Misplaced Pages

Probable low affinity copper uptake protein 2

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Protein-coding gene in the species Homo sapiens
SLC31A2
Identifiers
AliasesSLC31A2, COPT2, CTR2, hCTR2, solute carrier family 31 member 2
External IDsOMIM: 603088; MGI: 1333844; HomoloGene: 37536; GeneCards: SLC31A2; OMA:SLC31A2 - orthologs
Gene location (Human)
Chromosome 9 (human)
Chr.Chromosome 9 (human)
Chromosome 9 (human)Genomic location for SLC31A2Genomic location for SLC31A2
Band9q32Start113,150,976 bp
End113,164,140 bp
Gene location (Mouse)
Chromosome 4 (mouse)
Chr.Chromosome 4 (mouse)
Chromosome 4 (mouse)Genomic location for SLC31A2Genomic location for SLC31A2
Band4|4 B3Start62,180,799 bp
End62,216,648 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • parotid gland

  • inferior ganglion of vagus nerve

  • C1 segment

  • corpus callosum

  • Pons

  • subthalamic nucleus

  • Medulla Oblongata

  • monocyte

  • superior vestibular nucleus

  • decidua
Top expressed in
  • lacrimal gland

  • seminal vesicula

  • parotid gland

  • neural layer of retina

  • granulocyte

  • spermatid

  • submandibular gland

  • renal corpuscle

  • lip

  • gastrula
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

1318

20530

Ensembl

ENSG00000136867

ENSMUSG00000066152

UniProt

O15432

Q9CPU9

RefSeq (mRNA)

NM_001860

NM_001290518
NM_025286

RefSeq (protein)

NP_001851

NP_001277447
NP_079562

Location (UCSC)Chr 9: 113.15 – 113.16 MbChr 4: 62.18 – 62.22 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000136867 – Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000066152 – 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. Zhou B, Gitschier J (Aug 1997). "hCTR1: a human gene for copper uptake identified by complementation in yeast". Proc Natl Acad Sci U S A. 94 (14): 7481–6. Bibcode:1997PNAS...94.7481Z. doi:10.1073/pnas.94.14.7481. PMC 23847. PMID 9207117.
  6. "Entrez Gene: SLC31A2 solute carrier family 31 (copper transporters), member 2".

Further reading

Membrane proteins, carrier proteins: membrane transport proteins solute carrier (TC 2A)
By group
SLC1–10
(1):
(2):
(3):
(4):
(5):
(6):
(7):
(8):
(9):
(10):
SLC11–20
(11):
(12):
(13):
(14):
(15):
(16):
(17):
(18):
(19):
(20):
SLC21–30
(21):
(22):
(23):
(24):
(25):
(26):
(27):
(28):
(29):
(30):
SLC31–40
(31):
(32):
(33):
(34):
(35):
(36):
(37):
(38):
(39):
(40):
SLC41–48
(41):
(42):
(43):
(44):
(45):
(46):
(47):
(48):
SLCO1–4
Ion pumps
Symporter, Cotransporter
Antiporter (exchanger)
see also solute carrier disorders


Stub icon

This membrane protein–related article is a stub. You can help Misplaced Pages by expanding it.

Categories: