TEX29 testis expressed 29
Information
- Symbol
- TEX29
- Type
- protein-coding
- Description
- testis expressed 29
- Entrez Gene ID
- 121793
- Genome
- hg19
- Position
- chr13:111,972,989-111,996,595
- Genome
- hg38
- Position
- chr13:111,320,642-111,344,248
- HGNC
- HGNC:20370 HGNC
- Ensembl
- ENSG00000153495 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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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 |
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SYNONYM | C13orf16 |
SYNONYM | bA474D23.1 |
HGNC | HGNC:20370 HGNC |
Ensembl | ENSG00000153495 Ensembl |
AllianceGenome | HGNC:20370 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000283547.2 | hg38 | chr13 | 111,320,642 | 111,344,248 | 23,607 |
ENST00000283547.2 | hg19 | chr13 | 111,972,989 | 111,996,595 | 23,607 |
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