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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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Each of the F1 mice was 30 weeks old. Your basket is currently empty.

There was no significant paternal overtransmission of any other haplotype, nor was there maternal overtransmission of any haplotype. The black lines connecting boxes represent introns. Abbreviations are as follows: Q86UE6 Secondary accession number s: PhastCons conservation scores derived from multiple alignments of 45 vertebrate genomes to the human genome.

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Leucine-rich repeat transmembrane neuronal protein 1

Show all Align All. However, many other imprinted genes are not regulated by differential methylation within their own promoters, but are regulated instead by imprinted control centers which may be located many kilobases distant. Expression is also seen in the dorsal otic vesicle in the presumptive endolymphatic appendage. We also tested for association in a sample of Han Chinese families 23 but we found no significant bias in paternal or maternal transmission of any haplotype to schizophrenic people there were 65 paternal transmissions to 78 paternal nontransmissions of the haplotype.

Lrrtm1 interacts with markers MirMirMirPfam protein domain database More Orthologs of LRRTM1 were detected in databases derived from several vertebrate species but not in databases derived from Drosophila or C. These results suggest lrrfm1 endogenous LRRTM1 may have a role in intracellular trafficking within axons.


Similarly, in neuro-2a neuroblastoma cells myc-LRRTM1 c is not, but myc-lingo1 is d localized gend plasma membrane as detected by live-cell staining. Neural expression is present in the forebrain and midbrain with a sharp boundary across the central midbrain.

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

Database for complete collections of gene phylogenies More Anomalous cerebral asymmetry and language processing in schizophrenia. We analyzed methylation within 2 CpG islands that correspond to the predicted promoter and coding exon of LRRTM1, and a third island roughly 18 kb upstream of LRRTM1, in geme lymphoblastoid cell lines and 17 human post-mortem brain samples, but we did not find evidence that these CpG islands are differentially lrrt1m regions DMRs data not shown.

What good is genomic imprinting: At 10 and 11 dpc expression is restricted to the apical ectodermal ridge. A critique of Francks et gne. MGI growth cone Source: 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.

We screened the first two exons and predicted promoter of LRRTM1 for polymorphisms in 26 left-handers from the RD sample by denaturing high-performance liquid chromatography and sequencing, but we did not detect any polymorphisms that tagged rsrsrs haplotypeor that had overt disruptive effects on the predicted LRRTM1 protein entirely coded within exon 2.

View protein features Protein Feature View.

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

Comprehensive resource for the study of protein post-translational modifications PTMs in human, mouse and rat. No imprinted genes were known previously on chromosome 2p. View list of all current human gene IDs.

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However, this sample was not sufficiently large to test for heterogeneity of the association effect between these two patient groups.

The Journal of Neuroscience. We then found direct confirmatory evidence that LRRTM1 is lrrt1m imprinted gene in humans that shows a variable pattern of maternal downregulation. Click on a disease name to see all genes associated with that disease. Details of the Materials and methods are given in Supplementary information online. Leucine-rich repeat transmembrane tene protein 1.


Family-based association study of markers on chromosome 22 in schizophrenia using African-American, European-American, and Chinese families. It is useful for tracking sequence updates. Pfam protein domain database More The left-handedness risk haplotype is highlighted in bold. Transcript distribution was similar in more caudal sections with the addition of signal in dorsolateral thalamus Figure 4.

Genevisible search portal to normalized and curated expression data from Genevestigator More This entry has 1 described isoform and 3 potential isoforms that are computationally mapped. No detection of these genes was obtained in RT- controls.

The algorithm is described in the ISO standard. Thus, LRRTM1 is an ideal candidate gene for having an involvement in subtle developmental abnormalities of the central nervous system. SwissPalm database of S-palmitoylation events More Expression was intermediate in cerebellum, small intestine, spinal cord, stomach, testis, and uterus.