lymph node hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Enlargment (swelling) of a lymph node. (Human Phenotype Ontology, HP_0002716)
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25 gene mutations causing the lymph node hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BHLHE40 basic helix-loop-helix family, member e40
BIRC3 baculoviral IAP repeat containing 3
CARD11 caspase recruitment domain family, member 11
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
CISH cytokine inducible SH2-containing protein
CTSV cathepsin V
FAS Fas cell surface death receptor
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL2 interleukin 2
IL6ST interleukin 6 signal transducer
IRF2 interferon regulatory factor 2
ITGAL integrin, alpha L (antigen CD11A (p180), lymphocyte function-associated antigen 1; alpha polypeptide)
MARK2 MAP/microtubule affinity-regulating kinase 2
NFATC2 nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2
PDCD1LG2 programmed cell death 1 ligand 2
PRKDC protein kinase, DNA-activated, catalytic polypeptide
PTEN phosphatase and tensin homolog
PTPN2 protein tyrosine phosphatase, non-receptor type 2
PTPRC protein tyrosine phosphatase, receptor type, C
SPTA1 spectrin, alpha, erythrocytic 1
TANK TRAF family member-associated NFKB activator
TNIP1 TNFAIP3 interacting protein 1
TRAF3IP2 TRAF3 interacting protein 2
ZBTB46 zinc finger and BTB domain containing 46