lymphoid hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size, usually due to increased cell number, of lymphatic tissues (Mammalian Phenotype Ontology, MP_0000688)
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24 gene mutations causing the lymphoid hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CHD2 chromodomain helicase DNA binding protein 2
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FEN1 flap structure-specific endonuclease 1
FOXO3 forkhead box O3
HMGA1 high mobility group AT-hook 1
IL12RB2 interleukin 12 receptor, beta 2
IL2RA interleukin 2 receptor, alpha
KMT2A lysine (K)-specific methyltransferase 2A
MTUS1 microtubule associated tumor suppressor 1
OTUD7B OTU deubiquitinase 7B
PELI1 pellino E3 ubiquitin protein ligase 1
PPM1D protein phosphatase, Mg2+/Mn2+ dependent, 1D
PTEN phosphatase and tensin homolog
PTPRCAP protein tyrosine phosphatase, receptor type, C-associated protein
RC3H1 ring finger and CCCH-type domains 1
TBK1 TANK-binding kinase 1
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
TOM1L2 target of myb1-like 2 (chicken)
TRAF3IP2 TRAF3 interacting protein 2
UNG uracil-DNA glycosylase