Misplaced Pages

ZNF385D

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Protein-coding gene in the species Homo sapiens
ZNF385D
Identifiers
AliasesZNF385D, ZNF659, zinc finger protein 385D
External IDsHomoloGene: 11663; GeneCards: ZNF385D; OMA:ZNF385D - orthologs
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • ascending aorta

  • endothelial cell

  • left coronary artery

  • Achilles tendon

  • Brodmann area 23

  • right coronary artery

  • cerebellar cortex

  • cerebellar hemisphere

  • middle temporal gyrus

  • popliteal artery
    n/a
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

79750

n/a

Ensembl

n/a

n/a

UniProt

Q9H6B1

n/a

RefSeq (mRNA)

NM_024697

n/a

RefSeq (protein)

NP_078973

n/a

Location (UCSC)n/an/a
PubMed searchn/a
Wikidata
View/Edit Human

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

References

  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.
Stub icon

This article on a gene on human chromosome 3 is a stub. You can help Misplaced Pages by expanding it.

Categories: