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GENE AND PROTEIN SUMMARY

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Gene name

FZD9

Description

frizzled family receptor 9

Protein class

CD markers, G-protein coupled receptors, Mapped to UniProt SWISS-PROT, Potential transmembrane proteins, Potentially secreted proteins

Protein evidence

Only RNA

Entrez gene summary

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. [provided by RefSeq, Jul 2008]

External links

Ensembl, UniProt, Entrez gene, neXtProt, Antibodypedia

No of splice variants

1 in total
1 with predicted TM region
1 with predicted signal peptide

SUBCELLULAR LOCATION SUMMARY

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Pending subcellular analysis

NORMAL TISSUE & ORGAN SUMMARY

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Pending normal tissue analysis

CANCER TISSUE SUMMARY

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Pending cancer tissue analysis

CELL LINE SUMMARY

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RNA evidence

Low
 

Cell line

Cell origin

RNA abundance

IH staining

IF intensity

A-431 Skin Low

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-

A-549 Lung Low

-

-

CACO-2 Colon Low

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-

HEK 293 Embryonal kidney Low

-

-

HeLa Cervix Low

-

-

Hep-G2 Liver Low

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-

MCF-7 Pleural effusion Low

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-

PC-3 Bone marrow Not detected

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-

RT-4 Urinary bladder Not detected

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-

U-2 OS Bone Low

-

-

U-251 MG Brain Not detected

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-

ANTIBODY SUMMARY

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Pending antibodies