1. Panels
  2. Cytopenias and congenital anaemias
  3. CD36
Genes in panel
Prev Next
STRs in panel
Prev Next
Regions in panel
Prev Next

Cytopenias and congenital anaemias

Gene: CD36

Red List (low evidence)
CD36 (CD36 molecule)
EnsemblGeneIds (GRCh38): ENSG00000135218
EnsemblGeneIds (GRCh37): ENSG00000135218
OMIM: 173510, Gene2Phenotype
CD36 is in 1 panel

1 review

Arianna Tucci (Genomics England Curator)

Red List (low evidence)

The phenotype is not relevant for this panel, add to the bleeding disorder panel?
Created: 9 Mar 2017, 4:32 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Platelet glycoprotein IV deficiency 608404

Created: 9 Mar 2017, 4:32 p.m.

Panel version: 0.522

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • [Macrothrombocytopenia] (1)
OMIM
173510
Clinvar variants
Variants in CD36
Penetrance
Complete
Panels with this gene

History Filter Activity

11 Mar 2017, Gel status: 1

panel promoted to version 1

Arianna Tucci (Genomics England Curator)

Promoted to V1 on 11 March 2017, after internal review and discussion with the clinical team.

9 Mar 2017, Gel status: 1

Set Mode of Inheritance, Added New Source

Sarah Leigh (Genomics England Curator)

CD36 was added to Cytopaenias and congenital anaemiaspanel. Source: Expert Review Red Model of inheritance for gene CD36 was set to BIALLELIC, autosomal or pseudoautosomal

17 Feb 2017, Gel status: 0

Created

Louise Daugherty (Genomics England Curator)

CD36 was created by LouiseD

17 Feb 2017, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

CD36 was added to Cytopaenias and congenital anaemiaspanel. Sources: Radboud University Medical Center, Nijmegen