CDH10

Last updated
CDH10
Identifiers
Aliases CDH10 , cadherin 10
External IDs OMIM: 604555; MGI: 107436; HomoloGene: 68530; GeneCards: CDH10; OMA:CDH10 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001190450
NM_006727
NM_001317222
NM_001317224
NM_001362460

Contents

NM_009865
NM_001316758

RefSeq (protein)

NP_001304151
NP_001304153
NP_006718
NP_001349389
NP_001304153.1

NP_001303687
NP_033995

Location (UCSC) Chr 5: 24.49 – 24.64 Mb Chr 15: 18.82 – 19.01 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Cadherin 10 is a protein that in humans is encoded by the CDH10 gene. [5] [6]

Clinical significance

An association with autism has been suggested. [7]

See also

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000040731 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000022321 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 10".
  6. 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.
  7. 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. Bibcode:2009Natur.459..528W. doi:10.1038/nature07999. PMC   2943511 . PMID   19404256.

Further reading