HMGN3 high mobility group nucleosomal binding domain 3

Information
Symbol
HMGN3
Type
protein-coding
Description
high mobility group nucleosomal binding domain 3
Entrez Gene ID
9324
Genome
hg19
Position
chr6:79,910,962-79,944,399
Genome
hg38
Position
chr6:79,201,245-79,234,682
MIM
604502 OMIM
HGNC
HGNC:12312 HGNC
Ensembl
ENSG00000118418 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
14
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 :
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 PNAS-24
SYNONYM PNAS-25
SYNONYM TRIP7
MIM 604502 OMIM
HGNC HGNC:12312 HGNC
Ensembl ENSG00000118418 Ensembl
AllianceGenome HGNC:12312
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000706660.1 hg38 chr6 79,201,479 79,234,675 33,197
ENST00000703810.2 hg38 chr6 79,201,245 79,234,614 33,370
ENST00000275036.11 hg38 chr6 79,201,245 79,234,689 33,445
ENST00000706657.1 hg38 chr6 79,201,245 79,234,682 33,438
ENST00000706659.1 hg38 chr6 79,201,253 79,234,656 33,404
ENST00000620514.2 hg38 chr6 79,201,245 79,234,682 33,438
ENST00000344726.10 hg38 chr6 79,201,245 79,234,682 33,438
ENST00000703810.2 hg19 chr6 79,910,962 79,944,331 33,370
ENST00000344726.10 hg19 chr6 79,910,962 79,944,399 33,438
ENST00000620514.2 hg19 chr6 79,910,962 79,944,399 33,438
ENST00000706657.1 hg19 chr6 79,910,962 79,944,399 33,438
ENST00000275036.11 hg19 chr6 79,910,962 79,944,406 33,445
ENST00000706659.1 hg19 chr6 79,910,970 79,944,373 33,404
ENST00000706660.1 hg19 chr6 79,911,196 79,944,392 33,197
Genome browser