• Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. (nih.gov)
  • The protein belongs to the S9P family of ribosomal proteins. (nih.gov)
  • As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. (nih.gov)
  • Recently, the characteristics of a family of soluble carotenoid-binding proteins (Helical Carotenoid Proteins [HCPs]), paralogs of the N-terminal domain of OCP, were described. (nih.gov)
  • Here, we show that the latter genes encode carotenoid proteins (CTDHs). (nih.gov)
  • This family of proteins contains two subgroups with distinct characteristics. (nih.gov)
  • This gene encodes a member of the Kruppel family of C2H2-type zinc-finger transcription factor proteins. (novusbio.com)
  • While their genomic structure is distinct from other glycosyltransferases, fringe proteins have a fucose-specific beta-1,3-N-acetylglucosaminyltransferase activity that leads to elongation of O-linked fucose residues on Notch, which alters Notch signaling. (prosci-inc.com)
  • This gene product is predicted to be a single-pass type II Golgi membrane protein but it may also be secreted and proteolytically processed like the related proteins in mouse and Drosophila (PMID: 9187150). (prosci-inc.com)
  • This protein belongs to the aldehyde dehydrogenase family of proteins. (nih.gov)
  • This gene encodes a member of the aquaporin family of intrinsic membrane proteins that function as water-selective channels in the plasma membranes of many cells. (antibodies-online.com)
  • Peptide- specific antiserum bound in immunoblots to multiple SMORF proteins with a range of sizes predicted by smorf genes, confirming translation of multiple smorf gene products from these transcripts. (usda.gov)
  • All known 44 variant smorf genes are located in close chromosomal proximity to ves1 genes, which encode proteins that mediate cytoadhesion and contribute to immune evasion. (usda.gov)
  • The observed inhibition of fibronectin binding was confirmed by a reduction in the expression of genes encoding two major fibronectin-binding streptococcal surface proteins, Sof and SfbI. (microbiologyresearch.org)
  • Description: Description of target: This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. (iowaodes.com)
  • The ROR2 protein is part of a family of proteins known as receptor tyrosine kinases (RTKs), which play a role in chemical signaling within cells. (medlineplus.gov)
  • Fibroblast Growth Factors (FGFs) comprise a family of at least eighteen structurally realted proteins that are involved in a multitude of physiological and pathological cellular processes, including cell growth, differentation, angiogenesis, wound healing and tumorgenesis. (prospecbio.com)
  • The protein encoded by this gene belongs to the EGR family of Cys 2 His 2 -type zinc finger proteins. (wikipedia.org)
  • The UGT1 family constitutes a complex gene locus on human chromosome 2q37 and comprises 13 first exons that encode the unique N-terminal domains of the UGT1A proteins and exons 2 to 5 that encode the C-terminal domain, which is identical in all UGT1A family members ( Owens and Ritter, 1992 ). (aspetjournals.org)
  • The IFN-λ proteins are distinct from type-1 and type-2 IFNs in part because they signal through a unique receptor complex that is distinct from those used by type-1 and type-2 IFNs. (cytokinesociety.org)
  • Post-translational modification of host and viral proteins by ubiquitin (Ub) and Ub-like proteins, such as interferon stimulated gene product 15 (ISG15), plays a key role in response to infection. (cdc.gov)
  • Five distinct genes encode closely related FGF receptors, FGFR1 through 5. (rndsystems.com)
  • Four distinct genes encoding closely related FGF receptors, FGFR-1to -4 are known. (prospecbio.com)
  • The most updated annotation shows the gene spanning from 74,173,710 to 74,176,871 base pairs (3,161 bp) with location on the plus strand at position 15q24.1 (Chromosome 15). (wikipedia.org)
  • This gene was thought initially to be located on chromosome X, however, that location has been determined to correspond to a related pseudogene. (thermofisher.com)
  • The chromosome distribution and analysis for WGD-derived duplicated blocks revealed that the legume bZIP genes have expanded mainly by segmental duplication rather than tandem duplication. (datadryad.org)
  • The ADAMTS13 gene is mapped to chromosome 9q34 by genomic sequence analysis. (iowaodes.com)
  • The human EGR-1 protein contains (in its unprocessed form) 543 amino acids with a molecular weight of 57.5 kDa , and the gene is located on the chromosome 5 . (wikipedia.org)
  • The UGT2 family, in contrast, is encoded by separate genes clustered on chromosome 4q13 and consists of the UGT2A and UGT2B subfamilies. (aspetjournals.org)
  • It is linked to the TBCE gene on chromosome 1q42-43 which encodes for the tubulin-specific chaperone E protein [2-4]. (who.int)
  • Mutations in this gene have been associated with autosomal recessive spondylocostal dysostosis 3. (prosci-inc.com)
  • Mutations, amplification and overexpression of this gene, which alters cell cycle progression, are observed frequently in a variety of tumors and may contribute to tumorigenesis. (genetex.com)
  • At least 20 mutations in the ROR2 gene have been found to cause the autosomal recessive form of Robinow syndrome, a condition that affects the development of many parts of the body, particularly the bones. (medlineplus.gov)
  • Autosomal recessive inheritance means both copies of the gene in each cell have mutations. (medlineplus.gov)
  • More than 10 mutations in the ROR2 gene have been identified in people with a disorder called brachydactyly type B1. (medlineplus.gov)
  • Unlike the mutations that cause Robinow syndrome (described above), the ROR2 gene mutations that cause brachydactyly type B1 are described as "gain-of-function" because they appear to cause the ROR2 protein to be continuously active. (medlineplus.gov)
  • Afzal AR, Jeffery S. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B. Hum Mutat. (medlineplus.gov)
  • Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations. (medlineplus.gov)
  • Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B. Nat Genet. (medlineplus.gov)
  • Finally, it seems appropriate to consider the "sodium channel syndrome" (mutations in the gene of the α subunit of the sodium channel, SCN5A gene) as a single clinical entity that may manifest in a wide range of phenotypes, to thus have a better insight on these cardiac syndromes and potential outcomes for their clinical treatment. (bvsalud.org)
  • 500 mutations of this gene have been identified. (msdmanuals.com)
  • The ISLR gene have two known transcript isoforms on the plus strands: ISLR transcript variant 1 and ISLR transcript variant 2. (wikipedia.org)
  • The human gene of ISLR has two alternatively spliced identical isoforms. (wikipedia.org)
  • The mouse Pitx2 gene encodes three distinct protein isoforms (Pitx2a, b, c), and Pitx2c plays a determinant role in left-right atrium signaling from early somitogenesis onward 5 . (nature.com)
  • Alternatively spliced transcript variants encoding distinct isoforms exist. (cancerindex.org)
  • Two transcript variants encoding distinct isoforms have been identified for this gene. (novusbio.com)
  • Alternatively spliced transcript variants encoding distinct isoforms have been described. (thermofisher.com)
  • Multiple transcript variants encoding different isoforms have been found for this gene. (prosci-inc.com)
  • Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified. (abnova.com)
  • Alternatively spliced transcript variants encoding distinct isoforms have been reported. (utsouthwestern.edu)
  • Both variants encode for the same protein. (wikipedia.org)
  • Additionally, Bryson and Lanier found variants of this BGC in six other species in the mint family. (sciencedaily.com)
  • A potential postnatal treatment of Kabuki syndrome type 1 (KS1), caused by pathogenic variants in KMT2D encoding a histone-lysine methyltransferase, has emerged using a mouse model of KS1 (Kmt2d+/ßGeo). (bvsalud.org)
  • Floating-Harbor syndrome (FLHS) is a neurodevelopmental disorder (NDD) caused by truncating variants in exons 33 and 34 of the SNF2-related CREBBP activator protein gene (SRCAP). (bvsalud.org)
  • They all encode evolutionarily conserved glycosyltransferases that act in the Notch signaling pathway to define boundaries during embryonic development. (prosci-inc.com)
  • DOT1L is an evolutionarily conserved gene encoding a lysine methyltransferase (KMT) that methylates histone 3 lysine-79 (H3K79) and was not previously associated with a Mendelian disease in OMIM. (bvsalud.org)
  • This gene encodes a ribosomal protein that is a component of the 40S subunit. (nih.gov)
  • however, these fusions actually involve a ribosomal protein L22 pseudogene located at 3q26, and this gene actually maps to 1p36.3-p36.2. (ucsc.edu)
  • A patient with a MEN 1 gene mutation and one of the MEN 1 tumors is at risk of developing any of the other tumors later on. (msdmanuals.com)
