netrin G1

Summary
Gene Symbol
  • NTNG1
Aliases
  • KIAA0976
  • Lmnt1
  • Netrin-G1
  • netrin G1f
Organism
Homo sapiens (human)
NCBI Gene
22854
HGNC
23319
KEGG Gene ID
hsa:22854
PubChem
22854
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Developmental protein
  • Differentiation
  • Direct protein sequencing
  • Disulfide bond
  • EGF-like domain
  • GPI-anchor
  • Glycoprotein
  • Laminin EGF-like domain
  • Neurogenesis
  • Reference proteome
  • Repeat
  • Signal
Proteins
Displaying all 5 entries
UniProt Protein Name
Q5IEC8
X5DNW2
Q9Y2I2
  • Laminet-1
B4DKF0
Q5IEC3
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
netrin
Functional Category
  • E: Amino acid transport and metabolism
  • K: Transcription
  • T: Signal transduction mechanisms
KEGG BRITE Database
Orthology
K07522
Name
netrin-G1
References
Disease
The Human Phenotype Ontology
Displaying entries 21 - 30 of 50 in total
HPO ID HPO Term
HP:0002300 Mutism
HP:0002353 EEG abnormality
HP:0002360 Sleep abnormality
HP:0002371 Loss of speech
HP:0002376 Developmental regression
HP:0002505 Loss of ambulation
HP:0002540 Inability to walk
HP:0002650 Scoliosis
HP:0002793 Abnormal pattern of respiration
HP:0002808 Kyphosis
Displaying 1 entry
Disease ID Disease Name
ORPHA:3095
  • atypical Rett syndrome

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 8, 2025