SLITRK2 SLIT and NTRK like family member 2

Information
Symbol
SLITRK2
Type
protein-coding
Description
SLIT and NTRK like family member 2
Entrez Gene ID
84631
Genome
hg19
Position
chrX:144,899,347-144,911,374
Genome
hg38
Position
chrX:145,817,829-145,829,856
MIM
300561 OMIM
HGNC
HGNC:13449 HGNC
Ensembl
ENSG00000185985 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 10
Benign 0 4
Likely benign 0 14
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 52
Ranking
ClinVar
0
0
2
66
16
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 CXorf1
SYNONYM CXorf2
SYNONYM SLITL1
SYNONYM TMEM257
SYNONYM XLID111
MIM 300561 OMIM
HGNC HGNC:13449 HGNC
Ensembl ENSG00000185985 Ensembl
AllianceGenome HGNC:13449
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000335565.6 hg38 chrX 145,817,829 145,829,856 12,028
ENST00000370490.1 hg38 chrX 145,818,171 145,825,842 7,672
ENST00000335565.6 hg19 chrX 144,899,347 144,911,374 12,028
ENST00000370490.1 hg19 chrX 144,899,689 144,907,360 7,672
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