SLC11A1 solute carrier family 11 member 1

Information
Symbol
SLC11A1
Type
protein-coding
Description
solute carrier family 11 member 1
Entrez Gene ID
6556
Genome
hg19
Position
chr2:219,246,996-219,261,617
Genome
hg38
Position
chr2:218,382,273-218,396,894
MIM
600266 OMIM
HGNC
HGNC:10907 HGNC
Ensembl
ENSG00000018280 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 28
risk factor 0 4
Uncertain significance 0 100
Ranking
ClinVar
0
0
4
138
6
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
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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 LSH
SYNONYM NRAMP
SYNONYM NRAMP1
MIM 600266 OMIM
HGNC HGNC:10907 HGNC
Ensembl ENSG00000018280 Ensembl
AllianceGenome HGNC:10907
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000233202.11 hg38 chr2 218,382,273 218,396,894 14,622
ENST00000233202.11 hg19 chr2 219,246,996 219,261,617 14,622
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