type i diabetes mellitus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A diabetes mellitus that results from the body's failure to produce insulin and has_material_basis_in autoimmune destruction of insulin-producing beta cells of the pancreas. (Human Disease Ontology, DOID_9744)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100651
Similar Terms
Downloads & Tools

Genes

32 genes associated with the type i diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIRE autoimmune regulator
AKT2 v-akt murine thymoma viral oncogene homolog 2
COX1
COX2
COX3
CTNS cystinosin, lysosomal cystine transporter
DCAF17 DDB1 and CUL4 associated factor 17
EDA ectodysplasin A
EDA2R ectodysplasin A2 receptor
FOXP3 forkhead box P3
HNF1A HNF1 homeobox A
INS insulin
KCTD1 potassium channel tetramerization domain containing 1
LEMD3 LEM domain containing 3
LMNA lamin A/C
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
ND1
PDX1 pancreatic and duodenal homeobox 1
PSTPIP1 proline-serine-threonine phosphatase interacting protein 1
PTF1A pancreas specific transcription factor, 1a
SBDS Shwachman-Bodian-Diamond syndrome
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SLC19A2 solute carrier family 19 (thiamine transporter), member 2