SLC11A2

GENERAL INFORMATION

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Gene name

SLC11A2

Gene description

Solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2

Protein class

Disease related genes
Potential drug targets
Predicted intracellular proteins
Predicted membrane proteins
Transporters

Predicted localization

Intracellular,Membrane

Number of transcripts

15
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and membranous expression at variable levels in several different cell types.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 2 antibodies.
HPA032139 , HPA032140
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Salivary gland

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

SLC11A2 (HGNC Symbol)

Synonyms

DCT1, DMT1, NRAMP2

Description

Solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010]

Chromosome

12

Cytoband

q13.12

Chromosome location (bp)

50979401 - 51028566

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000110911 (version 78.38)

Entrez gene

4891

UniProt

P49281 (UniProt - Evidence at protein level)

neXtProt

NX_P49281

Antibodypedia

SLC11A2 antibodies


PROTEIN BROWSER

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ENST00000262051
 
ENST00000262052
 
ENST00000394904
 
ENST00000541174
 
ENST00000545993
 
ENST00000546488
 
ENST00000546743
 
ENST00000547198
 
ENST00000547579
 
ENST00000547688
 
ENST00000547732
 
ENST00000548150
 
ENST00000548193
 
ENST00000549110
 
ENST00000550714
 
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PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLC11A2-001 ENSP00000449200
ENST00000547688
P49281
Show all »
Show » Show » 590 64.7 No >9
SLC11A2-002 ENSP00000262052
ENST00000262052
P49281
Show all »
Show » Show » 561 61.5 No >9
SLC11A2-003 ENSP00000446914
ENST00000546743
F8W1P7
Show all »
Show » Show » 482 52.8 No >9
SLC11A2-005 ENSP00000444542
ENST00000541174
P49281
Show all »
Show » Show » 561 61.5 No >9
SLC11A2-006 ENSP00000262051
ENST00000262051
P49281
Show all »
Show » Show » 568 62.3 No >9
SLC11A2-007 ENSP00000446769
ENST00000547198
P49281
Show all »
Show » Show » 568 62.3 No >9
SLC11A2-008 ENSP00000442810
ENST00000545993
P49281
Show all »
Show » Show » 557 61 No >9
SLC11A2-010 ENSP00000447482
ENST00000547579
F8W1F2
Show all »
Show » Show » 150 16.5 No 4
SLC11A2-011 ENSP00000446984
ENST00000550714
F8W1C0
Show all »
Show » Show » 148 16.1 No 4
SLC11A2-012 ENSP00000450389
ENST00000546488
F8VR36
Show all »
Show » Show » 154 16.9 No 3
SLC11A2-014 ENSP00000447102
ENST00000547732
F8W154
Show all »
Show » Show » 98 10.6 No 2
SLC11A2-017 ENSP00000447334
ENST00000549110
F8VZL6
Show all »
Show » Show » 87 9.5 No 2
SLC11A2-020 ENSP00000449209
ENST00000548193
F8VWB0
Show all »
Show » Show » 149 16.3 No 2
SLC11A2-025 ENSP00000448273
ENST00000548150
Show » 3 0.4 No 0
SLC11A2-201 ENSP00000378364
ENST00000394904
P49281
Show all »
Show » Show » 590 64.7 No >9