NRGN neurogranin

Information
Symbol
NRGN
Type
protein-coding
Description
neurogranin
Entrez Gene ID
4900
Genome
hg19
Position
chr11:124,609,838-124,617,106
Genome
hg38
Position
chr11:124,739,942-124,747,210
MIM
602350 OMIM
HGNC
HGNC:8000 HGNC
Ensembl
ENSG00000154146 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
0
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 :
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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 RC3
SYNONYM hng
MIM 602350 OMIM
HGNC HGNC:8000 HGNC
Ensembl ENSG00000154146 Ensembl
AllianceGenome HGNC:8000
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000284292.11 hg38 chr11 124,739,942 124,747,210 7,269
ENST00000412681.2 hg38 chr11 124,740,045 124,747,206 7,162
ENST00000284292.11 hg19 chr11 124,609,838 124,617,106 7,269
ENST00000412681.2 hg19 chr11 124,609,941 124,617,102 7,162
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