CT45A7 cancer/testis antigen family 45 member A7
Information
- Symbol
- CT45A7
- Type
- protein-coding
- Description
- cancer/testis antigen family 45 member A7
- Entrez Gene ID
- 101060211
- Genome
- hg19
- Position
- chrX:134,945,946-134,953,994
- Genome
- hg38
- Position
- chrX:135,829,229-135,837,280
- HGNC
- HGNC:51260 HGNC
- Ensembl
- ENSG00000273696 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
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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2 |
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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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Category | : |
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Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CT45-5 |
SYNONYM | CT45-6 |
SYNONYM | CT45A5 |
SYNONYM | CT45A6 |
HGNC | HGNC:51260 HGNC |
Ensembl | ENSG00000273696 Ensembl |
AllianceGenome | HGNC:51260 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000610598.5 | hg38 | chrX | 135,829,229 | 135,837,280 | 8,052 |
ENST00000620885.1 | hg38 | chrX | 135,829,440 | 135,833,541 | 4,102 |
ENST00000610598.5 | hg19 | chrX | 134,945,946 | 134,953,994 | 8,049 |
ENST00000620885.1 | hg19 | chrX | 134,946,157 | 134,950,254 | 4,098 |
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