This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
Facts about Transmembrane O-methyltransferase.
Component of the cochlear hair cell's mechanotransduction (MET) machinery. Involved in the meeting of the asymmetric tip-link MET complicated.
Human | |
---|---|
Gene Name: | LRTOMT |
Uniprot: | Q8WZ04 |
Entrez: | 220074 |
Belongs to: |
---|
class I-like SAM-binding methyltransferase superfamily |
leucine rich transmembrane and 0-methyltransferase domain containing; TOMT
Mass (kDA):
32.155 kDA
Human | |
---|---|
Location: | 11q13.4 |
Sequence: | 11; NC_000011.10 (72080342..72110782) |
[Isoform 1]: Membrane; Single-pass membrane protein.; [Isoform 2]: Cytoplasm. Endoplasmic reticulum. Localized to the cell body of the cochlear hair cells, but is not present in the stereocilia (PubMed:28504928). Present but not restricted to the apical cistern, Hensen's body and the subsurface cistern (By similarity).
PMID: 18953341 by Ahmed Z.M., et al. Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID: 18794526 by Du X., et al. A catechol-O-methyltransferase that is essential for auditory function in mice and humans.