Variant: rs1553794464 

    present in Gene: ZBTB20-AS1;ZBTB20
    present in Chromosome: 3
    Position on Chromosome: 114350821
    Alleles of this Variant: -/C

rs1553794464 in ZBTB20-AS1;ZBTB20 gene and Dysmorphic features PMID 23032108 2013 Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.

PMID 27061120 2016 Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidism.

PMID 25017102 2014 Mutations in ZBTB20 cause Primrose syndrome.

PMID 19273596 2009 Zinc finger protein Zbtb20 is essential for postnatal survival and glucose homeostasis.

PMID 22180640 2012 A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features.

PMID 28462983 2017 Alterations in metabolic patterns have a key role in diagnosis and progression of primrose syndrome.

PMID 21567911 2011 Additional features of unique Primrose syndrome phenotype.

rs1553794464 in ZBTB20-AS1;ZBTB20 gene and Overgrowth PMID 28462983 2017 Alterations in metabolic patterns have a key role in diagnosis and progression of primrose syndrome.

PMID 27061120 2016 Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidism.

PMID 25017102 2014 Mutations in ZBTB20 cause Primrose syndrome.

PMID 23032108 2013 Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.

PMID 21567911 2011 Additional features of unique Primrose syndrome phenotype.

PMID 22180640 2012 A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features.

PMID 19273596 2009 Zinc finger protein Zbtb20 is essential for postnatal survival and glucose homeostasis.