ZNF761 zinc finger protein 761
Information
- Symbol
- ZNF761
- Type
- protein-coding
- Description
- zinc finger protein 761
- Entrez Gene ID
- 388561
- Genome
- hg19
- Position
- chr19:53,950,490-53,953,608
- Genome
- hg38
- Position
- chr19:53,447,237-53,450,354
- HGNC
- HGNC:23179 HGNC
- Ensembl
- ENSG00000160336 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 18 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
18 |
 |
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 | ZNF468 |
| HGNC | HGNC:23179 HGNC |
| Ensembl | ENSG00000160336 Ensembl |
| AllianceGenome | HGNC:23179 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000610928.4 | hg38 | chr19 | 53,431,993 | 53,450,331 | 18,339 |
| ENST00000432094.6 | hg38 | chr19 | 53,445,001 | 53,458,261 | 13,261 |
| ENST00000613950.1 | hg38 | chr19 | 53,447,237 | 53,450,354 | 3,118 |
| ENST00000651864.1 | hg38 | chr19 | 53,431,984 | 53,461,862 | 29,879 |
| ENST00000684525.1 | hg38 | chr19 | 53,431,984 | 53,458,261 | 26,278 |
| ENST00000684525.1 | hg19 | chr19 | 53,935,237 | 53,961,515 | 26,279 |
| ENST00000651864.1 | hg19 | chr19 | 53,935,237 | 53,965,116 | 29,880 |
| ENST00000610928.4 | hg19 | chr19 | 53,935,246 | 53,953,585 | 18,340 |
| ENST00000432094.6 | hg19 | chr19 | 53,948,254 | 53,961,515 | 13,262 |
| ENST00000613950.1 | hg19 | chr19 | 53,950,490 | 53,953,608 | 3,119 |
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