Genes on human chromosome 16

E3 ubiquitin-protein ligase SIAH1 is an enzyme that in humans is encoded by the SIAH1 gene.

F-box only protein 31 is a protein that in humans is encoded by the FBXO31 gene.

Forkhead box protein C2 (FOXC2) also known as forkhead-related protein FKHL14 (FKHL14), transcription factor FKH-14, or mesenchyme fork head protein 1 (MFH1) is a protein that in humans is encoded by the FOXC2 gene. FOXC2 is a member of the fork head box (FOX) family of transcription factors.

Insulin-like growth factor binding protein, acid labile subunit, also known as IGFALS, is a protein which in humans is encoded by the IGFALS gene.

Serine/threonine-protein phosphatase 4 catalytic subunit is an enzyme that in humans is encoded by the PPP4C gene.

AP-1 complex subunit gamma-1 is a protein that in humans is encoded by the AP1G1 gene.

Proline-rich transmembrane protein 2 is a protein that in humans is encoded by the PRRT2 gene.

Rho GDP-dissociation inhibitor 3 is a protein that in humans is encoded by the ARHGDIG gene.

BAI1-associated protein 3 is a protein that in humans is encoded by the BAIAP3 gene.

Cytoplasmic dynein 1 light intermediate chain 2 is a protein that in humans is encoded by the DYNC1LI2 gene.

NLRC3, short for NOD-like receptor family CARD domain containing 3, is an intracellular protein that plays a role in the immune system. It was previously known as nucleotide-binding oligomerization domain, leucine rich repeat and CARD domain containing 3 (NOD3) and CLR16.2. NLRC3 inhibits the activity of T cells. NLRC3 also inhibits the mTOR signalling pathway to block cellular proliferation.

Telomeric repeat-binding factor 2-interacting protein 1 also known as repressor activator protein 1 (Rap1) is a protein that in humans is encoded by the TERF2IP gene.

protein-coding gene in the species Homo sapiens

Exocyst complex component 3-like is a protein that in humans is encoded by the EXOC3L gene.

Protein ITFG3 also known as family with sequence similarity 234 member A (FAM234A) is a protein that in humans is encoded by the ITFG3 gene. Here, the gene is explored as encoded by mRNA found in Homo sapiens. The FAM234A gene is conserved in mice, rats, chickens, zebrafish, dogs, cows, frogs, chimpanzees, and rhesus monkeys. Orthologs of the gene can be found in at least 220 organisms including the tropical clawed frog, pandas, and Chinese hamsters. The gene is located at 16p13.3 and has a total of 19 exons. The mRNA has a total of 3224 bp and the protein has 552 aa. The molecular mass of the

Interferon regulatory factor 8 (IRF8) also known as interferon consensus sequence-binding protein (ICSBP), is a protein that in humans is encoded by the IRF8 gene. IRF8 is a transcription factor that plays critical roles in the regulation of lineage commitment and in myeloid cell maturation including the decision for a common myeloid progenitor (CMP) to differentiate into a monocyte precursor cell.

G protein-coupled receptor 114 is a protein encoded by the ADGRG5 gene. GPR114 is a member of the adhesion GPCR family. Adhesion GPCRs are characterized by an extended extracellular region often possessing N-terminal protein modules that is linked to a TM7 region via a domain known as the GPCR-Autoproteolysis INducing (GAIN) domain.

Mitochondrial import inner membrane translocase subunit TIM16 also known as presequence translocated-associated motor subunit PAM16, mitochondria-associated granulocyte macrophage CSF-signaling molecule, or presequence translocated-associated motor subunit PAM16 is a protein that in humans is encoded by the PAM16 gene.

mammalian protein found in Homo sapiens

SET domain containing 6 is a protein in humans that is encoded by the SETD6 gene.

Septin-1 is a protein that in humans is encoded by the SEPTIN1 gene. It was renamed from SEPT1 to avoid problems where Microsoft Excel would auto-correct the gene name to the date September 1.

Myosin light chain, phosphorylatable, fast skeletal muscle is a protein that in humans is encoded by the MYLPF gene. It is located on chromosome 16 in humans. Myosin light chain, phosphorylatable

Katanin p80 WD40-containing subunit B1 is a protein that in humans is encoded by the KATNB1 gene.

Septin 12 is a protein that in humans is encoded by the SEPT12 gene.

CCNF may also mean Canonical conjunctive normal form in Boolean algebra.

Iroquois-class homeodomain protein IRX-6, also known as Iroquois homeobox protein 6, is a protein that in humans is encoded by the IRX6 gene.

Leucine-rich repeat-containing protein 50 is a protein that in humans is encoded by the LRRC50 gene.

General transcription factor 3C polypeptide 1 is a protein that in humans is encoded by the GTF3C1 gene.

