RAB11B, member RAS oncogene family

Summary
Gene Symbol
  • RAB11B
Aliases
  • H-YPT3
Organism
Homo sapiens (human)
NCBI Gene
9230
HGNC
9761
PubChem
9230
Alliance of Genome Resources
JoGo
RAB11B
TogoVar
RAB11B
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Alternative splicing
  • Citrullination
  • Cytoplasmic vesicle
  • Direct protein sequencing
  • Disease variant
  • Endosome
  • GTP-binding
  • Glycoprotein
  • Hydrolase
  • Intellectual disability
  • Membrane
  • Methylation
  • Prenylation
  • Protein transport
  • Proteomics identification
  • Reference proteome
  • Synapse
Proteins
Displaying 1 entry
UniProt Protein Name
Q15907
  • GTP-binding protein YPT3
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 10 in total
GO Term Evidence Code PMID
Golgi apparatus
cytosol
synaptic vesicle
phagocytic vesicle membrane
synaptic vesicle membrane
GO Hierarchy
GO Hierarchy
Disease
The Human Phenotype Ontology
Displaying entries 1 - 10 of 39 in total
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000252 Microcephaly
HP:0000297 Facial hypotonia
HP:0000395 Prominent antihelix
HP:0000486 Strabismus
HP:0000505 Visual impairment
HP:0000540 Hypermetropia
HP:0000582 Upslanted palpebral fissure
HP:0000639 Nystagmus
HP:0000648 Optic atrophy
Displaying 1 entry
Disease ID Disease Name
OMIM:617807
  • neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter

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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: April 6, 2026