Human Gene NEUROD1 (ENST00000295108.4_6) from GENCODE V47lift37
  Description: neuronal differentiation 1, transcript variant 1 (from RefSeq NM_002500.5)
Gencode Transcript: ENST00000295108.4_6
Gencode Gene: ENSG00000162992.5_10
Transcript (Including UTRs)
   Position: hg19 chr2:182,541,194-182,545,244 Size: 4,051 Total Exon Count: 2 Strand: -
Coding Region
   Position: hg19 chr2:182,542,517-182,543,587 Size: 1,071 Coding Exon Count: 1 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsPathwaysOther NamesGeneReviewsModel Information
Methods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr2:182,541,194-182,545,244)mRNA (may differ from genome)Protein (356 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
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MalacardsMGIOMIMPubMedReactomeUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: NDF1_HUMAN
DESCRIPTION: RecName: Full=Neurogenic differentiation factor 1; Short=NeuroD; Short=NeuroD1; AltName: Full=Class A basic helix-loop-helix protein 3; Short=bHLHa3;
FUNCTION: Acts as a transcriptional activator: mediates transcriptional activation by binding to E box-containing promoter consensus core sequences 5'-CANNTG-3'. Associates with the p300/CBP transcription coactivator complex to stimulate transcription of the secretin gene as well as the gene encoding the cyclin-dependent kinase inhibitor CDKN1A. Contributes to the regulation of several cell differentiation pathways, like those that promote the formation of early retinal ganglion cells, inner ear sensory neurons, granule cells forming either the cerebellum or the dentate gyrus cell layer of the hippocampus, endocrine islet cells of the pancreas and enteroendocrine cells of the small intestine. Together with PAX6 or SIX3, is required for the regulation of amacrine cell fate specification. Also required for dendrite morphogenesis and maintenance in the cerebellar cortex. Associates with chromatin to enhancer regulatory elements in genes encoding key transcriptional regulators of neurogenesis (By similarity).
SUBUNIT: Interacts (via helix-loop-helix motif domain) with EP300 (via C-terminus) (By similarity). Heterodimer with TCF3/E47; the heterodimer is inhibited in presence of ID2, but not NR0B2, to E- box element. Efficient DNA-binding requires dimerization with another bHLH protein. Interacts with RREB1. Interacts with EP300; the interaction is inhibited by NR0B2. Interacts with TCF3; the interaction is inhibited by ID2.
SUBCELLULAR LOCATION: Cytoplasm (By similarity). Nucleus. Note=In pancreatic islet cells, shuttles to the nucleus in response to glucose stimulation (By similarity). Colocalizes with NR0B2 in the nucleus.
PTM: Phosphorylated. In islet cells, phosphorylated on Ser-274 upon glucose stimulation; which may be required for nuclear localization. In activated neurons, phosphorylated on Ser-335; which promotes dendritic growth. Phosphorylated by MAPK1; phosphorylation regulates heterodimerization and DNA-binding activities. Phosphorylation on Ser-266 and Ser-274 increases transactivation on the insulin promoter in glucose-stimulated insulinoma cells (By similarity).
DISEASE: Defects in NEUROD1 are the cause of maturity-onset diabetes of the young type 6 (MODY6) [MIM:606394]. MODY is a form of diabetes that is characterized by an autosomal dominant mode of inheritance, onset in childhood or early adulthood (usually before 25 years of age), a primary defect in insulin secretion and frequent insulin-independence at the beginning of the disease.
SIMILARITY: Contains 1 bHLH (basic helix-loop-helix) domain.
WEB RESOURCE: Name=GeneReviews; URL="http://www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/NEUROD1";

-  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: NEUROD1
Diseases sorted by gene-association score: diabetes mellitus, noninsulin-dependent* (1360), maturity-onset diabetes of the young 6* (1330), maturity-onset diabetes of the young* (167), diabetes mellitus, insulin-dependent, 7 (12), insulinoma (8), diarrhea 4, malabsorptive, congenital (7), large cell neuroendocrine carcinoma (7), pulmonary neuroendocrine tumor (6), neonatal diabetes mellitus (6), acth deficiency (5), branchiootic syndrome (5), retinitis pigmentosa 26 (4), diabetes mellitus, insulin-dependent (2), retinitis pigmentosa (1)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  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: 128.33 RPKM in Brain - Cerebellar Hemisphere
Total median expression: 237.93 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 -22.6099-0.228 Picture PostScript Text
3' UTR -238.201323-0.180 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
  InterPro Domains: Graphical view of domain structure
IPR011598 - HLH_dom
IPR022575 - Neurogenic_DUF
IPR016637 - TF_bHLH_NeuroD

Pfam Domains:
PF00010 - Helix-loop-helix DNA-binding domain
PF12533 - Neuronal helix-loop-helix transcription factor

SCOP Domains:
48371 - ARM repeat
47459 - HLH, helix-loop-helix DNA-binding domain
52058 - L domain-like

ModBase Predicted Comparative 3D Structure on Q13562
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 orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
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-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000978 RNA polymerase II core promoter proximal region sequence-specific DNA binding
GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding
GO:0001077 transcriptional activator activity, RNA polymerase II core promoter proximal region sequence-specific binding
GO:0001102 RNA polymerase II activating transcription factor binding
GO:0001105 RNA polymerase II transcription coactivator activity
GO:0003677 DNA binding
GO:0003682 chromatin binding
GO:0003690 double-stranded DNA binding
GO:0003700 transcription factor activity, sequence-specific DNA binding
GO:0003713 transcription coactivator activity
GO:0005515 protein binding
GO:0008134 transcription factor binding
GO:0043565 sequence-specific DNA binding
GO:0046982 protein heterodimerization activity
GO:0046983 protein dimerization activity
GO:0070888 E-box binding

Biological Process:
GO:0003326 pancreatic A cell fate commitment
GO:0003329 pancreatic PP cell fate commitment
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006366 transcription from RNA polymerase II promoter
GO:0006913 nucleocytoplasmic transport
GO:0007263 nitric oxide mediated signal transduction
GO:0007275 multicellular organism development
GO:0007399 nervous system development
GO:0009749 response to glucose
GO:0009952 anterior/posterior pattern specification
GO:0021542 dentate gyrus development
GO:0021549 cerebellum development
GO:0022008 neurogenesis
GO:0023019 signal transduction involved in regulation of gene expression
GO:0030073 insulin secretion
GO:0030154 cell differentiation
GO:0030902 hindbrain development
GO:0031018 endocrine pancreas development
GO:0035881 amacrine cell differentiation
GO:0035883 enteroendocrine cell differentiation
GO:0042493 response to drug
GO:0042593 glucose homeostasis
GO:0043010 camera-type eye development
GO:0043065 positive regulation of apoptotic process
GO:0045165 cell fate commitment
GO:0045597 positive regulation of cell differentiation
GO:0045664 regulation of neuron differentiation
GO:0045666 positive regulation of neuron differentiation
GO:0045893 positive regulation of transcription, DNA-templated
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0046426 negative regulation of JAK-STAT cascade
GO:0048562 embryonic organ morphogenesis
GO:0048666 neuron development
GO:0048839 inner ear development
GO:0050796 regulation of insulin secretion
GO:0051091 positive regulation of sequence-specific DNA binding transcription factor activity
GO:0060730 regulation of intestinal epithelial structure maintenance
GO:0071156 regulation of cell cycle arrest
GO:0071333 cellular response to glucose stimulus
GO:2000675 negative regulation of type B pancreatic cell apoptotic process
GO:2000679 positive regulation of transcription regulatory region DNA binding

Cellular Component:
GO:0005622 intracellular
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0090575 RNA polymerase II transcription factor complex