Genetic suppressor element 1 is a protein that in humans is encoded by the GSE1 gene.

Forkhead box protein F1 (FOXF1) is a protein that in humans is encoded by the FOXF1 gene.

Zinc finger protein 267 is a protein that in humans is encoded by the ZNF267 gene.

Bardet–Biedl syndrome 2 protein is a protein that in humans is encoded by the BBS2 gene.

Hyaluronan synthase 3 is an enzyme that in humans is encoded by the HAS3 gene.

Puratrophin-1 is a protein that in humans is encoded by the PLEKHG4 gene.

Bromodomain-containing protein 7 is a protein that in humans is encoded by the BRD7 gene.

Multidrug resistance-associated protein 9 is a protein that in humans is encoded by the ABCC12 gene.

CCR4-NOT transcription complex subunit 1 is a protein that in humans is encoded by the CNOT1 gene.

Iroquois-class homeodomain protein IRX-3, also known as Iroquois homeobox protein 3, is a protein that in humans is encoded by the IRX3 gene.

Nuclear factor of activated T-cells, cytoplasmic 3 is a protein that in humans is encoded by the NFATC3 gene.

Mu-crystallin homolog also known as NADP-regulated thyroid-hormone-binding protein (THBP) is a protein that in humans is encoded by the CRYM gene. Multiple alternatively spliced transcript variants have been found for this gene.

Centromere protein T is a protein that in humans is encoded by the CENPT gene.

Eukaryotic translation initiation factor 3 subunit C (eIF3c) is a protein that in humans is encoded by the EIF3C gene.

Zinc finger protein 598 (ZNF598) is a protein that in humans is encoded by the ZNF598 gene.

NEDD8-activating enzyme E1 regulatory subunit is a protein that in humans is encoded by the NAE1 gene.

Partitioning defective 6 homolog alpha is a protein that in humans is encoded by the PARD6A gene.

Nitrogen permease regulator-like 3 is a protein that in humans is encoded by the NPRL3 gene.

Branched chain ketoacid dehydrogenase kinase (BCKDK) is an enzyme encoded by the BCKDK gene on chromosome 16. This enzyme is part of the mitochondrial protein kinases family and it is a regulator of the valine, leucine, and isoleucine catabolic pathways. BCKDK is found in the mitochondrial matrix and the prevalence of it depends on the type of cell. Liver cells tend to have the lowest concentration of BCKDK, whereas skeletal muscle cells have the highest amount. Abnormal activity of this enzyme often leads to diseases such as maple syrup urine disease and cachexia.

UTP4 is a gene that encodes the protein Cirhin, the gene is also known as CIRH1A and NAIC. This protein contains a WD40 repeat and is localized to the nucleolus where it colocates with UTP15 and WDR43. Biallelic mutations to UTP4 have been associated with North American Indian childhood cirrhosis, a form of inherited cirrhosis of the liver occurring in American Indian children from the Abitibi region of northern Quebec.

Growth factor, augmenter of liver regeneration (ERV1 homolog, S. cerevisiae), also known as GFER, or Hepatopoietin is a protein which in humans is encoded by the GFER gene. This gene is also known as essential for respiration and vegatative growth, augmenter of liver regeneration, and growth factor of Erv1-like/Hepatic regenerative stimulation substance.

Golgi apparatus protein 1 is a protein that in humans is encoded by the GLG1 gene.

Contactin-associated protein-like 4 is a protein that in humans is encoded by the CNTNAP4 gene.

protein-coding gene in the species Homo sapiens

SLX4 (also known as BTBD12 and FANCP) is a protein involved in DNA repair, where it has important roles in the final steps of homologous recombination. Mutations in the gene are associated with the disease Fanconi anemia.

DNA-directed RNA polymerase II subunit RPB3 is an enzyme that in humans is encoded by the POLR2C gene.

thumb|Figure showing the retromer complex. The retromer complex recognizes cargo from the endosome. The VPS35-VPS26-VPS29 trimer forms the cargo recognition complex of the retromer. Vacuolar protein sorting ortholog 35 (VPS35) is a protein involved in autophagy and is implicated in neurodegenerative diseases, such as Parkinson's disease (PD) and Alzheimer's disease (AD). VPS35 is part of a complex called the retromer, which is responsible for transporting select cargo proteins between vesicular structures (e.g., endosomes, lysosomes, vacuoles) and the Golgi apparatus. Mutations in the VPS35 ge

Serine/arginine repetitive matrix protein 2 is a protein that in humans is encoded by the SRRM2 gene.

protein-coding gene in the species Homo sapiens

Cadherin-15 is a protein that in humans is encoded by the CDH15 gene.

Syntaxin-4 is a protein that in humans is encoded by the STX4 gene.

Nucleoside diphosphate kinase 3 is an enzyme that in humans is encoded by the NME3 gene.