MIER3 MIER family member 3

Information
Symbol
MIER3
Type
protein-coding
Description
MIER family member 3
Entrez Gene ID
166968
Genome
hg19
Position
chr5:56,215,429-56,247,945
Genome
hg38
Position
chr5:56,919,602-56,952,118
MIM
620100 OMIM
HGNC
HGNC:26678 HGNC
Ensembl
ENSG00000155545 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
28
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
MIM 620100 OMIM
HGNC HGNC:26678 HGNC
Ensembl ENSG00000155545 Ensembl
AllianceGenome HGNC:26678
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000381199.8 hg38 chr5 56,919,603 56,952,123 32,521
ENST00000409421.5 hg38 chr5 56,922,584 56,941,133 18,550
ENST00000381226.7 hg38 chr5 56,919,602 56,952,118 32,517
ENST00000381213.7 hg38 chr5 56,919,603 56,952,125 32,523
ENST00000381226.7 hg19 chr5 56,215,429 56,247,945 32,517
ENST00000381199.8 hg19 chr5 56,215,430 56,247,950 32,521
ENST00000381213.7 hg19 chr5 56,215,430 56,247,952 32,523
ENST00000409421.5 hg19 chr5 56,218,411 56,236,960 18,550
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