Communicating 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/C0009451
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Genes

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

Symbol Name
AQP1 aquaporin 1 (Colton blood group)
CCDC88C coiled-coil domain containing 88C
CCND2 cyclin D2
CDCA7 cell division cycle associated 7
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
DNAI1 dynein, axonemal, intermediate chain 1
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
FBN1 fibrillin 1
HELLS helicase, lymphoid-specific
HYDIN HYDIN, axonemal central pair apparatus protein
IFT122 intraflagellar transport 122
ISPD isoprenoid synthase domain containing
LAMC2 laminin, gamma 2
MPDZ multiple PDZ domain protein
MTOR mechanistic target of rapamycin (serine/threonine kinase)
P4HB prolyl 4-hydroxylase, beta polypeptide
PLAU plasminogen activator, urokinase
PTEN phosphatase and tensin homolog
PTPN13 protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase)
SEC24D SEC24 family member D
SIN3A SIN3 transcription regulator family member A
SKI SKI proto-oncogene
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC9A3R1 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1
ZBTB24 zinc finger and BTB domain containing 24