Homo sapiens Gene: NDEL1
Summary
InnateDB Gene IDBG-29031.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NDEL1
Gene Name nudE nuclear distribution E homolog (A. nidulans)-like 1
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000166579
Encoded Proteins
nudE nuclear distribution gene E homolog (A. nidulans)-like 1
nudE nuclear distribution gene E homolog (A. nidulans)-like 1
nudE nuclear distribution gene E homolog (A. nidulans)-like 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a coiled-coil protein that plays a role in multiple processes including cytoskeletal organization, cell signaling and neuron migration, outgrowth and maintenance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome X. [provided by RefSeq, Mar 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:8413131-8490411
Strand Forward strand
Band p13.1
Transcripts
ENST00000334527 ENSP00000333982
ENST00000380025 ENSP00000369364
ENST00000402554 ENSP00000384963
ENST00000580237 ENSP00000464154
ENST00000580738
ENST00000580012 ENSP00000463351
ENST00000579150
ENST00000582277 ENSP00000464441
ENST00000582490 ENSP00000462759
ENST00000583066
ENST00000582665 ENSP00000463430
ENST00000579880
ENST00000583683
ENST00000582812 ENSP00000462052
ENST00000581189
ENST00000584866 ENSP00000462458
ENST00000578172
ENST00000581679 ENSP00000464634
ENST00000585098 ENSP00000463492
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 61 experimentally validated interaction(s) in this database.
They are also associated with 7 interaction(s) predicted by orthology.
Experimentally validated
Total 61 [view]
Protein-Protein 61 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 7 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0008017 microtubule binding
GO:0032403 protein complex binding
GO:0043014 alpha-tubulin binding
GO:0048487 beta-tubulin binding
GO:0070012 oligopeptidase activity
Biological Process
GO:0000226 microtubule cytoskeleton organization
GO:0000278 mitotic cell cycle
GO:0001764 neuron migration
GO:0001833 inner cell mass cell proliferation
GO:0006508 proteolysis
GO:0007059 chromosome segregation
GO:0007100 mitotic centrosome separation
GO:0008090 retrograde axon cargo transport
GO:0010975 regulation of neuron projection development
GO:0016477 cell migration
GO:0021799 cerebral cortex radially oriented cell migration
GO:0021955 central nervous system neuron axonogenesis
GO:0031175 neuron projection development
GO:0032864 activation of Cdc42 GTPase activity
GO:0045773 positive regulation of axon extension
GO:0047496 vesicle transport along microtubule
GO:0048680 positive regulation of axon regeneration
GO:0051081 nuclear envelope disassembly
GO:0051642 centrosome localization
GO:0060052 neurofilament cytoskeleton organization
GO:1990138 neuron projection extension
Cellular Component
GO:0000776 kinetochore
GO:0000777 condensed chromosome kinetochore
GO:0005635 nuclear envelope
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005815 microtubule organizing center
GO:0005819 spindle
GO:0005829 cytosol
GO:0005871 kinesin complex
GO:0005874 microtubule
GO:0005875 microtubule associated complex
GO:0030424 axon
GO:0031252 cell leading edge
GO:0043203 axon hillock
GO:0044297 cell body
GO:0060053 neurofilament cytoskeleton
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Resolution of Sister Chromatid Cohesion pathway
Mitotic Prometaphase pathway
Separation of Sister Chromatids pathway
Cell Cycle pathway
M Phase pathway
Mitotic Anaphase pathway
Cell Cycle, Mitotic pathway
Mitotic Metaphase and Anaphase pathway
KEGG
INOH
PID NCI
Aurora A signaling
Lissencephaly gene (LIS1) in neuronal migration and development
Cross-References
SwissProt
TrEMBL J3KSF2 J3QL31
UniProt Splice Variant
Entrez Gene 81565
UniGene Hs.372123 Hs.666826 Hs.706901 Hs.739249 Hs.740680
RefSeq NM_001025579 NM_030808 XM_005256806 XM_006721581
HUGO HGNC:17620
OMIM 607538
CCDS CCDS11143 CCDS32564
HPRD 06340
IMGT
EMBL AC026130
GenPept
RNA Seq Atlas 81565