anorexia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A lack or loss of appetite for food (as a medical condition). (Human Phenotype Ontology, HP_0002039)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002039
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Genes

41 genes associated with the anorexia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
ARG1 arginase 1
ATM ATM serine/threonine kinase
C4A complement component 4A (Rodgers blood group)
CBS cystathionine-beta-synthase
CCND1 cyclin D1
COX1
COX2
COX3
GLA galactosidase, alpha
HLA-B major histocompatibility complex, class I, B
HMBS hydroxymethylbilane synthase
IL10 interleukin 10
IL12B interleukin 12B
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
MEFV Mediterranean fever
MLX MLX, MAX dimerization protein
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
MUT methylmalonyl CoA mutase
MYD88 myeloid differentiation primary response 88
ND1
NOD2 nucleotide-binding oligomerization domain containing 2
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
PTPN3 protein tyrosine phosphatase, non-receptor type 3
SLC39A4 solute carrier family 39 (zinc transporter), member 4
SLC46A1 solute carrier family 46 (folate transporter), member 1
STAT4 signal transducer and activator of transcription 4
TGFB1 transforming growth factor, beta 1
TLR4 toll-like receptor 4