ETDB embryonic testis differentiation homolog B
Information
- Symbol
- ETDB
- Type
- protein-coding
- Description
- embryonic testis differentiation homolog B
- Entrez Gene ID
- 100129515
- Genome
- hg19
- Position
- chrX:134,252,881-134,254,454
- Genome
- hg38
- Position
- chrX:135,118,955-135,120,526
- HGNC
- HGNC:44269 HGNC
- Ensembl
- ENSG00000224107 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 6 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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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| 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 | ETDA |
| SYNONYM | LINC00633 |
| HGNC | HGNC:44269 HGNC |
| Ensembl | ENSG00000224107 Ensembl |
| AllianceGenome | HGNC:44269 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000426364.5 | hg38 | chrX | 135,118,955 | 135,119,746 | 792 |
| ENST00000423661.1 | hg38 | chrX | 135,118,955 | 135,120,526 | 1,572 |
| ENST00000426364.5 | hg19 | chrX | 134,252,881 | 134,253,674 | 794 |
| ENST00000423661.1 | hg19 | chrX | 134,252,881 | 134,254,454 | 1,574 |
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