Browse our FLCN Proteins (FLCN)

On www.antibodies-online.com are 6 Folliculin (FLCN) Proteins from 4 different suppliers available. Additionally we are shipping FLCN Antibodies (88) and FLCN Kits (9) and many more products for this protein. A total of 112 FLCN products are currently listed.
Synonyms:
AU014660, B430214A04Rik, BHD, FLCL, flcn, wu:fe38g11, zgc:136982
list all proteins Gene Name GeneID UniProt
FLCN 216805 Q8QZS3
FLCN 303185 Q76JQ2
FLCN 201163 Q8NFG4

FLCN Proteins (FLCN) by Origin

More Proteins for FLCN Interaction Partners

Zebrafish Folliculin (FLCN) interaction partners

  1. Results show that zebrafish flcn is expressed during embryonic development with elevated expression levels in proliferating tissues of the zebrafish embryo.

Mouse (Murine) Folliculin (FLCN) interaction partners

  1. Based on the phenotypes of our preclinical models, the FLCN H255Y mutant protein has lost it tumour suppressive function leading to the clinical manifestations of BHD, whereas the FLCN K508R mutant protein may have a dominant negative effect on the function of wild-type FLCN in regulating kidney cell proliferation and, therefore, act as an oncoprotein

  2. FLCN regulates adipose tissue browning via mTOR (show FRAP1 Proteins) and the transcription factor TFE3 (show TFE3 Proteins)

  3. loss of FLCN results in a complete metabolic reprogramming of adipose tissues, resulting in enhanced oxidative metabolism.

  4. Tfe3 (show TFE3 Proteins) overexpression in HSPCs impaired long-term hematopoietic reconstitution in vivo, recapitulating the Flcn KO phenotype, and supporting the notion that abnormal activation of Tfe3 (show TFE3 Proteins) contributes to the Flcn KO phenotype. Flcn KO mice develop an acute histiocytic hyperplasia in multiple organs, suggesting a novel function for Flcn in macrophage development

  5. mTOR (show FRAP1 Proteins) inhibitor, sirolimus, suppresses the tumor's growth, suggesting that mTOR (show FRAP1 Proteins) inhibitors might be effective in control of FLCN-deficient RCC (show XRCC1 Proteins).

  6. we show that glycogen (show GYS1 Proteins) accumulates in kidneys from mice lacking FLCN and in renal tumors from a BHD patient

  7. Fnip1 and Fnip2 (show FNIP2 Proteins) play critical roles in kidney tumor suppression in cooperation with Flcn

  8. Folliculin (Flcn) inactivation leads to murine cardiac hypertrophy through mTORC1 deregulation.

  9. The FLCN-GABARAP (show GABARAP Proteins) association is modulated by the presence of either folliculin-interacting protein (FNIP)-1 or FNIP2 (show FNIP2 Proteins) and further regulated by ULK1 (show ULK1 Proteins).

  10. Flcn regulates apoptosis in lung epithelium via E-cadherin (show CDH1 Proteins)-LKB1 (show STK11 Proteins)-AMPK (show PRKAA1 Proteins) axis.

Human Folliculin (FLCN) interaction partners

  1. Seventy-six of 156 FLCN mutation carriers (120 probands and 36 sibs, 48.7%) had skin papules; however, cutaneous manifestations were so subtle that only one patient voluntarily consulted dermatologists. Japanese Asian BHD families have three FLCN mutational hotspots.

  2. A nonsense mutation of FLCN was found in a spontaneous pneumothorax family. The results expand the mutational spectrum of FLCN in patients with Birt-Hogg-Dube syndrome.

  3. the study describes the FLCN mutation spectrum in Danish Birt-Hogg-Dube (BHD) syndrome patients, and contributes to a better understanding of BHD syndrome and management of BHD patients.

  4. We report Smith-Magenis syndrome who presents bilateral renal tumors. This is most likely related to haploinsufficiency of FLCN gene, located in the deleted region

  5. For patients whose clinical features are atypical, detection of germline mutation in FLCN gene would help confirm diagnosis. The 2 mutations we reported would expand the mutation spectrum of FLCN gene associated with BHD syndrome

  6. DNA sequence analyses determined that there was a two base pair deletion in exon 4 of the FLCN gene, confirming the diagnosis of BHD syndrome.

  7. We identified a hitherto unreported pathogenic FLCN frameshift deletion c.563delT (p.Phe188Serfs*35) in a family of a 46-year-old woman presented with macrohematuria due to bilateral chromophobe renal carcinomas

  8. FLCN irregulation in lung cysts of primary spontaneous pneumothorax is not associated with promoter methylation.

  9. mTOR (show FRAP1 Proteins) inhibitor, sirolimus, suppresses the tumor's growth, suggesting that mTOR (show FRAP1 Proteins) inhibitors might be effective in control of FLCN-deficient RCC (show XRCC1 Proteins).

  10. we show that glycogen (show GYS1 Proteins) accumulates in kidneys from mice lacking FLCN and in renal tumors from a BHD patient

FLCN Protein Profile

Protein Summary

This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms.

Alternative names and synonyms associated with FLCN

  • folliculin (FLCN)
  • folliculin (flcn)
  • folliculin (Flcn)
  • AU014660 protein
  • B430214A04Rik protein
  • BHD protein
  • FLCL protein
  • flcn protein
  • wu:fe38g11 protein
  • zgc:136982 protein

Protein level used designations for Folliculin Proteins (FLCN)

folliculin , folliculin-like , birt-Hogg-Dube syndrome protein homolog , BHD skin lesion fibrofolliculoma protein , birt-Hogg-Dube syndrome protein

GENE ID SPECIES
454472 Pan troglodytes
698082 Macaca mulatta
496819 Xenopus (Silurana) tropicalis
678628 Danio rerio
100158392 Xenopus laevis
100395467 Callithrix jacchus
100431335 Pongo abelii
100470222 Ailuropoda melanoleuca
216805 Mus musculus
303185 Rattus norvegicus
201163 Homo sapiens
416503 Gallus gallus
479529 Canis lupus familiaris
526652 Bos taurus
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