Misplaced Pages

NTNG1
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 3ZYJ
Identifiers
Aliases	NTNG1, Lmnt1, netrin G1
External IDs	OMIM: 608818; MGI: 1934028; HomoloGene: 8949; GeneCards: NTNG1; OMA:NTNG1 - orthologs
Gene location (Human) Chr. Chromosome 1 (human) Band 1p13.3 Start 107,140,007 bp End 107,484,923 bp
Gene location (Mouse) Chr. Chromosome 3 (mouse) Band 3|3 F3 Start 109,687,356 bp End 110,051,327 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in lateral nuclear group of thalamus buccal mucosa cell Brodmann area 23 middle temporal gyrus primary visual cortex gonad testicle germinal epithelium entorhinal cortex superior frontal gyrus Top expressed in medial dorsal nucleus medial geniculate nucleus lateral geniculate nucleus sciatic nerve nucleus of stria terminalis subiculum piriform cortex ventral tegmental area habenula inferior colliculi More reference expression data BioGPS More reference expression data
Gene ontology Molecular function protein binding cell adhesion molecule binding cell-cell adhesion mediator activity Cellular component anchored component of membrane anchored component of plasma membrane membrane extracellular region plasma membrane Schaffer collateral - CA1 synapse glutamatergic synapse anchored component of presynaptic active zone membrane Biological process multicellular organism development cell differentiation axonogenesis nervous system development C-terminal protein lipidation modulation of chemical synaptic transmission synaptic membrane adhesion motor neuron axon guidance animal organ morphogenesis tissue development Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 22854 80883 Ensembl ENSG00000162631 ENSMUSG00000059857 UniProt Q9Y2I2 Q8R4G0 RefSeq (mRNA) NM_001113226 NM_001113228 NM_001312688 NM_014917 NM_001330665 NM_001372166 NM_001372167 NM_001372168 NM_001372169 NM_001372170 NM_001372171 NM_001163348 NM_001163349 NM_001163350 NM_001163351 NM_030699 NM_133488 RefSeq (protein) NP_001106697 NP_001106699 NP_001299617 NP_001317594 NP_055732 NP_001359095 NP_001359096 NP_001359097 NP_001359098 NP_001359099 NP_001359100 NP_001156820 NP_001156821 NP_001156822 NP_109624 NP_597995 Location (UCSC) Chr 1: 107.14 – 107.48 Mb Chr 3: 109.69 – 110.05 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Netrin-G1 is a protein that in humans is encoded by the NTNG1 gene.

Netrin G1 (NTNG1) belongs to a conserved family of proteins that act as axon guidance cues during vertebrate nervous system development (Nakashiba et al., 2000).

References

1. ^ GRCh38: Ensembl release 89: ENSG00000162631 – Ensembl, May 2017
2. ^ GRCm38: Ensembl release 89: ENSMUSG00000059857 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Nakashiba T, Ikeda T, Nishimura S, Tashiro K, Honjo T, Culotti JG, Itohara S (Sep 2000). "Netrin-G1: a novel glycosyl phosphatidylinositol-linked mammalian netrin that is functionally divergent from classical netrins". J Neurosci. 20 (17): 6540–50. doi:10.1523/JNEUROSCI.20-17-06540.2000. PMC 6772945. PMID 10964959.
6. ^ "Entrez Gene: NTNG1 netrin G1".

Further reading

• Nagase T, Ishikawa K, Suyama M, et al. (1999). "Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Res. 6 (1): 63–70. doi:10.1093/dnares/6.1.63. PMID 10231032.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Clark HF, Gurney AL, Abaya E, et al. (2003). "The Secreted Protein Discovery Initiative (SPDI), a Large-Scale Effort to Identify Novel Human Secreted and Transmembrane Proteins: A Bioinformatics Assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
• Lin JC, Ho WH, Gurney A, Rosenthal A (2004). "The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons". Nat. Neurosci. 6 (12): 1270–6. doi:10.1038/nn1148. PMID 14595443. S2CID 28353131.
• Zhang Z, Henzel WJ (2005). "Signal peptide prediction based on analysis of experimentally verified cleavage sites". Protein Sci. 13 (10): 2819–24. doi:10.1110/ps.04682504. PMC 2286551. PMID 15340161.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Fukasawa M, Aoki M, Yamada K, et al. (2004). "Case-control association study of human netrin G1 gene in Japanese schizophrenia". J. Med. Dent. Sci. 51 (2): 121–8. PMID 15508520.
• Aoki-Suzuki M, Yamada K, Meerabux J, et al. (2005). "A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia". Biol. Psychiatry. 57 (4): 382–93. doi:10.1016/j.biopsych.2004.11.022. PMID 15705354. S2CID 19932857.
• Borg I, Freude K, Kübart S, et al. (2005). "Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome". European Journal of Human Genetics. 13 (8): 921–7. doi:10.1038/sj.ejhg.5201429. PMID 15870826.
• Meerabux JM, Ohba H, Fukasawa M, et al. (2006). "Human netrin-G1 isoforms show evidence of differential expression". Genomics. 86 (1): 112–6. doi:10.1016/j.ygeno.2005.04.004. PMID 15901489.
• Archer HL, Evans JC, Millar DS, et al. (2006). "NTNG1 Mutations are a Rare Cause of Rett Syndrome". American Journal of Medical Genetics. 140 (7): 691–4. doi:10.1002/ajmg.a.31133. PMC 2577736. PMID 16502428.
• Gregory SG, Barlow KF, McLay KE, et al. (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315–21. Bibcode:2006Natur.441..315G. doi:10.1038/nature04727. PMID 16710414.
• Nectoux J, Girard B, Bahi-Buisson N, et al. (2007). "Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy". Pediatr. Neurol. 37 (4): 270–4. doi:10.1016/j.pediatrneurol.2007.06.002. PMID 17903671.

This article on a gene on human chromosome 1 is a stub. You can help Misplaced Pages by expanding it.

• v
• t
• e

• Genes on human chromosome 1
• Human chromosome 1 gene stubs
• Netrins