HDDC2 HD domain containing 2

Information
Symbol
HDDC2
Type
protein-coding
Description
HD domain containing 2
Entrez Gene ID
51020
Genome
hg19
Position
chr6:125,596,496-125,623,113
Genome
hg38
Position
chr6:125,275,350-125,301,967
HGNC
HGNC:21078 HGNC
Ensembl
ENSG00000111906 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
36
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 C6orf74
SYNONYM CGI-130
SYNONYM NS5ATP2
SYNONYM dJ167O5.2
HGNC HGNC:21078 HGNC
Ensembl ENSG00000111906 Ensembl
AllianceGenome HGNC:21078
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000608284.1 hg38 chr6 125,297,487 125,302,078 4,592
ENST00000608295.5 hg38 chr6 125,275,882 125,301,937 26,056
ENST00000398153.7 hg38 chr6 125,275,350 125,301,967 26,618
ENST00000398153.7 hg19 chr6 125,596,496 125,623,113 26,618
ENST00000608295.5 hg19 chr6 125,597,028 125,623,083 26,056
ENST00000608284.1 hg19 chr6 125,618,633 125,623,224 4,592
Genome browser