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Protein Coding Gene : Nln neurolysin (metallopeptidase M3 family)

Primary Identifier  MGI:1923055 Organism  mouse, laboratory
Chromosome  13 NCBI Gene Number  75805
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables peptidase activity and peptide binding activity. Acts upstream of or within regulation of gluconeogenesis and regulation of skeletal muscle fiber differentiation. Located in plasma membrane. Orthologous to human NLN (neurolysin).
PHENOTYPE: Mice homozygous for a null allele exhibit increased glucose tolerance, insulin sensitivity, and gluconeogensis. Mice also show decreased body weight and run less in a low intensity regime to exhaustion. [provided by MGI curators]
  • synonyms:
  • Nln,
  • RIKEN cDNA 4930472G13 gene,
  • expressed sequence C79345,
  • 4930472G13Rik,
  • C79345,
  • MGI:2145509,
  • neurolysin (metallopeptidase M3 family)

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

5 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For