self-mutilation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000742
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Genes

16 genes associated with the self-mutilation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADSL adenylosuccinate lyase
CREBBP CREB binding protein
DHCR7 7-dehydrocholesterol reductase
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NDE1 nudE neurodevelopment protein 1
NGF nerve growth factor (beta polypeptide)
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PAH phenylalanine hydroxylase
RAI1 retinoic acid induced 1
SLITRK1 SLIT and NTRK-like family, member 1
TMCO1 transmembrane and coiled-coil domains 1
TMEM231 transmembrane protein 231
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)