Beginning March 1, 2024, the University of Utah Department of Pathology and ARUP Laboratories will no longer host this mutation database. Our clinical variant data will be consolidated and shared with free publicly accessible databases such as ClinVar. For any questions or concerns related to the removal of this database from our website, please click here and one of our molecular genetics medical directors will review your submission and get back to you.

Hereditary Hemorrhagic Telangiectasia and ENG  

Initial release: January 2011
Last update: March 2021

The purpose of this database is to document all known ENG gene variants including sequence based changes and large deletion/duplications that have been linked to Hereditary Hemorrhagic Telangiectasia (HHT), as well as available associated clinical information and relevant citations. The Genebank sequences NC_000009.10 and NM_001114753.1 were used as reference sequences.

The basis for classification of variants with regards to clinical significance (benign, suspected benign, uncertain, suspected pathogenic, pathogenic) is varied and should be regarded as such. In general it is based on the opinion of the laboratory or laboratories reporting the mutation directly to the database, or via publication. If no classification is given this means that the available publications and other evidence have not been reviewed with regards to clinical significance for the purpose of classification in this database. Our goal is to provide available information regarding a mutation so that database users can evaluate the evidence for disease causation.

Database Information

The ENG database currently has 510 total entries.


When using this resource in publications please link to:​database/ENG/ENG_welcome.php

ARUP offers the following testing for HHT:

  • HHT PANEL: Sequencing and Deletion/Duplication (test 2009337)
  • HHT Familial Mutation, Targeted Sequencing (test 2001961)