pelger-huet anomaly Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9631)
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Genes

19 genes co-occuring with the disease pelger-huet anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
LBR lamin B receptor 1.70588
HGS hepatocyte growth factor-regulated tyrosine kinase substrate 1.24081
LMNB2 lamin B2 1.12994
RPS14 ribosomal protein S14 1.06732
LMNA lamin A/C 0.967502
LMNB1 lamin B1 0.773296
ASXL1 additional sex combs like transcriptional regulator 1 0.660404
TET2 tet methylcytosine dioxygenase 2 0.650113
EMD emerin 0.58939
CSF1R colony stimulating factor 1 receptor 0.546644
PDGFRB platelet-derived growth factor receptor, beta polypeptide 0.46466
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit 0.461639
EGR1 early growth response 1 0.432646
RUNX1 runt-related transcription factor 1 0.400453
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble 0.395235
ALPPL2 alkaline phosphatase, placental-like 2 0.218374
ALPP alkaline phosphatase, placental 0.218034
ALPL alkaline phosphatase, liver/bone/kidney 0.217352
WT1 Wilms tumor 1 0.201308