenosylhomocysteinase · See more »
ADNP (gene)
Activity-dependent neuroprotector homeobox is a protein that in humans is encoded by the ADNP gene.
New!!: Chromosome 20 and ADNP (gene) · See more »
Alagille syndrome
Alagille syndrome, Alagille-Watson syndrome or ALGS, is an autosomal dominant genetic disorder that affects the liver, heart, kidney, and other systems of the body.
New!!: Chromosome 20 and Alagille syndrome · See more »
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.
New!!: Chromosome 20 and Albright's hereditary osteodystrophy · See more »
APMAP
Adipocyte plasma membrane-associated protein is a protein that in humans is encoded by the APMAP gene.
New!!: Chromosome 20 and APMAP · See more »
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.
New!!: Chromosome 20 and Arbitrary unit · See more »
ARFGEF2
Brefeldin A-inhibited guanine nucleotide-exchange protein 2 is a protein that in humans is encoded by the ARFGEF2 gene.
New!!: Chromosome 20 and ARFGEF2 · See more »
Arterial tortuosity syndrome
Arterial tortuosity syndrome is a rare congenital connective tissue condition disorder characterized by elongation and generalized tortuosity of the major arteries including the aorta.
New!!: Chromosome 20 and Arterial tortuosity syndrome · See more »
Autosome
An autosome is a chromosome that is not an allosome (a sex chromosome).
New!!: Chromosome 20 and Autosome · See more »
Base pair
A base pair (bp) is a unit consisting of two nucleobases bound to each other by hydrogen bonds.
New!!: Chromosome 20 and Base pair · See more »
BCAS1
Breast carcinoma-amplified sequence 1 is a protein that in humans is encoded by the BCAS1 gene.
New!!: Chromosome 20 and BCAS1 · See more »
BLCAP
Bladder cancer-associated protein is a protein that in humans is encoded by the BLCAP gene.
New!!: Chromosome 20 and BLCAP · See more »
Bone morphogenetic protein 2
Bone morphogenetic protein 2 or BMP-2 belongs to the TGF-β superfamily of proteins.
New!!: Chromosome 20 and Bone morphogenetic protein 2 · See more »
BPIFB1
BPI fold containing family B, member 1 is a protein that in humans is encoded by the BPIFB1 gene.
New!!: Chromosome 20 and BPIFB1 · See more »
BPIFB4
BPI fold containing family B, member 4 is a protein that in humans is encoded by the BPIFB4 gene.
New!!: Chromosome 20 and BPIFB4 · See more »
C20orf27
UPF0687 protein C20orf27 is a protein that in humans is encoded by the C20orf27 gene.
New!!: Chromosome 20 and C20orf27 · See more »
Cathepsin A
Cathepsin A is an enzyme that is classified both as a cathepsin and a carboxypeptidase.
New!!: Chromosome 20 and Cathepsin A · See more »
Cell (biology)
The cell (from Latin cella, meaning "small room") is the basic structural, functional, and biological unit of all known living organisms.
New!!: Chromosome 20 and Cell (biology) · See more »
Centromere
The centromere is the specialized DNA sequence of a chromosome that links a pair of sister chromatids (a dyad).
New!!: Chromosome 20 and Centromere · See more »
Chromosome
A chromosome (from Ancient Greek: χρωμόσωμα, chromosoma, chroma means colour, soma means body) is a DNA molecule with part or all of the genetic material (genome) of an organism.
New!!: Chromosome 20 and Chromosome · See more »
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.
New!!: Chromosome 20 and Consensus CDS Project · See more »
CSRP2BP
CSRP2 binding protein is a protein that in humans is encoded by the CSRP2BP gene.
New!!: Chromosome 20 and CSRP2BP · See more »
CST9L
Cystatin-9-like is a protein that in humans is encoded by the CST9L gene.
New!!: Chromosome 20 and CST9L · See more »
CSTL1
Cystatin-like 1 is a protein that in humans is encoded by the CSTL1 gene.
New!!: Chromosome 20 and CSTL1 · See more »
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.
New!!: Chromosome 20 and CTCFL · See more »
CTNNBL1
Beta-catenin-like protein 1 is a protein that in humans is encoded by the CTNNBL1 gene.
