Absent Eyebrow Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Absence of the eyebrow. (Human Phenotype Ontology, HP_0002223)
External Link https://www.disgenet.org/browser/0/1/0/C0431448
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Genes

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

Symbol Name
ALX1 ALX homeobox 1
BRAF B-Raf proto-oncogene, serine/threonine kinase
CDH3 cadherin 3, type 1, P-cadherin (placental)
EDA ectodysplasin A
FRAS1 Fraser extracellular matrix complex subunit 1
HR hair growth associated
KRAS Kirsten rat sarcoma viral oncogene homolog
KRT85 keratin 85, type II
LMNA lamin A/C
MAP2K2 mitogen-activated protein kinase kinase 2
MBTPS2 membrane-bound transcription factor peptidase, site 2
RECQL4 RecQ protein-like 4
RIPK4 receptor-interacting serine-threonine kinase 4
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SOX18 SRY (sex determining region Y)-box 18
TTC7A tetratricopeptide repeat domain 7A
TWIST2 twist family bHLH transcription factor 2
UBE3B ubiquitin protein ligase E3B
UROS uroporphyrinogen III synthase