Pulmonary Artery Stenosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormal narrowing or constriction of the pulmonary artery, in the main pulmonary artery and/or in the left or right pulmonary artery branches. (Human Phenotype Ontology, HP_0004415)
External Link https://www.disgenet.org/browser/0/1/0/C0238397
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Genes

35 genes associated with the disease Pulmonary Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
A2ML1 alpha-2-macroglobulin-like 1
ARHGAP31 Rho GTPase activating protein 31
BCL11B B-cell CLL/lymphoma 11B (zinc finger protein)
BRAF B-Raf proto-oncogene, serine/threonine kinase
CLCN7 chloride channel, voltage-sensitive 7
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
ELN elastin
FAM58A family with sequence similarity 58, member A
GATA4 GATA binding protein 4
GATA6 GATA binding protein 6
GPC6 glypican 6
KAT6B K(lysine) acetyltransferase 6B
KRAS Kirsten rat sarcoma viral oncogene homolog
LTBP4 latent transforming growth factor beta binding protein 4
LZTR1 leucine-zipper-like transcription regulator 1
MGP matrix Gla protein
MRAS muscle RAS oncogene homolog
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
POLA1 polymerase (DNA directed), alpha 1, catalytic subunit
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RASA2 RAS p21 protein activator 2
RIT1 Ras-like without CAAX 1
RPL10 ribosomal protein L10
RRAS related RAS viral (r-ras) oncogene homolog
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
SNX10 sorting nexin 10
SOS1 son of sevenless homolog 1 (Drosophila)
SOS2 son of sevenless homolog 2 (Drosophila)
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
WNT4 wingless-type MMTV integration site family, member 4
WRN Werner syndrome, RecQ helicase-like
ZEB2 zinc finger E-box binding homeobox 2