To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

From Wikipedia, the free encyclopedia

CDH9
Identifiers
AliasesCDH9, cadherin 9
External IDsOMIM: 609974 MGI: 107433 HomoloGene: 9450 GeneCards: CDH9
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]

YouTube Encyclopedic

  • 1/4
    Views:
    7 745
    1 965
    350
    5 300
  • Breathing Matters
  • Hérnia diafragmática
  • Matthew T. Harting, MD, MS, Congenital Diaphragmatic Hernia
  • Congenital Diaphragmatic Hernia (CDH) - Diagnosis via Sonogram

Transcription

Clinical significance

An association with autism has been suggested.[7]

See also

References

  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:". 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.

External links

Further reading


This page was last edited on 17 October 2022, at 09:39
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.