TP53AIP1 tumor protein p53 regulated apoptosis inducing protein 1
Information
- Symbol
- TP53AIP1
- Type
- protein-coding
- Description
- tumor protein p53 regulated apoptosis inducing protein 1
- Entrez Gene ID
- 63970
- Genome
- hg19
- Position
- chr11:128,805,265-128,812,766
- Genome
- hg38
- Position
- chr11:128,935,370-128,942,871
- MIM
- 605426 OMIM
- HGNC
- HGNC:29984 HGNC
- Ensembl
- ENSG00000120471 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
16 |
![]() |
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
|
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 | P53AIP1 |
MIM | 605426 OMIM |
HGNC | HGNC:29984 HGNC |
Ensembl | ENSG00000120471 Ensembl |
AllianceGenome | HGNC:29984 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000458238.6 | hg38 | chr11 | 128,934,731 | 128,942,927 | 8,197 |
ENST00000531399.6 | hg38 | chr11 | 128,935,370 | 128,942,871 | 7,502 |
ENST00000602346.5 | hg38 | chr11 | 128,935,377 | 128,943,399 | 8,023 |
ENST00000530777.5 | hg38 | chr11 | 128,935,591 | 128,937,818 | 2,228 |
ENST00000458238.6 | hg19 | chr11 | 128,804,626 | 128,812,822 | 8,197 |
ENST00000531399.6 | hg19 | chr11 | 128,805,265 | 128,812,766 | 7,502 |
ENST00000602346.5 | hg19 | chr11 | 128,805,272 | 128,813,294 | 8,023 |
ENST00000530777.5 | hg19 | chr11 | 128,805,486 | 128,807,713 | 2,228 |
Genome browser