thymus hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Enlargement of the thymus. (Human Phenotype Ontology, HP_0010516)
External Link
Similar Terms
Downloads & Tools


25 gene mutations causing the thymus hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADRM1 adhesion regulating molecule 1
BHLHE40 basic helix-loop-helix family, member e40
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CDKN2A cyclin-dependent kinase inhibitor 2A
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CISH cytokine inducible SH2-containing protein
CYLD cylindromatosis (turban tumor syndrome)
ERAP1 endoplasmic reticulum aminopeptidase 1
FOXN1 forkhead box N1
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
IL10 interleukin 10
IL2RG interleukin 2 receptor, gamma
KLF13 Kruppel-like factor 13
LCN2 lipocalin 2
NFATC2 nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
PTTG1 pituitary tumor-transforming 1
RNASEL ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent)
SAC3D1 SAC3 domain containing 1
SIT1 signaling threshold regulating transmembrane adaptor 1
SOAT1 sterol O-acyltransferase 1
STK4 serine/threonine kinase 4
TBATA thymus, brain and testes associated
TNFSF10 tumor necrosis factor (ligand) superfamily, member 10
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor