GATAD2A GATA zinc finger domain containing 2A
Information
- Symbol
- GATAD2A
- Type
- protein-coding
- Description
- GATA zinc finger domain containing 2A
- Entrez Gene ID
- 54815
- Genome
- hg19
- Position
- chr19:19,538,336-19,619,736
- Genome
- hg38
- Position
- chr19:19,427,527-19,508,927
- MIM
- 614997 OMIM
- HGNC
- HGNC:29989 HGNC
- Ensembl
- ENSG00000167491 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 2 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 100 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
106 |
 |
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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| 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
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| Category | : |
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| 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 | p66alpha |
| MIM | 614997 OMIM |
| HGNC | HGNC:29989 HGNC |
| Ensembl | ENSG00000167491 Ensembl |
| AllianceGenome | HGNC:29989 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000404158.5 | hg38 | chr19 | 19,427,527 | 19,508,927 | 81,401 |
| ENST00000358713.7 | hg38 | chr19 | 19,458,466 | 19,508,927 | 50,462 |
| ENST00000360315.7 | hg38 | chr19 | 19,385,833 | 19,508,931 | 123,099 |
| ENST00000683918.1 | hg38 | chr19 | 19,405,675 | 19,508,932 | 103,258 |
| ENST00000360315.7 | hg19 | chr19 | 19,496,642 | 19,619,740 | 123,099 |
| ENST00000683918.1 | hg19 | chr19 | 19,516,484 | 19,619,741 | 103,258 |
| ENST00000404158.5 | hg19 | chr19 | 19,538,336 | 19,619,736 | 81,401 |
| ENST00000358713.7 | hg19 | chr19 | 19,569,275 | 19,619,736 | 50,462 |
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