Congenital Hydrocephalus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0020256
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Genes

37 genes associated with the disease Congenital Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
ADCYAP1R1 adenylate cyclase activating polypeptide 1 (pituitary) receptor type I
AP1S2 adaptor-related protein complex 1, sigma 2 subunit
AQP1 aquaporin 1 (Colton blood group)
BMP1 bone morphogenetic protein 1
CCDC88C coiled-coil domain containing 88C
CCND2 cyclin D2
CLDN10 claudin 10
DCDC2 doublecortin domain containing 2
DUSP2 dual specificity phosphatase 2
EML1 echinoderm microtubule associated protein like 1
FEN1 flap structure-specific endonuclease 1
FOLR1 folate receptor 1 (adult)
FOXC1 forkhead box C1
FZD3 frizzled class receptor 3
GMNC geminin coiled-coil domain containing
HTT huntingtin
HYDIN HYDIN, axonemal central pair apparatus protein
IFT122 intraflagellar transport 122
ISLR2 immunoglobulin superfamily containing leucine-rich repeat 2
ISPD isoprenoid synthase domain containing
KDM6A lysine (K)-specific demethylase 6A
KLF6 Kruppel-like factor 6
L1CAM L1 cell adhesion molecule
MPDZ multiple PDZ domain protein
NME7 NME/NM23 family member 7
PGPEP1 pyroglutamyl-peptidase I
POMK protein-O-mannose kinase
PRCP prolylcarboxypeptidase (angiotensinase C)
PSMG1 proteasome (prosome, macropain) assembly chaperone 1
RFX4 regulatory factor X, 4 (influences HLA class II expression)
SIN3A SIN3 transcription regulator family member A
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC12A7 solute carrier family 12 (potassium/chloride transporter), member 7
SNX27 sorting nexin family member 27
TRIM71 tripartite motif containing 71, E3 ubiquitin protein ligase
WDR81 WD repeat domain 81