SLC52A3

SLC52A3
Identifiers
Aliases	SLC52A3, BVVLS, BVVLS1, C20orf54, RFT2, RFVT3, bA371L19.1, hRFT2, solute carrier family 52 member 3
External IDs	MGI: 1916948 HomoloGene: 12324 GeneCards: SLC52A3
Gene location (Human) Chr. Chromosome 20 (human) Band 20p13 Start 760,080 bp End 776,015 bp
Gene location (Mouse) Chr. Chromosome 2 (mouse) Band 2|2 G3 Start 151,996,511 bp End 152,009,258 bp
Gene ontology Molecular function • riboflavin transporter activity Cellular component • integral component of membrane • apical plasma membrane • membrane • integral component of plasma membrane • plasma membrane Biological process • riboflavin metabolic process • sensory perception of sound • riboflavin transport Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	113278	69698
Ensembl	ENSG00000101276	ENSMUSG00000027463
UniProt	Q9NQ40	Q9D6X5
RefSeq (mRNA)	NM_033409	NM_001164819 NM_001164820 NM_027172
RefSeq (protein)	NP_212134	NP_001158291 NP_001158292 NP_081448
Location (UCSC)	Chr 20: 0.76 – 0.78 Mb	Chr 2: 152 – 152.01 Mb
PubMed search

113278

69698

ENSG00000101276

ENSMUSG00000027463

Q9NQ40

Q9D6X5

NM_033409

NM_001164819
NM_001164820
NM_027172

NP_212134

NP_001158291
NP_001158292
NP_081448

Solute carrier family 52 (riboflavin transporter), member 3, formerly known as chromosome 20 open reading frame 54 and riboflavin transporter 2, is a protein that in humans is encoded by the SLC52A3 gene.

This locus likely encodes a transmembrane protein that may function as a riboflavin transporter.

Mutations at this locus have been associated with Fazio–Londe disease and Brown-Vialetto-Van Laere syndrome.

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Wikipedia