MIEN1 migration and invasion enhancer 1

Information
Symbol
MIEN1
Type
protein-coding
Description
migration and invasion enhancer 1
Entrez Gene ID
84299
Genome
hg19
Position
chr17:37,885,411-37,886,763
Genome
hg38
Position
chr17:39,729,158-39,730,510
MIM
611802 OMIM
HGNC
HGNC:28230 HGNC
Ensembl
ENSG00000141741 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 2 0
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
18
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
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 C17orf37
SYNONYM C35
SYNONYM ORB3
SYNONYM RDX12
SYNONYM XTP4
MIM 611802 OMIM
HGNC HGNC:28230 HGNC
Ensembl ENSG00000141741 Ensembl
AllianceGenome HGNC:28230
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000394231.8 hg38 chr17 39,728,510 39,730,532 2,023
ENST00000577810.1 hg38 chr17 39,729,158 39,730,510 1,353
ENST00000394231.8 hg19 chr17 37,884,763 37,886,785 2,023
ENST00000577810.1 hg19 chr17 37,885,411 37,886,763 1,353
Genome browser