CDH9

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CDH9
Identifiers
AliasesCDH9, cadherin 9
External IDsMGI: 107433 HomoloGene: 9450 GeneCards: CDH9
Gene location (Human)
Chromosome 5 (human)
Chr.Chromosome 5 (human)[1]
Chromosome 5 (human)
Genomic location for CDH9
Genomic location for CDH9
Band5p14.1Start26,880,600 bp[1]
End27,121,150 bp[1]
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 MbChr 15: 16.73 – 16.86 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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

Clinical significance[edit]

An association with autism has been suggested.[7]

See also[edit]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000113100 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025370 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:".
  4. ^ "Mouse PubMed Reference:".
  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.

External links[edit]

Further reading[edit]