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KIF2A

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Protein-coding gene in the species Homo sapiens

KIF2A
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2GRY

Identifiers
AliasesKIF2A, CDCBM3, HK2, KIF2, kinesin heavy chain member 2A, kinesin family member 2A
External IDsOMIM: 602591; MGI: 108390; HomoloGene: 3320; GeneCards: KIF2A; OMA:KIF2A - orthologs
Gene location (Human)
Chromosome 5 (human)
Chr.Chromosome 5 (human)
Chromosome 5 (human)Genomic location for KIF2AGenomic location for KIF2A
Band5q12.1Start62,306,162 bp
End62,391,025 bp
Gene location (Mouse)
Chromosome 13 (mouse)
Chr.Chromosome 13 (mouse)
Chromosome 13 (mouse)Genomic location for KIF2AGenomic location for KIF2A
Band13|13 D2.1Start107,095,504 bp
End107,158,634 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • corpus callosum

  • ganglionic eminence

  • monocyte

  • sperm

  • ventricular zone

  • external globus pallidus

  • sural nerve

  • subthalamic nucleus

  • pars compacta

  • superior vestibular nucleus
Top expressed in
  • barrel cortex

  • blood

  • genital tubercle

  • habenula

  • tail of embryo

  • zygote

  • secondary oocyte

  • olfactory bulb

  • facial motor nucleus

  • spermatid
More reference expression data
BioGPS




More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

3796

16563

Ensembl

ENSG00000068796

ENSMUSG00000021693

UniProt

O00139

P28740

RefSeq (mRNA)

NM_004520
NM_001098511
NM_001243952
NM_001243953

NM_001145779
NM_008442
NM_001374727
NM_001378936
NM_001378937

NM_001378938
NM_001378939
NM_001378940

RefSeq (protein)

NP_001091981
NP_001230881
NP_001230882
NP_004511

NP_001139251
NP_032468
NP_001361656
NP_001365865
NP_001365866

NP_001365867
NP_001365868
NP_001365869

Location (UCSC)Chr 5: 62.31 – 62.39 MbChr 13: 107.1 – 107.16 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Kinesin-like protein KIF2A is a protein that in humans is encoded by the KIF2A gene. In mice, KIF2A is essential for proper neurogenesis and deficiency of KIF2A in mature neurons results in the loss of those neurons.

Kinesins, such as KIF2, are microtubule-associated motor proteins. For background information on kinesins, see MIM 148760.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000068796Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000021693Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Debernardi S, Fontanella E, De Gregorio L, Pierotti MA, Delia D (May 1997). "Identification of a novel human kinesin-related gene (HK2) by the cDNA differential display technique". Genomics. 42 (1): 67–73. doi:10.1006/geno.1997.4720. PMID 9177777.
  6. ^ "Entrez Gene: KIF2A kinesin heavy chain member 2A".
  7. Ruiz-Reig N, Chehade G, Hakanen J, Aittaleb M, Wierda K, De Wit J, et al. (November 2022). "KIF2A deficiency causes early-onset neurodegeneration". Proceedings of the National Academy of Sciences of the United States of America. 119 (46): e2209714119. Bibcode:2022PNAS..11909714R. doi:10.1073/pnas.2209714119. PMC 9674219. PMID 36343267.

Further reading

External links

  • Overview of all the structural information available in the PDB for UniProt: O00139 (Human Kinesin-like protein KIF2A) at the PDBe-KB.
PDB gallery
  • 2gry: Crystal structure of the human KIF2 motor domain in complex with ADP 2gry: Crystal structure of the human KIF2 motor domain in complex with ADP


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Proteins of the cytoskeleton
Human
Microfilaments
and ABPs
Myofilament
Actins
Myosins
Other
Other
Intermediate
filaments
Type 1/2
(Keratin,
Cytokeratin)
Epithelial keratins
(soft alpha-keratins)
Hair keratins
(hard alpha-keratins)
Ungrouped alpha
Not alpha
Type 3
Type 4
Type 5
Microtubules
and MAPs
Tubulins
MAPs
Kinesins
Dyneins
Microtubule organising proteins
Microtubule severing proteins
Other
Catenins
Membrane
Other
Nonhuman
See also: cytoskeletal defects
Categories:
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