Harmonizome 3.0

like-glycosyltransferase

This gene encodes a member of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, and may carry out the synthesis of glycoprotein and glycosphingolipid sugar chains. It may also be involved in the addition of a repeated disaccharide unit. The protein encoded by this gene is the glycotransferase that adds the final xylose and glucuronic acid to alpha-dystroglycan and thereby allows alpha-dystroglycan to bind ligands including laminin 211 and neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized by cognitive disability and abnormal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2018]

LARGE antisense RNA 1

LARGE intronic transcript 1

ng>neuromedinng> B receptor

This gene encodes a 7-transmembrane G protein-coupled receptor that binds ng>neuromedinng> B, which is a growth factor and mitogen for gastrointestinal epithelial tissue and for normal and neoplastic lung. This receptor may play a role in smooth muscle contraction, neuronal responses, and the regulation of cell growth. Antagonists of this receptor have a potential therapeutic use in inhibiting tumor cell growth. Polymorphisms in this gene may be associated with a susceptibility for schizophrenia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]

ng>neuromedinng> U receptor 2

This gene encodes a protein from the G-protein coupled receptor 1 family. This protein is a receptor for ng>neuromedinng> U, which is a neuropeptide that is widely distributed in the gut and central nervous system. This receptor plays an important role in the regulation of food intake and body weight. [provided by RefSeq, Jul 2008]

ng>neuromedinng> U receptor 1

Enables ng>neuromedinng> U binding activity and ng>neuromedinng> U receptor activity. Involved in several processes, including calcium-mediated signaling; chloride transport; and positive regulation of calcium-mediated signaling. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

ng>neuromedinng> U

This gene encodes a member of the ng>neuromedinng> family of neuropeptides. The encoded protein is a precursor that is proteolytically processed to generate a biologically active neuropeptide that plays a role in pain, stress, immune-mediated inflammatory diseases and feeding regulation. Increased expression of this gene was observed in renal, pancreatic and lung cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. Some of these isoforms may undergo similar processing to generate the mature peptide. [provided by RefSeq, Jul 2015]

ng>neuromedinng> S

This gene encodes a member of the ng>neuromedinng> family of neuropeptides. The encoded preproprotein is proteolytically processed to generate a biologically active neuropeptide that plays a role in the regulation of circadian rhythm, anorexigenic action, antidiuretic action, cardiovascular function and stimulation of oxytocin and vasopressin release. [provided by RefSeq, May 2016]

ng>neuromedinng> B

This gene encodes a member of the bombesin-like family of neuropeptides, which negatively regulate eating behavior. The encoded protein may regulate colonic smooth muscle contraction through binding to its cognate receptor, the ng>neuromedinng> B receptor (NMBR). Polymorphisms of this gene may be associated with hunger, weight gain and obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]

discs, ng>largeng> (Drosophila) homolog-associated protein 2

The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014]

discs, ng>largeng> (Drosophila) homolog-associated protein 3

Predicted to enable PDZ domain binding activity; molecular adaptor activity; and scaffold protein binding activity. Predicted to be involved in modulation of chemical synaptic transmission and protein-containing complex assembly. Predicted to be located in plasma membrane. Predicted to be active in several cellular components, including cholinergic synapse; glutamatergic synapse; and neuromuscular junction. [provided by Alliance of Genome Resources, Mar 2025]

discs, ng>largeng> (Drosophila) homolog-associated protein 1

Predicted to enable molecular adaptor activity. Predicted to be a structural constituent of postsynaptic density. Predicted to be involved in several processes, including aggresome assembly; protein localization to synapse; and regulation of proteasomal protein catabolic process. Predicted to be located in plasma membrane. Predicted to be active in glutamatergic synapse and postsynaptic density, intracellular component. [provided by Alliance of Genome Resources, Mar 2025]

discs, ng>largeng> (Drosophila) homolog-associated protein 4

The product of this gene is a membrane-associated guanylate kinase found at the postsynaptic density in neuronal cells. It is a signaling molecule that can interact with potassium channels and receptors, as well as other signaling molecules. The protein encoded by this gene can interact with PSD-95 through its guanylate kinase domain and may be involved in clustering PSD-95 in the postsynaptic density region. The encoded protein is one of at least four similar proteins that have been found. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

discs, ng>largeng> (Drosophila) homolog-associated protein 5

Predicted to enable microtubule binding activity. Predicted to be involved in several processes, including centrosome localization; kinetochore assembly; and mitotic spindle organization. Located in cytosol; nucleus; and spindle. [provided by Alliance of Genome Resources, Mar 2025]

ribosomal protein, ng>largeng>, P2 pseudogene 2

ribosomal protein, ng>largeng>, P0 pseudogene 10

ribosomal protein, ng>largeng>, P0 pseudogene

ribosomal protein, ng>largeng>, P1 pseudogene 12

ribosomal protein, ng>largeng>, P1 pseudogene 13

ribosomal protein, ng>largeng>, P1 pseudogene 10

ribosomal protein, ng>largeng>, P1 pseudogene 11

ribosomal protein, ng>largeng>, P0 pseudogene 11

potassium channel, calcium activated ng>largeng> conductance subfamily M alpha, member 1

This gene encodes the alpha subunit of calcium-activated BK channel. The encoded protein is involved in several physiological processes including smooth muscle contraction, neurotransmitter release and neuronal excitability. Mutations in this gene are associated with a spectrum of neurological disorders including Paroxysmal Nonkinesigenic Dyskinesia 3, Idiopathic Generalized Epilepsy 16 and Liang-Wang syndrome. [provided by RefSeq, Aug 2022]

DNA primase ng>largeng> subunit-like

ribosomal protein, ng>largeng>, P1 pseudogene 1

ribosomal protein, ng>largeng>, P1 pseudogene 3

ribosomal protein, ng>largeng>, P1 pseudogene 4

ribosomal protein, ng>largeng>, P1 pseudogene 5

ribosomal protein, ng>largeng>, P1 pseudogene 7

ribosomal protein, ng>largeng>, P1 pseudogene 8

ribosomal protein, ng>largeng>, P1 pseudogene 9

discs, ng>largeng> homolog 3 (Drosophila)

This gene encodes a member of the membrane-associated guanylate kinase protein family. The encoded protein may play a role in clustering of NMDA receptors at excitatory synapses. It may also negatively regulate cell proliferation through interaction with the C-terminal region of the adenomatosis polyposis coli tumor suppressor protein. Mutations in this gene have been associated with X-linked cognitive disability. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2009]

discs, ng>largeng> homolog 2 (Drosophila)

This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family. The encoded protein forms a heterodimer with a related family member that may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. Multiple transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described, but their full-length nature is not known. [provided by RefSeq, Dec 2008]

discs, ng>largeng> homolog 5 (Drosophila)

This gene encodes a member of the family of discs ng>largeng> (DLG) homologs, a subset of the membrane-associated guanylate kinase (MAGUK) superfamily. The MAGUK proteins are composed of a catalytically inactive guanylate kinase domain, in addition to PDZ and SH3 domains, and are thought to function as scaffolding molecules at sites of cell-cell contact. The protein encoded by this gene localizes to the plasma membrane and cytoplasm, and interacts with components of adherens junctions and the cytoskeleton. It is proposed to function in the transmission of extracellular signals to the cytoskeleton and in the maintenance of epithelial cell structure. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]

discs, ng>largeng> homolog 1 (Drosophila)

This gene encodes a multi-domain scaffolding protein that is required for normal development. This protein may have a role in septate junction formation, signal transduction, cell proliferation, synaptogenesis and lymphocyte activation. A multitude of transcript variants deriving from alternative splicing and the use of multiple alternate promoter have been observed, including some splice variants that may be specific to brain and other tissues. An upstream uORF may regulate translation at some splice variants of this gene. [provided by RefSeq, Sep 2018]

discs, ng>largeng> homolog 4 (Drosophila)

This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family. It heteromultimerizes with another MAGUK protein, DLG2, and is recruited into NMDA receptor and potassium channel clusters. These two MAGUK proteins may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ng>largeng> tumor suppressor kinase 2

This gene encodes a serine/threonine protein kinase belonging to the LATS tumor suppressor family. The protein localizes to centrosomes during interphase, and early and late metaphase. It interacts with the centrosomal proteins aurora-A and ajuba and is required for accumulation of gamma-tubulin and spindle formation at the onset of mitosis. It also interacts with a negative regulator of p53 and may function in a positive feedback loop with p53 that responds to cytoskeleton damage. Additionally, it can function as a co-repressor of androgen-responsive gene expression. [provided by RefSeq, Jul 2008]

ng>largeng> tumor suppressor kinase 1

The protein encoded by this gene is a putative serine/threonine kinase that localizes to the mitotic apparatus and complexes with cell cycle controller CDC2 kinase in early mitosis. The protein is phosphorylated in a cell-cycle dependent manner, with late prophase phosphorylation remaining through metaphase. The N-terminal region of the protein binds CDC2 to form a complex showing reduced H1 histone kinase activity, indicating a role as a negative regulator of CDC2/cyclin A. In addition, the C-terminal kinase domain binds to its own N-terminal region, suggesting potential negative regulation through interference with complex formation via intramolecular binding. Biochemical and genetic data suggest a role as a tumor suppressor. This is supported by studies in knockout mice showing development of soft-tissue sarcomas, ovarian stromal cell tumors and a high sensitivity to carcinogenic treatments. [provided by RefSeq, Apr 2017]

ribosomal protein, ng>largeng>, P0 pseudogene

ribosomal protein, ng>largeng>, P0 pseudogene 8

ribosomal protein, ng>largeng>, P0 pseudogene 1

ribosomal protein, ng>largeng>, P0 pseudogene 3

ribosomal protein, ng>largeng>, P0 pseudogene 2

ribosomal protein, ng>largeng>, P0 pseudogene 5

ribosomal protein, ng>largeng>, P0 pseudogene 4

ribosomal protein, ng>largeng>, P0 pseudogene 7

ribosomal protein, ng>largeng>, P0 pseudogene 6

Predicted to enable ng>largeng> ribosomal subunit rRNA binding activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in cytoplasmic translation. Predicted to be located in ribosome. Predicted to be part of cytosolic ng>largeng> ribosomal subunit. [provided by Alliance of Genome Resources, Mar 2025]

ribosomal protein, ng>largeng>, P2

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a ng>largeng> 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal phosphoprotein that is a component of the 60S subunit. The protein, which is a functional equivalent of the E. coli L7/L12 ribosomal protein, belongs to the L12P family of ribosomal proteins. It plays an important role in the elongation step of protein synthesis. Unlike most ribosomal proteins, which are basic, the encoded protein is acidic. Its C-terminal end is nearly identical to the C-terminal ends of the ribosomal phosphoproteins P0 and P1. The P2 protein can interact with P0 and P1 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

ribosomal protein, ng>largeng>, P1

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a ng>largeng> 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal phosphoprotein that is a component of the 60S subunit. The protein, which is a functional equivalent of the E. coli L7/L12 ribosomal protein, belongs to the L12P family of ribosomal proteins. It plays an important role in the elongation step of protein synthesis. Unlike most ribosomal proteins, which are basic, the encoded protein is acidic. Its C-terminal end is nearly identical to the C-terminal ends of the ribosomal phosphoproteins P0 and P2. The P1 protein can interact with P0 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Two alternatively spliced transcript variants that encode different proteins have been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

ribosomal protein, ng>largeng>, P0

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a ng>largeng> 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which is the functional equivalent of the E. coli L10 ribosomal protein, belongs to the L10P family of ribosomal proteins. It is a neutral phosphoprotein with a C-terminal end that is nearly identical to the C-terminal ends of the acidic ribosomal phosphoproteins P1 and P2. The P0 protein can interact with P1 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Transcript variants derived from alternative splicing exist; they encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

mitochondrial assembly of ribosomal ng>largeng> subunit 1

Enables mitochondrial ng>largeng> ribosomal subunit binding activity. Involved in negative regulation of mitochondrial translation and ribosomal ng>largeng> subunit biogenesis. Located in cytosol and mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

discs, ng>largeng> (Drosophila) homolog-associated protein 5 pseudogene 1

ng>largeng> 60S subunit nuclear export GTPase 1

This gene encodes a protein related to the yeast ng>largeng> subunit GTPase 1. The encoded protein is necessary for cell viability and may localize in the endoplasmic reticulum, nucleus and cytoplasm.[provided by RefSeq, Feb 2009]

GTPase, very ng>largeng> interferon inducible pseudogene 1

Predicted to enable GTP binding activity. Predicted to be located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

GTPase, very ng>largeng> interferon inducible pseudogene 2

ribosomal protein, ng>largeng>, P2 pseudogene 3

ribosomal protein, ng>largeng> P2, pseudogene 1

ribosomal protein, ng>largeng>, P2 pseudogene 5

ribosomal protein, ng>largeng>, P2 pseudogene 4

calpain 2, (m/II) ng>largeng> subunit

The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct ng>largeng>, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the ng>largeng> subunit of the ubiquitous enzyme, calpain 2. Multiple heterogeneous transcriptional start sites in the 5' UTR have been reported. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

calpain 1, (mu/I) ng>largeng> subunit

The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct ng>largeng>, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the ng>largeng> subunit of the ubiquitous enzyme, calpain 1. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]

ribosomal protein, ng>largeng>, P1 pseudogene 2

ribosomal protein, ng>largeng>, P1 pseudogene 6

LARGE xylosyl- and glucuronyltransferase 2

Predicted to enable dystroglycan binding activity; glucuronosyltransferase activity; and xylosyltransferase activity. Involved in protein O-linked mannosylation. Predicted to be located in intracellular membrane-bounded organelle. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025]

LARGE xylosyl- and glucuronyltransferase 1

This gene encodes a member of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, and may carry out the synthesis of glycoprotein and glycosphingolipid sugar chains. It may also be involved in the addition of a repeated disaccharide unit. The protein encoded by this gene is the glycotransferase that adds the final xylose and glucuronic acid to alpha-dystroglycan and thereby allows alpha-dystroglycan to bind ligands including laminin 211 and neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized by cognitive disability and abnormal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2018]

From DGIdb Drug Targets 2026

interacting proteins for the LARGE NEUROMEDIN N drug from theDGIdb Drug Targets 2026 dataset.

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hematologic diseases; hepatitis, toxic; ng>largeng>-cell lymphomas; lymphoma, ng>largeng> b-cell, diffuse; mucositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease b-cell lymphomas; lymphoma, b-cell; lymphoma, ng>largeng> b-cell, diffuse; lymphoma, ng>largeng>-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, ng>largeng> b-cell, diffuse; lymphoma, ng>largeng>-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse; lymphoma, ng>largeng>-cell, diffuse; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse; lymphoma, ng>largeng>-cell, diffuse; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease ng>largeng>-cell lymphomas; lymphoma, ng>largeng> b-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse; lymphoma, ng>largeng>-cell, diffuse; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse; lymphoma, ng>largeng>-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, ng>largeng> b-cell, diffuse; lymphoma, ng>largeng>-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ng>neuromedinng> in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From GO Molecular Function Annotations 2015

genes performing the ng>neuromedinng> u binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the ng>neuromedinng> u receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the ng>neuromedinng> b receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the ng>neuromedinng> u receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ng>neuromedinng> C (pig) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [¹²⁵I]ng>neuromedinng> U-23 (rat) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [¹²⁵I]ng>neuromedinng> U-8 (pig) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [¹²⁵I]ng>neuromedinng> U-25 (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ng>neuromedinng> B (1-30) (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurotensin/ng>neuromedinng> N protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ng>Neuromedinng> U receptor, type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ng>Neuromedinng> U receptor, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ng>Neuromedinng> U, amidation site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ng>Neuromedinng> B receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bombesin/ng>neuromedinng>-B/ranatensin peptide family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ng>Neuromedinng> U, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ng>Neuromedinng> U receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From GO Molecular Function Annotations 2023

genes performing the type 1 ng>neuromedinng> U receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the type 2 ng>neuromedinng> U receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the ng>neuromedinng> U receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the ng>neuromedinng> U binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the ng>neuromedinng> B receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the ng>neuromedinng> U receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2025

genes performing the ng>neuromedinng> K receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the type 1 ng>neuromedinng> U receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the type 2 ng>neuromedinng> U receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the ng>neuromedinng> U receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the ng>neuromedinng> U binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the ng>neuromedinng> U receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the ng>neuromedinng> B receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the NEUROMEDIN B drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the NEUROMEDIN B (1-30) (HUMAN) drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the NEUROMEDIN C drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the NEUROMEDIN S-33 drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the NEUROMEDIN U-23 drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the NEUROMEDIN U-25 drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the NEUROMEDIN U-8 drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the [125I]NEUROMEDIN U-23 (RAT) drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the [125I]NEUROMEDIN U-25 (HUMAN) drug from theDGIdb Drug Targets 2026 dataset.

From DGIdb Drug Targets 2026

interacting proteins for the [125I]NEUROMEDIN U-8 (PIG) drug from theDGIdb Drug Targets 2026 dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the organellar ng>largeng> ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial ng>largeng> ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytosolic ng>largeng> ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the gamma-tubulin ng>largeng> complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ng>largeng> ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the preribosome, ng>largeng> subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cytosolic ng>largeng> ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chloroplast ng>largeng> ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the organellar ng>largeng> ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial ng>largeng> ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the gamma-tubulin ng>largeng> complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ng>largeng> ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ng>largeng> latent transforming growth factor-beta complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plastid ng>largeng> ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From CORUM Protein Complexes

proteins in the ng>Largeng> Drosha complex protein complex from the CORUM Protein Complexes dataset.

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lymphoma, ng>Largeng> B-Cell, Diffuse from the curated CTD Gene-Disease Associations dataset.

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carcinoma, ng>Largeng> Cell from the curated CTD Gene-Disease Associations dataset.

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lymphoma, ng>Largeng>-Cell, Anaplastic from the curated CTD Gene-Disease Associations dataset.

From CTD Gene-Disease Associations

genes/proteins associated with the disease Male Infertility with ng>Largeng>-Headed, Multiflagellar, Polyploid Spermatozoa from the curated CTD Gene-Disease Associations dataset.

From dbGAP Gene-Trait Associations

genes associated with the trait Lymphoma, ng>Largeng> B-Cell, Diffuse in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

From DISEASES Experimental Gene-Disease Association Evidence Scores

genes associated with the disease ng>largeng> intestine cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease anaplastic ng>largeng> cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease thymus ng>largeng> cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ng>largeng> cell medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ng>largeng> intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ng>largeng> intestine lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease lung ng>largeng> cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ovarian ng>largeng>-cell neuroendocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease t-cell ng>largeng> granular lymphocyte leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease diffuse ng>largeng> b-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ng>largeng> cell carcinoma with rhabdoid phenotype in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ng>largeng> cell acanthoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease pulmonary ng>largeng> cell neuroendocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ng>largeng> cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From GAD Gene-Disease Associations

genes associated with the disease follicular lymphoma to diffuse ng>largeng>-cell lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, ng>largeng> cell; carcinoma, squamous cell; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, ng>largeng> cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, follicular; lymphoma, ng>largeng> b-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease adipocyte size, ng>largeng> subcutaneous abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease diffuse ng>largeng>-cell subtype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease diarrhea; lymphoma, ng>largeng> b-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma; carcinoma, ng>largeng> cell; colorectal neoplasms; leukemia, lymphoid; lung neoplasms; neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; leukemia, lymphocytic, chronic, b-cell; lymphoma, ng>largeng> b-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse; lymphoma, non-hodgkin; lymphoma, t-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease diffuse ng>largeng> b-cell lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, ng>largeng> b-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease leukemia, ng>largeng> granular lymphocytic; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease clonal t-cell ng>largeng> granular lymphocyte disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease arthritis; felty's syndrome; ng>largeng> granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, b-cell; lymphoma, follicular; lymphoma, ng>largeng> b-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease ng>largeng> cell lymphoblastic lymphoma; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, ng>largeng> cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, ng>largeng> cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ng>largeng> in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Crohn's disease_Intestine - ng>Largeng> Intestine - Colon (MMHCC)_GSE6731 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during LGLL - ng>Largeng> granular lymphocytic leukemia_Peripheral blood mononuclear cell_GSE10631 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Cancer of Colon_Intestine - ng>Largeng> Intestine - Colon (MMHCC)_GSE4107 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

From GO Biological Process Annotations 2015

genes participating in the ribosomal ng>largeng> subunit biogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the rna polymerase i transcriptional preinitiation complex assembly at the promoter for the nuclear ng>largeng> rrna transcript biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the ribosomal ng>largeng> subunit assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of ng>largeng> conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of transcription of nuclear ng>largeng> rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of transcription of nuclear ng>largeng> rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the transcription of nuclear ng>largeng> rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of transcription of nuclear ng>largeng> rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of ng>largeng> conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the ribosomal ng>largeng> subunit export from nucleus biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the organellar ng>largeng> ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the mitochondrial ng>largeng> ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the gamma-tubulin ng>largeng> complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the preribosome, ng>largeng> subunit precursor cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the ng>largeng> ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the cytosolic ng>largeng> ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the ng>largeng> conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the ribosomal ng>largeng> subunit binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GWAS Catalog SNP-Phenotype Associations

genes associated with the ng>Largeng> B-cell lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

From GWAS Catalog SNP-Phenotype Associations

genes associated with the ng>Largeng> artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Coronary artery disease or ng>largeng> artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

