Inherited non-medullary thyroid cancer
Gene: MINPP1EnsemblGeneIds (GRCh38): ENSG00000107789
EnsemblGeneIds (GRCh37): ENSG00000107789
OMIM: 605391, Gene2Phenotype
MINPP1 is in 6 panels
3 reviews
Emma Woodward (Manchester Centre for Genomic Medicine)
insufficient evidence linking germline mutation with NMTC predispositionCreated: 13 Jun 2017, 2:18 p.m.
insufficient evidence linking germline mutation with NMTC predispositionCreated: 13 Jun 2017, 2:18 p.m.
Fiona Lalloo (Manchester Centre for Genomic Medicine)
A single publication with one case of follicular thyroid ca and one adenoma. No other evidence available. No clinical utilityCreated: 9 Jun 2017, 9:25 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Thyroid carcinoma, follicular 188470
- OMIM
- 605391
- Clinvar variants
- Variants in MINPP1
- Penetrance
- Complete
- Publications
- Panels with this gene
History Filter Activity
panel promoted to version 1
Sarah Leigh (Genomics England Curator)All genes have been reviewed and the reviews evaluated. 07.08.2017
Created
Sarah Leigh (Genomics England Curator)MINPP1 was created by sleigh
Added New Source
Sarah Leigh (Genomics England Curator)MINPP1 was added to Inherited non-medullary thyroid cancerpanel. Sources: Radboud University Medical Center, Nijmegen