PHF23 PHD finger protein 23
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 46 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
46 |
 |
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 | hJUNE-1b |
| MIM | 612910 OMIM |
| HGNC | HGNC:28428 HGNC |
| Ensembl | ENSG00000040633 Ensembl |
| AllianceGenome | HGNC:28428 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000613632.4 | hg38 | chr17 | 7,235,626 | 7,239,279 | 3,654 |
| ENST00000454255.6 | hg38 | chr17 | 7,235,287 | 7,238,930 | 3,644 |
| ENST00000320316.8 | hg38 | chr17 | 7,235,038 | 7,239,457 | 4,420 |
| ENST00000576955.5 | hg38 | chr17 | 7,235,038 | 7,239,455 | 4,418 |
| ENST00000571362.5 | hg38 | chr17 | 7,235,029 | 7,239,439 | 4,411 |
| ENST00000571362.5 | hg19 | chr17 | 7,138,348 | 7,142,758 | 4,411 |
| ENST00000576955.5 | hg19 | chr17 | 7,138,357 | 7,142,774 | 4,418 |
| ENST00000320316.8 | hg19 | chr17 | 7,138,357 | 7,142,776 | 4,420 |
| ENST00000454255.6 | hg19 | chr17 | 7,138,606 | 7,142,249 | 3,644 |
| ENST00000613632.4 | hg19 | chr17 | 7,138,945 | 7,142,598 | 3,654 |
Genome browser