×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
28734020
2017
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations.
26059845
2016
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency.
26608600
2016
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiency.
25581745
2015
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
26111865
2015
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism.
25557026
2015
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
Recombinant human growth hormone replacement in a Japanese man with a novel PROP1 gene mutation (R112X).
22111336
2011
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
Mutations and pituitary morphology in a series of 82 patients with PROP1 gene defects.
22024773
2011
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
Mutations and pituitary morphology in a series of 82 patients with PROP1 gene defects.
22024773
2011
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency.
21132537
2011
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
W194XProp1 and S156insTProp1, both of which have intact DNA-binding domain, show a different DNA-binding activity to the Prop1-binding element in human Pit-1 gene.
20381582
2010
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
UNIPROT
Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD).
19128366
2009
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD).
19128366
2009
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.
17526936
2006
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
Biomarker
disease
GENOMICS_ENGLAND
PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.
16984240
2006
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
16735499
2006
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency.
17526949
2006
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.
17526936
2006
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.
16984240
2006
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domain.
15941866
2005
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
15963055
2005
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects.
16131601
2005
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
CausalMutation
disease
CLINVAR
Long-term growth hormone therapy in adulthood results in significant linear growth in siblings with a PROP-1 gene mutation.
15472175
2004
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
UNIPROT
A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies.
15531542
2004
×
Entrez Id:
5626
Gene Symbol:
PROP1
PROP1
0.700
GeneticVariation
disease
CLINVAR
PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis.
15472232
2004