Gene Symbol:
GREB1L
HGNC:31042
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
18q11.1-q11.2
Filters:

Definitive classifications

renal hypodysplasia/aplasia 3
AD
09/30/2020
Evaluated
10/15/2020
Submitted
Illumina
Evidence: The GREB1L gene is located on chromosome 18 at q11.1-11.2 and encodes the GREB1 like retinoic acid r... Read more

Strong classifications

renal hypodysplasia/aplasia 3
Submitted as: OMIM:617805
AD
11/22/2022
Evaluated
11/30/2023
Submitted

Moderate classifications

renal hypodysplasia/aplasia 3
Submitted as: OMIM:617805
AD
01/04/2018
Evaluated
03/02/2021
Submitted

Supportive classifications

bilateral renal agenesis
Submitted as: Orphanet:1848
AR
09/14/2021
Evaluated
09/14/2021
Submitted
renal agenesis, unilateral
Submitted as: Orphanet:93100
AD
09/14/2021
Evaluated
09/14/2021
Submitted

Limited classifications

renal hypodysplasia/aplasia 3
Submitted as: OMIM:617805
AD
07/31/2018
Evaluated
03/02/2021
Submitted
hearing loss, autosomal dominant 80
Submitted as: OMIM:619274
AD
11/17/2022
Evaluated
11/30/2023
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.