Genes on human chromosome 6

Probable lysosomal cobalamin transporter is a protein that in humans is encoded by the LMBRD1 gene.

Neurensin-1 is a protein that in humans is encoded by the NRSN1 gene.

protein-coding gene in the species Homo sapiens

protein family

Dual specificity protein phosphatase 22 is an enzyme that in humans is encoded by the DUSP22 gene.

Olfactory receptor 12D3 is a protein that in humans is encoded by the OR12D3 gene.

Splicing factor 3B subunit 5 is a protein that in humans is encoded by the SF3B5 gene.

Histone H2B type 1-H is a protein that in humans is encoded by the HIST1H2BH gene.

NHL repeat-containing protein 1 is a protein that in humans is encoded by the NHLRC1 gene.

Akirin-2 is a protein that in humans is encoded by the AKIRIN2 gene.

SAM pointed domain-containing Ets transcription factor is a protein that in humans is encoded by the SPDEF gene.

protein-coding gene in the species Homo sapiens

cAMP-dependent protein kinase inhibitor beta is a protein that in humans is encoded by the PKIB gene.

Histone H2A type 1-J is a protein that in humans is encoded by the HIST1H2AJ gene.

Beta-taxilin is a protein that in humans is encoded by the TXLNB gene.

Differentially expressed in FDCP 6 homolog is a protein that in humans is encoded by the DEF6 gene.

Golgi-associated PDZ and coiled-coil motif-containing protein is a protein that in humans is encoded by the GOPC gene.

Dynein light chain Tctex-type 1 is a protein that in humans is encoded by the DYNLT1 gene.

Histone H1.1 is a protein that in humans is encoded by the HIST1H1A gene.

Serpin B9 is a protein that in humans is encoded by the SERPINB9 gene. Serpin B9 is an inhibitor of Granzyme B (GzmB). GzmB is a potent cytotoxic molecule that is secreted by cytotoxic T lymphocytes and natural killer (NK) cells to induce apoptosis in target cells during an immune response. Serpin B9, expressed in the cytosol and nucleus, thus protects from apoptosis by cytotoxic T lymphocytes and NK cells.

Corneodesmosin is a protein that in humans is encoded by the CDSN gene.

Heme-binding protein 2 is a protein that in humans is encoded by the HEBP2 gene.

Zinc finger protein PLAGL1 is a protein that in humans is encoded by the PLAGL1 gene.

FYVE, RhoGEF and PH domain-containing protein 2 (FGD2), also known as zinc finger FYVE domain-containing protein 4 (ZFYVE4), is a protein that in humans is encoded by the FGD2 gene.

Cyclic GMP-AMP synthase is a protein that in humans is encoded by the CGAS gene. It's an enzyme, a nucleotidyltransferase, a cyclic GMP-AMP synthase. == References ==

C6orf58 is a human gene located at locus 6q22.33 of chromosome 6 and encodes for UPF0762, a protein which is subsequently secreted after cleavage of a signal peptide. DUF781, which is the singular identifiable domain in UPF0762, is tied to liver development in an orthologous protein in zebrafish. The function of the human UPF0762 is not yet well characterized.

Dysbindin, short for dystrobrevin-binding protein 1, is a protein constituent of the dystrophin-associated protein complex (DPC) of skeletal muscle cells. It is also a part of BLOC-1, or biogenesis of lysosome-related organelles complex 1.In humans, dysbindin is encoded by the DTNBP1 gene.

Mas-related G-protein coupled receptor MRG is a protein that in humans is encoded by the MAS1L gene.

thumb|Oscillations of Runx2 mRNA levels. Runt-related transcription factor 2 (RUNX2) also known as core-binding factor subunit alpha-1 (CBF-alpha-1) is a protein that in humans is encoded by the RUNX2 gene. RUNX2 is a key transcription factor associated with osteoblast differentiation.

Osteopetrosis-associated transmembrane protein 1 is a protein that in humans is encoded by the OSTM1 gene. It is required for osteoclast and melanocyte maturation and function.

TATA box-binding protein-like protein 1 is a protein that in humans is encoded by the TBPL1 gene.

mammalian protein found in Homo sapiens

protein-coding gene in the species Homo sapiens

The Abelson helper integration site 1 (AHI1) is a protein coding gene that is known for the critical role it plays in brain development. Proper cerebellar and cortical development in the human brain depends heavily on AHI1. The AHI1 gene is prominently expressed in the embryonic hindbrain and forebrain. AHI1 specifically encodes the Jouberin protein and mutations in the expression of the gene is known to cause specific forms of Joubert syndrome. Joubert syndrome is autosomal recessive and is characterized by the brain malformations and mental retardation that AHI1 mutations have the potential

NADPH oxidase 3 is an enzyme that in humans is encoded by the NOX3 gene.

Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 is an enzyme that in humans is encoded by the DHX16 gene.

Olfactory receptor 5V1 is a protein that in humans is encoded by the OR5V1 gene.

sex-specific cell surface antigen in mammals

Histone H2B type 1-M is a protein that in humans is encoded by the HIST1H2BM gene.

Molybdenum cofactor biosynthesis protein 1 is a protein that in humans and other animals, fungi, and cellular slime molds, is encoded by the MOCS1 gene.

High-mobility group protein HMG-I/HMG-Y is a protein that in humans is encoded by the HMGA1 gene.

Alpha-(1,3)-fucosyltransferase is an enzyme that in humans is encoded by the FUT9 gene.

NADH:ubiquinone oxidoreductase complex assembly factor 4, (NDUFAF4) also known as Hormone-regulated proliferation-associated protein of 20 kDa, (HRPAP20) or C6orf66 is a protein that in humans is encoded by the NDUFAF4 gene. NDUFAF4 is a mitochondrial assembly protein involved in the assembly of NADH dehydrogenase (ubiquinone) also known as complex I, which is located in the mitochondrial inner membrane and is the largest of the five complexes of the electron transport chain. Mutations in this gene have been associated with complex I deficiency and infantile mitochondrial encephalomyopathy. El

Diphosphoinositol polyphosphate phosphohydrolase 1 is an enzyme that in humans is encoded by the NUDT3 gene.

HLA class II histocompatibility antigen, DQ(6) alpha chain is a protein that in humans is encoded by the HLA-DQA2 gene. Also known as HLA-DXA or DAAP-381D23.2, it is part of the human leukocyte antigen system.

Radial spoke head protein 4 homolog A, also known as radial spoke head-like protein 3, is a protein that in humans is encoded by the RSPH4A gene.

InterPro Family

mammalian protein found in Homo sapiens

CARMIL1 is a protein that in humans is encoded by the CARMIL1 gene. The gene is also known as LRRC16, LRRC16A, CARMIL, or CARMIL1a.

HLA class I histocompatibility antigen, alpha chain F is a protein that in humans is encoded by the HLA-F gene. It is an empty intracellular molecule that encodes a non-classical heavy chain anchored to the membrane and forming a heterodimer with a β-2 microglobulin light chain. It belongs to the HLA class I heavy chain paralogues that separate from most of the HLA heavy chains. HLA-F is localized in the endoplasmic reticulum and Golgi apparatus, and is also unique in the sense that it exhibits few polymorphisms in the human population relative to the other HLA genes; however, there have been

Spliceosome RNA helicase BAT1 is an enzyme that in humans is encoded by the BAT1 gene.

Solute carrier family 17 (organic anion transporter), member 3 is a protein that in humans is encoded by the SLC17A3 gene.

Tripartite motif containing 38 is a protein that in humans is encoded by the TRIM38 gene.

POU domain, class 3, transcription factor 2 is a protein that in humans is encoded by the POU3F2 gene.

Magnesium transporter MRS2 homolog, mitochondrial is a protein that in humans is encoded by the MRS2 gene.

Superoxide dismutase 2, mitochondrial (SOD2), also known as manganese-dependent superoxide dismutase (MnSOD), is an enzyme which in humans is encoded by the SOD2 gene on chromosome 6. A related pseudogene has been identified on chromosome 1. Alternative splicing of this gene results in multiple transcript variants. This gene is a member of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. This protein binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen p

Cilia And Flagella Associated Protein 206 (CFAP206) is a gene that in humans encodes a protein “DUF3508”. This protein has a function that is not currently very well understood. Other known aliases are “dJ382I10.1, UPF0704 Protein C6orf165.” In humans, the gene coding sequence is 56,501 base pairs long, with an mRNA of 2,215 base pairs, and a protein sequence of 622 amino acids. The C6orf165 gene is conserved in chimpanzee, rhesus monkey, dog, cow, mouse, rat, chicken, zebrafish, mosquito, frog, and more C6orf165 is rarely expressed in humans, with relatively high expression in brain, lungs (t

Radial spoke head protein 3 homolog (RSPH3), also known as radial spoke head-like protein 2 (RSHL2), is a protein that in humans is encoded by the RSPH3 gene.

Histone H1.4 is a protein that in humans is encoded by the HIST1H1E gene.

protein-coding gene in the species Homo sapiens