SPATA2L spermatogenesis associated 2 like
Information
- Symbol
- SPATA2L
- Type
- protein-coding
- Description
- spermatogenesis associated 2 like
- Entrez Gene ID
- 124044
- Genome
- hg19
- Position
- chr16:89,762,765-89,768,113
- Genome
- hg38
- Position
- chr16:89,696,357-89,701,705
- HGNC
- HGNC:28393 HGNC
- Ensembl
- ENSG00000158792 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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66 |
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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 |
Search Word
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 | C16orf76 |
SYNONYM | tamo |
HGNC | HGNC:28393 HGNC |
Ensembl | ENSG00000158792 Ensembl |
AllianceGenome | HGNC:28393 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000335360.11 | hg38 | chr16 | 89,696,357 | 89,701,705 | 5,349 |
ENST00000289805.10 | hg38 | chr16 | 89,696,357 | 89,701,705 | 5,349 |
ENST00000289805.10 | hg19 | chr16 | 89,762,765 | 89,768,113 | 5,349 |
ENST00000335360.11 | hg19 | chr16 | 89,762,765 | 89,768,113 | 5,349 |
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