TLCD5 TLC domain containing 5
Information
- Symbol
- TLCD5
- Type
- protein-coding
- Description
- TLC domain containing 5
- Entrez Gene ID
- 219902
- Genome
- hg19
- Position
- chr11:120,196,005-120,201,527
- Genome
- hg38
- Position
- chr11:120,325,296-120,330,818
- HGNC
- HGNC:28280 HGNC
- Ensembl
- ENSG00000181264 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 38 |
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 |
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 |
---|---|
SYNONYM | TMEM136 |
HGNC | HGNC:28280 HGNC |
Ensembl | ENSG00000181264 Ensembl |
AllianceGenome | HGNC:28280 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000529187.1 | hg38 | chr11 | 120,325,307 | 120,333,682 | 8,376 |
ENST00000314475.6 | hg38 | chr11 | 120,325,296 | 120,330,818 | 5,523 |
ENST00000375095.3 | hg38 | chr11 | 120,325,299 | 120,333,686 | 8,388 |
ENST00000314475.6 | hg19 | chr11 | 120,196,005 | 120,201,527 | 5,523 |
ENST00000375095.3 | hg19 | chr11 | 120,196,008 | 120,204,395 | 8,388 |
ENST00000529187.1 | hg19 | chr11 | 120,196,016 | 120,204,391 | 8,376 |
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