fg syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An X-linked disease characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern. (Human Disease Ontology, DOID_14711)
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Genes

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

Symbol Name Standardized Value
MED12 mediator complex subunit 12 2.74168
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family) 1.46451
IGBP1 immunoglobulin (CD79A) binding protein 1 1.41972
PRKX protein kinase, X-linked 1.4092
RCOR1 REST corepressor 1 1.16649
STXBP1 syntaxin binding protein 1 0.990222
MYBPC1 myosin binding protein C, slow type 0.984321
DLG3 discs, large homolog 3 (Drosophila) 0.983479
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3 0.980952
REST RE1-silencing transcription factor 0.939534
YWHAE tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon 0.88434
BBOX1 butyrobetaine (gamma), 2-oxoglutarate dioxygenase (gamma-butyrobetaine hydroxylase) 1 0.877786
MID2 midline 2 0.874919
ALAS2 5'-aminolevulinate synthase 2 0.80977
CKM creatine kinase, muscle 0.703536
AFF2 AF4/FMR2 family, member 2 0.674713
PPP2R4 protein phosphatase 2A activator, regulatory subunit 4 0.606152
COL4A5 collagen, type IV, alpha 5 0.60147
L1CAM L1 cell adhesion molecule 0.578106
FLNA filamin A, alpha 0.457864
FMR1 fragile X mental retardation 1 0.358183