Spinal Muscular Atrophies of Childhood Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A spinal muscular atrophy that is associated with the survival of motor neuron protein. (Human Disease Ontology, DOID_0060160)
Similar Terms
Downloads & Tools

Genes

7 genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BIRC2 baculoviral IAP repeat containing 2
GTF2H2 general transcription factor IIH, polypeptide 2, 44kDa
HSPG2 heparan sulfate proteoglycan 2
NAIP NLR family, apoptosis inhibitory protein
SERF1A small EDRK-rich factor 1A (telomeric)
SMN1 survival of motor neuron 1, telomeric
SMN2 survival of motor neuron 2, centromeric