ZNF469 protein, human MeSH Supplementary Concept Data 2025

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MeSH Supplementary: ZNF469 protein, human
Unique ID: C530065
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C530065
Entry Term(s): zinc-finger protein 469, human
Registry Numbers: 0
Heading Mapped to: *Transcription Factors
Frequency: 29
Note: mutation leads to brittle cornea syndrome; GenBank AC135049
Source: Am J Hum Genet 2008 May;82(5):1217-22
Indexing Information: Zinc Fingers
Date of Entry: 2008/07/15
Revision Date: 2008/07/16

ZNF469 protein, human Preferred

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