SLC41A3

Protein-coding gene in the species Homo sapiens
SLC41A3
Identifiers
AliasesSLC41A3, SLC41A1-L2, solute carrier family 41 member 3
External IDsOMIM: 610803 MGI: 1918949 HomoloGene: 23052 GeneCards: SLC41A3
Gene location (Human)
Chromosome 3 (human)
Chr.Chromosome 3 (human)[1]
Chromosome 3 (human)
Genomic location for SLC41A3
Genomic location for SLC41A3
Band3q21.2-q21.3Start126,006,357 bp[1]
End126,101,561 bp[1]
Gene location (Mouse)
Chromosome 6 (mouse)
Chr.Chromosome 6 (mouse)[2]
Chromosome 6 (mouse)
Genomic location for SLC41A3
Genomic location for SLC41A3
Band6|6 D1Start90,581,707 bp[2]
End90,623,394 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • prefrontal cortex

  • ascending aorta

  • middle temporal gyrus

  • left adrenal gland

  • amygdala

  • right coronary artery

  • anterior pituitary

  • Brodmann area 9

  • popliteal artery

  • gastrocnemius muscle
Top expressed in
  • interventricular septum

  • right ventricle

  • triceps brachii muscle

  • sternocleidomastoid muscle

  • digastric muscle

  • extraocular muscle

  • temporal muscle

  • quadriceps femoris muscle

  • vastus lateralis muscle

  • tibialis anterior muscle
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • cation transmembrane transporter activity
  • protein binding
Cellular component
  • integral component of membrane
  • membrane
  • plasma membrane
Biological process
  • cation transport
  • cation transmembrane transport
  • transmembrane transport
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

54946

71699

Ensembl

ENSG00000114544

ENSMUSG00000030089

UniProt

Q96GZ6

Q921R8

RefSeq (mRNA)

NM_001008485
NM_001008486
NM_001008487
NM_001164475
NM_017836

NM_001037493
NM_027868

RefSeq (protein)
NP_001008485
NP_001008486
NP_001008487
NP_001157947
NP_060306

NP_001008486.1

NP_001032570
NP_082144

Location (UCSC)Chr 3: 126.01 – 126.1 MbChr 6: 90.58 – 90.62 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 41, member 3 is a protein that in humans is encoded by the SLC41A3 gene.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000114544 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030089 – 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. ^ "Entrez Gene: Solute carrier family 41, member 3". Retrieved 2011-09-28.

Further reading

  • Wabakken T, Rian E, Kveine M, Aasheim HC (July 2003). "The human solute carrier SLC41A1 belongs to a novel eukaryotic subfamily with homology to prokaryotic MgtE Mg2+ transporters". Biochemical and Biophysical Research Communications. 306 (3): 718–24. doi:10.1016/S0006-291X(03)01030-1. PMID 12810078.
  • v
  • t
  • e
By group
SLC1–10
(1):
(2):
(3):
(4):
(5):
(6):
(7):
(8):
  • Na+/Ca2+ exchanger
(9):
(10):
SLC11–20
(11):
(12):
(13):
(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


Stub icon

This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e