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ZNF385D

From Wikipedia, the free encyclopedia
ZNF385D
Identifiers
AliasesZNF385D, ZNF659, zinc finger protein 385D
External IDsHomoloGene: 11663; GeneCards: ZNF385D; OMA:ZNF385D - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_024697

n/a

RefSeq (protein)

NP_078973

n/a

Location (UCSC)n/an/a
PubMed search[1]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.[2] It has been implicated in dyslexia.[3]

References

[edit]
  1. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. ^ "Entrez Gene: Zinc finger protein 385D". Retrieved 2018-11-20.
  3. ^ 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.