SLAIN2 SLAIN motif family member 2

Information
Symbol
SLAIN2
Type
protein-coding
Description
SLAIN motif family member 2
Entrez Gene ID
57606
Genome
hg19
Position
chr4:48,343,546-48,428,218
Genome
hg38
Position
chr4:48,341,529-48,426,201
MIM
610492 OMIM
HGNC
HGNC:29282 HGNC
Ensembl
ENSG00000109171 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 1 4
Uncertain significance 0 84
Ranking
ClinVar
0
0
0
90
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 KIAA1458
MIM 610492 OMIM
HGNC HGNC:29282 HGNC
Ensembl ENSG00000109171 Ensembl
AllianceGenome HGNC:29282
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000264313.11 hg38 chr4 48,341,529 48,426,201 84,673
ENST00000512093.5 hg38 chr4 48,377,901 48,425,015 47,115
ENST00000264313.11 hg19 chr4 48,343,546 48,428,218 84,673
ENST00000512093.5 hg19 chr4 48,379,918 48,427,032 47,115
Genome browser