MTNAP1 mitochondrial nucleoid associated protein 1
Information
- Symbol
- MTNAP1
- Type
- protein-coding
- Description
- mitochondrial nucleoid associated protein 1
- Entrez Gene ID
- 55028
- Genome
- hg19
- Position
- chr17:71,228,572-71,245,098
- Genome
- hg38
- Position
- chr17:73,232,433-73,248,959
- MIM
- 620717 OMIM
- HGNC
- HGNC:29601 HGNC
- Ensembl
- ENSG00000141219 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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20 |
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2 |
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 |
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 | |||
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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 | C17orf80 |
SYNONYM | HLC-8 |
SYNONYM | MIG3 |
SYNONYM | SPEP1 |
MIM | 620717 OMIM |
HGNC | HGNC:29601 HGNC |
Ensembl | ENSG00000141219 Ensembl |
AllianceGenome | HGNC:29601 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000359042.6 | hg38 | chr17 | 73,232,622 | 73,248,947 | 16,326 |
ENST00000577615.5 | hg38 | chr17 | 73,232,465 | 73,247,530 | 15,066 |
ENST00000582793.1 | hg38 | chr17 | 73,233,226 | 73,247,455 | 14,230 |
ENST00000268942.12 | hg38 | chr17 | 73,232,637 | 73,248,874 | 16,238 |
ENST00000255557.8 | hg38 | chr17 | 73,232,233 | 73,245,339 | 13,107 |
ENST00000426147.6 | hg38 | chr17 | 73,232,662 | 73,245,344 | 12,683 |
ENST00000535032.7 | hg38 | chr17 | 73,232,433 | 73,248,959 | 16,527 |
ENST00000255557.8 | hg19 | chr17 | 71,228,372 | 71,241,478 | 13,107 |
ENST00000535032.7 | hg19 | chr17 | 71,228,572 | 71,245,098 | 16,527 |
ENST00000577615.5 | hg19 | chr17 | 71,228,604 | 71,243,669 | 15,066 |
ENST00000359042.6 | hg19 | chr17 | 71,228,761 | 71,245,086 | 16,326 |
ENST00000268942.12 | hg19 | chr17 | 71,228,776 | 71,245,013 | 16,238 |
ENST00000426147.6 | hg19 | chr17 | 71,228,801 | 71,241,483 | 12,683 |
ENST00000582793.1 | hg19 | chr17 | 71,229,365 | 71,243,594 | 14,230 |
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