MESP2 mesoderm posterior bHLH transcription factor 2

Information
Symbol
MESP2
Type
protein-coding
Description
mesoderm posterior bHLH transcription factor 2
Entrez Gene ID
145873
Genome
hg19
Position
chr15:90,319,563-90,321,985
Genome
hg38
Position
chr15:89,776,332-89,778,754
MIM
605195 OMIM
HGNC
HGNC:29659 HGNC
Ensembl
ENSG00000188095 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 84
Likely pathogenic 0 26
Benign 0 34
Likely benign 0 536
Conflicting classifications of pathogenicity 0 28
not provided 0 4
Uncertain significance 0 240
Ranking
ClinVar
0
0
80
798
22
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 SCDO2
SYNONYM bHLHc6
MIM 605195 OMIM
HGNC HGNC:29659 HGNC
Ensembl ENSG00000188095 Ensembl
AllianceGenome HGNC:29659
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000560219.2 hg38 chr15 89,760,591 89,778,754 18,164
ENST00000341735.5 hg38 chr15 89,776,332 89,778,754 2,423
ENST00000560219.2 hg19 chr15 90,303,822 90,321,985 18,164
ENST00000341735.5 hg19 chr15 90,319,563 90,321,985 2,423
Genome browser