hydrops fetalis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema. (Human Phenotype Ontology, HP_0001789)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001789
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Genes

42 genes associated with the hydrops fetalis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGGF1 angiogenic factor with G patch and FHA domains 1
ALG1 ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
BSND barttin CLCNK-type chloride channel accessory beta subunit
CCBE1 collagen and calcium binding EGF domains 1
CDAN1 codanin 1
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
COL11A1 collagen, type XI, alpha 1
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COL2A1 collagen, type II, alpha 1
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
FAT4 FAT atypical cadherin 4
FIG4 FIG4 phosphoinositide 5-phosphatase
FLNB filamin B, beta
FLT4 fms-related tyrosine kinase 4
GBA glucosidase, beta, acid
GBE1 glucan (1,4-alpha-), branching enzyme 1
GUSB glucuronidase, beta
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
HADHB hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
IFT80 intraflagellar transport 80
KLF1 Kruppel-like factor 1 (erythroid)
LBR lamin B receptor
NEK1 NIMA-related kinase 1
NEU1 sialidase 1 (lysosomal sialidase)
PKLR pyruvate kinase, liver and RBC
PMM2 phosphomannomutase 2
PTH1R parathyroid hormone 1 receptor
RAPSN receptor-associated protein of the synapse
RYR1 ryanodine receptor 1 (skeletal)
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SOX18 SRY (sex determining region Y)-box 18
TRIP11 thyroid hormone receptor interactor 11
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60
WNT7A wingless-type MMTV integration site family, member 7A