LRRTM1 leucine rich repeat transmembrane neuronal 1 [ (human)]. Gene ID: , updated on 7-Dec This gene is imprinted, being predominantly expressed from the paternal allele and showing a variable pattern of maternal down-regulation. May be associated . Leucine-rich repeat transmembrane neuronal protein 1. Gene. Lrrtm1. Organism. Mus musculus (Mouse). Status. Reviewed-Annotation score: Annotation.

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Expression is also seen in the dorsal otic vesicle in the presumptive endolymphatic appendage. Also, expression within the fetal human thalamus is more restricted as compared to the mouse, with staining relatively limited lrrt1 dorsomedial regions that have been implicated in schizophrenia.

Supplementary Information doc 86K Click here to view. Protein interaction database and analysis system More ENSG Expressed in organ shighest expression level in caudate nucleus.

LRRTM1 – leucine rich repeat transmembrane neuronal 1

The striking signal in caudate and putamen in human Figure 4 was not present in mouse, at least not at E15 and in adult. LRRTM1 aids in the assembly of complex retinogenciulate synapses in mice, which are believed to help process complex visual signals. Abnormal asymmetry in language association cortex in autism. While the OMIM database is open to the public, users seeking information lrrhm1 a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.

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Please consider making a donation now and again in the future. In adult brain expression is most prominent in the forebraain, particularly in the thalamus and in the cortical areas including hippocampus, piriform and posterior cingulate. Database for complete collections of gene phylogenies More Four distinct tokens exist: H-Invitational Database, human transcriptome db More In the present study we have used genetic association mapping and gene-functional analysis to identify a novel imprinted gene on 2p12, LRRTM1, that we propose is responsible lrrhm1 causing the linkages of this chromosomal region to human handedness and schizophrenia.


Accelerated evolution of conserved noncoding sequences in humans.

RCSB PDB – Gene View – LRRTM1 – leucine rich repeat transmembrane neuronal 1

Views Read Edit View history. LRRTM1 is the first gene linked to increased odds of being left-handedwhen inherited from the father’s side. Introduction Left—right asymmetrical function is egne conserved feature of vertebrate central nervous systems. Handedness, brain asymmetry and schizophrenia are likely to be etiologically complex traits with gens, or many, genetic and environmental influences.

Integrated resource of protein families, domains and functional sites More There are no other genes within 1.

Our website will not work properly. Chordata Protein Annotation Program.

However, biallelic expression was found in 15 out of 18 brains, and LRRTM1 was expressed at similar levels from both alleles in the adult human cerebral cortex of five individuals hene biallelic expression analyzed by quantitative PCR.

The displayed sequence is further processed into a mature form. Genevisible search portal to normalized and curated expression data from Genevestigator More Warning You are using a web browser that we do not support. March 6, Last modified: Merlin—rapid analysis of dense genetic maps using sparse gene flow trees.

LRRTM1 leucine rich repeat transmembrane neuronal 1 [ (human)]

Parallel patterns of evolution in the genomes and transcriptomes of humans and chimpanzees. Use several keywords to find the most relevant results: We are determined to keep this website freely accessible. Similarly to embryonic brain, LRRTM1 was expressed at similar levels that is, krrtm1 in all analyzed regions of left and right adult human cerebral cortex several different cortical regions from five individuals were analyzed by quantitative PCR.


Human Protein Atlas More This is version of the entry and version 2 of the sequence. Developmental Gene Expression 7.

Leucine-rich repeat transmembrane neuronal protein 1

MGI Extracellular region or secreted extracellular matrix Source: Biochem Biophys Res Commun. It lists the nodes as they appear rlrtm1 in the taxonomic tree, with the more general grouping listed first. Asymmetry of fetal cerebral hemispheres: This track represents the gene-structure on the genome.

In developing mice, Lrrtm1 was expressed at embryonic day 13 and Supplementary Information accompanies the paper on the Molecular Psychiatry website http: Author manuscript; available in PMC Nov Protein Spotlight The hands to say it – Issue 91 of February Brain morphology appears grossly normal, except for rare cases of anomalous ventroculomegaly.

The block in LTP could be rescued by expression of full-length Lrrtm2 or Lrrtm2 lacking its intracellular domain, but not by Lrrtm4