Anonychia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Aplasia of the nail. (Human Phenotype Ontology, HP_0001798)
External Link https://www.disgenet.org/browser/0/1/0/C0265998
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Genes

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

Symbol Name
ACTG2 actin, gamma 2, smooth muscle, enteric
ARID1B AT rich interactive domain 1B (SWI1-like)
ATP6V1B2 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2
COL17A1 collagen, type XVII, alpha 1
COL2A1 collagen, type II, alpha 1
DSP desmoplakin
GRHL2 grainyhead-like 2 (Drosophila)
HOXA13 homeobox A13
ITGA6 integrin, alpha 6
ITGB4 integrin, beta 4
JUP junction plakoglobin
KRT16 keratin 16, type I
KRT17 keratin 17, type I
KRT6A keratin 6A, type II
KRT6B keratin 6B, type II
LAMA3 laminin, alpha 3
LAMB3 laminin, beta 3
LAMC2 laminin, gamma 2
LMX1B LIM homeobox transcription factor 1, beta
NOG noggin
PLEC plectin
RIPK4 receptor-interacting serine-threonine kinase 4
ROR2 receptor tyrosine kinase-like orphan receptor 2
RSPO4 R-spondin 4
SOX9 SRY (sex determining region Y)-box 9
TBC1D24 TBC1 domain family, member 24
TP63 tumor protein p63
WNT10A wingless-type MMTV integration site family, member 10A
WNT7A wingless-type MMTV integration site family, member 7A
ZBTB20 zinc finger and BTB domain containing 20