Congenital Hypoplasia Of Thymus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0685891
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Genes

34 genes associated with the disease Congenital Hypoplasia Of Thymus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AK2 adenylate kinase 2
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
ATM ATM serine/threonine kinase
CELF2 CUGBP, Elav-like family member 2
COMT catechol-O-methyltransferase
DCLRE1C DNA cross-link repair 1C
DGCR2 DiGeorge syndrome critical region gene 2
FBXO7 F-box protein 7
FOXI3 forkhead box I3
FOXN1 forkhead box N1
G6PC3 glucose 6 phosphatase, catalytic, 3
GP1BB glycoprotein Ib (platelet), beta polypeptide
HIRA histone cell cycle regulator
IL2RG interleukin 2 receptor, gamma
JMJD1C jumonji domain containing 1C
NEK9 NIMA-related kinase 9
PEX5 peroxisomal biogenesis factor 5
POLR1C polymerase (RNA) I polypeptide C, 30kDa
POLR1D polymerase (RNA) I polypeptide D, 16kDa
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RORC RAR-related orphan receptor C
RREB1 ras responsive element binding protein 1
SEC24C SEC24 family member C
SKIV2L superkiller viralicidic activity 2-like (S. cerevisiae)
TBX1 T-box 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TNF tumor necrosis factor
TP63 tumor protein p63
TTC37 tetratricopeptide repeat domain 37
TTC7A tetratricopeptide repeat domain 7A
UFD1 ubiquitin recognition factor in ER associated degradation 1
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1