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Gene : KIF5A Homo sapiens

Name  ? kinesin family member 5A Cytological Location  12q13.3
Brief Description  kinesin family member 5A
description  This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10. [provided by RefSeq, Jul 2008]
  • synonyms:
  • NKHC,
  • KIF5A,
  • D12S1889,
  • spastic paraplegia 10 (autosomal dominant),
  • SPG10,
  • NM_004984,
  • ALS25,
  • U06698,
  • uc001sor.2,
  • OTTHUMG00000170143,
  • MY050,
  • SPG10,
  • HGNC:6323,
  • NKHC,
  • NEIMY,
  • MY050,
  • D12S1889
  • identifiers:
  • 3798,
  • ENSG00000155980,
  • KIF5A

Genome feature

Region: gene ? Length: 36595  
Location: 12:57550039-57586633 Cyto location: 12q13.3

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Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


3 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



359 SN Ps

5 Cross References

19 Data Sets

50 Homologues

0 Located Features

97 Rna Seq Results