WHCR Gene

Name Wolf-Hirschhorn syndrome chromosome region
Description Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008 [PubMed 18932224]).[supplied by OMIM, Nov 2010]
Synonyms PRDS
NCBI Gene ID 7467
API
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Predicted Functions View WHCR's ARCHS4 Predicted Functions.
Co-expressed Genes View WHCR's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View WHCR's ARCHS4 Predicted Functions.

Functional Associations

WHCR has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.

Click the + buttons to view associations for WHCR from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with WHCR gene/protein from the curated CTD Gene-Disease Associations dataset.