PREDICTED: Homo sapiens cingulin (CGN), transcript variant X2, misc_RN - 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.

BioProject
Related BioProject entry
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.
Gene
Link to related Genes
PubMed (RefSeq)
Link to RefSeq PubMed articles

PREDICTED: Homo sapiens cingulin (CGN), transcript variant X2, misc_RNA
PREDICTED: Homo sapiens cingulin (CGN), transcript variant X2, misc_RNA
gi|2217269420|ref|XR_921902.3|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide