netrin G1

Summary
Gene Symbol
  • NTNG1
Aliases
  • KIAA0976
  • Lmnt1
  • Netrin-G1
  • netrin G1f
Organism
Homo sapiens (human)
External Links
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
KEGG BRITE Database
Orthology
K07522
Name
netrin-G1
References
Disease
Disease Ontology
Displaying entries 1 - 10 of 39 in total
DO ID Disease Name Source
DOID:0080199 colorectal carcinoma
DOID:10003 sensorineural hearing loss
DOID:1059 intellectual disability
DOID:10907 microcephaly
DOID:10908 hydrocephalus
DOID:11832 visual epilepsy
DOID:11963 esophagitis
DOID:1206 Rett syndrome
DOID:12849 autistic disorder
DOID:13832 patent ductus arteriosus
The Human Phenotype Ontology
Displaying entries 11 - 20 of 50 in total
HPO ID HPO Term
HP:0001288 Gait disturbance
HP:0001319 Neonatal hypotonia
HP:0001332 Dystonia
HP:0001337 Tremor
HP:0001510 Growth delay
HP:0001773 Short foot
HP:0002066 Gait ataxia
HP:0002123 Generalized myoclonic seizure
HP:0002186 Apraxia
HP:0002194 Delayed gross motor development
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: August 19, 2024