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GeneQ14877933· pop 7· linked from 4 articles

Also known as DCDC2A, DFNB66, NPHP19, RU2, RU2S, doublecortin domain containing 2, NSC

Gen der Spezies Homo sapiens

Gene data

DCDC2
Name
doublecortin domain containing 2
Type
protein-coding
Aliases
DCDC2A, DFNB66, NPHP19, NSC, RU2, RU2S

This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2013].

via MyGene.info

Gene · Ensembl

doublecortin domain containing 2

Symbol
DCDC2
Biotype
Protein coding
Organism
Homo sapiens
Location
6:24,171,747-24,383,300
Strand
Reverse (−)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

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