Gene Symbol:
HPRT1
HGNC:5157
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
Xq26.2-q26.3
Filters:

Definitive classifications

hypoxanthine guanine phosphoribosyltransferase partial deficiency
Submitted as: OMIM:300323
XLR
07/22/2015
Evaluated
11/25/2020
Submitted
Lesch-Nyhan syndrome
Submitted as: OMIM:300322
XLR
07/22/2015
Evaluated
11/25/2020
Submitted
Lesch-Nyhan syndrome
Submitted as: OMIM:300322
XL
06/12/2018
Evaluated
03/02/2021
Submitted
Lesch-Nyhan syndrome
Submitted as: OMIM:300322
XL
07/22/2015
Evaluated
09/11/2023
Submitted
Lesch-Nyhan syndrome
XL
07/08/2022
Evaluated
04/21/2024
Submitted

Strong classifications

Lesch-Nyhan syndrome
Submitted as: OMIM:300322
XL
11/04/2022
Evaluated
11/30/2023
Submitted
hypoxanthine guanine phosphoribosyltransferase partial deficiency
Submitted as: OMIM:300323
XL
09/17/2021
Evaluated
11/30/2023
Submitted

Supportive classifications

Lesch-Nyhan syndrome
Submitted as: Orphanet:510
XL
09/14/2021
Evaluated
09/14/2021
Submitted
hypoxanthine guanine phosphoribosyltransferase partial deficiency
Submitted as: Orphanet:79233
XL
09/14/2021
Evaluated
09/14/2021
Submitted

The GenCC data are available free of restriction under a CC0 1.0 Universal (CC0 1.0) Public Domain Dedication. The GenCC requests that you give attribution to GenCC and the contributing sources whenever possible and appropriate. The accepted Flagship manuscript is now available from Genetics in Medicine (https://www.gimjournal.org/article/S1098-3600(22)00746-8/fulltext).

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. The GenCC does not independently verify the submitted information. Though the information is obtained from sources believed to be reliable, no warranty, expressed or implied, is made regarding accuracy, adequacy, completeness, reliability or usefulness of any information. This disclaimer applies to both isolated and aggregate uses of the information. The information is provided on an "as is" basis, collected through periodic submission and therefore may not represent the most up-to-date information from the submitters. If you have questions about the medical relevance of information contained on this website, please see a healthcare professional; if you have questions about specific gene-disease claims, please contact the relevant sources; and if you have questions about the representation of the data on this website, please contact gencc@thegencc.org.