ULK2 Summary

This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2008]

ULK2 Details

Gene Symbol : ULK2

Gene Name : Unc-51 like autophagy activating kinase 2

Chromosome : CHR 17: 198,679,25-197,708,27

Locus : 17p11.2

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APOL2 Summary

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. [provided by RefSeq, Jul 2008]

APOL2 Details

Gene Symbol : APOL2

Gene Name : Apolipoprotein L2

Chromosome : CHR 22: 362,399,53-362,262,08

Locus : 22q12.3

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