SYTL2 synaptotagmin like 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 24 |
Uncertain significance | 0 | 204 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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236 |
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2 |
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
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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 |
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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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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 | CHR11SYT |
SYNONYM | EXO4 |
SYNONYM | PPP1R151 |
SYNONYM | SGA72M |
SYNONYM | SLP2 |
SYNONYM | SLP2A |
MIM | 612880 OMIM |
HGNC | HGNC:15585 HGNC |
Ensembl | ENSG00000137501 Ensembl |
AllianceGenome | HGNC:15585 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000529581.5 | hg38 | chr11 | 85,694,726 | 85,719,138 | 24,413 |
ENST00000634661.1 | hg38 | chr11 | 85,695,195 | 85,757,725 | 62,531 |
ENST00000533892.5 | hg38 | chr11 | 85,695,035 | 85,719,098 | 24,064 |
ENST00000524452.5 | hg38 | chr11 | 85,695,195 | 85,757,725 | 62,531 |
ENST00000525702.5 | hg38 | chr11 | 85,694,288 | 85,715,137 | 20,850 |
ENST00000389960.8 | hg38 | chr11 | 85,694,224 | 85,811,159 | 116,936 |
ENST00000359152.10 | hg38 | chr11 | 85,694,229 | 85,811,141 | 116,913 |
ENST00000389958.7 | hg38 | chr11 | 85,694,726 | 85,719,168 | 24,443 |
ENST00000528231.5 | hg38 | chr11 | 85,694,742 | 85,758,003 | 63,262 |
ENST00000527523.5 | hg38 | chr11 | 85,695,086 | 85,811,141 | 116,056 |
ENST00000316356.8 | hg38 | chr11 | 85,694,275 | 85,811,129 | 116,855 |
ENST00000359152.10 | hg19 | chr11 | 85,405,272 | 85,522,184 | 116,913 |
ENST00000316356.8 | hg19 | chr11 | 85,405,318 | 85,522,172 | 116,855 |
ENST00000389958.7 | hg19 | chr11 | 85,405,769 | 85,430,211 | 24,443 |
ENST00000389960.8 | hg19 | chr11 | 85,405,267 | 85,522,202 | 116,936 |
ENST00000524452.5 | hg19 | chr11 | 85,406,238 | 85,468,768 | 62,531 |
ENST00000525702.5 | hg19 | chr11 | 85,405,331 | 85,426,180 | 20,850 |
ENST00000527523.5 | hg19 | chr11 | 85,406,129 | 85,522,184 | 116,056 |
ENST00000528231.5 | hg19 | chr11 | 85,405,785 | 85,469,046 | 63,262 |
ENST00000529581.5 | hg19 | chr11 | 85,405,769 | 85,430,181 | 24,413 |
ENST00000533892.5 | hg19 | chr11 | 85,406,078 | 85,430,141 | 24,064 |
ENST00000634661.1 | hg19 | chr11 | 85,406,238 | 85,468,768 | 62,531 |
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