TPT1 tumor protein, translationally-controlled 1
Information
- Symbol
- TPT1
- Type
- protein-coding
- Description
- tumor protein, translationally-controlled 1
- Entrez Gene ID
- 7178
- Genome
- hg19
- Position
- chr13:45,907,606-45,915,419
- Genome
- hg38
- Position
- chr13:45,333,471-45,341,284
- MIM
- 600763 OMIM
- HGNC
- HGNC:12022 HGNC
- Ensembl
- ENSG00000133112 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
risk factor | 0 | 8 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
10 |
![]() |
8 |
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
|
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 |
Type | ID |
---|---|
SYNONYM | HRF |
SYNONYM | TCTP |
SYNONYM | p02 |
SYNONYM | p23 |
MIM | 600763 OMIM |
HGNC | HGNC:12022 HGNC |
Ensembl | ENSG00000133112 Ensembl |
AllianceGenome | HGNC:12022 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000616577.4 | hg38 | chr13 | 45,333,471 | 45,341,284 | 7,814 |
ENST00000379060.8 | hg38 | chr13 | 45,337,198 | 45,341,122 | 3,925 |
ENST00000309246.9 | hg38 | chr13 | 45,338,185 | 45,341,086 | 2,902 |
ENST00000379055.5 | hg38 | chr13 | 45,337,302 | 45,341,158 | 3,857 |
ENST00000379056.5 | hg38 | chr13 | 45,336,873 | 45,341,212 | 4,340 |
ENST00000530705.6 | hg38 | chr13 | 45,333,471 | 45,341,183 | 7,713 |
ENST00000530705.6 | hg19 | chr13 | 45,907,606 | 45,915,318 | 7,713 |
ENST00000616577.4 | hg19 | chr13 | 45,907,606 | 45,915,419 | 7,814 |
ENST00000379056.5 | hg19 | chr13 | 45,911,008 | 45,915,347 | 4,340 |
ENST00000379060.8 | hg19 | chr13 | 45,911,333 | 45,915,257 | 3,925 |
ENST00000379055.5 | hg19 | chr13 | 45,911,437 | 45,915,293 | 3,857 |
ENST00000309246.9 | hg19 | chr13 | 45,912,320 | 45,915,221 | 2,902 |
Genome browser