×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
GeneticVariation
disease
BEFREE
This region contains the genes of FAM84A, NBAS, DDX1, MYCNOS and MYCN , of which haploinsufficiency or mutations of the MYCN gene is associated with Feingold syndrome .
22842076
2012
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
Biomarker
disease
CTD_human
Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes.
21532573
2011
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
GeneticVariation
disease
BEFREE
We hypothesized that mutations or deletions of highly conserved non-coding elements (HCNEs) at the MYCN locus could lead to its misregulation and thereby to FS and/or IOA.
21224895
2011
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
GeneticVariation
disease
BEFREE
Knockout (KO) of either c-myc or N-myc genes in neural stem and precursor cells (NSC) driven by nestin-cre impairs mouse brain growth and mutation of N-myc also causes microcephaly in humans in Feingold Syndrome .
20651942
2010
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
Biomarker
disease
CTD_human
Clinical presentation of the family was suggestive of Feingold syndrome , and genetic testing of the MYCN gene confirmed the diagnosis.
19852433
2009
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
ChromosomalRearrangement
disease
ORPHANET
Genotype-phenotype correlations in MYCN -related Feingold syndrome .
18470948
2008
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
GermlineCausalMutation
disease
ORPHANET
Genotype-phenotype correlations in MYCN -related Feingold syndrome .
18470948
2008
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
GermlineCausalMutation
disease
ORPHANET
We show here that heterozygous mutations in the gene MYCN are present in Feingold syndrome .
15821734
2005
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
GeneticVariation
disease
BEFREE
We show here that heterozygous mutations in the gene MYCN are present in Feingold syndrome .
15821734
2005
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
ChromosomalRearrangement
disease
ORPHANET
We show here that heterozygous mutations in the gene MYCN are present in Feingold syndrome .
15821734
2005
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
Biomarker
disease
BEFREE
MODED : microcephaly-oculo-digito-esophageal-duodenal syndrome .
9268091
1997
×
Entrez Id:
4613
Gene Symbol:
MYCN
MYCN
0.650
CausalMutation
disease
CLINVAR