1. Genes and Genomic Entities
  2. HRG

HRG

histidine rich glycoprotein
OMIM: 142640, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green HRG in Inherited bleeding disorders

Level 3: Haemostasis disorders
Level 2: Haematological and immunological disorders
Version 1.177

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Eligibility statement prior genetic testing
  • Radboud University Medical Center, Nijmegen
  • Other
  • Expert Review Green
  • BRIDGE Study Tier 1 Gene
Phenotypes
  • Histidine-rich glycoprotein deficiency
  • Thrombophiliadue to elevated HRG
  • Thrombophilia due to HRG deficiency
  • Thrombophilia due to elevated HRG 613116
  • Thrombophilia due to HRG deficiency 613116
Tags
  • missense
Green HRG in Thrombophilia with a likely monogenic cause


Version 2.5
Latest signed off version: v2.2 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • Thrombophilia due to HRG deficiency, OMIM:613116