FXYD5 FXYD domain containing ion transport regulator 5
Information
- Symbol
- FXYD5
- Type
- protein-coding
- Description
- FXYD domain containing ion transport regulator 5
- Entrez Gene ID
- 53827
- Genome
- hg19
- Position
- chr19:35,645,633-35,657,664
- Genome
- hg38
- Position
- chr19:35,154,730-35,166,761
- MIM
- 606669 OMIM
- HGNC
- HGNC:4029 HGNC
- Ensembl
- ENSG00000089327 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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26 |
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2 |
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 | DYSAD |
| SYNONYM | HSPC113 |
| SYNONYM | IWU1 |
| SYNONYM | KCT1 |
| SYNONYM | OIT2 |
| SYNONYM | PRO6241 |
| SYNONYM | RIC |
| MIM | 606669 OMIM |
| HGNC | HGNC:4029 HGNC |
| Ensembl | ENSG00000089327 Ensembl |
| AllianceGenome | HGNC:4029 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000541435.6 | hg38 | chr19 | 35,154,753 | 35,169,859 | 15,107 |
| ENST00000423817.7 | hg38 | chr19 | 35,154,942 | 35,169,879 | 14,938 |
| ENST00000342879.7 | hg38 | chr19 | 35,154,773 | 35,169,880 | 15,108 |
| ENST00000392219.7 | hg38 | chr19 | 35,154,735 | 35,169,881 | 15,147 |
| ENST00000392217.3 | hg38 | chr19 | 35,164,035 | 35,169,881 | 5,847 |
| ENST00000392218.6 | hg38 | chr19 | 35,154,730 | 35,159,999 | 5,270 |
| ENST00000590686.5 | hg38 | chr19 | 35,154,753 | 35,169,865 | 15,113 |
| ENST00000588699.5 | hg38 | chr19 | 35,154,787 | 35,169,879 | 15,093 |
| ENST00000543307.5 | hg38 | chr19 | 35,154,730 | 35,166,761 | 12,032 |
| ENST00000392218.6 | hg19 | chr19 | 35,645,633 | 35,650,902 | 5,270 |
| ENST00000543307.5 | hg19 | chr19 | 35,645,633 | 35,657,664 | 12,032 |
| ENST00000392219.7 | hg19 | chr19 | 35,645,638 | 35,660,784 | 15,147 |
| ENST00000541435.6 | hg19 | chr19 | 35,645,656 | 35,660,762 | 15,107 |
| ENST00000590686.5 | hg19 | chr19 | 35,645,656 | 35,660,768 | 15,113 |
| ENST00000342879.7 | hg19 | chr19 | 35,645,676 | 35,660,783 | 15,108 |
| ENST00000588699.5 | hg19 | chr19 | 35,645,690 | 35,660,782 | 15,093 |
| ENST00000423817.7 | hg19 | chr19 | 35,645,845 | 35,660,782 | 14,938 |
| ENST00000392217.3 | hg19 | chr19 | 35,654,938 | 35,660,784 | 5,847 |
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