New!!: Chromosome 20 and CTNNBL1 · See more »
DBNDD2
Dysbindin domain-containing protein 2 is a protein that in humans is encoded by the DBNDD2 gene.
New!!: Chromosome 20 and DBNDD2 · See more »
DDX27
DEAD (Asp-Glu-Ala-Asp) box polypeptide 27, also known as DDX27, is a human gene.
New!!: Chromosome 20 and DDX27 · See more »
DEFB118
Beta-defensin 118 is a protein that in humans is encoded by the DEFB118 gene.
New!!: Chromosome 20 and DEFB118 · See more »
DEFB119
Beta-defensin 119 is a protein that in humans is encoded by the DEFB119 gene.
New!!: Chromosome 20 and DEFB119 · See more »
DEFB126
Beta-defensin 126 is a protein that in humans is encoded by the DEFB126 gene.
New!!: Chromosome 20 and DEFB126 · See more »
DEFB127
Beta-defensin 127 is a protein that in humans is encoded by the DEFB127 gene.
New!!: Chromosome 20 and DEFB127 · See more »
DEFB129
Beta-defensin 129 is a protein that in humans is encoded by the DEFB129 gene.
New!!: Chromosome 20 and DEFB129 · See more »
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.
New!!: Chromosome 20 and DLGAP4 · See more »
DNA
Deoxyribonucleic acid (DNA) is a thread-like chain of nucleotides carrying the genetic instructions used in the growth, development, functioning and reproduction of all known living organisms and many viruses.
New!!: Chromosome 20 and DNA · See more »
DNA annotation
DNA annotation or genome annotation is the process of identifying the locations of genes and all of the coding regions in a genome and determining what those genes do.
New!!: Chromosome 20 and DNA annotation · See more »
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.
New!!: Chromosome 20 and DNAJC5 · See more »
EDEM2
ER degradation-enhancing alpha-mannosidase-like 2 is an enzyme that in humans is encoded by the EDEM2 gene.
New!!: Chromosome 20 and EDEM2 · See more »
Endothelin 3
Endothelin-3 is a protein that in humans is encoded by the EDN3 gene.
New!!: Chromosome 20 and Endothelin 3 · See more »
Ensembl genome database project
Ensembl genome database project is a joint scientific project between the European Bioinformatics Institute and the Wellcome Trust Sanger Institute, which was launched in 1999 in response to the imminent completion of the Human Genome Project.
New!!: Chromosome 20 and Ensembl genome database project · See more »
ENTPD6
Ectonucleoside triphosphate diphosphohydrolase 6 is an enzyme that in humans is encoded by the ENTPD6 gene.
New!!: Chromosome 20 and ENTPD6 · See more »
Enzyme
Enzymes are macromolecular biological catalysts.
New!!: Chromosome 20 and Enzyme · See more »
ESF1
ESF1 homolog is a protein that in humans is encoded by the ESF1 gene.
New!!: Chromosome 20 and ESF1 · See more »
Euchromatin
Euchromatin is a lightly packed form of chromatin (DNA, RNA, and protein) that is enriched in genes, and is often (but not always) under active transcription.
New!!: Chromosome 20 and Euchromatin · See more »
FASTKD5
FAST kinase domain-containing protein 5 (FASTKD5) is a protein that in humans is encoded by the FASTKD5 gene on chromosome 20.
New!!: Chromosome 20 and FASTKD5 · See more »
Fatal insomnia
Fatal insomnia is an extremely rare sleep disorder which is typically inherited and results in death within a few months to a few years after onset.
New!!: Chromosome 20 and Fatal insomnia · See more »
FITM2
Fat storage-inducing transmembrane protein 2 is a protein that in humans is encoded by the FITM2 gene.
New!!: Chromosome 20 and FITM2 · See more »
G banding
G-banding, G banding, or Giemsa banding is a technique used in cytogenetics to produce a visible karyotype by staining condensed chromosomes.
New!!: Chromosome 20 and G banding · See more »
Galactosialidosis
Galactosialidosis is a lysosomal storage disease.
New!!: Chromosome 20 and Galactosialidosis · See more »
GC-content
In molecular biology and genetics, GC-content (or guanine-cytosine content) is the percentage of nitrogenous bases on a DNA or RNA molecule that are either guanine or cytosine (from a possibility of four different ones, also including adenine and thymine in DNA and adenine and uracil in RNA).
