abnormal hair pattern Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the distribution of hair growth. (Human Phenotype Ontology, HP_0010720)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0010720
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Genes

30 genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
IL2RA interleukin 2 receptor, alpha 1.54733
C6ORF10 chromosome 6 open reading frame 10 1.41648
SLC16A12 solute carrier family 16, member 12 1.30315
LOC100288310 uncharacterized LOC100288310 1.18475
MALRD1 MAM and LDL receptor class A domain containing 1 1.14276
STX17 syntaxin 17 1.09906
ITK IL2-inducible T-cell kinase 1.00025
ST8SIA5 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5 0.997335
NTM neurotrimin 0.990592
APOLD1 apolipoprotein L domain containing 1 0.988702
ST3GAL3 ST3 beta-galactoside alpha-2,3-sialyltransferase 3 0.982743
CPVL carboxypeptidase, vitellogenic-like 0.924992
MICA MHC class I polypeptide-related sequence A 0.91273
DPCR1 diffuse panbronchiolitis critical region 1 0.911485
IQSEC3 IQ motif and Sec7 domain 3 0.909447
ZNF217 zinc finger protein 217 0.901003
OPCML opioid binding protein/cell adhesion molecule-like 0.895681
ALPK1 alpha-kinase 1 0.889988
BTNL2 butyrophilin-like 2 0.8881
EHMT2 euchromatic histone-lysine N-methyltransferase 2 0.86204
ACOX1 acyl-CoA oxidase 1, palmitoyl 0.856898
STARD13 StAR-related lipid transfer (START) domain containing 13 0.853672
UNC5C unc-5 homolog C (C. elegans) 0.844452
THSD4 thrombospondin, type I, domain containing 4 0.823019
DCBLD1 discoidin, CUB and LCCL domain containing 1 0.81905
FNDC3B fibronectin type III domain containing 3B 0.77023
SPATA5 spermatogenesis associated 5 0.74151
CSMD1 CUB and Sushi multiple domains 1 0.727711
ZNF677 zinc finger protein 677 0.596548
UBE2E2 ubiquitin-conjugating enzyme E2E 2 0.595129