eczema Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin. (Human Disease Ontology, DOID_2723)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000964
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Genes

73 genes associated with the eczema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALAS2 5'-aminolevulinate synthase 2
ARID1B AT rich interactive domain 1B (SWI1-like)
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
BTD biotinidase
C5 complement component 5
CARD14 caspase recruitment domain family, member 14
CASP8 caspase 8, apoptosis-related cysteine peptidase
CASR calcium-sensing receptor
CD3G CD3g molecule, gamma (CD3-TCR complex)
COMT catechol-O-methyltransferase
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
DHCR7 7-dehydrocholesterol reductase
DOCK8 dedicator of cytokinesis 8
EDA ectodysplasin A
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain
FECH ferrochelatase
FERMT1 fermitin family member 1
FLG filaggrin
FOXP3 forkhead box P3
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GP1BB glycoprotein Ib (platelet), beta polypeptide
HDAC4 histone deacetylase 4
HIRA histone cell cycle regulator
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
IL7R interleukin 7 receptor
KANSL1 KAT8 regulatory NSL complex subunit 1
KRT1 keratin 1, type II
KRT16 keratin 16, type I
KRT9 keratin 9, type I
LBR lamin B receptor
LIG4 ligase IV, DNA, ATP-dependent
MBTPS2 membrane-bound transcription factor peptidase, site 2
MCCC2 methylcrotonoyl-CoA carboxylase 2 (beta)
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
NCF4 neutrophil cytosolic factor 4, 40kDa
NOD2 nucleotide-binding oligomerization domain containing 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
PAH phenylalanine hydroxylase
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PGM3 phosphoglucomutase 3
PIGA phosphatidylinositol glycan anchor biosynthesis, class A
PTPRC protein tyrosine phosphatase, receptor type, C
RBCK1 RanBP-type and C3HC4-type zinc finger containing 1
RBM8A RNA binding motif protein 8A
SAT1 spermidine/spermine N1-acetyltransferase 1
SBDS Shwachman-Bodian-Diamond syndrome
SHOC2 soc-2 suppressor of clear homolog (C. elegans)
SLC30A2 solute carrier family 30 (zinc transporter), member 2
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
SLCO2A1 solute carrier organic anion transporter family, member 2A1
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SPINK5 serine peptidase inhibitor, Kazal type 5
SRD5A3 steroid 5 alpha-reductase 3
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
SUOX sulfite oxidase
TBX1 T-box 1
TMC6 transmembrane channel-like 6
TMC8 transmembrane channel-like 8
TP63 tumor protein p63
TRAF6 TNF receptor-associated factor 6, E3 ubiquitin protein ligase
TRPM1 transient receptor potential cation channel, subfamily M, member 1
UBE3B ubiquitin protein ligase E3B
UFD1L ubiquitin fusion degradation 1 like (yeast)
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1
ZAP70 zeta-chain (TCR) associated protein kinase 70kDa
ZNF750 zinc finger protein 750