FAM223A family with sequence similarity 223 member A
Information
- Symbol
- FAM223A
- Type
- ncRNA
- Description
- family with sequence similarity 223 member A
- Entrez Gene ID
- 100132967
- Genome
- hg19
- Position
- chrX:153,799,479-153,800,191
- Genome
- hg38
- Position
- chrX:154,571,248-154,571,960
- HGNC
- HGNC:30612 HGNC
- Ensembl
- ENSG00000279245 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Ranking
ClinVar | |
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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 |
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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 |
Type | ID |
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SYNONYM | CXorf52 |
SYNONYM | LINC00204A |
SYNONYM | NCRNA00204 |
SYNONYM | NCRNA00204A |
SYNONYM | SPCX |
HGNC | HGNC:30612 HGNC |
Ensembl | ENSG00000279245 Ensembl |
AllianceGenome | HGNC:30612 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000625204.1 | hg38 | chrX | 154,571,248 | 154,571,960 | 713 |
ENST00000625204.1 | hg19 | chrX | 153,799,479 | 153,800,191 | 713 |
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