NDUFC2 NADH:ubiquinone oxidoreductase subunit C2
Information
- Symbol
- NDUFC2
- Type
- protein-coding
- Description
- NADH:ubiquinone oxidoreductase subunit C2
- Entrez Gene ID
- 4718
- Genome
- hg19
- Position
- chr11:77,779,343-77,790,908
- Genome
- hg38
- Position
- chr11:78,068,297-78,079,862
- MIM
- 603845 OMIM
- HGNC
- HGNC:7706 HGNC
- Ensembl
- ENSG00000151366 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 4 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
10 |
 |
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
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | B14.5b |
| SYNONYM | CI-B14.5b |
| SYNONYM | HLC-1 |
| SYNONYM | MC1DN36 |
| SYNONYM | NADHDH2 |
| MIM | 603845 OMIM |
| HGNC | HGNC:7706 HGNC |
| Ensembl | ENSG00000151366 Ensembl |
| AllianceGenome | HGNC:7706 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000527806.1 | hg38 | chr11 | 78,068,349 | 78,079,841 | 11,493 |
| ENST00000534029.5 | hg38 | chr11 | 78,069,856 | 78,079,819 | 9,964 |
| ENST00000528164.1 | hg38 | chr11 | 78,072,864 | 78,079,861 | 6,998 |
| ENST00000525085.1 | hg38 | chr11 | 78,069,858 | 78,079,819 | 9,962 |
| ENST00000281031.5 | hg38 | chr11 | 78,068,297 | 78,079,862 | 11,566 |
| ENST00000281031.5 | hg19 | chr11 | 77,779,343 | 77,790,908 | 11,566 |
| ENST00000527806.1 | hg19 | chr11 | 77,779,395 | 77,790,887 | 11,493 |
| ENST00000534029.5 | hg19 | chr11 | 77,780,902 | 77,790,865 | 9,964 |
| ENST00000525085.1 | hg19 | chr11 | 77,780,904 | 77,790,865 | 9,962 |
| ENST00000528164.1 | hg19 | chr11 | 77,783,910 | 77,790,907 | 6,998 |
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