TIGAR TP53 induced glycolysis regulatory phosphatase
Information
- Symbol
- TIGAR
- Type
- protein-coding
- Description
- TP53 induced glycolysis regulatory phosphatase
- Entrez Gene ID
- 57103
- Genome
- hg19
- Position
- chr12:4,430,379-4,469,194
- Genome
- hg38
- Position
- chr12:4,321,213-4,360,028
- MIM
- 610775 OMIM
- HGNC
- HGNC:1185 HGNC
- Ensembl
- ENSG00000078237 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 2 | 0 |
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
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
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 | C12orf5 |
| SYNONYM | FR2BP |
| MIM | 610775 OMIM |
| HGNC | HGNC:1185 HGNC |
| Ensembl | ENSG00000078237 Ensembl |
| AllianceGenome | HGNC:1185 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000635110.1 | hg38 | chr12 | 4,307,763 | 4,354,549 | 46,787 |
| ENST00000179259.6 | hg38 | chr12 | 4,321,213 | 4,360,028 | 38,816 |
| ENST00000635110.1 | hg19 | chr12 | 4,416,929 | 4,463,715 | 46,787 |
| ENST00000179259.6 | hg19 | chr12 | 4,430,379 | 4,469,194 | 38,816 |
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