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Gene : LCAT Homo sapiens

Name  ? lecithin-cholesterol acyltransferase Cytological Location  16q22.1
Brief Description  lecithin-cholesterol acyltransferase
Description  This gene encodes the extracellular cholesterol esterifying enzyme, lecithin-cholesterol acyltransferase. The esterification of cholesterol is required for cholesterol transport. Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency. [provided by RefSeq, Jul 2008]
  • synonyms:
  • uc002euy.2,
  • LCAT,
  • phosphatidylcholine--sterol O-acyltransferase,
  • OTTHUMG00000137551,
  • HGNC:6522,
  • NM_000229
  • identifiers:
  • 3931,
  • ENSG00000213398,
  • LCAT

Genome feature

Region: gene ? Length: 4371  
Location: 16:67939750-67944120 reverse strand Cyto location: 16q22.1


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

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Disease

2 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

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

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Other

3753 SN Ps

5 Cross References

19 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results