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- Table of Contents
Facts about Pleckstrin homology domain-containing family M member 1.
Positively regulates lysosome peripheral distribution and ruffled border formation in osteoclasts (By similarity). May be involved in negative regulation of endocytic transport from early endosome to late endosome/lysosome implicating its association with Rab7 (PubMed:20943950).
Human | |
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Gene Name: | PLEKHM1 |
Uniprot: | Q9Y4G2 |
Entrez: | 9842 |
Belongs to: |
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No superfamily |
162 kDa adapter protein; AP162; hsa-mir-4315-1; KIAA0356; microRNA 4315-1; PH domain-containing family M member 1
Mass (kDA):
117.443 kDA
Human | |
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Location: | 17q21.31 |
Sequence: | 17; NC_000017.11 (45434262..45490775, complement) |
Expressed in placenta, liver, prostate, thymus, spleen, ovary, colon, colon carcinoma and peripheral blood lymphocytes (PBL). Weakly expressed in brain, lung, kidney, and testis. No expression in heart, skeletal muscle, pancreas and small intestine. Predominantly expressed in the breast carcinoma cell line MCF-7.
Cytoplasm. Endosome membrane. Lysosome. Lysosome membrane. Localizes to the external membrane of autolysosomes (PubMed:25498145). In case of infection colocalizes with Salmonella typhimurium sifA in proximity of Salmonella-containing vacuole (SCV) (PubMed:25500191).
PMID: 12820725 by Hartel-Schenk S., et al. Novel adapter protein AP162 connects a sialyl-Le(x)-positive mucin with an apoptotic signal transduction pathway.
PMID: 17404618 by van Wesenbeeck L., et al. Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans.