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Gene : GSN Homo sapiens

Name  ? gelsolin Cytological Location  9q33.2
Brief Description  gelsolin
Description  The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000020584,
  • AGEL,
  • NM_000177,
  • X04412,
  • gelsolin (amyloidosis, Finnish type),
  • amyloidosis, Finnish type,
  • HGNC:4620,
  • DKFZp313L0718,
  • ADF,
  • uc064vkv.1,
  • GSN
  • identifiers:
  • 2934,
  • ENSG00000148180,
  • GSN

Genome feature

Region: gene ? Length: 131362  
Location: 9:121201483-121332844 Cyto location: 9q33.2


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

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Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

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Gene Ontology

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Other

599 SN Ps

5 Cross References

19 Data Sets

0 Homologues

0 Located Features

97 Rna Seq Results