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Gene : APOO Homo sapiens

Name  ? apolipoprotein O Cytological Location  Xp22.11
Brief Description  apolipoprotein O
Description  This gene is a member of the apolipoprotein family. Members of this protein family are involved in the transport and metabolism of lipids. The encoded protein associates with HDL, LDL and VLDL lipoproteins and is characterized by chondroitin-sulfate glycosylation. This protein may be involved in preventing lipid accumulation in the myocardium in obese and diabetic patients. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 4, 5, 12 and 16.[provided by RefSeq, Sep 2009]
  • synonyms:
  • mitochondrial contact site and cristae organizing system subunit 26,
  • MIC26,
  • FAM121B,
  • MIC26,
  • APOO,
  • My025,
  • MICOS26,
  • Mic23,
  • MICOS26,
  • HGNC:28727,
  • My025,
  • BC016814,
  • uc004dax.4,
  • Mic23,
  • FAM121B,
  • OTTHUMG00000021259,
  • MGC4825,
  • NM_024122,
  • family with sequence similarity 121B
  • identifiers:
  • 79135,
  • ENSG00000184831,
  • APOO

Genome feature

Region: gene ? Length: 74591  
Location: X:23833348-23907938 reverse strand Cyto location: Xp22.11

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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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]


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



3740 SN Ps

5 Cross References

16 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results