CDH9

Last updated
CDH9
Identifiers
Aliases CDH9 , cadherin 9
External IDs OMIM: 609974; MGI: 107433; HomoloGene: 9450; GeneCards: CDH9; OMA:CDH9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_016279

NM_009869

RefSeq (protein)

NP_057363

NP_033999

Location (UCSC) Chr 5: 26.88 – 27.12 Mb Chr 15: 16.73 – 16.86 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Cadherin 9 is a protein that in humans is encoded by the CDH9 gene. [5] [6]

Contents

Clinical significance

An association with autism has been suggested. [7]

See also

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000113100 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000025370 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: cadherin 9".
  6. 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.
  7. 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. Bibcode:2009Natur.459..528W. doi:10.1038/nature07999. PMC   2943511 . PMID   19404256.

Further reading