ZNF711 zinc finger protein 711
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 6 |
| Likely pathogenic | 0 | 12 |
| Benign | 0 | 44 |
| Likely benign | 0 | 38 |
| Conflicting classifications of pathogenicity | 0 | 8 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 160 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
24 |
 |
218 |
 |
4 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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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 | CMPX1 |
| SYNONYM | MRX65 |
| SYNONYM | MRX97 |
| SYNONYM | XLID97 |
| SYNONYM | ZNF4 |
| SYNONYM | ZNF5 |
| SYNONYM | ZNF6 |
| SYNONYM | Zfp711 |
| SYNONYM | dJ75N13.1 |
| MIM | 314990 OMIM |
| HGNC | HGNC:13128 HGNC |
| Ensembl | ENSG00000147180 Ensembl |
| AllianceGenome | HGNC:13128 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000373165.7 | hg38 | chrX | 85,244,032 | 85,273,360 | 29,329 |
| ENST00000276123.7 | hg38 | chrX | 85,244,084 | 85,271,921 | 27,838 |
| ENST00000360700.4 | hg38 | chrX | 85,244,765 | 85,273,362 | 28,598 |
| ENST00000674551.1 | hg38 | chrX | 85,243,991 | 85,273,357 | 29,367 |
| ENST00000674551.1 | hg19 | chrX | 84,498,997 | 84,528,363 | 29,367 |
| ENST00000373165.7 | hg19 | chrX | 84,499,038 | 84,528,366 | 29,329 |
| ENST00000276123.7 | hg19 | chrX | 84,499,090 | 84,526,927 | 27,838 |
| ENST00000360700.4 | hg19 | chrX | 84,499,771 | 84,528,368 | 28,598 |
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