CDH9

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

CDH9
Identifiers
AliasesCDH9, cadherin 9
External IDsOMIM: 609974 MGI: 107433 HomoloGene: 9450 GeneCards: CDH9
Gene location (Human)
Chr.Chromosome 5 (human)[1]
Band5p14.1Start26,880,597 bp[1]
End27,121,150 bp[1]
Orthologs
SpeciesHumanMouse
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 MbChr 15: 16.73 – 16.86 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Clinical significance

An association with autism has been suggested.[7]

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000113100 - Ensembl, May 2017
  2. 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. doi:10.1038/nature07999. PMC 2943511. PMID 19404256.

Further reading


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