ETFBKMT electron transfer flavoprotein subunit beta lysine methyltransferase

Information
Symbol
ETFBKMT
Type
protein-coding
Description
electron transfer flavoprotein subunit beta lysine methyltransferase
Entrez Gene ID
254013
Genome
hg19
Position
chr12:31,812,622-31,826,048
Genome
hg38
Position
chr12:31,659,688-31,673,114
MIM
615256 OMIM
HGNC
HGNC:28739 HGNC
Ensembl
ENSG00000139160 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
6
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
HGNC HGNC:28739 HGNC
SYNONYM C12orf72
SYNONYM ETFB-KMT
SYNONYM METTL20
MIM 615256 OMIM
Ensembl ENSG00000139160 Ensembl
AllianceGenome HGNC:28739
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000357721.3 hg38 chr12 31,659,688 31,673,114 13,427
ENST00000538391.1 hg38 chr12 31,661,937 31,668,382 6,446
ENST00000395763.7 hg38 chr12 31,659,187 31,668,967 9,781
ENST00000412352.6 hg38 chr12 31,647,160 31,668,075 20,916
ENST00000538463.5 hg38 chr12 31,659,688 31,668,380 8,693
ENST00000412352.6 hg19 chr12 31,800,094 31,821,009 20,916
ENST00000395763.7 hg19 chr12 31,812,121 31,821,901 9,781
ENST00000538463.5 hg19 chr12 31,812,622 31,821,314 8,693
ENST00000357721.3 hg19 chr12 31,812,622 31,826,048 13,427
ENST00000538391.1 hg19 chr12 31,814,871 31,821,316 6,446
Genome browser