-  Descriptions from all associated GenBank mRNAs
  HQ426678 - Homo sapiens clone 22 ceramide kinase-like isoform 8 mRNA, complete cds.
JF290420 - Homo sapiens ceramide kinase-like protein isoform 8 mRNA, complete cds.
AJ697857 - Homo sapiens partial mRNA for ceramide kinase-like protein (CERKL gene), variant 3.
AB593070 - Homo sapiens NEUROD1 mRNA for neurogenic differentiation factor 1, complete cds, clone: HP05315-RBd13F05.
AB593068 - Homo sapiens NEUROD1 mRNA for neurogenic differentiation factor 1, complete cds, clone: HP05315-RBb12B09.
AB593071 - Homo sapiens NEUROD1 mRNA for neurogenic differentiation factor 1, complete cds, clone: HP05315-RBd77G05.
AB593069 - Homo sapiens NEUROD1 mRNA for neurogenic differentiation factor 1, complete cds, clone: HP05315-RBb30G01.
D82347 - Homo sapiens mRNA for NeuroD, complete cds.
JD097069 - Sequence 78093 from Patent EP1572962.
BC009046 - Homo sapiens neurogenic differentiation 1, mRNA (cDNA clone MGC:9038 IMAGE:3873419), complete cds.
JD234317 - Sequence 215341 from Patent EP1572962.
JD284458 - Sequence 265482 from Patent EP1572962.
JD499130 - Sequence 480154 from Patent EP1572962.
JB759088 - Sequence 13 from Patent WO2013102203.
JD287393 - Sequence 268417 from Patent EP1572962.
JD244098 - Sequence 225122 from Patent EP1572962.
JD268741 - Sequence 249765 from Patent EP1572962.
JD233742 - Sequence 214766 from Patent EP1572962.
BT019731 - Homo sapiens neurogenic differentiation 1 mRNA, complete cds.
DQ891560 - Synthetic construct clone IMAGE:100004190; FLH178062.01X; RZPDo839G12126D neurogenic differentiation 1 (NEUROD1) gene, encodes complete protein.
AK313799 - Homo sapiens cDNA, FLJ94416, highly similar to Homo sapiens neurogenic differentiation 1 (NEUROD1), mRNA.
KJ891691 - Synthetic construct Homo sapiens clone ccsbBroadEn_01085 NEUROD1 gene, encodes complete protein.
KR709663 - Synthetic construct Homo sapiens clone CCSBHm_00004997 NEUROD1 (NEUROD1) mRNA, encodes complete protein.
KR709664 - Synthetic construct Homo sapiens clone CCSBHm_00004998 NEUROD1 (NEUROD1) mRNA, encodes complete protein.
KR709665 - Synthetic construct Homo sapiens clone CCSBHm_00005000 NEUROD1 (NEUROD1) mRNA, encodes complete protein.
KR709666 - Synthetic construct Homo sapiens clone CCSBHm_00005002 NEUROD1 (NEUROD1) mRNA, encodes complete protein.
DQ894747 - Synthetic construct Homo sapiens clone IMAGE:100009207; FLH178058.01L; RZPDo839G12125D neurogenic differentiation 1 (NEUROD1) gene, encodes complete protein.
KU178230 - Homo sapiens neurogenic differentiation 1 isoform 1 (NEUROD1) mRNA, partial cds.
KU178231 - Homo sapiens neurogenic differentiation 1 isoform 2 (NEUROD1) mRNA, complete cds, alternatively spliced.
AB385071 - Synthetic construct DNA, clone: pF1KB5244, Homo sapiens NEUROD1 gene for neurogenic differentiation factor 1, complete cds, without stop codon, in Flexi system.
CU679237 - Synthetic construct Homo sapiens gateway clone IMAGE:100017085 5' read NEUROD1 mRNA.
GQ904713 - Homo sapiens neurogenic differentiation factor 1 (NEUROD1) mRNA, partial cds.
U80578 - Human basic helix-loop-helix transcription factor (NeuroD) mRNA, partial cds.
U36472 - Human putative neuroD homolog mRNA, partial cds.
U50823 - Human neurod mRNA, partial cds.
JD394719 - Sequence 375743 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein Q13562 (Reactome details) participates in the following event(s):

R-HSA-210746 Regulation of gene expression in endocrine-committed (NEUROG3+) progenitor cells
R-HSA-186712 Regulation of beta-cell development
R-HSA-1266738 Developmental Biology

-  Other Names for This Gene
  Alternate Gene Symbols: B2R9I8, BHLHA3, ENST00000295108.1, ENST00000295108.2, ENST00000295108.3, F1T0E1, NDF1_HUMAN, NEUROD, NM_002500, O00343, Q13340, Q13562, Q5U095, Q96TH0, Q99455, Q9UEC8, uc317ljv.1, uc317ljv.2
UCSC ID: ENST00000295108.4_6
RefSeq Accession: NM_002500.5
Protein: Q13562 (aka NDF1_HUMAN)

-  GeneReviews for This Gene
  GeneReviews article(s) related to gene NEUROD1:
rp-overview (Nonsyndromic Retinitis Pigmentosa Overview)
dmn (Permanent Neonatal Diabetes Mellitus)
mody-ov (Maturity-Onset Diabetes of the Young Overview)

-  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.