Adult solid tumours for rare disease
Gene: AIPEnsemblGeneIds (GRCh38): ENSG00000110711
EnsemblGeneIds (GRCh37): ENSG00000110711
OMIM: 605555, Gene2Phenotype
AIP is in 5 panels
1 review
Helen Brittain (Genomics England Curator)
Comment on list classification: Could be of relevance for recruits with a pituitary adenoma as part of the multiple tumour category for example, therefore added to this panelCreated: 27 Feb 2018, 1:23 p.m.
AIP gene is tested for in NHS service in relation to familial pituitary adenomaCreated: 27 Feb 2018, 1:22 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Pituitary adenoma 1, multiple types 102200
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Pituitary adenoma 1, multiple types 102200
- OMIM
- 605555
- Clinvar variants
- Variants in AIP
- Penetrance
- Incomplete
- Publications
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)5th March 2018 - promoted to version 1 after expert review and internal clinical review.
Gene classified by Genomics England curator
Helen Brittain (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Gene classified by Genomics England curator
Helen Brittain (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Helen Brittain (Genomics England Curator)AIP was added to Adult solid tumours for rare disease panel. Sources: Literature
Created
Helen Brittain (Genomics England Curator)AIP was created by Helen Brittain