Sequence Detail

ID/Version

Q8R4G0 Q69ZU3 Q8R4F8 Q9ESR5 Q8R4F5 Q9ESR6 Q9ESR3 Q8R4F4 Q68FE5 Q8R4F9 Q8R4F7 Q8R4F6 Q9ESR8 Q9ESR4 Q9ESR7 Q8R4F3 (UniProt | EBI)

Last sequence update: 2005-01-04
Last annotation update: 2024-03-27

Sequence description from provider

RecName: Full=Netrin-G1;AltName: Full=Laminet-1;Flags: Precursor;

Provider

SWISS-PROT

Sequence

Polypeptide 539 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Ntng1	netrin G1	27	105	3	12

Sequence references in MGI

J:64213 Nakashiba T, et al., Netrin-G1: a novel glycosyl phosphatidylinositol-linked mammalian netrin that is functionally divergent from classical netrins. J Neurosci. 2000 Sep 1;20(17):6540-50
J:74494 Nakashiba T, et al., Complementary expression and neurite outgrowth activity of netrin-G subfamily members. Mech Dev. 2002 Feb;111(1-2):47-60
J:75881 Yin Y, et al., Laminets: laminin- and netrin-related genes expressed in distinct neuronal subsets. Mol Cell Neurosci. 2002 Mar;19(3):344-58
J:92575 Okazaki N, et al., Prediction of the coding sequences of mouse homologues of KIAA gene: IV. The complete nucleotide sequences of 500 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries. DNA Res. 2004 Jun 30;11(3):205-18
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:287131 Heimer G, et al., Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia. Hum Mutat. 2020 Feb;41(2):476-486