New!!: Chromosome 20 and GC-content · See more »
Gdnf-inducible zinc finger protein 1
GDNF-inducible zinc finger protein 1 is a protein in humans that is encoded by the GZF1 gene.
New!!: Chromosome 20 and Gdnf-inducible zinc finger protein 1 · See more »
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
New!!: Chromosome 20 and Gene · See more »
Gene prediction
In computational biology, gene prediction or gene finding refers to the process of identifying the regions of genomic DNA that encode genes.
New!!: Chromosome 20 and Gene prediction · See more »
Glutathione synthetase
Glutathione synthetase (GSS) (EC 6.3.2.3) is the second enzyme in the glutathione (GSH) biosynthesis pathway.
New!!: Chromosome 20 and Glutathione synthetase · See more »
GMEB2
Glucocorticoid modulatory element-binding protein 2 is a protein that in humans is encoded by the GMEB2 gene.
New!!: Chromosome 20 and GMEB2 · See more »
Gs alpha subunit
The Gs alpha subunit (Gαs, Gsα, or Gs protein) is a heterotrimeric G protein subunit that activates the cAMP-dependent pathway by activating adenylyl cyclase.
New!!: Chromosome 20 and Gs alpha subunit · See more »
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.
New!!: Chromosome 20 and HUGO Gene Nomenclature Committee · See more »
Human
Humans (taxonomically Homo sapiens) are the only extant members of the subtribe Hominina.
New!!: Chromosome 20 and Human · See more »
Human genome
The human genome is the 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.
New!!: Chromosome 20 and Human genome · See more »
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.
New!!: Chromosome 20 and ITPA · See more »
JAG1
Jagged1 (JAG1) is one of five cell surface proteins (ligands) that interact with 4 receptors in the mammalian Notch signaling pathway.
New!!: Chromosome 20 and JAG1 · See more »
JPH2
Junctophilin 2, also known as JPH2, is a protein which in humans is encoded by the JPH2 gene.
New!!: Chromosome 20 and JPH2 · See more »
Karyotype
A karyotype is the number and appearance of chromosomes in the nucleus of a eukaryotic cell.
New!!: Chromosome 20 and Karyotype · See more »
KIZ (gene)
Kizuna centrosomal protein is a protein that in humans is encoded by the KIZ gene.
New!!: Chromosome 20 and KIZ (gene) · See more »
Kua-UEV
Ubiquitin-conjugating enzyme E2 variant 1, also known as Kua-UEV, is a human gene.
New!!: Chromosome 20 and Kua-UEV · See more »
LIME1
Lck-interacting transmembrane adapter 1 is a protein that in humans is encoded by the LIME1 gene.
New!!: Chromosome 20 and LIME1 · See more »
Locus (genetics)
A locus (plural loci) in genetics is a fixed position on a chromosome, like the position of a gene or a marker (genetic marker).
New!!: Chromosome 20 and Locus (genetics) · See more »
LZTS3
Leucine zipper, putative tumor suppressor family member 3 is a protein in humans that is encoded by the LZTS3 gene.
New!!: Chromosome 20 and LZTS3 · See more »
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.
New!!: Chromosome 20 and Maturity onset diabetes of the young · See more »
Mitosis
In cell biology, mitosis is a part of the cell cycle when replicated chromosomes are separated into two new nuclei.
New!!: Chromosome 20 and Mitosis · See more »
MROH8
MROH8 is a protein that in humans is encoded by the MROH8 gene.
New!!: Chromosome 20 and MROH8 · See more »
NAPB
Beta-soluble NSF attachment protein is a protein that in humans is encoded by the NAPB gene.
New!!: Chromosome 20 and NAPB · See more »
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).
New!!: Chromosome 20 and National Center for Biotechnology Information · See more »
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis (NCL) is the general name for a family of at least eight genetically separate neurodegenerative disorders that result from excessive accumulation of lipopigments (lipofuscin) in the body's tissues.
New!!: Chromosome 20 and Neuronal ceroid lipofuscinosis · See more »
NOL5A
Nucleolar protein 56 is a protein that in humans is encoded by the NOP56 gene.
New!!: Chromosome 20 and NOL5A · See more »
Non-coding RNA
A non-coding RNA (ncRNA) is an RNA molecule that is not translated into a protein.
New!!: Chromosome 20 and Non-coding RNA · See more »
NRSN2
Neurensin-2 is a protein that in humans is encoded by the NRSN2 gene.
New!!: Chromosome 20 and NRSN2 · See more »
OTOR
Otoraplin is a protein that in humans is encoded by the OTOR gene.
New!!: Chromosome 20 and OTOR · See more »
PANK2 (gene)
Pantothenate kinase 2, mitochondrial is an enzyme that in humans is encoded by the PANK2 gene.
New!!: Chromosome 20 and PANK2 (gene) · See more »
Pantothenate kinase-associated neurodegeneration
Pantothenate kinase-associated neurodegeneration (PKAN), also known as neurodegeneration with brain iron accumulation 1 (NBIA1), also called Hallervorden–Spatz syndrome, is a degenerative disease of the brain that can lead to parkinsonism, dystonia, dementia, and ultimately death.
New!!: Chromosome 20 and Pantothenate kinase-associated neurodegeneration · See more »
PKIG
cAMP-dependent protein kinase inhibitor gamma is a protein that in humans is encoded by the PKIG gene.
New!!: Chromosome 20 and PKIG · See more »
PLAGL2
Zinc finger protein PLAGL2 is a protein that in humans is encoded by the PLAGL2 gene.
New!!: Chromosome 20 and PLAGL2 · See more »
POLR3F
DNA-directed RNA polymerase III subunit RPC6 is an enzyme that in humans is encoded by the POLR3F gene.
New!!: Chromosome 20 and POLR3F · See more »
PRIC285
Peroxisomal proliferator-activated receptor A interacting complex 285, also known as PRIC285, is a human gene.
New!!: Chromosome 20 and PRIC285 · See more »
PRNP
PRNP (PRioN Protein) is the human gene encoding for the major prion protein PrP (for prion protein), also known as CD230 (cluster of differentiation 230).
New!!: Chromosome 20 and PRNP · See more »
Protein
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
New!!: Chromosome 20 and Protein · See more »
Pseudogene
Pseudogenes are segments of DNA that are related to real genes.
New!!: Chromosome 20 and Pseudogene · See more »
PXMP4
Peroxisomal membrane protein 4 is a protein that in humans is encoded by the PXMP4 gene.
New!!: Chromosome 20 and PXMP4 · See more »
R3HDML
R3H domain containing-like is a protein in humans that is encoded by the R3HDML gene.
New!!: Chromosome 20 and R3HDML · See more »
Reference genome
A reference genome (also known as a reference assembly) is a digital nucleic acid sequence database, assembled by scientists as a representative example of a species' set of genes.
New!!: Chromosome 20 and Reference genome · See more »
RTFDC1
RTFDC1 is a protein that in humans is encoded by the RTFDC1 gene.
New!!: Chromosome 20 and RTFDC1 · See more »
SALL4
Sal-like protein 4 (SALL4) is a transcription factor encoded by a member of the Spalt-like (SALL) gene family, SALL4.
New!!: Chromosome 20 and SALL4 · See more »
SERINC3
Serine incorporator 3 is a protein that in humans is encoded by the SERINC3 gene.
New!!: Chromosome 20 and SERINC3 · See more »
SLC2A4RG
SLC2A4 regulator is a protein that in humans is encoded by the SLC2A4RG gene.
New!!: Chromosome 20 and SLC2A4RG · See more »
SLX4IP
SLX4 interacting protein is a protein that in humans is encoded by the SLX4IP gene.
New!!: Chromosome 20 and SLX4IP · See more »
SPATA2
Spermatogenesis-associated protein 2 is a protein that in humans is encoded by the SPATA2 gene.
New!!: Chromosome 20 and SPATA2 · See more »
SPEF1
Sperm flagellar protein 1 is a protein that in humans is encoded by the SPEF1 gene.
New!!: Chromosome 20 and SPEF1 · See more »
SRXN1
Sulfiredoxin-1 is a protein that in humans is encoded by the SRXN1 gene.
New!!: Chromosome 20 and SRXN1 · See more »
STAU1
Double-stranded RNA-binding protein Staufen homolog 1 is a protein that in humans is encoded by the STAU1 gene.
