EPGN epithelial mitogen

Information
Symbol
EPGN
Type
protein-coding
Description
epithelial mitogen
Entrez Gene ID
255324
Genome
hg19
Position
chr4:75,174,187-75,182,506
Genome
hg38
Position
chr4:74,308,470-74,316,789
MIM
618717 OMIM
HGNC
HGNC:17470 HGNC
Ensembl
ENSG00000182585 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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 ALGV3072
SYNONYM EPG
SYNONYM PRO9904
MIM 618717 OMIM
HGNC HGNC:17470 HGNC
Ensembl ENSG00000182585 Ensembl
AllianceGenome HGNC:17470
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000503098.5 hg38 chr4 74,308,534 74,314,637 6,104
ENST00000502358.5 hg38 chr4 74,308,534 74,314,637 6,104
ENST00000509145.5 hg38 chr4 74,308,534 74,314,637 6,104
ENST00000514968.5 hg38 chr4 74,308,534 74,314,637 6,104
ENST00000332112.8 hg38 chr4 74,308,487 74,313,590 5,104
ENST00000413830.6 hg38 chr4 74,308,470 74,316,789 8,320
ENST00000505212.5 hg38 chr4 74,308,534 74,314,637 6,104
ENST00000413830.6 hg19 chr4 75,174,187 75,182,506 8,320
ENST00000332112.8 hg19 chr4 75,174,204 75,179,307 5,104
ENST00000502358.5 hg19 chr4 75,174,251 75,180,354 6,104
ENST00000503098.5 hg19 chr4 75,174,251 75,180,354 6,104
ENST00000505212.5 hg19 chr4 75,174,251 75,180,354 6,104
ENST00000509145.5 hg19 chr4 75,174,251 75,180,354 6,104
ENST00000514968.5 hg19 chr4 75,174,251 75,180,354 6,104
Genome browser