Human Gene KIF5C (ENST00000435030.1) from GENCODE V47lift37
  Description: kinesin family member 5C (from HGNC KIF5C)
Gencode Transcript: ENST00000435030.1
Gencode Gene: ENSG00000168280.12
Transcript (Including UTRs)
   Position: hg19 chr2:149,632,819-149,883,273 Size: 250,455 Total Exon Count: 26 Strand: +
Coding Region
   Position: hg19 chr2:149,633,187-149,868,190 Size: 235,004 Coding Exon Count: 25 

Page IndexSequence and LinksPrimersMalaCardsCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr2:149,632,819-149,883,273)mRNA (may differ from genome)Protein (957 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblExonPrimerGeneCardsHGNC
MalacardsMGIPubMedUniProtKBWikipedia

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: KIF5C
Diseases sorted by gene-association score: cortical dysplasia, complex, with other brain malformations 2* (1330), complex cortical dysplasia with other brain malformations (19), spastic paraplegia 10, autosomal dominant (7), microcephaly (2)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 129.35 RPKM in Brain - Cerebellar Hemisphere
Total median expression: 1298.41 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -220.20368-0.598 Picture PostScript Text
3' UTR -955.603689-0.259 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  Pfam Domains:
PF00225 - Kinesin motor domain
PF16796 - Microtubule binding

SCOP Domains:
52540 - P-loop containing nucleoside triphosphate hydrolases

ModBase Predicted Comparative 3D Structure on Q9UFW7
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologGenome BrowserNo ortholog
Gene DetailsGene Details Gene DetailsGene Details 
Gene SorterGene Sorter Gene SorterGene Sorter 
 RGDEnsembl WormBase 
    Protein Sequence 
    Alignment 

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0003777 microtubule motor activity

Biological Process:
GO:0007018 microtubule-based movement


-  Descriptions from all associated GenBank mRNAs
  BC002721 - Homo sapiens kinesin family member 5C, mRNA (cDNA clone IMAGE:3627474), partial cds.
BC025961 - Homo sapiens kinesin family member 5C, mRNA (cDNA clone IMAGE:3627269), partial cds.
AB011103 - Homo sapiens KIAA0531 mRNA for KIAA0531 protein.
BC017298 - Homo sapiens kinesin family member 5C, mRNA (cDNA clone IMAGE:5017583), partial cds.
AB384491 - Synthetic construct DNA, clone: pF1KA0531, Homo sapiens KIF5C gene for kinesin family member 5C, complete cds, without stop codon, in Flexi system.
BC127772 - Homo sapiens kinesin family member 5C, mRNA (cDNA clone IMAGE:40128992), partial cds.
BC110287 - Homo sapiens kinesin family member 5C, mRNA (cDNA clone MGC:111478 IMAGE:5165262), complete cds.
KJ904493 - Synthetic construct Homo sapiens clone ccsbBroadEn_13887 KIF5C gene, encodes complete protein.
JD485612 - Sequence 466636 from Patent EP1572962.
JD109013 - Sequence 90037 from Patent EP1572962.
JD109014 - Sequence 90038 from Patent EP1572962.
JD472988 - Sequence 454012 from Patent EP1572962.
JD394991 - Sequence 376015 from Patent EP1572962.
JD256380 - Sequence 237404 from Patent EP1572962.
AB073396 - Homo sapiens primary neuroblastoma cDNA, clone:Nbla04137, full insert sequence.
AB209191 - Homo sapiens mRNA for Kinesin heavy chain isoform 5C variant protein.
AL117393 - Homo sapiens mRNA; cDNA DKFZp566O183 (from clone DKFZp566O183).
AK126689 - Homo sapiens cDNA FLJ44735 fis, clone BRACE3026456.
JD552721 - Sequence 533745 from Patent EP1572962.
JD532754 - Sequence 513778 from Patent EP1572962.
JD044394 - Sequence 25418 from Patent EP1572962.
AL050070 - Homo sapiens mRNA; cDNA DKFZp566B0746 (from clone DKFZp566B0746).
JD471690 - Sequence 452714 from Patent EP1572962.
JD369482 - Sequence 350506 from Patent EP1572962.
JD312974 - Sequence 293998 from Patent EP1572962.
JD256026 - Sequence 237050 from Patent EP1572962.
JD036370 - Sequence 17394 from Patent EP1572962.
JD529000 - Sequence 510024 from Patent EP1572962.
JD203113 - Sequence 184137 from Patent EP1572962.
JD200247 - Sequence 181271 from Patent EP1572962.
JD247252 - Sequence 228276 from Patent EP1572962.
JD290517 - Sequence 271541 from Patent EP1572962.
JD085366 - Sequence 66390 from Patent EP1572962.
JD381333 - Sequence 362357 from Patent EP1572962.
JD299839 - Sequence 280863 from Patent EP1572962.
JD531175 - Sequence 512199 from Patent EP1572962.
JD379311 - Sequence 360335 from Patent EP1572962.
JD048184 - Sequence 29208 from Patent EP1572962.
JD327728 - Sequence 308752 from Patent EP1572962.
JD360850 - Sequence 341874 from Patent EP1572962.
JD245298 - Sequence 226322 from Patent EP1572962.
JD298175 - Sequence 279199 from Patent EP1572962.
JD299685 - Sequence 280709 from Patent EP1572962.
JD098051 - Sequence 79075 from Patent EP1572962.
JD354612 - Sequence 335636 from Patent EP1572962.
JD417415 - Sequence 398439 from Patent EP1572962.
JD059012 - Sequence 40036 from Patent EP1572962.
JD052060 - Sequence 33084 from Patent EP1572962.
JD241268 - Sequence 222292 from Patent EP1572962.
JD468658 - Sequence 449682 from Patent EP1572962.
JD261759 - Sequence 242783 from Patent EP1572962.
JD241151 - Sequence 222175 from Patent EP1572962.
JD333491 - Sequence 314515 from Patent EP1572962.
JD146711 - Sequence 127735 from Patent EP1572962.
JD302131 - Sequence 283155 from Patent EP1572962.
AF010146 - Homo sapiens kinesin heavy chain homolog mRNA, partial cds.

-  Other Names for This Gene
  Alternate Gene Symbols: AB011103, DKFZp566O183 , Q9UFW7, Q9UFW7_HUMAN, uc320dmy.1
UCSC ID: ENST00000435030.1
RefSeq Accession: NM_004522.3
Protein: Q9UFW7

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.