NDUFA4L2 NDUFA4 mitochondrial complex associated like 2
Information
- Symbol
- NDUFA4L2
- Type
- protein-coding
- Description
- NDUFA4 mitochondrial complex associated like 2
- Entrez Gene ID
- 56901
- Genome
- hg19
- Position
- chr12:57,628,686-57,630,887
- Genome
- hg38
- Position
- chr12:57,234,903-57,237,104
- HGNC
- HGNC:29836 HGNC
- Ensembl
- ENSG00000185633 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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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| 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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| 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 | COXFA4L2 |
| SYNONYM | MISTRH |
| SYNONYM | NUOMS |
| HGNC | HGNC:29836 HGNC |
| Ensembl | ENSG00000185633 Ensembl |
| AllianceGenome | HGNC:29836 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000393825.5 | hg38 | chr12 | 57,234,905 | 57,240,692 | 5,788 |
| ENST00000556732.1 | hg38 | chr12 | 57,235,080 | 57,237,092 | 2,013 |
| ENST00000554503.6 | hg38 | chr12 | 57,234,903 | 57,237,104 | 2,202 |
| ENST00000554503.6 | hg19 | chr12 | 57,628,686 | 57,630,887 | 2,202 |
| ENST00000393825.5 | hg19 | chr12 | 57,628,688 | 57,634,475 | 5,788 |
| ENST00000556732.1 | hg19 | chr12 | 57,628,863 | 57,630,875 | 2,013 |
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