  • A rare type of X-linked HSP, however, has been associated with a myelin protein gene mutation. (medscape.com)
  • Furthermore, they also suggest that calmodulin genes diversified into subfamilies before speciation of Triticum and Aegilops diploid species. (huji.ac.il)
  • Number of Gene Ontology (GO) annotations for this target, consisting of the sum of GO Functions and GO Processes. (nih.gov)
  • What pathways are this gene/protein implicaed in? (cancerindex.org)
  • A BGC is a group of genes located close together in the genome that are involved in the same metabolic pathways. (sciencedaily.com)
  • The BGC cluster of the beautyberry plant contains genes that encode two distinct terpenoid pathways. (sciencedaily.com)
  • These pathways control the activity of genes needed at specific times, and they regulate the interactions between cells as organs and tissues are forming. (medlineplus.gov)
  • PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. (antibodypedia.com)
  • The PKC family of serine/threonine kinases, including PRKCB1 (PKC beta I), is activated intracellularly by signal transduction pathways. (thermofisher.cn)
  • The receptor tyrosine kinase (RTK)-like orphan receptor (ROR)2 belongs to a conserved family of tyrosine kinase receptors that play important roles in some developmental processes, such as chondrogenesis, osteoblastogenesis, and neural differentiation [ 6 , 7 ]. (oncotarget.com)
  • Additional splicing events for FGFR-1 to -3, involving the C-terminal half of the IgIII domain encoded by two mutually exclusive alternative exons, generate FGF receptors with alternative IgIII domains (IIIb and IIIc). (prospecbio.com)
  • PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. (antibodypedia.com)
  • These studies have not, however, identified distinct subtype-specific functions for these receptors in vivo. (aspetjournals.org)
  • Nautilus shows a compact, minimalist genome with few encoding genes and slow evolutionary rates in both non-coding and coding regions among known cephalopods. (nature.com)
  • Conclusions: In summary, this genome-wide identification, characterization and expression analysis of legume bZIP genes provides valuable information for understanding the molecular functions and evolution of the legume bZIP transcription factor family, and highlights potential legume bZIP genes involved in regulating tissue development and abiotic stress responses. (datadryad.org)
  • Together, Lanier and Bryson discovered something highly unusual in the beautyberry genome from the mint family. (sciencedaily.com)
  • We are learning that the physical location of genes within the genome is important," Bryson said. (sciencedaily.com)
  • An outbreak of respiratory disease in Ugandan chimpanzees provides insight into how virus infection can shape the genome and lead to differences in the cell receptor gene that regulate susceptibility to infection. (virology.ws)
  • Further analysis revealed that Aegilops tauschii, the presumed diploid donor of the D-genome of hexaploid wheat, lacks a subfamily-1 calmodulin gene homologue, whereas diploid species related to the progenitors of the A and B genomes do contain such genes. (huji.ac.il)
  • A protein [virus protein, genome-linked by a capsid architecture with 32 distinct cup-shaped depressions. (cdc.gov)
  • Importantly, multiple genomic innovations including gene losses, independent contraction and expansion of specific gene families and their associated regulatory networks likely moulded the evolution of the nautilus pinhole eye. (nature.com)
  • To begin this process, we have isolated two mouse genomic clones encoding alpha 2-AR subtypes and expressed these genes in COS-7 cells for binding studies. (aspetjournals.org)
  • Recent genomic characterization has revealed a high degree of diversity, with vOTUs showing less than 25% amino acids identities within the family. (cdc.gov)
  • The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. (nih.gov)
  • It encodes a membrane-associated tyrosine kinase that has been implicated in the control of cell growth. (cancerindex.org)
  • The report covers research from the authors' laboratories on the structure and regulation of UDP-glucuronosyltransferase (UGT) genes, glucuronidation of xenobiotics and endobiotics, the toxicological relevance of UGTs, the role of UGT polymorphisms in cancer susceptibility, and gene therapy for UGT deficiencies. (aspetjournals.org)
  • Since genes are composed of a given alphabet (A, T, C, G) with fixed pairing properties A-T and C-G, probes can be constructed that attract gene transcripts extracted from cell tissues and cultures. (lu.se)
  • The encoded protein acts as a transcriptional activator. (novusbio.com)
  • In this study, we characterized the general topology of smorf genes, and investigated the gene repertoire, transcriptional profile, and SMORF expression in two distinct Babesia bovis strains, T2Bo and Mo7. (usda.gov)
  • Expression profile of differentially-regulated genes during progression of androgen-independent growth in human prostate cancer cells. (nih.gov)
  • Search the gene expression profiles from curated DataSets in the Gene Expression Omnibus (GEO) repository. (cancerindex.org)
  • Expression varies depending on the nature of the gene. (origene.com)
  • Expression data further revealed that the legume bZIP genes were expressed constitutively or in an organ-specific, development-dependent manner playing roles in multiple seed developmental stages and tissues. (datadryad.org)
  • We also detected several key legume bZIP genes involved in drought- and salt-responses by comparing fold changes of expression values in drought-stressed or salt-stressed roots and leaves. (datadryad.org)
  • We have investigated the developmental expression and subcellular localization of synapsin III, the newest member of the synapsin family, in cultured mouse hippocampal neurons. (jneurosci.org)
  • Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. (genetex.com)
  • This protein has been shown to interact with tumor suppressor protein Rb and the expression of this gene is regulated positively by Rb. (genetex.com)
  • Compared with non-tumorous tissues, both mRNA expression and protein product of ROR2 and Wnt5a genes were significantly increased in NSCLC. (oncotarget.com)
  • It has a distinct pattern of expression in the brain, and its induction has been shown to be associated with neuronal activity. (wikipedia.org)
  • Each member of the PKC family has a specific expression profile and is believed to play a distinct role. (antibodypedia.com)
  • Bone marrow & Lymphoid tissues Brain Breast and female reproductive system Connective & Soft tissue Endocrine tissues Eye Gastrointestinal tract Kidney & Urinary bladder Liver & Gallbladder Lymphoid Male reproductive system Muscle tissues Myeloid Pancreas Proximal digestive tract Respiratory system Skin * nTPM: Normalized TPM levels represent consensus gene expression calculated using two data sets. (antibodypedia.com)
  • Studies on rodent UGT genes have demonstrated that the transcription factors hepatocyte nuclear factor 1 (HNF1) and CAAT-enhancer binding protein are important positive regulators of UGT expression in the liver (Hansen et al. (aspetjournals.org)
  • How Reliable Are Gene Expression-Based and Immunohistochemical Biomarkers Assessed on a Core-Needle Biopsy? (lu.se)
  • A brief introduction to high throughput technologies for measuring and analyzing gene expression is given. (lu.se)
  • The main emphasis is on supervised machine learning methods for classification and prediction of tumor gene expression profiles. (lu.se)
  • Using such probes, one can obtain a fingerprint of the gene expression activity in a macroscopic sample. (lu.se)
  • Microarrays are one such tool that allows for the study of expression of thousands of genes simultaneously. (lu.se)
  • In what follows we limit ourselves to the analysis of gene expression measurements obtained using microarrays with small spots of DNA fixed to glass slides. (lu.se)
  • Levels of gene expression are measured using a preparation of fluorescently labeled tissue RNA (copies of DNA), together with reference RNA labeled with a different fluorochrome, hybridized onto the slides. (lu.se)
  • Despite the availability of six completely sequenced legume genomes, a comprehensive investigation of bZIP family members in legumes has yet to be presented. (datadryad.org)
  • This collaboration with Buell's team led Hamberger's graduate students, Abigail Bryson and Emily Lanier, to discover how several genomes of the mint family have evolved and how these chemistries have emerged over the past 60 million to 70 million years. (sciencedaily.com)
  • As the sequencing and gene annotation projects of entire genomes of many species are headed towards completion (see, e.g. [13] ), massive mapping efforts in biology are now focused on how the genes interact. (lu.se)
