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 | |
---|---|
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0 |
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0 |
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0 |
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76 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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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 |
Type | ID |
---|---|
SYNONYM | D6S45 |
SYNONYM | NELF-E |
SYNONYM | RD |
SYNONYM | RDBP |
SYNONYM | RDP |
MIM | 154040 OMIM |
HGNC | HGNC:13974 HGNC |
Ensembl | ENSG00000204356 Ensembl |
AllianceGenome | HGNC:13974 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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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