Early Detection Research Network

KIF1A

Aliases:
This biomarker is also known as:
  • UNC104,
  • Kinesin-Like Protein KIF1A,
  • HUnc-104,
  • KIF1A,
  • C2orf20,
  • Microtubule-Based Motor KIF1A,
  • Tmp_locus_27,
  • MRD9,
  • SPG30,
  • HSN2C,
  • ATSV,
  • Axonal Transport Of Synaptic Vesicles,
  • Chromosome 2 Open Reading Frame 20,
  • Unc-104- And KIF1A-Related Protein,
  • Kinesin Family Member 1A,
  • Axonal Transporter Of Synaptic Vesicles,
  • Spastic Paraplegia 30 (Autosomal Recessive),
  • Kinesin, Heavy Chain, Member 1A, Homolog Of Mouse,

Description…

From NCBI Entrez Gene: The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Apr 2012]

Datasets

There are no datasets associated with this biomarker.

Attributes
QA State: Curated
Type: Gene
HGNC Name: KIF1A

The following organs have data associated with this biomarker…

Attributes

Phase: One
QA State: Curated

Overview

No additional data available.

Performance Comment

KIF1A is one of eight genes on a panel of differentially methylated genes from normal and OSCC clinical samples from patients with heterogenous risk profiles chosen for further validation.  The eight genes are: HOXA9, NID2, GATA4, KIF1A, EDNRB, MCAM, DCC, and CALCA.

This biomarker is currently being annotated or is under review. You must be logged in or do not have permission to view any additional information. Contact Heather Kincaid at heather.kincaid@jpl.nasa.gov if you should have access to this biomarker.

No associated publications found.