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Gene: SLC4A11 (solute carrier family 4 member 11) Homo sapiens
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Symbol: SLC4A11
Name: solute carrier family 4 member 11
Description: Exhibits ion transmembrane transporter activity and protein dimerization activity. Involved in anion transport; cellular cation homeostasis; and monovalent inorganic cation transport. Localizes to apical plasma membrane and basolateral plasma membrane. Implicated in Fuchs' endothelial dystrophy; congenital hereditary endothelial dystrophy of cornea; and corneal dystrophy-perceptive deafness syndrome.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: bicarbonate transporter related protein 1; BTR1; CDPD; CDPD1; CHED; CHED2; corneal dystrophy and perceptive deafness 1; corneal endothelial dystrophy 2 (autosomal recessive); dJ794I6.2; MGC126418; MGC126419; NABC1; sodium bicarbonate transporter-like protein 11; sodium-coupled borate cotransporter 1; solute carrier family 4, sodium bicarbonate transporter-like, member 11; solute carrier family 4, sodium borate transporter, member 11
Orthologs:
Mus musculus (house mouse) : Slc4a11 (solute carrier family 4, sodium bicarbonate transporter-like, member 11)  MGI  Alliance
Rattus norvegicus (Norway rat) : Slc4a11 (solute carrier family 4 member 11)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Slc4a11 (solute carrier family 4 member 11)
Pan paniscus (bonobo/pygmy chimpanzee) : SLC4A11 (solute carrier family 4 member 11)
Canis lupus familiaris (dog) : SLC4A11 (solute carrier family 4 member 11)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Slc4a11 (solute carrier family 4 member 11)
Sus scrofa (pig) : SLC4A11 (solute carrier family 4 member 11)
Chlorocebus sabaeus (African green monkey) : SLC4A11 (solute carrier family 4 member 11)
Heterocephalus glaber (naked mole-rat) : Slc4a11 (solute carrier family 4 member 11)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl203,227,417 - 3,239,559 (-)EnsemblGRCh38hg38GRCh38
GRCh38203,227,417 - 3,241,484 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37203,208,063 - 3,222,109 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36203,156,063 - 3,166,373 (-)NCBINCBI36hg18NCBI36
Build 34203,156,063 - 3,166,373NCBI
Celera203,270,026 - 3,281,861 (-)NCBI
Cytogenetic Map20p13NCBI
HuRef203,156,372 - 3,168,190 (-)NCBIHuRef
CHM1_1203,208,125 - 3,219,949 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
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References - curated
References - uncurated

Genomics

Comparative Map Data
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miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SLC4A11
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1320941
Created: 2005-01-12
Species: Homo sapiens
Last Modified: 2020-04-28
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.