NELFE negative elongation factor complex member E

Information
Symbol
NELFE
Type
protein-coding
Description
negative elongation factor complex member E
Entrez Gene ID
7936
Genome
hg19
Position
chr6:31,919,864-31,926,748
Genome
hg38
Position
chr6:31,952,087-31,958,971
MIM
154040 OMIM
HGNC
HGNC:13974 HGNC
Ensembl
ENSG00000204356 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
76
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
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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 D6S45
SYNONYM NELF-E
SYNONYM RD
SYNONYM RDBP
SYNONYM RDP
MIM 154040 OMIM
HGNC HGNC:13974 HGNC
Ensembl ENSG00000204356 Ensembl
AllianceGenome HGNC:13974
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000375425.9 hg38 chr6 31,952,229 31,958,852 6,624
ENST00000375429.8 hg38 chr6 31,952,087 31,958,971 6,885
ENST00000444811.6 hg38 chr6 31,952,229 31,958,960 6,732
ENST00000625905.1 hg38 chr6 31,957,400 31,958,446 1,047
ENST00000375429.8 hg19 chr6 31,919,864 31,926,748 6,885
ENST00000375425.9 hg19 chr6 31,920,006 31,926,629 6,624
ENST00000444811.6 hg19 chr6 31,920,006 31,926,737 6,732
ENST00000625905.1 hg19 chr6 31,925,177 31,926,223 1,047
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