Homo sapiens casein kinase 2 alpha 1 (CSNK2A1), transcript variant 3, - 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.

Okur-Chung neurodevelopmental syndrome: Implications for phenotype and genotype expansion. [Mol Genet Genomic Med. 2024]
Okur-Chung neurodevelopmental syndrome: Implications for phenotype and genotype expansion.
Nan H, Chu M, Zhang J, Jiang D, Wang Y, Wu L. Mol Genet Genomic Med. 2024 Mar; 12(3):e2398.
CSNK2A1 confers gemcitabine resistance to pancreatic ductal adenocarcinoma via inducing autophagy. [Cancer Lett. 2024]
CSNK2A1 confers gemcitabine resistance to pancreatic ductal adenocarcinoma via inducing autophagy.
Liu ZD, Shi YH, Xu QC, Zhao GY, Zhu YQ, Li FX, Ma MJ, Ye JY, Huang XT, Wang XY, et al. Cancer Lett. 2024 Mar 31; 585:216640. Epub 2024 Jan 28.
Systematic discovery of protein interaction interfaces using AlphaFold and experimental validation. [Mol Syst Biol. 2024]
Systematic discovery of protein interaction interfaces using AlphaFold and experimental validation.
Lee CY, Hubrich D, Varga JK, Schäfer C, Welzel M, Schumbera E, Djokic M, Strom JM, Schönfeld J, Geist JL, et al. Mol Syst Biol. 2024 Feb; 20(2):75-97. Epub 2024 Jan 15.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the CSNK2A1 gene.
RefSeq protein product
See the reference protein sequence for casein kinase II subunit alpha isoform b (NP_808228.1).

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
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 casein kinase 2 alpha 1 (CSNK2A1), transcript variant 3, mRNA
Homo sapiens casein kinase 2 alpha 1 (CSNK2A1), transcript variant 3, mRNA
gi|1676325020|ref|NM_177560.3|

Nucleotide
Optic Atrophies, Hereditary
Optic Atrophies, Hereditary
Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, ...<br/>Year introduced: 2000(1989)

MeSH
Corticobasal Degeneration
Corticobasal Degeneration
Rare progressive neurological disorder characterized by Parkinsonism, cortical atrophy of multiple areas of the brain including the cerebral cortex and the basal ganglia, cogn...<br/>Year introduced: 2022

MeSH

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide