GeneID: 432


Common Name: ZNF385D Type: Gene
Chromosome: 3 (NC_000003.12) Locus: NM_024697.3 (ZNF385D)
HUGO Symbol: ZNF385D Full Name: zinc finger protein 385D
Exons: 8 Introns: 7

The ZNF385D has been implicated in schizophrenia and attention deficit hyperactivity disorder (ADHD) and shown to be associated with reading disability and language impairement in GWAS analyses. These findings highlight a role by ZNF385D in the development of various neurocognitive traits and its potential implication in neural development. Genetic variance in ZNF385D associated with disease severity in β-thalassaemia HbE patients.

Synonyms: ZNF659


Number of entries/variants: 1


Sequence Viewer

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Publications / Origin

  1. Sherva R, Sripichai O, Abel K, Ma Q, Whitacre J, Angkachatchai V, Makarasara W, Winichagoon P, Svasti S, Fucharoen S, Braun A, Farrer LA, Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study., BMC Med. Genet. , 11(0), 51, 2010 PubMed
  2. Eicher JD, Powers NR, Miller LL, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst T, Frazier J, Kaufmann WE, Keating B, Kenet T, Kennedy D, Mostofsky S, Murray SS, Sowell ER, Bartsch H, Kuperman JM, Brown TT, Hagler DJ, Dale AM, Jernigan TL, St Pourcain B, Davey Smith G, Ring SM, Gruen JR, , Genome-wide association study of shared components of reading disability and language impairment., Genes Brain Behav, 12(8), 792-801, 2013 PubMed
Created on 2021-07-08 13:02:59, Last reviewed on (Show full history)

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