ZNF18 zinc finger protein 18
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
38 |
 |
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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| 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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| 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 | HDSG1 |
| SYNONYM | KOX11 |
| SYNONYM | ZKSCAN6 |
| SYNONYM | ZNF535 |
| SYNONYM | ZSCAN38 |
| SYNONYM | Zfp535 |
| MIM | 194524 OMIM |
| HGNC | HGNC:12969 HGNC |
| Ensembl | ENSG00000154957 Ensembl |
| AllianceGenome | HGNC:12969 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000580613.5 | hg38 | chr17 | 11,977,445 | 11,992,917 | 15,473 |
| ENST00000322748.7 | hg38 | chr17 | 11,977,445 | 11,997,372 | 19,928 |
| ENST00000454073.7 | hg38 | chr17 | 11,977,452 | 11,997,457 | 20,006 |
| ENST00000580306.7 | hg38 | chr17 | 11,977,439 | 11,997,475 | 20,037 |
| ENST00000580306.7 | hg19 | chr17 | 11,880,756 | 11,900,792 | 20,037 |
| ENST00000580613.5 | hg19 | chr17 | 11,880,762 | 11,896,234 | 15,473 |
| ENST00000322748.7 | hg19 | chr17 | 11,880,762 | 11,900,689 | 19,928 |
| ENST00000454073.7 | hg19 | chr17 | 11,880,769 | 11,900,774 | 20,006 |
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