ANKFY1 ankyrin repeat and FYVE domain containing 1
Information
- Symbol
- ANKFY1
- Type
- protein-coding
- Description
- ankyrin repeat and FYVE domain containing 1
- Entrez Gene ID
- 51479
- Genome
- hg19
- Position
- chr17:4,068,368-4,167,142
- Genome
- hg38
- Position
- chr17:4,165,074-4,263,847
- MIM
- 607927 OMIM
- HGNC
- HGNC:20763 HGNC
- Ensembl
- ENSG00000185722 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 70 |
| Likely benign | 0 | 62 |
| Uncertain significance | 0 | 128 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
6 |
 |
254 |
 |
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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| 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 | ANKHZN |
| SYNONYM | BTBD23 |
| SYNONYM | ZFYVE14 |
| MIM | 607927 OMIM |
| HGNC | HGNC:20763 HGNC |
| Ensembl | ENSG00000185722 Ensembl |
| AllianceGenome | HGNC:20763 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000341657.9 | hg38 | chr17 | 4,163,821 | 4,263,979 | 100,159 |
| ENST00000570535.5 | hg38 | chr17 | 4,165,074 | 4,263,847 | 98,774 |
| ENST00000574367.5 | hg38 | chr17 | 4,166,274 | 4,263,956 | 97,683 |
| ENST00000341657.9 | hg19 | chr17 | 4,067,115 | 4,167,274 | 100,160 |
| ENST00000570535.5 | hg19 | chr17 | 4,068,368 | 4,167,142 | 98,775 |
| ENST00000574367.5 | hg19 | chr17 | 4,069,568 | 4,167,251 | 97,684 |
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