kinesin family member 1B

Summary
Gene Symbol
  • KIF1B
Organism
Homo sapiens (human)
NCBI Gene
23095
PubChem
23095
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Acetylation
  • Alternative splicing
  • Apoptosis
  • Charcot-Marie-Tooth disease
  • Coiled coil
  • Cytoplasmic vesicle
  • Cytoskeleton
  • Disease variant
  • Isomerase
  • Membrane
  • Microtubule
  • Mitochondrion
  • Motor protein
  • Neurodegeneration
  • Phosphoprotein
  • Reference proteome
  • Synapse
Proteins
Displaying 1 entry
UniProt Protein Name
O60333
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 12 in total
GO Term Evidence Code PMID
cytoplasm
mitochondrion
mitochondrion
kinesin complex
microtubule
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
kinesin
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 5 entries
DO ID Disease Name Source
DOID:0110154 Charcot-Marie-Tooth disease type 2A1
DOID:2152 ovary epithelial cancer
DOID:2377 multiple sclerosis
DOID:684 hepatocellular carcinoma
DOID:769 neuroblastoma
Ortholog
Displaying entries 71 - 74 of 74 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
117027219 RHIFE03197
118889697 BALMU22113
122228623 PANLE10048
123779086 URSAM06401

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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 7, 2025