LRTOMT

Identifiers

LRTOMT, CFAP111, DFNB63, LRRC51, leucine rich transmembrane and O-methyltransferase domain containing

External IDs

Gene ontology
Molecular function	• methyltransferase activity • transferase activity • O-methyltransferase activity • L-dopa O-methyltransferase activity • catechol O-methyltransferase activity • orcinol O-methyltransferase activity
Cellular component	• cytoplasm • integral component of membrane • membrane • plasma membrane
Biological process	• methylation • auditory receptor cell development • sensory perception of sound • catecholamine catabolic process • catecholamine metabolic process • neurotransmitter catabolic process
Sources:Amigo / QuickGO

Orthologs

Species

Human

Mouse

Entrez


220074


791260


n/a


ENSMUSG00000078630


Q8WZ04 Q96E66


A1Y9I9

RefSeq (mRNA)

NM_001145307 NM_001145308 NM_001145309 NM_001145310 NM_001205138
NM_001271471 NM_145309 NM_001318803


NM_001081679 NM_001282088

RefSeq (protein)

NP_001138780.1 NP_001138781.1 NP_001138782.1 NP_001138779.1 NP_001192067.1
NP_001258400.1 NP_660352.1 NP_001305732.1


NP_001075148 NP_001269017

Location (UCSC)

n/a

PubMed search

n/a

Leucine rich transmembrane and O-methyltransferase domain containing is a protein that in humans is encoded by the LRTOMT gene.

Mutations in LRTOMT are associated to non syndromic deafness .