From GWASdb SNP-Disease Associations

genes associated with the disease ng>largeng> intestine cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

From GWASdb SNP-Phenotype Associations

genes associated with the inflammation of the ng>largeng> intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ng>largeng> intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

From GWASdb SNP-Phenotype Associations

genes associated with the neoplasm of the ng>largeng> intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> sella turcica phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> placenta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> hands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> iliac wings phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> artery calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the contractures of the ng>largeng> joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> hyperpigmented retinal spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the medial calcification of ng>largeng> arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the decreased number of ng>largeng> peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> joint dislocations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> cafe-au-lait macules with irregular margins phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> sternal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the neoplasm of the ng>largeng> intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> beaked nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> posterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the inflammation of the ng>largeng> intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> fleshy ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> intestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the abnormal ng>largeng> intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> clumps of pigment irregularly distributed along hair shaft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> eyes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> foramen magnum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> for gestational age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the ng>largeng> central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the abnormality of the ng>largeng> intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, ng>Largeng>-Cell, Ki-1 phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, ng>Largeng>-Cell, Diffuse phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, ng>Largeng>-Cell, Immunoblastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia, ng>Largeng> Granular Lymphocytic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, ng>Largeng> B-Cell, Diffuse phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Carcinoma, ng>Largeng> Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, ng>Largeng>-Cell, Anaplastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, ng>Largeng>-Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbamoyl-phosphate synthase, ng>largeng> subunit, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal RNA ng>largeng> subunit methyltransferase E protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ng>Largeng> neutral amino acids transporter small subunit 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C2, calpain, ng>largeng> subunit, domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal RNA ng>largeng> subunit methyltransferase F-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase/3-isopropylmalate dehydratase ng>largeng> subunit, alpha/beta/alpha, subdomain 1/3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Citrate synthase-like, ng>largeng> alpha subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA primase ng>largeng> subunit, eukaryotic/archaeal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Very ng>largeng> inducible GTPASE (VLIG)-type guanine nucleotide-binding (G) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase/3-isopropylmalate dehydratase ng>largeng> subunit, alpha/beta/alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribonucleotide reductase ng>largeng> subunit, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbamoyl-phosphate synthetase ng>largeng> subunit-like, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CD81 antigen, ng>largeng> extracellular loop domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbamoyl-phosphate synthase, ng>largeng> subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Iron hydrogenase, ng>largeng> subunit, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA primase, ng>largeng> subunit, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Disks ng>largeng> 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase/3-isopropylmalate dehydratase ng>largeng> subunit, alpha/beta/alpha, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbamoyl-phosphate synthetase, ng>largeng> subunit oligomerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbamoyl-phosphate synthase ng>largeng> subunit, CPSase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the U2 snRNP auxilliary factor, ng>largeng> subunit, splicing factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribonucleotide reductase ng>largeng> subunit, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the increased ng>largeng> intestine adenocarcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the ng>largeng> lymphoid organs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ng>largeng> intestine morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ng>largeng> intestine placement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the ng>largeng> intestinal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the ng>largeng> penis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the ng>largeng> anterior fontanelle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ng>largeng> intestinal transit time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the ng>largeng> orbits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ng>largeng> intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the ng>largeng> ureter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From Pathway Commons Protein-Protein Interactions

interacting proteins for LARGE from the Pathway Commons Protein-Protein Interactions dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-A7CR-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A4XK-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-8043-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-G8-6324-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-G8-6325-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GR-7353-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A4BB-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A86F-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A82F-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GS-A9TT-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-8062-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GR-7351-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-G8-6907-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-8061-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GS-A9TX-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GR-A4D4-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GR-A4D9-01B-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-A7CX-01A-12R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-A7CW-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-G8-6326-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GR-A4D6-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A6HO-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A7DS-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GS-A9TU-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GS-A9TQ-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-VB-A8QN-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GS-A9TV-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A7Q1-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-A7CQ-01A-11R-A38C-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-RQ-A6JB-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-A6HN-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FA-8693-01A-11R-2404-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-8047-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-G8-6914-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-8046-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-8041-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-GR-A4D5-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FM-8000-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-G8-6909-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-G8-6906-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-RQ-A68N-01A-11R-A31O-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Lymphoid Neoplasm Diffuse ng>Largeng> B-cell Lymphoma_DLBC_TCGA-FF-8042-01A-11R-2213-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.