  • The family Caliciviridae includes viruses with single-stranded, positive-sense RNA genomes of 7.4-8.3 kb. (cdc.gov)
  • The inheritance in different families can be autosomal dominant, autosomal recessive or either X-linked dominant or recessive. (jefferson.edu)
  • HSP may also be classified as autosomal dominant, autosomal recessive, or X-linked, and each type has several subtypes, which are based on the location of the gene. (medscape.com)
  • Total count of NCBI Gene Reference Into Function hits for target listed in parenthesis, and summary table with links to publications per PMID with the specific text in article that includes the reported target. (nih.gov)
  • This includes viruses in the Nairoviridae family that encode a viral homologue of the ovarian tumor protease (vOTU). (cdc.gov)
  • Studies suggest this is a tumor suppressor gene . (wikipedia.org)
  • Using subfamily-specific DNA probes, calmodulin genes were identified and the chromosomal location of each subfamily was determined by Southern analysis of selected aneuploid lines. (huji.ac.il)
  • The PITX gene encode the paired-like homeodomain transcription factor family. (nature.com)
  • The molecular sequence of this clone aligns with the gene accession number as a point of reference only. (origene.com)
  • Sequence analysis using degenerate primers identified additional smorf genes in each strain, and demonstrated that the smorf gene repertoire varies between strains, with conserved and unique genes in both. (usda.gov)
  • The other clone (M alpha 2-10H) closely resembles the human alpha 2-C10 subtype in sequence but binds with significantly lower affinity to yohimbine and rauwolscine, members of a distinct class of bulky alpha 2-selective antagonists commonly used to evaluate alpha 2-AR function in vivo. (aspetjournals.org)
  • The ROR2 gene provides instructions for making a protein whose function is not well understood. (medlineplus.gov)
  • Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene. (ucsc.edu)
  • Interindividual UGT variability likely plays an important role in drug efficacy and xenobiotic toxicity, as well as in hormonal regulation and certain diseases, which in some cases may be amenable to therapeutic manipulations including gene therapy. (aspetjournals.org)
  • Overview of Multiple Endocrine Neoplasias (MEN) The multiple endocrine neoplasia (MEN) syndromes comprise 4 genetically distinct familial diseases involving adenomatous hyperplasia and malignant tumors in several endocrine glands. (msdmanuals.com)
  • The presentation of degenerative disease in focal areas of the cerebral cortex is the hallmark of the family of diseases referred to as frontotemporal dementia (also termed frontotemporal lobar degeneration). (medscape.com)
  • It could be involved in the hypothalamic regulation of body weight.This gene encodes a member of the Tubby family of bipartite transcription factors. (avivasysbio.com)
  • These studies have provided fundamental insights into UGT gene structure and regulation, isozyme substrate selectivity, and interindividual variability. (aspetjournals.org)
  • Structure and Tissue-Specific Regulation of UGT Genes (P.I.M., P.A.G., Y.I., A.J.H. (aspetjournals.org)
  • Here, we report on the isolation and characterization of calmodulin cDNAs corresponding to 10 genes from hexaploid (bread) wheat (Triticum aestivum). (huji.ac.il)
  • Studies on the mechanisms that regulate UGT genes, in a temporal and tissue-specific manner, should contribute significantly to understanding the basis for these differences. (aspetjournals.org)
  • The new molecular adaptations Hamberger and his team have found open the door for future applications of natural plant products from the mint family. (sciencedaily.com)
  • Molecular cloning and ligand binding studies have shown the alpha 2 class of adrenergic receptor (alpha 2-AR) to be a family of at least three related subtypes in humans. (aspetjournals.org)
  • The molecular interactions of genes and gene products underlie fundamental questions of biology. (lu.se)
  • The protein encoded by this gene belongs to the biotin and lipoic acid synthetases family. (abnova.com)
  • The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance throughout the cell cycle. (genetex.com)
  • Cloning of two mouse genes encoding alpha 2-adrenergic receptor subtypes and identification of a single amino acid in the mouse alpha 2-C10 homolog responsible for an interspecies variation in antagonist binding. (aspetjournals.org)
