Homo sapiens solute carrier organic anion transporter family member 2A - 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.

Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review. [Am J Med Genet A. 2024]
Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review.
Kimball TN, Rivero-García P, Barrera-Godínez A, Domínguez-Cherit J. Am J Med Genet A. 2024 Mar; 194(3):e63446. Epub 2023 Nov 1.
Evaluation of ADRB2 and OATP2A1 genetic polymorphisms in Indian patients with primary open-angle glaucoma. [Pharmacogenet Genomics. 2024]
Evaluation of ADRB2 and OATP2A1 genetic polymorphisms in Indian patients with primary open-angle glaucoma.
Gowtham L, Halder N, Singh SB, Angmo D, Jayasundar R, Dada T, Velpandian T. Pharmacogenet Genomics. 2024 Jan 1; 34(1):20-24. Epub 2023 Nov 1.
Identification of three novel mutations in SLCO2A1 in Asian-Indians with Pachydermoperiostosis. [Indian J Med Res. 2023]
Identification of three novel mutations in SLCO2A1 in Asian-Indians with Pachydermoperiostosis.
Pasumarthi D, Ranganath P, Mandal K, Lakshmi ND, Dalal A, Aggarwal S. Indian J Med Res. 2023 Sep; 158(3):319-323.

RefSeq protein product
See the reference protein sequence for solute carrier organic anion transporter family member 2A1 (NP_005621.2).

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
Probe
Related Probe entry
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
Order TALEN/CRISPR clone [GeneCopoeia Inc.]
Order TALEN/CRISPR clone
GeneCopoeia Inc.
Order qPCR primer [GeneCopoeia Inc.]
Order qPCR primer
GeneCopoeia Inc.
Order full-length cDNA clone [GeneCopoeia Inc.]
Order full-length cDNA clone
GeneCopoeia Inc.
UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser

Homo sapiens solute carrier organic anion transporter family member 2A1 (SLCO2A1...
Homo sapiens solute carrier organic anion transporter family member 2A1 (SLCO2A1), mRNA
gi|1673110479|ref|NM_005630.3|

Nucleotide
Homo sapiens TGFB induced factor homeobox 1 (TGIF1), transcript variant 1, mRNA
Homo sapiens TGFB induced factor homeobox 1 (TGIF1), transcript variant 1, mRNA
gi|1751363270|ref|NM_170695.5|

Nucleotide
Homo sapiens peptidase, mitochondrial processing subunit alpha (PMPCA), transcri...
Homo sapiens peptidase, mitochondrial processing subunit alpha (PMPCA), transcript variant 1, mRNA; nuclear gene for mitochondrial product
gi|1519311703|ref|NM_015160.3|

Nucleotide
LOC100897849 [Galendromus occidentalis]
LOC100897849 [Galendromus occidentalis]
Gene ID:100897849

Gene
SPATA21 spermatogenesis associated 21 [Homo sapiens]
SPATA21 spermatogenesis associated 21 [Homo sapiens]
Gene ID:374955

Gene

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide