Atrichia With Papular Lesions Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Atrichia with papular lesions is a rare inherited form of alopecia characterized by irreversible hair loss during the neonatal period on all hear-bearing areas of the body, later associated with the development of papular lesions all over the body and preferentially on the face and extensor surfaces of the extremities. (Orphanet Rare Disease Ontology, Orphanet_86819)
External Link https://www.disgenet.org/browser/0/1/0/C1859592
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Genes

65 genes associated with the disease Atrichia With Papular Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADCY9 adenylate cyclase 9
AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AKT1 v-akt murine thymoma viral oncogene homolog 1
ANXA5 annexin A5
APRT adenine phosphoribosyltransferase
AS3MT arsenite methyltransferase
ATG5 autophagy related 5
CCNA1 cyclin A1
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CEBPE CCAAT/enhancer binding protein (C/EBP), epsilon
DAP death-associated protein
DAPK2 death-associated protein kinase 2
DCTN4 dynactin 4 (p62)
F2 coagulation factor II (thrombin)
F2RL1 coagulation factor II (thrombin) receptor-like 1
F3 coagulation factor III (thromboplastin, tissue factor)
FANCB Fanconi anemia, complementation group B
FAS Fas cell surface death receptor
FGF13 fibroblast growth factor 13
FGFR1 fibroblast growth factor receptor 1
FLT3 fms-related tyrosine kinase 3
GTF2H1 general transcription factor IIH, polypeptide 1, 62kDa
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HOXB2 homeobox B2
HR hair growth associated
ITGAM integrin, alpha M (complement component 3 receptor 3 subunit)
KAT2A K(lysine) acetyltransferase 2A
KDM3B lysine (K)-specific demethylase 3B
KHDRBS1 KH domain containing, RNA binding, signal transduction associated 1
LEF1 lymphoid enhancer-binding factor 1
LMNA lamin A/C
LMNB2 lamin B2
MAPK3 mitogen-activated protein kinase 3
MATN1 matrilin 1, cartilage matrix protein
MFAP1 microfibrillar-associated protein 1
MYC v-myc avian myelocytomatosis viral oncogene homolog
NCAM1 neural cell adhesion molecule 1
NPM1 nucleophosmin (nucleolar phosphoprotein B23, numatrin)
NUP62 nucleoporin 62kDa
ODC1 ornithine decarboxylase 1
PEG10 paternally expressed 10
PML promyelocytic leukemia
PPARG peroxisome proliferator-activated receptor gamma
PRAM1 PML-RARA regulated adaptor molecule 1
PRF1 perforin 1 (pore forming protein)
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRKCA protein kinase C, alpha
PRKCB protein kinase C, beta
PRRT2 proline-rich transmembrane protein 2
PTK2B protein tyrosine kinase 2 beta
RAB40B RAB40B, member RAS oncogene family
RARA retinoic acid receptor, alpha
RXRA retinoid X receptor, alpha
SQSTM1 sequestosome 1
TACR1 tachykinin receptor 1
TOP2B topoisomerase (DNA) II beta 180kDa
TP73 tumor protein p73
TRIB3 tribbles pseudokinase 3
TSHR thyroid stimulating hormone receptor
TWIST1 twist family bHLH transcription factor 1
VAV1 vav 1 guanine nucleotide exchange factor
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
ZBTB16 zinc finger and BTB domain containing 16
ZMPSTE24 zinc metallopeptidase STE24