NEUROD2 neuronal differentiation 2

Information
Symbol
NEUROD2
Type
protein-coding
Description
neuronal differentiation 2
Entrez Gene ID
4761
Genome
hg19
Position
chr17:37,760,021-37,764,173
Genome
hg38
Position
chr17:39,603,768-39,607,920
MIM
601725 OMIM
HGNC
HGNC:7763 HGNC
Ensembl
ENSG00000171532 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 2
Benign 0 8
Likely benign 0 12
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 76
Ranking
ClinVar
0
0
6
94
4
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM DEE72
SYNONYM EIEE72
SYNONYM NDRF
SYNONYM bHLHa1
MIM 601725 OMIM
HGNC HGNC:7763 HGNC
Ensembl ENSG00000171532 Ensembl
AllianceGenome HGNC:7763
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000302584.5 hg38 chr17 39,603,768 39,607,920 4,153
ENST00000302584.5 hg19 chr17 37,760,021 37,764,173 4,153
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