Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

FST (follistatin)

Identity

Other namesFS
HGNC FST
Location 5q11.2
Note

Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 

External links

Nomenclature
HGNCFST   3971
Entrez_GeneFST  10468  follistatin
Cards
GeneCardsFST
EnsemblFST [Search_View]   ENSG00000134363 [Gene_View]
GenatlasFST
GeneLynxFST
eGenomeFST
euGene10468
Genomic and cartography
GoldenPathFST  -  5q11.2   chr5:52812352-52817661 +  5q11.2   [Description]    (hg18-March_2006)
EnsemblFST - 5q11.2 [CytoView]
NCBIMapview
OMIMDisease map [OMIM]
HomoloGeneFST
Gene and transcription
GenbankBC004107 [ ENTREZ ]
GenbankCR541813 [ ENTREZ ]
GenbankDQ893433 [ ENTREZ ]
GenbankDQ896745 [ ENTREZ ]
RefSeqNM_006350 [ SRS ]    NM_006350 [ ENTREZ ]
RefSeqNM_013409 [ SRS ]    NM_013409 [ ENTREZ ]
RefSeqAC_000048 [ SRS ]    AC_000048 [ ENTREZ ]
RefSeqAC_000137 [ SRS ]    AC_000137 [ ENTREZ ]
RefSeqNC_000005 [ SRS ]    NC_000005 [ ENTREZ ]
RefSeqNT_006713 [ SRS ]    NT_006713 [ ENTREZ ]
RefSeqNW_001838934 [ SRS ]    NW_001838934 [ ENTREZ ]
RefSeqNW_922607 [ SRS ]    NW_922607 [ ENTREZ ]
AceViewFST AceView - NCBI
UnigeneHs.9914 [ SRS ]    Hs.9914 [ NCBI ]     HS9914 [ spliceNest ]
Fast-db3876 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtP19883 [ SRS]    P19883 [ EXPASY ]     P19883 [ INTERPRO ]     P19883 [ UNIPROT ]
PrositePS00282 KAZAL [ SRS ]    PS00282 KAZAL [ Expasy ]
PrositePS51364 TB [ SRS ]    PS51364 TB [ Expasy ]
InterproIPR003645 Fol_N [ SRS ]    IPR003645 Fol_N [ EBI ]
InterproIPR015204 Fol_N_sub [ SRS ]    IPR015204 Fol_N_sub [ EBI ]
InterproIPR002350 Prot_inh_Kazal [ SRS ]    IPR002350 Prot_inh_Kazal [ EBI ]
CluSTrP19883
PfamPF09120 EGF-like_subdom [ SRS ]    PF09120 EGF-like_subdom [ Sanger ]    pfam09120 [ NCBI-CDD ]
PfamPF00050 Kazal_1 [ SRS ]    PF00050 Kazal_1 [ Sanger ]    pfam00050 [ NCBI-CDD ]
SmartSM00274 FOLN [EMBL]
SmartSM00280 KAZAL [EMBL]
BlocksP19883
PDB2B0U [ SRS ]    2B0U [ PdbSum ],   2B0U [ IMB ]   2B0U [ RSDB ]
PDB2P6A [ SRS ]    2P6A [ PdbSum ],   2P6A [ IMB ]   2P6A [ RSDB ]
HPRD00641
Protein Interaction databases
DIPP19883
IntActP19883
Polymorphism : SNP, mutations, diseases
OMIM136470;184700    [ map ]   
GENECLINICS136470;184700
SNPFST [dbSNP-NCBI]  
SNPNM_006350 [SNP-NCI]  
SNPNM_013409 [SNP-NCI]  
SNPFST [GeneSNPs - Utah]  FST] [HGBASE - SRS]
HAPMAPFST [HAPMAP]  
HGMDFST
General knowledge
Family BrowserFST [UCSC Family Browser]
SOURCENM_006350
SOURCENM_013409
SMDHs.9914
SAGEHs.9914
GOnegative regulation of transcription from RNA polymerase II promoter [Amigo]  negative regulation of transcription from RNA polymerase II promoter
GOprotein binding [Amigo]  protein binding
GOextracellular region [Amigo]  extracellular region
GOmulticellular organismal development [Amigo]  multicellular organismal development
GOactivin inhibitor activity [Amigo]  activin inhibitor activity
GOnegative regulation of follicle-stimulating hormone secretion [Amigo]  negative regulation of follicle-stimulating hormone secretion
GOpositive regulation of hair follicle development [Amigo]  positive regulation of hair follicle development
KEGGTGF-beta signaling pathway
PubGeneFST
TreeFamFST
CTD10468 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbeFST Related clones (RZPD - Berlin)
PubMed
PubMed42 Pubmed reference(s) in LocusLink
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written09-2002Dessen P, Le Minor S
Updated03-2008Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Aug 11 20:11:48 2008


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

j.l.huret@chu-poitiers.fr.