PSMD9 proteasome 26S subunit, non-ATPase 9
Information
- Symbol
- PSMD9
- Type
- protein-coding
- Description
- proteasome 26S subunit, non-ATPase 9
- Entrez Gene ID
- 5715
- Genome
- hg19
- Position
- chr12:122,326,696-122,356,203
- Genome
- hg38
- Position
- chr12:121,888,790-121,918,297
- MIM
- 603146 OMIM
- HGNC
- HGNC:9567 HGNC
- Ensembl
- ENSG00000110801 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
28 |
 |
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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| 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 | Rpn4 |
| SYNONYM | p27 |
| MIM | 603146 OMIM |
| HGNC | HGNC:9567 HGNC |
| Ensembl | ENSG00000110801 Ensembl |
| AllianceGenome | HGNC:9567 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000541212.6 | hg38 | chr12 | 121,888,790 | 121,918,297 | 29,508 |
| ENST00000542602.1 | hg38 | chr12 | 121,888,786 | 121,916,399 | 27,614 |
| ENST00000261817.6 | hg38 | chr12 | 121,888,771 | 121,917,863 | 29,093 |
| ENST00000261817.6 | hg19 | chr12 | 122,326,677 | 122,355,769 | 29,093 |
| ENST00000542602.1 | hg19 | chr12 | 122,326,692 | 122,354,305 | 27,614 |
| ENST00000541212.6 | hg19 | chr12 | 122,326,696 | 122,356,203 | 29,508 |
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