SYTL4 synaptotagmin like 4

Information
Symbol
SYTL4
Type
protein-coding
Description
synaptotagmin like 4
Entrez Gene ID
94121
Genome
hg19
Position
chrX:99,926,780-99,987,110
Genome
hg38
Position
chrX:100,671,783-100,732,123
MIM
300723 OMIM
HGNC
HGNC:15588 HGNC
Ensembl
ENSG00000102362 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
not provided 6 0
Uncertain significance 0 36
Ranking
ClinVar
0
0
2
44
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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
TypeID
SYNONYM SLP4
MIM 300723 OMIM
HGNC HGNC:15588 HGNC
Ensembl ENSG00000102362 Ensembl
AllianceGenome HGNC:15588
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000685623.1 hg38 chrX 100,671,783 100,732,123 60,341
ENST00000263033.9 hg38 chrX 100,675,897 100,732,121 56,225
ENST00000372981.1 hg38 chrX 100,684,696 100,732,120 47,425
ENST00000372989.6 hg38 chrX 100,674,491 100,732,121 57,631
ENST00000276141.10 hg38 chrX 100,674,494 100,731,534 57,041
ENST00000685623.1 hg19 chrX 99,926,780 99,987,110 60,331
ENST00000372989.6 hg19 chrX 99,929,488 99,987,108 57,621
ENST00000276141.10 hg19 chrX 99,929,491 99,986,522 57,032
ENST00000263033.9 hg19 chrX 99,930,894 99,987,108 56,215
ENST00000372981.1 hg19 chrX 99,939,693 99,987,107 47,415
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