ENST00000445930.7 PSMC6
Information
- Transcript ID
- ENST00000445930.7
- Genome
- hg38
- Position
- chr14:52,707,200-52,728,590
- Strand
- +
- CDS length
- 1,170
- Amino acid length
- 390
- Gene symbol
- PSMC6
- Gene type
- protein-coding
- Gene description
- proteasome 26S subunit, ATPase 6
- Gene Entrez Gene ID
- 5706
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| 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
|
| Category | : |
|
| 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 | |||||||||||||||
Exon
| Exon number | Start | Stop |
|---|---|---|
| 1 | 52,707,200 | 52,707,304 |
| 2 | 52,708,309 | 52,708,388 |
| 3 | 52,708,483 | 52,708,522 |
| 4 | 52,708,764 | 52,708,816 |
| 5 | 52,711,101 | 52,711,168 |
| 6 | 52,711,410 | 52,711,524 |
| 7 | 52,713,881 | 52,713,968 |
| 8 | 52,718,081 | 52,718,142 |
| 9 | 52,718,229 | 52,718,352 |
| 10 | 52,718,977 | 52,719,038 |
| 11 | 52,720,861 | 52,720,981 |
| 12 | 52,721,110 | 52,721,190 |
| 13 | 52,723,965 | 52,724,036 |
| 14 | 52,727,499 | 52,728,590 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 52,707,220 | 52,707,304 |
| 2 | CDS | 52,708,309 | 52,708,388 |
| 3 | CDS | 52,708,483 | 52,708,522 |
| 4 | CDS | 52,708,764 | 52,708,816 |
| 5 | CDS | 52,711,101 | 52,711,168 |
| 6 | CDS | 52,711,410 | 52,711,524 |
| 7 | CDS | 52,713,881 | 52,713,968 |
| 8 | CDS | 52,718,081 | 52,718,142 |
| 9 | CDS | 52,718,229 | 52,718,352 |
| 10 | CDS | 52,718,977 | 52,719,038 |
| 11 | CDS | 52,720,861 | 52,720,981 |
| 12 | CDS | 52,721,110 | 52,721,190 |
| 13 | CDS | 52,723,965 | 52,724,036 |
| 14 | CDS | 52,727,499 | 52,727,617 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr14 | 53,173,918 | 53,195,308 | Link |
CDS sequence
ATGGCGGACCCTAGAGATAAGGCGCTTCAGGACTACCGCAAGAAGTTGCTTGAACACAAGGAGATCGACGGCCGTCTTAAGGAGTTAAGGGAACAATTAAAAGAACTTACCAAGCAGTATGAAAAGTCTGAAAATGATCTGAAGGCCCTACAGAGTGTTGGGCAGATCGTGGGTGAAGTGCTTAAACAGTTAACTGAAGAAAAATTCATTGTTAAAGCTACCAATGGACCAAGATATGTTGTGGGTTGTCGTCGACAGCTTGACAAAAGTAAGCTGAAGCCAGGAACAAGAGTTGCTTTGGATATGACTACACTAACTATCATGAGATATTTGCCGAGAGAGGTGGATCCACTGGTTTATAACATGTCTCATGAGGACCCTGGGAATGTTTCTTATTCTGAGATTGGAGGGCTATCAGAACAGATCCGGGAATTAAGAGAGGTGATAGAATTACCTCTTACAAACCCAGAGTTATTTCAGCGTGTAGGAATAATACCTCCAAAAGGCTGTTTGTTATATGGACCACCAGGTACGGGAAAAACACTCTTGGCACGAGCCGTTGCTAGCCAGCTGGACTGCAATTTCTTAAAGGTTGTATCTAGTTCTATTGTAGACAAGTACATTGGTGAAAGTGCTCGTTTGATCAGAGAAATGTTTAATTATGCTAGAGATCATCAACCATGCATCATTTTTATGGATGAAATAGATGCTATTGGTGGTCGTCGGTTTTCTGAGGGTACTTCAGCTGACAGAGAGATTCAGAGAACGTTAATGGAGTTACTGAATCAAATGGATGGATTTGATACTCTGCATAGAGTTAAAATGATCATGGCTACAAACAGACCAGATACACTGGATCCTGCTTTGCTGCGTCCAGGAAGATTAGATAGAAAAATACATATTGATTTGCCAAATGAACAAGCAAGATTAGACATACTGAAAATCCATGCAGGTCCCATTACAAAGCATGGTGAAATAGATTATGAAGCAATTGTGAAGCTTTCGGATGGCTTTAATGGAGCAGATCTGAGAAATGTTTGTACTGAAGCAGGTATGTTCGCAATTCGTGCTGATCATGATTTTGTAGTACAGGAAGACTTCATGAAAGCAGTCAGAAAAGTGGCTGATTCTAAGAAGCTGGAGTCTAAATTGGACTACAAACCTGTGTAA
Amino sequence
MADPRDKALQDYRKKLLEHKEIDGRLKELREQLKELTKQYEKSENDLKALQSVGQIVGEVLKQLTEEKFIVKATNGPRYVVGCRRQLDKSKLKPGTRVALDMTTLTIMRYLPREVDPLVYNMSHEDPGNVSYSEIGGLSEQIRELREVIELPLTNPELFQRVGIIPPKGCLLYGPPGTGKTLLARAVASQLDCNFLKVVSSSIVDKYIGESARLIREMFNYARDHQPCIIFMDEIDAIGGRRFSEGTSADREIQRTLMELLNQMDGFDTLHRVKMIMATNRPDTLDPALLRPGRLDRKIHIDLPNEQARLDILKIHAGPITKHGEIDYEAIVKLSDGFNGADLRNVCTEAGMFAIRADHDFVVQEDFMKAVRKVADSKKLESKLDYKPV*