SLC13A5

Protein-coding gene in humans
SLC13A5
Identifiers
AliasesSLC13A5, EIEE25, NACT, mIndy, solute carrier family 13 member 5, INDY, DEE25
External IDsOMIM: 608305; MGI: 3037150; HomoloGene: 21941; GeneCards: SLC13A5; OMA:SLC13A5 - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)[1]
Chromosome 17 (human)
Genomic location for SLC13A5
Genomic location for SLC13A5
Band17p13.1Start6,684,719 bp[1]
End6,713,377 bp[1]
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)[2]
Chromosome 11 (mouse)
Genomic location for SLC13A5
Genomic location for SLC13A5
Band11|11 B4Start72,132,815 bp[2]
End72,158,048 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lobe of liver

  • parotid gland

  • tibia

  • nucleus accumbens

  • caudate nucleus

  • cingulate gyrus

  • Brodmann area 9

  • prefrontal cortex

  • putamen

  • ganglionic eminence
Top expressed in
  • calvaria

  • molar

  • spermatocyte

  • body of femur

  • spermatid

  • seminiferous tubule

  • stria vascularis

  • fossa

  • superior frontal gyrus

  • condyle
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • transporter activity
  • tricarboxylic acid transmembrane transporter activity
  • symporter activity
  • succinate transmembrane transporter activity
  • sodium:dicarboxylate symporter activity
  • citrate transmembrane transporter activity
Cellular component
  • integral component of membrane
  • integral component of plasma membrane
  • membrane
  • plasma membrane
Biological process
  • tricarboxylic acid transport
  • succinate transmembrane transport
  • ion transport
  • succinate transport
  • sodium ion transport
  • transmembrane transport
  • tricarboxylic acid transmembrane transport
  • citrate transport
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

284111

237831

Ensembl

ENSG00000141485

ENSMUSG00000020805

UniProt

Q86YT5

Q67BT3

RefSeq (mRNA)

NM_001143838
NM_001284509
NM_001284510
NM_177550

NM_001004148
NM_001372402
NM_001372403

RefSeq (protein)

NP_001137310
NP_001271438
NP_001271439
NP_808218

NP_001004148
NP_001359331
NP_001359332

Location (UCSC)Chr 17: 6.68 – 6.71 MbChr 11: 72.13 – 72.16 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 13 (sodium-dependent citrate transporter), member 5 also known as the Na+/citrate cotransporter or mIndy is a protein that in humans is encoded by the SLC13A5 gene.[5] It is the mammalian homolog of the fly Indy gene.

Function

SLC13A5 is a tricarboxylate plasma transporter with a preference for citrate.[5]

Clinical significance

In 2014, by means of exome sequencing it was determined that a genetic mutation of the SLC13A5 gene is the cause of a rare citrate transporter disorder.[6] Mutations in SLC13A5 cause autosomal recessive epileptic encephalopathy with seizure onset in the first days of life.[6] Those afflicted suffer from seizures, global developmental delay, movement disorder and hypotonia.

Reduced expression of this gene is associated with longer lifespan in many organisms, including some non-human primates. Increased expression is associated with type 2 diabetes and non-alcoholic fatty liver disease. A sugary diet upregulates the expression of the gene, and so does Interleukin 6 signaling.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000141485 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020805 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: Solute carrier family 13 (sodium-dependent citrate transporter), member 5".
  6. ^ a b Thevenon J, Milh M, Feillet F, St-Onge J, Duffourd Y, Jugé C, et al. (July 2014). "Mutations in SLC13A5 cause autosomal-recessive epileptic encephalopathy with seizure onset in the first days of life". American Journal of Human Genetics. 95 (1): 113–20. doi:10.1016/j.ajhg.2014.06.006. PMC 4085634. PMID 24995870.
  7. ^ von Loeffelholz C, Lieske S, Neuschäfer-Rube F, Willmes DM, Raschzok N, Sauer IM, et al. (August 2017). "The human longevity gene homolog INDY and interleukin-6 interact in hepatic lipid metabolism". Hepatology. 66 (2): 616–630. doi:10.1002/hep.29089. PMC 5519435. PMID 28133767.

Further reading

  • Pajor AM (February 2006). "Molecular properties of the SLC13 family of dicarboxylate and sulfate transporters". Pflügers Archiv. 451 (5): 597–605. doi:10.1007/s00424-005-1487-2. PMC 1866268. PMID 16211368.
  • Inoue K, Zhuang L, Ganapathy V (December 2002). "Human Na+ -coupled citrate transporter: primary structure, genomic organization, and transport function". Biochemical and Biophysical Research Communications. 299 (3): 465–71. doi:10.1016/S0006-291X(02)02669-4. PMID 12445824.
  • Gopal E, Miyauchi S, Martin PM, Ananth S, Srinivas SR, Smith SB, Prasad PD, Ganapathy V (January 2007). "Expression and functional features of NaCT, a sodium-coupled citrate transporter, in human and rat livers and cell lines". American Journal of Physiology. Gastrointestinal and Liver Physiology. 292 (1): G402-8. doi:10.1152/ajpgi.00371.2006. PMID 16973915. S2CID 18725925.
  • Benjamin DJ, Cesarini D, van der Loos MJ, Dawes CT, Koellinger PD, Magnusson PK, Chabris CF, Conley D, Laibson D, Johannesson M, Visscher PM (May 2012). "The genetic architecture of economic and political preferences". Proceedings of the National Academy of Sciences of the United States of America. 109 (21): 8026–31. Bibcode:2012PNAS..109.8026B. doi:10.1073/pnas.1120666109. PMC 3361436. PMID 22566634.
  • Inoue K, Zhuang L, Maddox DM, Smith SB, Ganapathy V (August 2003). "Human sodium-coupled citrate transporter, the orthologue of Drosophila Indy, as a novel target for lithium action". The Biochemical Journal. 374 (Pt 1): 21–6. doi:10.1042/BJ20030827. PMC 1223593. PMID 12826022.

External links

  • tessresearch.org - A foundation dedicated to SLC13A5 disorders.
  • v
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By group
SLC1–10
(1):
(2):
(3):
(4):
(5):
(6):
(7):
(8):
  • Na+/Ca2+ exchanger
(9):
(10):
SLC11–20
(11):
(12):
(13):
  • human Na+-sulfate/carboxylate cotransporter
(14):
(15):
(16):
(17):
(18):
(19):
(20):
SLC21–30
(21):
(22):
(23):
  • Na+-dependent ascorbic acid transporter
(24):
  • Na+/(Ca2+-K+) exchanger
(25):
(26):
(27):
(28):
(29):
(30):
SLC31–40
(31):
(32):
(33):
(34):
(35):
(36):
(37):
(38):
(39):
(40):
  • basolateral iron transporter
SLC41–48
(41):
(42):
(43):
  • Na+-independent, system-L like amino-acid transporter
(44):
(45):
(46):
(47):
(48):
SLCO1–4
Symporter, Cotransporter
  • Na+/K+,Cl
  • Na+/Pi3
  • Na+/Cl
  • Na+/glucose
  • Na+/I
  • Cl/K+
Antiporter (exchanger)
  • Na+/H+
  • Na+/Ca2+
    • Na+/(Ca2+-K+) - Cl/HCO
      3
      (Band 3)
  • Cl-formate
  • Cl-oxalate
see also solute carrier disorders

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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