Homo sapiens solute carrier family 52 member 2 (SLC52A2), transcript v - Nucleotide

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.
Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...
Show in Genome Data Viewer
Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2. [Free Radic Res. 2022]
Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2.
Tolomeo M, Chimienti G, Lanza M, Barbaro R, Nisco A, Latronico T, Leone P, Petrosillo G, Liuzzi GM, Ryder B, et al. Free Radic Res. 2022 Jul-Aug; 56(7-8):511-525. Epub 2022 Dec 8.
A dual-activity topoisomerase complex regulates mRNA translation and turnover. [Nucleic Acids Res. 2022]
A dual-activity topoisomerase complex regulates mRNA translation and turnover.
Su S, Xue Y, Sharov A, Zhang Y, Lee SK, Martindale JL, Li W, Ku WL, Zhao K, De S, et al. Nucleic Acids Res. 2022 Jul 8; 50(12):7013-7033.
Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2. [IUBMB Life. 2022]
Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2.
Console L, Tolomeo M, Cosco J, Massey K, Barile M, Indiveri C. IUBMB Life. 2022 Jul; 74(7):618-628. Epub 2021 Aug 24.

RefSeq alternative splicing
See 29 reference mRNA sequence splice variants for the SLC52A2 gene.
RefSeq protein product
See the reference protein sequence for solute carrier family 52, riboflavin transporter, member 2 isoform 1 (NP_001350049.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
BioSystems
BioSystems
CCDS
Link to Consensus CDS
Components (Core)
Links to Core components
Full text in PMC
Free full text articles in PMC
Functional Class
Functional class of the sequence domain architecture
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

Ensembl [Ensembl]
Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser

Homo sapiens solute carrier family 52 member 2 (SLC52A2), transcript variant 6, ...
Homo sapiens solute carrier family 52 member 2 (SLC52A2), transcript variant 6, mRNA
gi|1677530788|ref|NM_001363120.2|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide