unc-51-like kinase 2 (C. elegans) | |
Hgncid: | 13480 |
Symbol: | ULK2 |
Entrezgene: | 9706 |
Omim: | 608650 |
Refseq: | NM_014683 |
Uniprot: | Q8IYT8 |
Ecnumber: | 2.7.11.1 |
Chromosome: | 17 |
Arm: | p |
Band: | 11.2 |
Unc-51-like kinase 2 (C. elegans) also known as ULK2 is an enzyme which in humans is encoded by the ULK2 gene.[1] The gene is located within the Smith–Magenis syndrome region on chromosome 17.
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.[2] ULK2 and the GTPase activating protein SynGAP function cooperatively in axon formation.[3]