CRTAM cytotoxic and regulatory T cell molecule
Information
- Symbol
- CRTAM
- Type
- protein-coding
- Description
- cytotoxic and regulatory T cell molecule
- Entrez Gene ID
- 56253
- Genome
- hg19
- Position
- chr11:122,709,208-122,743,351
- Genome
- hg38
- Position
- chr11:122,838,500-122,872,643
- MIM
- 612597 OMIM
- HGNC
- HGNC:24313 HGNC
- Ensembl
- ENSG00000109943 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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40 |
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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
[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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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Target data | : |
MGeND data only
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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 |
---|---|
SYNONYM | CD355 |
MIM | 612597 OMIM |
HGNC | HGNC:24313 HGNC |
Ensembl | ENSG00000109943 Ensembl |
AllianceGenome | HGNC:24313 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000227348.9 | hg38 | chr11 | 122,838,500 | 122,872,643 | 34,144 |
ENST00000533709.1 | hg38 | chr11 | 122,862,303 | 122,872,637 | 10,335 |
ENST00000227348.9 | hg19 | chr11 | 122,709,208 | 122,743,351 | 34,144 |
ENST00000533709.1 | hg19 | chr11 | 122,733,011 | 122,743,345 | 10,335 |
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