| Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.700 | Biomarker | disease | GENOMICS_ENGLAND | Role of GLI2 in hypopituitarism phenotype. | 25878059 | 2015 | ||||
|
0.700 | GeneticVariation | disease | UNIPROT | Novel heterozygous nonsense GLI2 mutations in patients with hypopituitarism and ectopic posterior pituitary lobe without holoprosencephaly. | 20685856 | 2010 | ||||
|
0.700 | GeneticVariation | disease | CLINVAR | Novel heterozygous nonsense GLI2 mutations in patients with hypopituitarism and ectopic posterior pituitary lobe without holoprosencephaly. | 20685856 | 2010 | ||||
|
0.700 | Biomarker | disease | GENOMICS_ENGLAND | Novel heterozygous nonsense GLI2 mutations in patients with hypopituitarism and ectopic posterior pituitary lobe without holoprosencephaly. | 20685856 | 2010 | ||||
|
0.700 | GeneticVariation | disease | UNIPROT | GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum? | 17096318 | 2006 | ||||
|
0.700 | Biomarker | disease | GENOMICS_ENGLAND | GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum? | 17096318 | 2006 | ||||
|
0.700 | GeneticVariation | disease | CLINVAR | Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. | 14581620 | 2003 | ||||
|
0.700 | GeneticVariation | disease | UNIPROT | Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. | 14581620 | 2003 | ||||
|
0.700 | Biomarker | disease | GENOMICS_ENGLAND | Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. | 14581620 | 2003 | ||||
|
0.700 | Biomarker | disease | GENOMICS_ENGLAND | |||||||
|
0.700 | Biomarker | disease | CTD_human | |||||||
|
0.700 | CausalMutation | disease | CLINVAR |