HSFX4 heat shock transcription factor family, X-linked member 4
Information
- Symbol
- HSFX4
- Type
- protein-coding
- Description
- heat shock transcription factor family, X-linked member 4
- Entrez Gene ID
- 101927685
- Genome
- hg19
- Position
- chrX:149,097,791-149,099,505
- Genome
- hg38
- Position
- chrX:149,929,573-149,931,287
- HGNC
- HGNC:52398 HGNC
- Ensembl
- ENSG00000283463 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 6 | 0 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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4 |
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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
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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000457775.3 | hg38 | chrX | 149,929,573 | 149,931,287 | 1,715 |
ENST00000457775.3 | hg19 | chrX | 149,097,791 | 149,099,505 | 1,715 |
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