GGA3 golgi associated, gamma adaptin ear containing, ARF binding protein 3
Information
- Symbol
- GGA3
- Type
- protein-coding
- Description
- golgi associated, gamma adaptin ear containing, ARF binding protein 3
- Entrez Gene ID
- 23163
- Genome
- hg19
- Position
- chr17:73,232,694-73,257,687
- Genome
- hg38
- Position
- chr17:75,236,599-75,261,606
- MIM
- 606006 OMIM
- HGNC
- HGNC:17079 HGNC
- Ensembl
- ENSG00000125447 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 28 |
| Likely benign | 0 | 22 |
| Uncertain significance | 0 | 102 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
10 |
 |
140 |
 |
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
|
| 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 |
|---|---|
| MIM | 606006 OMIM |
| HGNC | HGNC:17079 HGNC |
| Ensembl | ENSG00000125447 Ensembl |
| AllianceGenome | HGNC:17079 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000582717.5 | hg38 | chr17 | 75,238,238 | 75,262,363 | 24,126 |
| ENST00000538886.5 | hg38 | chr17 | 75,236,599 | 75,261,600 | 25,002 |
| ENST00000578348.5 | hg38 | chr17 | 75,237,284 | 75,262,361 | 25,078 |
| ENST00000582486.5 | hg38 | chr17 | 75,237,427 | 75,262,361 | 24,935 |
| ENST00000537686.6 | hg38 | chr17 | 75,236,599 | 75,261,606 | 25,008 |
| ENST00000537686.6 | hg19 | chr17 | 73,232,694 | 73,257,687 | 24,994 |
| ENST00000538886.5 | hg19 | chr17 | 73,232,694 | 73,257,681 | 24,988 |
| ENST00000582717.5 | hg19 | chr17 | 73,234,319 | 73,258,444 | 24,126 |
| ENST00000578348.5 | hg19 | chr17 | 73,233,379 | 73,258,442 | 25,064 |
| ENST00000582486.5 | hg19 | chr17 | 73,233,522 | 73,258,442 | 24,921 |
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