ZNF726 zinc finger protein 726
Information
- Symbol
- ZNF726
- Type
- protein-coding
- Description
- zinc finger protein 726
- Entrez Gene ID
- 730087
- Genome
- hg19
- Position
- chr19:24,097,688-24,117,286
- Genome
- hg38
- Position
- chr19:23,914,886-23,934,484
- HGNC
- HGNC:32462 HGNC
- Ensembl
- ENSG00000213967 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
---|
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
[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 | ZNF92P3 |
HGNC | HGNC:32462 HGNC |
Ensembl | ENSG00000213967 Ensembl |
AllianceGenome | HGNC:32462 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000594466.6 | hg38 | chr19 | 23,914,886 | 23,934,484 | 19,599 |
ENST00000334589.9 | hg38 | chr19 | 23,914,877 | 23,945,159 | 30,283 |
ENST00000575986.1 | hg38 | chr19 | 23,914,919 | 23,944,713 | 29,795 |
ENST00000531821.6 | hg38 | chr19 | 23,914,882 | 23,921,541 | 6,660 |
ENST00000525354.6 | hg38 | chr19 | 23,914,876 | 23,923,893 | 9,018 |
ENST00000525354.6 | hg19 | chr19 | 24,097,678 | 24,106,695 | 9,018 |
ENST00000334589.9 | hg19 | chr19 | 24,097,679 | 24,127,961 | 30,283 |
ENST00000531821.6 | hg19 | chr19 | 24,097,684 | 24,104,343 | 6,660 |
ENST00000594466.6 | hg19 | chr19 | 24,097,688 | 24,117,286 | 19,599 |
ENST00000575986.1 | hg19 | chr19 | 24,097,721 | 24,127,515 | 29,795 |
Genome browser