  • And it is confirmed that the ADAMTS13 gene encodes the von Willebrand factor-cleaving protease (VWFCP). (iowaodes.com)
  • This gene is a member of the protein-tyrosine kinase oncogene family. (cancerindex.org)
  • In humans, the immunoglobulin super family containing leucine-rich repeat (ISLR) protein is encoded by the ISLR gene. (wikipedia.org)
  • EGR-1 (Early growth response protein 1) also known as ZNF268 (zinc finger protein 268) or NGFI-A (nerve growth factor-induced protein A) is a protein that in humans is encoded by the EGR1 gene . (wikipedia.org)
  • Description of the protein which includes the UniProt Function and the NCBI Gene Summary. (nih.gov)
  • Description: RNA profiling data sets generated by the Mouse ENCODE project. (nih.gov)
  • FUNCTION: [Summary is not available for the mouse gene. (utsouthwestern.edu)
  • Bioinformatics studies also revealed the existence of genes coding for homologs of CTD. (nih.gov)
  • Once the abnormal gene products are better understood, specific medical treatments may emerge. (medscape.com)
  • 7 Primers designed to amplify the partial groEL gene encoding heat-shock protein of Anaplasma phagocytophilum EphplgroELF (5′-ATGGTATGCAGTTTGATCGC-3′) and EphplgroELR (5′-TCTACTCTGTCTTTGCGTTC-3′) were used and expected to yield a 625-bp product for Anaplasma phagocytophilum and for Anaplasma platys , respectively. (who.int)
  • A single nucleotide polymorphism in the human gene encoding the HRV C receptor, CDHR3 (cadherin-related family member 3, pictured), is associated with severe disease and asthma. (virology.ws)
  • However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. (origene.com)
  • Gene symbols, accession ids and various other target identifiers. (nih.gov)
  • Smorf genes have multiple semi- conserved and variable blocks, and a large hypervariable insertion in 20 of the 44 genes defines two major branches of the family, termed smorf A and smorf B. A total of 32 smorf genes are simultaneously transcribed in brain sequestered T2Bo strain B. bovis. (usda.gov)
  • pendent of those associated with cretory ducts, columnar epithelia the KRAS gene is more frequent- other key mechanistic characteris- lining the gastrointestinal tract and ly mutated in human cancer, which tics of IARC Group 1 carcinogens. (who.int)
  • FGF activity is mediated by a family of type I transmembrane tyrosine kinases, which undergo dimerization and autophosphorylation after ligand binding. (rndsystems.com)
  • The biological activities of the FGFs are mediated by a family if type I transmembrane tyrosine kinases which undergo dimerization and autophosphorylation after ligand binding. (prospecbio.com)
  • We report 8 patients from 7 Jordanian families, 6 of whom underwent genetic testing and were found to have a 12 bp (155-166 del) deletion within the tubulin-specific chaperone E (TBCE gene) in exon 3 at 1q42-43. (who.int)
  • The availability of genetic testing enables accurate diagnosis of affected children, discovery of carriers and prospective counselling as well as prenatal diagnosis of Sanjad Sakati syndrome in high-risk families. (who.int)
  • This case series reports 8 patients with Sanjad Sakati syndrome from 7 families in Jordan, 6 of whom had genetic testing. (who.int)
  • Family members are offered genetic screening. (msdmanuals.com)
  • This gene encodes a member of the hepatoma-derived growth factor family. (thermofisher.com)
  • This gene is a member of the fringe gene family which also includes radical and manic fringe genes. (prosci-inc.com)
  • Synapsin III, the newest member of the synapsin family, was identified recently. (jneurosci.org)
  • This gene encodes a member of the SLC2A facilitative glucose transporter family. (nih.gov)
  • This gene encodes a member of the adenylate kinase family, which is involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate groups among adenine nucleotides. (antikoerper-online.de)
  • This gene encodes a member of the glyceraldehyde-3-phosphate dehydrogenase protein family. (aipunuobio.com)
  • Over 160 distinct rhinovirus genotypes are grouped into types A, B, and C. The latter cause about 50% of all human upper respiratory tract infections, and have been associated with influenza-like symptoms and acute asthma exacerbations in children. (virology.ws)
  • The human IFN-λ gene family includes 4 distinct genes: IFNL1, IFNL2, IFNL3, and IFNL4. (cytokinesociety.org)
  • Approved gene symbol with link to HUGO Gene Nomenclature Committee. (nih.gov)