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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:
  • Mic23,
  • My025,
  • HGNC:28727,
  • MICOS26,
  • FAM121B,
  • NM_024122,
  • family with sequence similarity 121B,
  • APOO,
  • MIC26,
  • My025,
  • uc004dax.4,
  • mitochondrial contact site and cristae organizing system subunit 26,
  • Mic23,
  • BC016814,
  • OTTHUMG00000021259,
  • FAM121B,
  • MGC4825,
  • MIC26,
  • MICOS26
  • identifiers:
  • 79135,
  • ENSG00000184831,
  • APOO

Genome feature

Region: gene ? Length: 74593  
Location: X:23833348-23907940 reverse strand Cyto location: Xp22.11


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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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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

280 SN Ps

5 Cross References

16 Data Sets

7 Homologues

0 Located Features

90 Rna Seq Results