NOPCHAP1 NOP protein chaperone 1
Information
- Symbol
- NOPCHAP1
- Type
- protein-coding
- Description
- NOP protein chaperone 1
- Entrez Gene ID
- 121053
- Genome
- hg19
- Position
- chr12:105,380,094-105,411,403
- Genome
- hg38
- Position
- chr12:104,986,316-105,017,625
- HGNC
- HGNC:28628 HGNC
- Ensembl
- ENSG00000151131 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
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 | C12orf45 |
| SYNONYM | DDSR1 |
| HGNC | HGNC:28628 HGNC |
| Ensembl | ENSG00000151131 Ensembl |
| AllianceGenome | HGNC:28628 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000622317.5 | hg38 | chr12 | 104,986,338 | 105,060,827 | 74,490 |
| ENST00000552951.7 | hg38 | chr12 | 104,986,316 | 105,017,625 | 31,310 |
| ENST00000280749.5 | hg38 | chr12 | 104,986,339 | 104,994,720 | 8,382 |
| ENST00000637147.1 | hg38 | chr12 | 104,986,338 | 105,048,677 | 62,340 |
| ENST00000552951.7 | hg19 | chr12 | 105,380,094 | 105,411,403 | 31,310 |
| ENST00000637147.1 | hg19 | chr12 | 105,380,116 | 105,442,455 | 62,340 |
| ENST00000622317.5 | hg19 | chr12 | 105,380,116 | 105,454,605 | 74,490 |
| ENST00000280749.5 | hg19 | chr12 | 105,380,117 | 105,388,498 | 8,382 |
| Key | Value |
|---|---|
| strand | + |
| start | 105,380,097 |
| Gene Symbol | C12orf45 |
| Entrez GeneId | 121,053 |
| Chr Band | 12q23.3 |
| end | 105,388,504 |
| chr | chr12 |
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