MYRF myelin regulatory factor

Information
Symbol
MYRF
Type
protein-coding
Description
myelin regulatory factor
Entrez Gene ID
745
Genome
hg19
Position
chr11:61,520,108-61,555,990
Genome
hg38
Position
chr11:61,752,636-61,788,518
MIM
608329 OMIM
HGNC
HGNC:1181 HGNC
Ensembl
ENSG00000124920 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 8 46
Likely pathogenic 0 54
Benign 0 62
Likely benign 0 68
Conflicting classifications of pathogenicity 0 6
Uncertain significance 0 156
Ranking
ClinVar
0
0
24
324
34
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 11orf9
SYNONYM C11orf9
SYNONYM CUGS
SYNONYM MMERV
SYNONYM MRF
SYNONYM Ndt80
SYNONYM pqn-47
MIM 608329 OMIM
HGNC HGNC:1181 HGNC
Ensembl ENSG00000124920 Ensembl
AllianceGenome HGNC:1181
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000278836.10 hg38 chr11 61,752,636 61,788,518 35,883
ENST00000265460.9 hg38 chr11 61,755,389 61,788,517 33,129
ENST00000278836.10 hg19 chr11 61,520,108 61,555,990 35,883
ENST00000265460.9 hg19 chr11 61,522,861 61,555,989 33,129
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