ZNF385D

ZNF385D
Identifiers
Aliases	ZNF385D, ZNF659, zinc finger protein 385D
External IDs	HomoloGene: 11663 GeneCards: ZNF385D
Gene location (Human)
Chr.	Chromosome 3 (human)[1]
End	22,373,321 bp[1]
RNA expression pattern
	Top expressed in
	left coronary artery; ; thoracic aorta; ; ascending aorta; ; colon; ; testicle; ; stomach; ; tendon;
	More reference expression data
	n/a
Gene ontology
Molecular function	zinc ion binding; p53 binding; metal ion binding; RNA binding; nucleic acid binding;
Cellular component	nucleus;
Biological process	intrinsic apoptotic signaling pathway by p53 class mediator;
	Sources:Amigo / QuickGO
Orthologs
	79750
	n/a
	ENSG00000151789
	n/a
	Q9H6B1
	n/a
	NM_024697
	n/a
	NP_078973
	n/a
	Wikidata
View/Edit Human

ZNF385D is a gene on chromosome 3 that encodes for the zinc finger protein 385, a zinc finger protein.[3] It has been implicated in dyslexia.[4]

References

GRCh38: Ensembl release 89: ENSG00000151789 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: Zinc finger protein 385D". Retrieved 2018-11-20.
Guidi LG, Velayos-Baeza A, Martinez-Garay I, Monaco AP, Paracchini S, Bishop DV, Molnár Z (November 2018). "The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on" (PDF). The European Journal of Neuroscience. 48 (10): 3212–3233. doi:10.1111/ejn.14149. PMC 6282621. PMID 30218584.

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