Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10763
Gene name Gene Name - the full gene name approved by the HGNC.
Nestin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NES
Synonyms (NCBI Gene) Gene synonyms aliases
Nbla00170
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q23.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the intermediate filament protein family and is expressed primarily in nerve cells. [provided by RefSeq, Sep 2011]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020595 hsa-miR-155-5p Proteomics 18668040
MIRT035540 hsa-miR-125b-5p Luciferase reporter assay 23016664
MIRT035540 hsa-miR-125b-5p Luciferase reporter assay 23016664
MIRT035540 hsa-miR-125b-5p Luciferase reporter assay 23016664
MIRT438696 hsa-miR-432-5p Flow, Immunocytochemistry, Luciferase reporter assay, qRT-PCR, Western blot 24657437
Transcription factors
Transcription factor Regulation Reference
MYCN Activation 15117961
SOX10 Unknown 19845757
SOX9 Unknown 19845757
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000086 Process G2/M transition of mitotic cell cycle IDA 19384922
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 26496610, 28514442, 30021884
GO:0005737 Component Cytoplasm IDA 19384922
GO:0005882 Component Intermediate filament IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600915 7756 ENSG00000132688
Protein
UniProt ID P48681
Protein name Nestin
Protein function Required for brain and eye development. Promotes the disassembly of phosphorylated vimentin intermediate filaments (IF) during mitosis and may play a role in the trafficking and distribution of IF proteins and other cellular factors to daughter
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00038 Filament 7 160 Intermediate filament protein Coiled-coil
PF00038 Filament 178 312 Intermediate filament protein Coiled-coil
Tissue specificity TISSUE SPECIFICITY: CNS stem cells.
Sequence
MEGCMGEESFQMWELNRRLEAYLARVKALEEQNELLSAELGGLRAQSADTSWRAHADDEL
AALRALVDQRWREKHAAEVARDNLAEELEGVAGRCQQLRLARERTTEEVARNRRAVEAEK
CARAWLSSQVAELERELEALRVAHEEERVGLNAQAACAPR
CPAPPRGPPAPAPEVEELAR
RLGEAWRGAVRGYQERVAHMETSLGQARERLGRAVQGAREGRLELQQLQAERGGLLERRA
ALEQRLEGRWQERLRATEKFQLAVEALEQEKQGLQSQIAQVLEGRQQLAHLKMSLSLEVA
TYRTLLEAENSR
LQTPGGGSKTSLSFQDPKLELQFPRTPEGRRLGSLLPVLSPTSLPSPL
PATLETPVPAFLKNQEFLQARTPTLASTPIPPTPQAPSPAVDAEIRAQDAPLSLLQTQGG
RKQAPEPLRAEARVAIPASVLPGPEEPGGQRQEASTGQSPEDHASLAPPLSPDHSSLEAK
DGESGGSRVFSICRGEGEGQIWGLVEKETAIEGKVVSSLQQEIWEEEDLNRKEIQDSQVP
LEKETLKSLGEEIQESLKTLENQSHETLERENQECPRSLEEDLETLKSLEKENKELLKDV
EVVRPLEKEAVGQLKPTGKEDTQTLQSLQKENQELMKSLEGNLETFLFPGTENQELVSSL
QENLESLTALEKENQEPLRSPEVGDEEALRPLTKENQEPLRSLEDENKEAFRSLEKENQE
PLKTLEEEDQSIVRPLETENHKSLRSLEEQDQETLRTLEKETQQRRRSLGEQDQMTLRPP
EKVDLEPLKSLDQEIARPLENENQEFLKSLKEESVEAVKSLETEILESLKSAGQENLETL
KSPETQAPLWTPEEINQGAMNPLEKEIQEPLESVEVNQETFRLLEEENQESLRSLGAWNL
ENLRSPEEVDKESQRNLEEEENLGKGEYQESLRSLEEEGQELPQSADVQRWEDTVEKDQE
LAQESPPGMAGVENEDEAELNLREQDGFTGKEEVVEQGELNATEEVWIPGEGHPESPEPK
EQRGLVEGASVKGGAEGLQDPEGQSQQVGAPGLQAPQGLPEAIEPLVEDDVAPGGDQASP
EVMLGSEPAMGESAAGAEPGPGQGVGGLGDPGHLTREEVMEPPLEEESLEAKRVQGLEGP
RKDLEEAGGLGTEFSELPGKSRDPWEPPREGREESEAEAPRGAEEAFPAETLGHTGSDAP
SPWPLGSEEAEEDVPPVLVSPSPTYTPILEDAPGPQPQAEGSQEASWGVQGRAEALGKVE
SEQEELGSGEIPEGPQEEGEESREESEEDELGETLPDSTPLGFYLRSPTSPRWDPTGEQR
PPPQGETGKEGWDPAVLASEGLEAPPSEKEEGEEGEEECGRDSDLSEEFEDLGTEAPFLP
GVPGEVAEPLGQVPQLLLDPAAWDRDGESDGFADEEESGEEGEEDQEEGREPGAGRWGPG
SSVGSLQALSSSQRGEFLESDSVSVSVPWDDSLRGAVAGAPKTALETESQDSAEPSGSEE
ESDPVSLEREDKVPGPLEIPSGMEDAGPGADIIGVNGQGPNLEGKSQHVNGGVMNGLEQS
EEVGQGMPLVSEGDRGSPFQEEEGSALKTSWAGAPVHLGQGQFLKFTQREGDRESWSSGE
D
Sequence length 1621
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Epilepsy Epilepsy, Tonic-Clonic, Familial, Epilepsy, Tonic-Clonic, Symptomatic rs113994140, rs28937874, rs1589762127, rs104894166, rs28939075, rs2134001459, rs104894167, rs119488099, rs119488100, rs387906420, rs121917752, rs121918622, rs281865564, rs387907313, rs397514670
View all (165 more)
16137769
Associations from Text Mining
Disease Name Relationship Type References
Ameloblastoma Associate 33395399
Coronary Disease Associate 18724036
Glioblastoma Associate 34948016, 36333778
Lung Neoplasms Associate 37784249
Lymphoma Extranodal NK T Cell Associate 34872521
Melanoma Associate 20882037, 39273022
Multiple Myeloma Associate 24329895
Neoplasm Metastasis Associate 37379245, 39273022
Neoplasms Associate 27312238, 33251771, 39273022
Oncogene Addiction Associate 17167184