Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 GeneticVariation disease BEFREE In vitro studies showed that the <i>POU1F1</i> c.605delC mutation codes for a truncated protein with reduced transactivation capacity on its downstream effectors, viz., growth hormone (<i>GH</i>) and prolactin (<i>PRL</i>) causing severe CPHD. 31022740 2019
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 GeneticVariation disease BEFREE The proband, born to consanguineous parents, presented with proportional growth failure (height 108.8 cm, -3.48 SDS), combined pituitary hormone deficiency (GH, TSH, PRL and gonadotropins) and a suprasellar mass with optic chiasm invasion, compatible with a diagnosis of chiasmatic hypothalamic glioma, as revealed by MRI. 23831233 2013
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 GeneticVariation disease BEFREE We identified a de novo heterozygous 522,009-bp deletion involving LHX4 in a patient with CPHD (GH, TSH, PRL, LH, and FSH deficiencies), anterior pituitary hypoplasia, ectopic posterior pituitary, and underdeveloped sella turcica. 20534763 2010
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 Biomarker disease BEFREE Therefore, abnormalities of the POU1F1 gene are known to be responsible for a phenotype causing combined pituitary hormone deficiency (CPHD) involving growth hormone, prolactin and thyrotropin. 18059085 2008
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 GeneticVariation disease BEFREE PROP1 and POU1F: Recessive mutations within the pituitary-specific transcription factor Prophet of Pit1, or PROP1, are associated with CPHD (GH, prolactin [PRL] and TSH deficiency with additional LH and FSH deficiency). 18174732 2007
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 GeneticVariation disease BEFREE Mutations of the PROP1 gene lead to combined pituitary hormone deficiency (CPHD), which is characterized by a deficiency of GH, TSH, LH/FSH, PRL and, less frequently, ACTH. 16984240 2006
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 Biomarker disease BEFREE Two patients with childhood onset of CPHD (GH, PRL, TSH, LH, FSH) caused by a genetic defect (GA296del mutation) of the Prop1 gene. 15302300 2004
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 Biomarker disease BEFREE The pituitary transcription factor Pit-1 is expressed during the later differentiation stages of anterior pituitary development and Pit-1 mutations have been identified as the cause of a combined pituitary hormone deficiency (CPHD) for GH, prolactin and TSH. 10698595 1999
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 Biomarker disease BEFREE Pit-1 gene mutations result in complete growth hormone (GH) and PRL deficiencies and variable degrees of TSH deficiency, producing the clinical syndrome of combined pituitary hormone deficiency (CPHD). 9588494 1998
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 GeneticVariation disease BEFREE Mutations in the Pit-1 gene account for a form of combined pituitary hormone deficiency for GH, Prolactin (Prl) and TSH (CPHD). 9439906 1997
Entrez Id: 5617
Gene Symbol: PRL
PRL
0.100 Biomarker disease BEFREE Mutations in the Pit-1 gene result in insufficient expression of this factor, accounting for a form of combined pituitary hormone deficiency for growth hormone (GH), prolactin, and thyroid-stimulating hormone. 8805025 1996