HEMGN hemogen

Information
Symbol
HEMGN
Type
protein-coding
Description
hemogen
Entrez Gene ID
55363
Genome
hg19
Position
chr9:100,689,073-100,707,138
Genome
hg38
Position
chr9:97,926,791-97,944,856
MIM
610715 OMIM
HGNC
HGNC:17509 HGNC
Ensembl
ENSG00000136929 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
54
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 CT155
SYNONYM EDAG
SYNONYM EDAG-1
SYNONYM NDR
MIM 610715 OMIM
HGNC HGNC:17509 HGNC
Ensembl ENSG00000136929 Ensembl
AllianceGenome HGNC:17509
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000259456.7 hg38 chr9 97,926,791 97,944,856 18,066
ENST00000616898.2 hg38 chr9 97,926,791 97,938,172 11,382
ENST00000616898.2 hg19 chr9 100,689,073 100,700,454 11,382
ENST00000259456.7 hg19 chr9 100,689,073 100,707,138 18,066
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