VOOZH about

URL: https://en.wikipedia.org/wiki/Frizzled-9

⇱ Frizzled-9 - Wikipedia


Jump to content
From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
FZD9
Identifiers
AliasesFZD9, CD349, FZD3, frizzled class receptor 9
External IDsOMIM: 601766; MGI: 1313278; HomoloGene: 2619; GeneCards: FZD9; OMA:FZD9 - orthologs
Gene location (Human)
πŸ‘ Chromosome 7 (human)
Chr.Chromosome 7 (human)[1]
Band7q11.23Start73,433,778 bp[1]
End73,436,120 bp[1]
Gene location (Mouse)
πŸ‘ Chromosome 5 (mouse)
Chr.Chromosome 5 (mouse)[2]
Band5 G2|5 75.08 cMStart135,277,792 bp[2]
End135,280,084 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • cartilage tissue

  • muscle of thigh

  • gastrocnemius muscle

  • amygdala

  • cingulate gyrus

  • anterior cingulate cortex

  • prefrontal cortex

  • C1 segment

  • hypothalamus

  • right frontal lobe
Top expressed in
  • rib

  • myotome

  • soleus muscle

  • lumbar subsegment of spinal cord

  • lumbar spine

  • ventricular zone

  • stria vascularis

  • plantaris muscle

  • larynx

  • extensor digitorum longus muscle
More reference expression data
BioGPS
πŸ‘ Image
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

8326

14371

Ensembl

ENSG00000188763

ENSMUSG00000049551

UniProt

O00144

Q9R216

RefSeq (mRNA)

NM_003508

NM_010246

RefSeq (protein)

NP_003499

NP_034376

Location (UCSC)Chr 7: 73.43 – 73.44 MbChr 5: 135.28 – 135.28 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Frizzled-9 (Fz-9) is a protein that in humans is encoded by the FZD9 gene.[5][6][7] Fz-9 has also been designated as CD349 (cluster of differentiation 349).

Function

[edit]

Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.[7]

References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000188763 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049551 – 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. ^ Wang YK, Samos CH, Peoples R, PΓ©rez-Jurado LA, Nusse R, Francke U (Mar 1997). "A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23". Human Molecular Genetics. 6 (3): 465–72. doi:10.1093/hmg/6.3.465. PMID 9147651.
  6. ^ Wang YK, SpΓΆrle R, Paperna T, Schughart K, Francke U (Apr 1999). "Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome". Genomics. 57 (2): 235–48. doi:10.1006/geno.1999.5773. PMID 10198163.
  7. ^ a b "Entrez Gene: FZD9 frizzled homolog 9 (Drosophila)".

Further reading

[edit]

External links

[edit]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.