APOL2

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Apolipoprotein L, 2
Identifiers
Symbols APOL2 ; APOL-II; APOL3
External IDs OMIM607252 MGI2444921 HomoloGene12785 GeneCards: APOL2 Gene
RNA expression pattern
PBB GE APOL2 221013 s at tn.png
PBB GE APOL2 221653 x at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 23780 239552
Ensembl ENSG00000128335 ENSMUSG00000056656
UniProt Q9BQE5 A2VDH7
RefSeq (mRNA) NM_030882 NM_001081970
RefSeq (protein) NP_112092 NP_001075439
Location (UCSC) Chr 22:
36.62 – 36.64 Mb
Chr 15:
77.75 – 77.76 Mb
PubMed search [1] [2]

Apolipoprotein L2 is a protein that in humans is encoded by the APOL2 gene.[1][2][3]

This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene.[3]

References[edit]

  1. ^ Dunham I, Shimizu N, Roe BA, Chissoe S, Hunt AR, Collins JE, Bruskiewich R, Beare DM, Clamp M, Smink LJ, Ainscough R, Almeida JP, Babbage A, Bagguley C, Bailey J, Barlow K, Bates KN, Beasley O, Bird CP, Blakey S, Bridgeman AM, Buck D, Burgess J, Burrill WD, O'Brien KP, et al. (Dec 1999). "The DNA sequence of human chromosome 22". Nature 402 (6761): 489–95. doi:10.1038/990031. PMID 10591208. 
  2. ^ Page NM, Butlin DJ, Lomthaisong K, Lowry PJ (May 2001). "The human apolipoprotein L gene cluster: identification, classification, and sites of distribution". Genomics 74 (1): 71–8. doi:10.1006/geno.2001.6534. PMID 11374903. 
  3. ^ a b "Entrez Gene: APOL2 apolipoprotein L, 2". 

Further reading[edit]