CHTF8 chromosome transmission fidelity factor 8
Information
- Symbol
- CHTF8
- Type
- protein-coding
- Description
- chromosome transmission fidelity factor 8
- Entrez Gene ID
- 54921
- Genome
- hg19
- Position
- chr16:69,151,913-69,166,491
- Genome
- hg38
- Position
- chr16:69,118,010-69,132,588
- MIM
- 613202 OMIM
- HGNC
- HGNC:24353 HGNC
- Ensembl
- ENSG00000168802 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 18 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
22 |
 |
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 | CTF8 |
| SYNONYM | DERPC |
| MIM | 613202 OMIM |
| HGNC | HGNC:24353 HGNC |
| Ensembl | ENSG00000168802 Ensembl |
| AllianceGenome | HGNC:24353 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000522091.1 | hg38 | chr16 | 69,120,461 | 69,132,578 | 12,118 |
| ENST00000398235.6 | hg38 | chr16 | 69,119,811 | 69,132,146 | 12,336 |
| ENST00000518041.5 | hg38 | chr16 | 69,118,134 | 69,121,492 | 3,359 |
| ENST00000448552.7 | hg38 | chr16 | 69,118,010 | 69,132,588 | 14,579 |
| ENST00000523421.5 | hg38 | chr16 | 69,118,122 | 69,132,567 | 14,446 |
| ENST00000448552.7 | hg19 | chr16 | 69,151,913 | 69,166,491 | 14,579 |
| ENST00000523421.5 | hg19 | chr16 | 69,152,025 | 69,166,470 | 14,446 |
| ENST00000518041.5 | hg19 | chr16 | 69,152,037 | 69,155,395 | 3,359 |
| ENST00000398235.6 | hg19 | chr16 | 69,153,714 | 69,166,049 | 12,336 |
| ENST00000522091.1 | hg19 | chr16 | 69,154,364 | 69,166,481 | 12,118 |
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