MYNN myoneurin

Information
Symbol
MYNN
Type
protein-coding
Description
myoneurin
Entrez Gene ID
55892
Genome
hg19
Position
chr3:169,491,184-169,507,504
Genome
hg38
Position
chr3:169,773,396-169,789,716
MIM
606042 OMIM
HGNC
HGNC:14955 HGNC
Ensembl
ENSG00000085274 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 1 0
association 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
30
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 OSZF
SYNONYM SBBIZ1
SYNONYM ZBTB31
SYNONYM ZNF902
MIM 606042 OMIM
HGNC HGNC:14955 HGNC
Ensembl ENSG00000085274 Ensembl
AllianceGenome HGNC:14955
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000544106.5 hg38 chr3 169,774,265 169,789,716 15,452
ENST00000349841.10 hg38 chr3 169,773,396 169,789,716 16,321
ENST00000356716.8 hg38 chr3 169,773,427 169,787,544 14,118
ENST00000349841.10 hg19 chr3 169,491,184 169,507,504 16,321
ENST00000356716.8 hg19 chr3 169,491,215 169,505,332 14,118
ENST00000544106.5 hg19 chr3 169,492,053 169,507,504 15,452
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