craniofrontonasal 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_14737)
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Genes

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

Symbol Name Standardized Value
EFNB1 ephrin-B1 3.39303
PJA1 praja ring finger 1, E3 ubiquitin protein ligase 1.86232
ALX3 ALX homeobox 3 1.31799
ALX1 ALX homeobox 1 1.30576
NCK2 NCK adaptor protein 2 1.28348
STARD8 StAR-related lipid transfer (START) domain containing 8 1.25167
EFNA2 ephrin-A2 1.17421
EPHB2 EPH receptor B2 1.09923
EFNB2 ephrin-B2 1.07614
OPHN1 oligophrenin 1 0.974642
ALX4 ALX homeobox 4 0.974221
PTPN13 protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase) 0.835607
SLC9A3R1 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1 0.737054
EPHB4 EPH receptor B4 0.700722
SP7 Sp7 transcription factor 0.634742
EPHA2 EPH receptor A2 0.513417
EDA ectodysplasin A 0.337608
CALB2 calbindin 2 0.313552
FGFR3 fibroblast growth factor receptor 3 0.271174
GJA1 gap junction protein, alpha 1, 43kDa 0.246448
FGFR2 fibroblast growth factor receptor 2 0.23666