Name | apolipoprotein A-II |
Symbol | APOA2 |
Aliases | |
Gene Product | - apolipoprotein A-II precursor
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Category | |
UniGene |
Hs.237658
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Reference Sequence |
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OMIM and SNP |
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Locus |
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Summary | Apolipoprotein (Apo-) A-II is the second most abundant protein of the high density lipoprotein particles. The apo-A-II gene consists of 4 exons and 3 introns. The four exons encode the 5' untranslated region, pre-peptide, a short N-terminal domain and a C-terminal domain composed of a variable number of lipid-binding amphipathic helices. Familial apo-A-II deficiency may result from a splice-junction alteration which blocks splicing of intron 3 from the primary transcript and result the formation of a non-functional mRNA. |
Gene Ontology | |
Expression | EST (658 ESTs, 49 libraries) |
Tissue | Breadth ? |
CPM ? |
brain |  |  | colon |  |  | germ cell |  |  | heart |  |  | kidney |  |  | liver |  |  | lung |  |  | mammary gland |  |  | muscle |  |  | placenta |  |  | spleen |  |  | testis |  |  | uncharacterized tissue |  |  | whole body |  |  |
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SAGE (3728446 tags, 69 libraries) |
Tissue | Breadth ? |
CPM ? |
brain |  |  | colon |  |  | eye |  |  | heart |  |  | kidney |  |  | liver |  |  | lung |  |  | mammary gland |  |  | mesothelial tissue |  |  | nervous |  |  | ovary |  |  | pancreas |  |  | prostate |  |  | skin |  |  | uncharacterized tissue |  |  |
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Evidence | Mutation in Renal Amyloidosis
- Benson MD, Liepnieks JJ, Yazaki M, Yamashita T, Hamidi Asl K, Guenther B, Kluve-Beckerman B, Benson MD, Liepnieks JJ, Yazaki M, Yamashita T, Hamidi Asl K, Guenther B, Kluve-Beckerman B A new human hereditary amyloidosis: the result of a stop-codon mutation inthe apolipoprotein AII gene. Genomics 2001 Mar 15;72(3):272-7.
Other key publications related to this gene
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