New!!: Chromosome 20 and STAU1 · See more »
STK35L1
STK35L1 is a protein that in humans is encoded by the STK35 (serine/threonine kinase 35) gene.
New!!: Chromosome 20 and STK35L1 · See more »
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.
New!!: Chromosome 20 and SUN domain-containing protein 5 · See more »
TASP1
Threonine aspartase 1 is an enzyme that in humans is encoded by the TASP1 gene.
New!!: Chromosome 20 and TASP1 · See more »
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).
New!!: Chromosome 20 and Tissue transglutaminase · See more »
TMEPAI
Transmembrane prostate androgen-induced protein is a protein that in humans is encoded by the PMEPA1 gene.
New!!: Chromosome 20 and TMEPAI · See more »
Transmissible spongiform encephalopathy
Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, are a group of progressive, invariably fatal, conditions that affect the brain (encephalopathies) and nervous system of many animals, including humans.
New!!: Chromosome 20 and Transmissible spongiform encephalopathy · See more »
TTPAL
Tocopherol (alpha) transfer protein-like is a protein that in humans is encoded by the TTPAL gene.
New!!: Chromosome 20 and TTPAL · See more »
UCKL1
Uridine-cytidine kinase-like 1 is an enzyme that in humans is encoded by the UCKL1 gene.
New!!: Chromosome 20 and UCKL1 · See more »
UCSC Genome Browser
The UCSC Genome Browser is an on-line, and downloadable, genome browser hosted by the University of California, Santa Cruz (UCSC).
New!!: Chromosome 20 and UCSC Genome Browser · See more »
UniProt
UniProt is a freely accessible database of protein sequence and functional information, many entries being derived from genome sequencing projects.
New!!: Chromosome 20 and UniProt · See more »
UQCC
Ubiquinol-cytochrome c reductase complex chaperone CBP3 homolog is an enzyme that in humans is encoded by the UQCC gene.
New!!: Chromosome 20 and UQCC · See more »
VAPB
Vesicle-associated membrane protein-associated protein B/C is a protein that in humans is encoded by the VAPB gene.
New!!: Chromosome 20 and VAPB · See more »
Waardenburg syndrome
Waardenburg syndrome is a rare genetic disorder most often characterized by varying degrees of deafness, minor defects in structures arising from the neural crest, and pigmentation changes.
New!!: Chromosome 20 and Waardenburg syndrome · See more »
YTHDF1
YTH domain family, member 1 is a protein that in humans is encoded by the YTHDF1 gene.
New!!: Chromosome 20 and YTHDF1 · See more »
ZFP64
Zinc finger protein 64 homolog, isoforms 1 and 2 is a protein that in humans is encoded by the ZFP64 gene.
New!!: Chromosome 20 and ZFP64 · See more »
ZGPAT
Zinc finger CCCH-type with G patch domain-containing protein is a protein that in humans is encoded by the ZGPAT gene.
New!!: Chromosome 20 and ZGPAT · See more »
ZHX3
Zinc fingers and homeoboxes protein 3 is a protein that in humans is encoded by the ZHX3 gene.
New!!: Chromosome 20 and ZHX3 · See more »
Zinc finger protein 334
Zinc finger protein 334 is a protein that in humans is encoded by the ZNF334 gene.
New!!: Chromosome 20 and Zinc finger protein 334 · See more »
Zinc finger protein 343
Zinc finger protein 343 is a protein that in humans is encoded by the ZNF343 gene.
New!!: Chromosome 20 and Zinc finger protein 343 · See more »
Zinc finger swim-type containing 3
Zinc finger SWIM-type containing 3 is a protein that in humans is encoded by the ZSWIM3 gene.
New!!: Chromosome 20 and Zinc finger swim-type containing 3 · See more »
ZMYND8
Protein kinase C-binding protein 1 is an enzyme that in humans is encoded by the ZMYND8 gene.
New!!: Chromosome 20 and ZMYND8 · See more »
ZNF133
Zinc finger protein 133 is a protein that in humans is encoded by the ZNF133 gene.
New!!: Chromosome 20 and ZNF133 · See more »
Redirects here:
Chromosome 20 (human), Chromosomes, human, pair 20, Human Chromosome 20, Human chromosome 20.
References
[1] https://en.wikipedia.org/wiki/Chromosome_20
