NELFCD negative elongation factor complex member C/D

Information
Symbol
NELFCD
Type
protein-coding
Description
negative elongation factor complex member C/D
Entrez Gene ID
51497
Genome
hg19
Position
chr20:57,556,311-57,570,168
Genome
hg38
Position
chr20:58,981,256-58,995,113
MIM
605297 OMIM
HGNC
HGNC:15934 HGNC
Ensembl
ENSG00000101158 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 42
Ranking
ClinVar
0
0
0
44
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 :
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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 HSPC130
SYNONYM NELF-C
SYNONYM NELF-D
SYNONYM TH1
SYNONYM TH1L
MIM 605297 OMIM
HGNC HGNC:15934 HGNC
Ensembl ENSG00000101158 Ensembl
AllianceGenome HGNC:15934
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000602795.6 hg38 chr20 58,981,208 58,995,131 13,924
ENST00000652272.2 hg38 chr20 58,981,256 58,995,113 13,858
ENST00000602795.6 hg19 chr20 57,556,263 57,570,186 13,924
ENST00000652272.2 hg19 chr20 57,556,311 57,570,168 13,858
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