PREDICTED: Homo sapiens myosin XVIIIB (MYO18B), transcript variant X12 - 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.

Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery. [Nat Commun. 2022]
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.
Havugimana PC, Goel RK, Phanse S, Youssef A, Padhorny D, Kotelnikov S, Kozakov D, Emili A. Nat Commun. 2022 Jul 13; 13(1):4043. Epub 2022 Jul 13.
Myosin18B predicts favorable prognosis of cutaneous squamous-cell carcinoma. [Genes Genomics. 2021]
Myosin18B predicts favorable prognosis of cutaneous squamous-cell carcinoma.
Cao C, Zhang C, Sun Y, Mu Z, Shen Q. Genes Genomics. 2021 Apr; 43(4):371-378. Epub 2021 Feb 8.
Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism. [Am J Med Genet A. 2021]
Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism.
Altuame FD, Haldeman-Englert C, Cupler E, Al Muhaizea MA, Al-Zaidan HI, Hashem M, Alkuraya FS. Am J Med Genet A. 2021 Feb; 185(2):370-376. Epub 2020 Nov 11.

RefSeq protein product
See the reference protein sequence for unconventional myosin-XVIIIb isoform X9 (XP_054182023.1).

BioProject
Related BioProject entry
Protein
Protein sequence from Nucleotide coding region
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
Gene
Link to related Genes
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

Order Myo18b cDNA clone/Protein/Antibody/RNAi [OriGene]
Order Myo18b cDNA clone/Protein/Antibody/RNAi
OriGene

PREDICTED: Homo sapiens myosin XVIIIB (MYO18B), transcript variant X12, mRNA
PREDICTED: Homo sapiens myosin XVIIIB (MYO18B), transcript variant X12, mRNA
gi|2462585730|ref|XM_054326048.1|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide