CDH9

From Wikipedia, the free encyclopedia
Jump to: navigation, search
CDH9
Identifiers
Aliases CDH9
External IDs MGI: 107433 HomoloGene: 9450 GeneCards: 1007
Genetically Related Diseases
Disease Name References
coronary artery disease
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_016279

NM_009869

RefSeq (protein)

NP_057363.3

n/a

Location (UCSC) Chr 5: 26.88 – 27.12 Mb Chr 15: 16.78 – 16.86 Mb
PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Cadherin 9 is a protein that in humans is encoded by the CDH9 gene.[1][2]

Clinical significance[edit]

An association with autism has been suggested.[3]

See also[edit]

References[edit]

  1. ^ "Entrez Gene: cadherin 9". 
  2. ^ Suzuki S, Sano K, Tanihara H (April 1991). "Diversity of the cadherin family: evidence for eight new cadherins in nervous tissue". Cell Regulation 2 (4): 261–70. doi:10.1091/mbc.2.4.261. PMC 361775. PMID 2059658. 
  3. ^ Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, et al. (May 2009). "Common genetic variants on 5p14.1 associate with autism spectrum disorders". Nature 459 (7246): 528–33. doi:10.1038/nature07999. PMC 2943511. PMID 19404256. 

Further reading[edit]