SLC38A11 solute carrier family 38 member 11

Information
Symbol
SLC38A11
Type
protein-coding
Description
solute carrier family 38 member 11
Entrez Gene ID
151258
Genome
hg19
Position
chr2:165,750,864-165,812,035
Genome
hg38
Position
chr2:164,894,354-164,955,525
MIM
616526 OMIM
HGNC
HGNC:26836 HGNC
Ensembl
ENSG00000169507 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
56
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 :
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 AVT2
MIM 616526 OMIM
HGNC HGNC:26836 HGNC
Ensembl ENSG00000169507 Ensembl
AllianceGenome HGNC:26836
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409149.7 hg38 chr2 164,898,329 164,955,486 57,158
ENST00000303735.8 hg38 chr2 164,896,186 164,955,525 59,340
ENST00000409058.5 hg38 chr2 164,898,334 164,955,477 57,144
ENST00000409662.5 hg38 chr2 164,898,374 164,955,246 56,873
ENST00000685975.1 hg38 chr2 164,894,354 164,955,525 61,172
ENST00000685975.1 hg19 chr2 165,750,864 165,812,035 61,172
ENST00000303735.8 hg19 chr2 165,752,696 165,812,035 59,340
ENST00000409149.7 hg19 chr2 165,754,839 165,811,996 57,158
ENST00000409058.5 hg19 chr2 165,754,844 165,811,987 57,144
ENST00000409662.5 hg19 chr2 165,754,884 165,811,756 56,873
Genome browser