You are viewing an incomplete version of our website. Please click to reload the website as full version.

Browse our Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing (LRTOMT) ELISA Kits

Full name:
Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing ELISA Kits (LRTOMT)
On www.antibodies-online.com are 0 Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing (LRTOMT) ELISA Kits from different suppliers available. Additionally we are shipping Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing Antibodies (8) and Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing Proteins (7) and many more products for this protein. A total of 15 Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing products are currently listed.
Synonyms:
1700008D07Rik, Comt2, DFNB63, F930017I19Rik, LRRC51, Lrtomt, RGD1561509, RGD1565856
list all ELISA KIts Gene Name GeneID UniProt
Mouse LRTOMT LRTOMT 69358 Q9DAK8
Rat LRTOMT LRTOMT 293156 B6CZ61
Human LRTOMT LRTOMT 220074 Q96E66 , Q8WZ04

Show all synonyms

More ELISA Kits for Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing Interaction Partners

Mouse (Murine) Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing (LRTOMT) interaction partners

Human Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing (LRTOMT) interaction partners

  1. LRTOMT gene is the second cause of congenital hearing impairment in Moroccan patients.

  2. A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame.

  3. A genome wide linkage analysis of nonsyndromic deafness segregating in a consanguineous Pakistani family (PKDF537) was used to identify DFNB63, a new locus for congenital profound sensorineural hearing loss.

  4. Mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.

Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing (LRTOMT) Antigen Profile

Antigen Summary

This gene includes two transcript forms. The short form has one open reading frame (ORF), which encodes the leucine-rich repeats (LRR)-containing protein of unknown function. This protein is called LRTOMT1 or LRRC51. The long form has two alternative ORFs\; the upstream ORF has the same translation start codon as used in the short form and the resulting transcript is a candidate for nonsense-mediated decay, and the downstream ORF encodes a different protein, which is a transmembrane catechol-O-methyltransferase and is called LRTOMT2, TOMT or COMT2. The COMT2 is essential for auditory and vestibular function. Defects in the COMT2 can cause nonsyndromic deafness. Alternatively spliced transcript variants from each transcript form have been found for this gene.

Alternative names and synonyms associated with Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing (LRTOMT)

  • leucine rich repeat containing 51 (Lrrc51) Elisa Kit
  • leucine rich transmembrane and O-methyltransferase domain containing (LRTOMT) Elisa Kit
  • leucine-rich repeat-containing protein 51 (LRRC51) Elisa Kit
  • O-methyltransferase domain containing (Tomt) Elisa Kit
  • transmembrane O-methyltransferase (Tomt) Elisa Kit
  • 1700008D07Rik Elisa Kit
  • Comt2 Elisa Kit
  • DFNB63 Elisa Kit
  • F930017I19Rik Elisa Kit
  • LRRC51 Elisa Kit
  • Lrtomt Elisa Kit
  • RGD1561509 Elisa Kit
  • RGD1565856 Elisa Kit

Protein level used designations for LRTOMT

leucine-rich repeat-containing protein 51 , leucine rich transmembrane and 0-methyltransferase domain containing , transmembrane O-methyltransferase , leucine rich repeat containing 51 , catechol O-methyltransferase 2 , leucine rich transmembrane and O-methyltransferase domain containing , catechol-O-methyltransferase 2

GENE ID SPECIES
69358 Mus musculus
293156 Rattus norvegicus
220074 Homo sapiens
718286 Macaca mulatta
748243 Pan troglodytes
515066 Bos taurus
308868 Rattus norvegicus
791260 Mus musculus
Did you look for something else?