GREB1L - Gene browser

GREB1L

GREB1 like retinoic acid receptor coactivator

HCNC Approved Symbol: GREB1L (HGNC:31042)
Genomic Coordinates: 18:21,242,232 - 21,526,112 (18q11.1-q11.2)
Synonyms: FLJ13687, C18orf6, KIAA1772
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

11Patients

In total, 11 patients were diagnosed with a variant in the GREB1L gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

011
Patient count

Single kidney: 3 (27.3%)
Patient Count: 3 (27.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (27.3%)
Hearing loss: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)
Mental retardation: 1 (9.1%)
Patient Count: 1 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (9.1%)
Abnormality of the heart: 1 (9.1%)
Patient Count: 1 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (9.1%)
Genitourinary abnormality: 1 (9.1%)
Patient Count: 1 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (9.1%)