SLC4A11

GENERAL INFORMATION

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Gene name

SLC4A11

Gene description

Solute carrier family 4, sodium borate transporter, member 11

Protein class

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

Predicted localization

Intracellular,Membrane

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (salivary gland, thyroid gland)
GTEx:Tissue enhanced (salivary gland, thyroid gland)

Protein evidence

Evidence at protein level

Protein localization

General cytoplasmic expression.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining not consistent with RNA expression data. External characterization data supports antibody staining.

Data reliability

Uncertain based on 1 antibody.
HPA018120
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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
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (salivary gland, thyroid gland)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (salivary gland, thyroid gland)

Organ

Expression



GENE INFORMATION

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Gene name

SLC4A11 (HGNC Symbol)

Synonyms

BTR1, CDPD1, CHED2, dJ794I6.2, FECD4, NaBC1

Description

Solute carrier family 4, sodium borate transporter, member 11 (HGNC Symbol)

Entrez gene summary

This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]

Chromosome

20

Cytoband

p13

Chromosome location (bp)

3227417 - 3239190

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000088836 (version 78.38)

Entrez gene

83959

UniProt

Q8NBS3 (UniProt - Evidence at protein level)

neXtProt

NX_Q8NBS3

Antibodypedia

SLC4A11 antibodies


PROTEIN BROWSER

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ENST00000380056
 
ENST00000380059
 
ENST00000437836
 
ENST00000539553
 
 
 
 


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)

SLC4A11-001 ENSP00000369399
ENST00000380059
Q8NBS3
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Show » Show » 918 103.1 No >9
SLC4A11-002 ENSP00000369396
ENST00000380056
Q8NBS3
Show all »
Show » Show » 891 99.6 No >9
SLC4A11-003 ENSP00000441370
ENST00000539553
Q8NBS3
Show all »
Show » Show » 875 98.2 No >9
SLC4A11-007 ENSP00000404271
ENST00000437836
V9GXZ2
Show all »
Show » 105 11.8 No 0