pallister-hall syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9248)
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Genes

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

Symbol Name Standardized Value
GLI3 GLI family zinc finger 3 2.88351
KLF10 Kruppel-like factor 10 1.53568
MECOM MDS1 and EVI1 complex locus 1.50184
KIF7 kinesin family member 7 1.45836
SHH sonic hedgehog 1.40701
MKKS McKusick-Kaufman syndrome 1.29134
HCN3 hyperpolarization activated cyclic nucleotide gated potassium channel 3 1.27126
SAP18 Sin3A-associated protein, 18kDa 1.25907
GAS1 growth arrest-specific 1 1.16008
KIF27 kinesin family member 27 1.07278
PTCH1 patched 1 0.963309
ZIC3 Zic family member 3 0.939119
SMO smoothened, frizzled class receptor 0.921736
RAB23 RAB23, member RAS oncogene family 0.883111
CDON cell adhesion associated, oncogene regulated 0.849536
CCM2 cerebral cavernous malformation 2 0.799103
GLI1 GLI family zinc finger 1 0.792951
PTCH2 patched 2 0.770844
HIP1 huntingtin interacting protein 1 0.756156
LRP2 low density lipoprotein receptor-related protein 2 0.743547
ZIC2 Zic family member 2 0.740299
WNT11 wingless-type MMTV integration site family, member 11 0.704742
SIX3 SIX homeobox 3 0.60108
MEGF6 multiple EGF-like-domains 6 0.567997
DHCR7 7-dehydrocholesterol reductase 0.46655
GLI2 GLI family zinc finger 2 0.418768
ALLC allantoicase 0.368888
PPP2R4 protein phosphatase 2A activator, regulatory subunit 4 0.23353
POMC proopiomelanocortin 0.18651
TBX1 T-box 1 0.167224