Homo sapiens Gene: KIF21A | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-26836.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | KIF21A | ||||||||||||||||||
Gene Name | kinesin family member 21A | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000139116 | ||||||||||||||||||
Encoded Proteins |
kinesin family member 21A
kinesin family member 21A
kinesin family member 21A
kinesin family member 21A
kinesin family member 21A
kinesin family member 21A
kinesin family member 21A
kinesin family member 21A
kinesin family member 21A
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Protein Structure | |||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 12:39293228-39443390 | ||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||
Band | q12 | ||||||||||||||||||
Transcripts | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||||||||||||||
SwissProt | |||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | |||||||||||||||||||
UniGene | Hs.374201 | ||||||||||||||||||
RefSeq | NM_001173463 NM_001173464 NM_001173465 NM_017641 XM_005269007 XM_005269008 XM_005269009 XM_005269010 XM_005269012 XM_005269013 XM_006719493 XM_006719494 XM_006719495 XM_006719496 | ||||||||||||||||||
HUGO | |||||||||||||||||||
OMIM | |||||||||||||||||||
CCDS | CCDS31773 CCDS53774 CCDS53775 CCDS53776 | ||||||||||||||||||
HPRD | 10506 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | |||||||||||||||||||
GenPept | |||||||||||||||||||
RNA Seq Atlas | |||||||||||||||||||