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Gene : APOC1 Homo sapiens

Name  ? apolipoprotein C1 Cytological Location  19q13.32
Brief Description  apolipoprotein C1
Description  This gene encodes a member of the apolipoprotein C1 family. This gene is expressed primarily in the liver, and it is activated when monocytes differentiate into macrophages. The encoded protein plays a central role in high density lipoprotein (HDL) and very low density lipoprotein (VLDL) metabolism. This protein has also been shown to inhibit cholesteryl ester transfer protein in plasma. A pseudogene of this gene is located 4 kb downstream in the same orientation, on the same chromosome. This gene is mapped to chromosome 19, where it resides within a apolipoprotein gene cluster. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Sep 2016]
  • synonyms:
  • NM_001321065,
  • uc002pac.2,
  • OTTHUMG00000180844,
  • X00570,
  • Apo-CI,
  • apo-CIB,
  • apolipoprotein C-I,
  • ApoC-I,
  • HGNC:607,
  • APOC1,
  • apoC-IB
  • identifiers:
  • 341,
  • ENSG00000130208,
  • APOC1

Genome feature

Region: gene ? Length: 5022  
Location: 19:44914325-44919346 Cyto location: 19q13.32

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Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

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Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



260 SNPs

5 Cross References

16 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results