CT47A11 cancer/testis antigen family 47 member A11
Information
- Symbol
- CT47A11
- Type
- protein-coding
- Description
- cancer/testis antigen family 47 member A11
- Entrez Gene ID
- 255313
- Genome
- hg19
- Position
- chrX:120,067,694-120,071,012
- Genome
- hg38
- Position
- chrX:120,933,840-120,937,158
- MIM
- 300592 OMIM
- HGNC
- HGNC:27397 HGNC
- Ensembl
- ENSG00000226929 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 |
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 |
Type | ID |
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SYNONYM | CT47.11 |
MIM | 300592 OMIM |
HGNC | HGNC:27397 HGNC |
Ensembl | ENSG00000226929 Ensembl |
AllianceGenome | HGNC:27397 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000457020.3 | hg38 | chrX | 120,933,840 | 120,937,158 | 3,319 |
ENST00000457020.3 | hg19 | chrX | 120,067,694 | 120,071,012 | 3,319 |
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