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Gene : DCDC2 Homo sapiens

Name  ? doublecortin domain containing 2 Cytological Location  6p22.3
Brief Description  doublecortin domain containing 2
Description  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]
  • synonyms:
  • uc003ndx.4,
  • NPHP19,
  • DCDC2A,
  • HGNC:18141,
  • RU2S,
  • deafness, autosomal recessive 66,
  • DFNB66,
  • KIAA1154,
  • RU2,
  • NSC,
  • NPHP19,
  • RU2,
  • NM_016356,
  • DFNB66,
  • AB032980,
  • DCDC2A,
  • OTTHUMG00000016275,
  • DCDC2
  • identifiers:
  • 51473,
  • ENSG00000146038,
  • DCDC2

Genome feature

Region: gene ? Length: 211538  
Location: 6:24171755-24383292 reverse strand Cyto location: 6p22.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


3 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3753 SN Ps

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results