ZEB2 - Gene browser

ZEB2

zinc finger E-box binding homeobox 2

HCNC Approved Symbol: ZEB2 (HGNC:14881)
Genomic Coordinates: 2:144,384,081 - 144,520,119 (2q22.3)
Synonyms: KIAA0569, SIP-1, SIP1, ZFHX1B
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

29Patients

In total, 29 patients were diagnosed with a variant in the ZEB2 gene.

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

029
Patient count

Microcephaly: 10 (34.5%)
Patient Count: 10 (34.5%)
% of total patients presenting each phenotype is shown in parentheses.
10 (34.5%)
Global developmental delay: 9 (31.0%)
Patient Count: 9 (31.0%)
% of total patients presenting each phenotype is shown in parentheses.
9 (31.0%)
Global development delay: 5 (17.2%)
Patient Count: 5 (17.2%)
% of total patients presenting each phenotype is shown in parentheses.
5 (17.2%)
Failure to thrive: 5 (17.2%)
Patient Count: 5 (17.2%)
% of total patients presenting each phenotype is shown in parentheses.
5 (17.2%)
Pointed chin: 5 (17.2%)
Patient Count: 5 (17.2%)
% of total patients presenting each phenotype is shown in parentheses.
5 (17.2%)