Lacrimation Abnormality Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormality of tear production. (Human Phenotype Ontology, HP_0000632)
External Link https://www.disgenet.org/browser/0/1/0/C4021801
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Genes

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

Symbol Name
ARID1A AT rich interactive domain 1A (SWI-like)
ARID1B AT rich interactive domain 1B (SWI1-like)
ARID2 AT rich interactive domain 2 (ARID, RFX-like)
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CHD7 chromodomain helicase DNA binding protein 7
CLIP2 CAP-GLY domain containing linker protein 2
DPF2 D4, zinc and double PHD fingers family 2
ELN elastin
EYA1 EYA transcriptional coactivator and phosphatase 1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
LIFR leukemia inhibitory factor receptor alpha
LIMK1 LIM domain kinase 1
OCRL oculocerebrorenal syndrome of Lowe
PAX3 paired box 3
RFC2 replication factor C (activator 1) 2, 40kDa
SCN9A sodium channel, voltage gated, type IX alpha subunit
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SIX1 SIX homeobox 1
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SMARCC2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2
SMARCE1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
SOX11 SRY (sex determining region Y)-box 11
SOX4 SRY (sex determining region Y)-box 4
TBL2 transducin (beta)-like 2
TP63 tumor protein p63
TWIST2 twist family bHLH transcription factor 2
UBR1 ubiquitin protein ligase E3 component n-recognin 1