Protein Domain : Zinc finger protein 469 IPR039270

Type  Family
Description  Zinc finger protein 469 (ZNF469) is found in chordates and is uncharacterised. Mutations in the ZNF469 gene are associated with brittle cornea syndrome, an autosomal-recessive disorder characterised by a thin cornea that tends to perforate, causing progressive visual loss and blindness [ ]. The protein contains several C2H2-type zinc fingers.
Short Name  ZNF469

0 Child Features

0 Gene Families

0 Genes

0 Ontology Annotations

0 Parent Features

0 Publications

USDA
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