NAA40 N-alpha-acetyltransferase 40, NatD catalytic subunit
Information
- Symbol
- NAA40
- Type
- protein-coding
- Description
- N-alpha-acetyltransferase 40, NatD catalytic subunit
- Entrez Gene ID
- 79829
- Genome
- hg19
- Position
- chr11:63,706,474-63,724,791
- Genome
- hg38
- Position
- chr11:63,939,002-63,957,319
- MIM
- 619999 OMIM
- HGNC
- HGNC:25845 HGNC
- Ensembl
- ENSG00000110583 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
20 |
 |
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 | NAT11 |
| SYNONYM | NatD |
| SYNONYM | PATT1 |
| SYNONYM | hNatD |
| MIM | 619999 OMIM |
| HGNC | HGNC:25845 HGNC |
| Ensembl | ENSG00000110583 Ensembl |
| AllianceGenome | HGNC:25845 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000377793.9 | hg38 | chr11 | 63,939,002 | 63,957,319 | 18,318 |
| ENST00000542163.1 | hg38 | chr11 | 63,939,248 | 63,954,519 | 15,272 |
| ENST00000539656.5 | hg38 | chr11 | 63,939,002 | 63,954,586 | 15,585 |
| ENST00000539656.5 | hg19 | chr11 | 63,706,474 | 63,722,058 | 15,585 |
| ENST00000377793.9 | hg19 | chr11 | 63,706,474 | 63,724,791 | 18,318 |
| ENST00000542163.1 | hg19 | chr11 | 63,706,720 | 63,721,991 | 15,272 |
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