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
OrthoDB (Group)
Group level
Eukaryota
Group Name
RAB
Functional Category
  • T: Signal transduction mechanisms
  • U: Intracellular trafficking, secretion, and vesicular transport
Displaying 1 entry
Gene Ontology
GTP binding
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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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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