Alacrima Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Absence of tear secretion. (Human Phenotype Ontology, HP_0000522)
External Link https://www.disgenet.org/browser/0/1/0/C0344505
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Genes

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

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
CLDN10 claudin 10
DST dystonin
ELP1 elongator acetyltransferase complex subunit 1
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GMPPA GDP-mannose pyrophosphorylase A
NGLY1 N-glycanase 1
PAX1 paired box 1
POMC proopiomelanocortin
SERPINB2 serpin peptidase inhibitor, clade B (ovalbumin), member 2
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SETBP1 SET binding protein 1
SOX10 SRY (sex determining region Y)-box 10