ZNF385D

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]

ZNF385D
Identifiers
Aliases	ZNF385D, ZNF659, zinc finger protein 385D
External IDs	HomoloGene: 11663 GeneCards: ZNF385D
Gene location (Human) Chr. Chromosome 3 (human)[1] Band 3p24.3 Start 21,412,218 bp[1] End 22,373,321 bp[1]
Gene ontology Molecular function • zinc ion binding • p53 binding • metal ion binding • RNA binding • nucleic acid binding Cellular component • cell nucleus Biological process • intrinsic apoptotic signaling pathway by p53 class mediator Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	79750	n/a
Ensembl	ENSG00000151789	n/a
UniProt	Q9H6B1	n/a
RefSeq (mRNA)	NM_024697	n/a
RefSeq (protein)	NP_078973	n/a
Location (UCSC)	Chr 3: 21.41 – 22.37 Mb	n/a
PubMed search	[2]	n/a
Wikidata
View/Edit Human

References

1. GRCh38: Ensembl release 89: ENSG00000151789 - Ensembl, May 2017
2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
3. "Entrez Gene: Zinc finger protein 385D". Retrieved 2018-11-20.
4. 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.