Netrin G1

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NTNG1
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases NTNG1, Lmnt1, netrin G1
External IDs MGI: 1934028 HomoloGene: 8949 GeneCards: NTNG1
Genetically Related Diseases
anorexia nervosa[1]
RNA expression pattern
PBB GE NTNG1 206713 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001113226
NM_001113228
NM_001312688
NM_014917
NM_001330665

RefSeq (protein)

NP_001106697
NP_001106699
NP_001299617
NP_001317594
NP_055732

Location (UCSC) Chr 1: 107.14 – 107.48 Mb Chr 3: 109.78 – 110.14 Mb
PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Netrin-G1 is a protein that in humans is encoded by the NTNG1 gene.[4][5]

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).[supplied by OMIM][5]

References[edit]

  1. ^ "Diseases that are genetically associated with NTNG1 view/edit references on wikidata". 
  2. ^ "Human PubMed Reference:". 
  3. ^ "Mouse PubMed Reference:". 
  4. ^ 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. PMID 10964959. 
  5. ^ a b "Entrez Gene: NTNG1 netrin G1". 

Further reading[edit]