laron syndrome 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_9521)
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Genes

24 genes co-occuring with the disease laron syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GHR growth hormone receptor 2.91164
IGF1 insulin-like growth factor 1 (somatomedin C) 2.24045
IGFBP3 insulin-like growth factor binding protein 3 1.66916
CKAP2 cytoskeleton associated protein 2 1.31755
STAT5B signal transducer and activator of transcription 5B 1.24558
VGLL3 vestigial-like family member 3 0.973801
GHRHR growth hormone releasing hormone receptor 0.918024
POU1F1 POU class 1 homeobox 1 0.90732
PROP1 PROP paired-like homeobox 1 0.742735
IGFALS insulin-like growth factor binding protein, acid labile subunit 0.72329
INS insulin 0.645375
GH1 growth hormone 1 0.634349
LHX3 LIM homeobox 3 0.540442
IGFBP2 insulin-like growth factor binding protein 2, 36kDa 0.533861
HESX1 HESX homeobox 1 0.428891
CHMP2B charged multivesicular body protein 2B 0.42289
IGFBP1 insulin-like growth factor binding protein 1 0.355972
PITX2 paired-like homeodomain 2 0.237009
GHRH growth hormone releasing hormone 0.235964
VASP vasodilator-stimulated phosphoprotein 0.207578
JAK2 Janus kinase 2 0.196139
TOP3A topoisomerase (DNA) III alpha 0.192971
PRL prolactin 0.185016
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone) 0.166768