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UDP-galactose translocator

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(Redirected from SLC35A2) Protein found in humans
SLC35A2
Identifiers
AliasesSLC35A2, CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL, solute carrier family 35 member A2
External IDsOMIM: 314375; MGI: 1345297; HomoloGene: 136614; GeneCards: SLC35A2; OMA:SLC35A2 - orthologs
Gene location (Human)
X chromosome (human)
Chr.X chromosome (human)
X chromosome (human)Genomic location for SLC35A2Genomic location for SLC35A2
BandXp11.23Start48,903,180 bp
End48,911,958 bp
Gene location (Mouse)
X chromosome (mouse)
Chr.X chromosome (mouse)
X chromosome (mouse)Genomic location for SLC35A2Genomic location for SLC35A2
BandX A1.1|X 3.56 cMStart7,750,267 bp
End7,760,731 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • secondary oocyte

  • bronchial epithelial cell

  • palpebral conjunctiva

  • stromal cell of endometrium

  • mucosa of transverse colon

  • olfactory zone of nasal mucosa

  • mucosa of sigmoid colon

  • rectum

  • epithelium of nasopharynx

  • right uterine tube
Top expressed in
  • left colon

  • Paneth cell

  • cumulus cell

  • ascending aorta

  • aortic valve

  • crypt of lieberkuhn of small intestine

  • motor neuron

  • lobe of prostate

  • seminal vesicula

  • lacrimal gland
More reference expression data
BioGPS




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

7355

22232

Ensembl

ENSG00000102100

ENSMUSG00000031156

UniProt

P78381

Q9R0M8

RefSeq (mRNA)
NM_005660
NM_001032289
NM_001042498
NM_001282647
NM_001282648

NM_001282649
NM_001282650
NM_001282651

NM_001083937
NM_078484

RefSeq (protein)
NP_001027460
NP_001035963
NP_001269576
NP_001269577
NP_001269578

NP_001269579
NP_001269580
NP_005651

NP_001077406
NP_511039

Location (UCSC)Chr X: 48.9 – 48.91 MbChr X: 7.75 – 7.76 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

UDP-galactose translocator is a protein that in humans is encoded by the SLC35A2 gene.

Somatic loss-of-function variants in the SLC35A2 gene were originally associated with focal epilepsy with radiographically nonlesional epilepsy. Later it was discovered that individuals with somatic variants in SLC35A2 have a mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE), which is a subtype of frontal lobe epilepsy.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000102100Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000031156Ensembl, 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. Hara T, Yamauchi M, Takahashi E, Hoshino M, Aoki K, Ayusawa D, Kawakita M (November 1993). "The UDP-galactose translocator gene is mapped to band Xp11.23-p11.22 containing the Wiskott-Aldrich syndrome locus". Somatic Cell and Molecular Genetics. 19 (6): 571–5. doi:10.1007/BF01233383. PMID 8128316. S2CID 10466290.
  6. "Entrez Gene: SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2".
  7. Winawer MR, Griffin NG, Samanamud J, Baugh EH, Rathakrishnan D, Ramalingam S, Zagzag D, Schevon CA, Dugan P, Hegde M, Sheth SA, McKhann GM, Doyle WK, Grant GA, Porter BE, Mikati MA, Muh CR, Malone CD, Bergin AM, Peters JM, McBrian DK, Pack AM, Akman CI, LaCoursiere CM, Keever KM, Madsen JR, Yang E, Lidov HG, Shain C, Allen AS, Canoll PD, Crino PB, Poduri AH, Heinzen EL (June 2018). "Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy". Ann Neurol. 83 (6): 1133–46. doi:10.1002/ana.25243. PMC 6105543. PMID 29679388.
  8. Bonduelle T, Hartlieb T, Baldassari S, Sim NS, Kim SH, Kang HC, et al. (January 2021). "Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)". Acta Neuropathologica Communications. 9 (1): 3. doi:10.1186/s40478-020-01085-3. PMC 7788938. PMID 33407896.

Further reading

Membrane proteins, carrier proteins: membrane transport proteins solute carrier (TC 2A)
By group
SLC1–10
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SLC11–20
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SLC21–30
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SLC31–40
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SLC41–48
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SLCO1–4
Ion pumps
Symporter, Cotransporter
Antiporter (exchanger)
see also solute carrier disorders
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