ptosis Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description An eye disease characterized by the drooping or falling of the upper or lower eyelid. (Human Disease Ontology, DOID_0060260)
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Genes

16 genes co-occuring with the biological term ptosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
COLQ collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
ECEL1 endothelin converting enzyme-like 1
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
FOXL2 forkhead box L2
KIF21A kinesin family member 21A
LARS leucyl-tRNA synthetase
OPA1 optic atrophy 1 (autosomal dominant)
PABPN1 poly(A) binding protein, nuclear 1
PISRT1 polled intersex syndrome regulated transcript 1 (non-protein coding RNA)
POLG polymerase (DNA directed), gamma
RYR1 ryanodine receptor 1 (skeletal)
TUBB3 tubulin, beta 3 class III
TWIST1 twist family bHLH transcription factor 1
ZFHX4 zinc finger homeobox 4