CDH10

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Cadherin 10, type 2 (T2-cadherin)
Identifiers
Symbol CDH10
External IDs OMIM604555 MGI107436 HomoloGene68530 GeneCards: CDH10 Gene
Orthologs
Species Human Mouse
Entrez 1008 320873
Ensembl ENSG00000040731 ENSMUSG00000022321
UniProt Q9Y6N8 P70408
RefSeq (mRNA) NM_001190450 NM_009865
RefSeq (protein) NP_006718 NP_033995
Location (UCSC) Chr 5:
24.49 – 24.65 Mb
Chr 15:
18.82 – 19.01 Mb
PubMed search [1] [2]

Cadherin 10 is a protein that in humans is encoded by the CDH10 gene.[1][2]

Clinical significance[edit]

An association with autism has been suggested.[3]

See also[edit]

References[edit]

  1. ^ "Entrez Gene: cadherin 10". 
  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]