NME4 NME/NM23 nucleoside diphosphate kinase 4
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 42 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
48 |
 |
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
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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 | |||||||||||
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| 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
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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 | NDPK-D |
| SYNONYM | NM23H4 |
| SYNONYM | nm23-H4 |
| MIM | 601818 OMIM |
| HGNC | HGNC:7852 HGNC |
| Ensembl | ENSG00000103202 Ensembl |
| AllianceGenome | HGNC:7852 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000620944.4 | hg38 | chr16 | 397,192 | 400,753 | 3,562 |
| ENST00000219479.7 | hg38 | chr16 | 397,199 | 400,754 | 3,556 |
| ENST00000397722.5 | hg38 | chr16 | 396,725 | 400,746 | 4,022 |
| ENST00000450036.1 | hg38 | chr16 | 397,742 | 400,416 | 2,675 |
| ENST00000621774.4 | hg38 | chr16 | 397,192 | 400,753 | 3,562 |
| ENST00000382940.8 | hg38 | chr16 | 397,209 | 400,506 | 3,298 |
| ENST00000397722.5 | hg19 | chr16 | 446,725 | 450,746 | 4,022 |
| ENST00000620944.4 | hg19 | chr16 | 447,192 | 450,753 | 3,562 |
| ENST00000621774.4 | hg19 | chr16 | 447,192 | 450,753 | 3,562 |
| ENST00000219479.7 | hg19 | chr16 | 447,199 | 450,754 | 3,556 |
| ENST00000382940.8 | hg19 | chr16 | 447,209 | 450,506 | 3,298 |
| ENST00000450036.1 | hg19 | chr16 | 447,742 | 450,416 | 2,675 |
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