CDH9

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Cadherin 9, type 2 (T1-cadherin)
Identifiers
Symbols CDH9 ; MGC125386
External IDs OMIM609974 MGI107433 HomoloGene9450 GeneCards: CDH9 Gene
Orthologs
Species Human Mouse
Entrez 1007 12565
Ensembl ENSG00000113100 ENSMUSG00000025370
UniProt Q9ULB4 P70407
RefSeq (mRNA) NM_016279 NM_009869
RefSeq (protein) NP_057363 NP_033999
Location (UCSC) Chr 5:
26.88 – 27.12 Mb
Chr 15:
16.78 – 16.86 Mb
PubMed search [1] [2]

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 Regul. 2 (4): 261–70. doi:10.1091/mbc.2.4.261. PMC 361775. PMID 2059658. 
  3. ^ Wang K, Zhang H, Ma D 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]