SLC8B1 solute carrier family 8 member B1

Information
Symbol
SLC8B1
Type
protein-coding
Description
solute carrier family 8 member B1
Entrez Gene ID
80024
Genome
hg19
Position
chr12:113,736,576-113,772,914
Genome
hg38
Position
chr12:113,298,771-113,335,109
MIM
609841 OMIM
HGNC
HGNC:26175 HGNC
Ensembl
ENSG00000089060 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
74
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
Category :
Search word :
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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 NCKX6
SYNONYM NCLX
SYNONYM SLC24A6
MIM 609841 OMIM
HGNC HGNC:26175 HGNC
Ensembl ENSG00000089060 Ensembl
AllianceGenome HGNC:26175
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000546737.5 hg38 chr12 113,299,777 113,332,947 33,171
ENST00000549069.5 hg38 chr12 113,299,332 113,306,844 7,513
ENST00000202831.7 hg38 chr12 113,298,767 113,335,120 36,354
ENST00000552014.5 hg38 chr12 113,298,759 113,335,030 36,272
ENST00000680972.1 hg38 chr12 113,298,771 113,335,109 36,339
ENST00000550047.5 hg38 chr12 113,298,781 113,308,843 10,063
ENST00000202831.7 hg19 chr12 113,736,572 113,772,925 36,354
ENST00000552014.5 hg19 chr12 113,736,564 113,772,835 36,272
ENST00000546737.5 hg19 chr12 113,737,582 113,770,752 33,171
ENST00000549069.5 hg19 chr12 113,737,137 113,744,649 7,513
ENST00000550047.5 hg19 chr12 113,736,586 113,746,648 10,063
ENST00000680972.1 hg19 chr12 113,736,576 113,772,914 36,339
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