MYRFL myelin regulatory factor like

Information
Symbol
MYRFL
Type
protein-coding
Description
myelin regulatory factor like
Entrez Gene ID
196446
Genome
hg19
Position
chr12:70,219,007-70,352,877
Genome
hg38
Position
chr12:69,825,227-69,959,097
HGNC
HGNC:26316 HGNC
Ensembl
ENSG00000166268 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
8
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
SYNONYM C12orf15
SYNONYM C12orf28
SYNONYM bcm1377
HGNC HGNC:26316 HGNC
Ensembl ENSG00000166268 Ensembl
AllianceGenome HGNC:26316
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000552032.7 hg38 chr12 69,825,227 69,959,097 133,871
ENST00000299350.5 hg38 chr12 69,935,956 69,958,598 22,643
ENST00000547771.6 hg38 chr12 69,825,316 69,959,097 133,782
ENST00000535034.5 hg38 chr12 69,932,536 69,958,607 26,072
ENST00000552032.7 hg19 chr12 70,219,007 70,352,877 133,871
ENST00000547771.6 hg19 chr12 70,219,096 70,352,877 133,782
ENST00000535034.5 hg19 chr12 70,326,316 70,352,387 26,072
ENST00000299350.5 hg19 chr12 70,329,736 70,352,378 22,643
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