MSTN myostatin

Information
Symbol
MSTN
Type
protein-coding
Description
myostatin
Entrez Gene ID
2660
Genome
hg19
Position
chr2:190,920,426-190,927,455
Genome
hg38
Position
chr2:190,055,700-190,062,729
MIM
601788 OMIM
HGNC
HGNC:4223 HGNC
Ensembl
ENSG00000138379 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 8 54
Likely benign 0 28
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 78
Ranking
ClinVar
0
0
16
134
2
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 GDF8
SYNONYM MSLHP
MIM 601788 OMIM
HGNC HGNC:4223 HGNC
Ensembl ENSG00000138379 Ensembl
AllianceGenome HGNC:4223
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000260950.5 hg38 chr2 190,055,700 190,062,729 7,030
ENST00000260950.5 hg19 chr2 190,920,426 190,927,455 7,030
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