PREDICTED: Homo sapiens multiple EGF like domains 10 (MEGF10), transcr - 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.

[A family with early onset myopathy caused by MEGF10 gene defect and literature review]. [Zhonghua Er Ke Za Zhi. 2023]
[A family with early onset myopathy caused by MEGF10 gene defect and literature review].
Lin YF, Wu XY, Yang L, Cheng GQ, Huang Y, Zhuang DY. Zhonghua Er Ke Za Zhi. 2023 Mar 2; 61(3):261-265.
Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course. [Acta Myol. 2022]
Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course.
Croci C, Traverso M, Baratto S, Iacomino M, Pedemonte M, Caroli F, Scala M, Bruno C, Fiorillo C. Acta Myol. 2022; 41(3):111-116. Epub 2022 Sep 30.
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. [Genes (Basel). 2021]
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population.
AlMuhaizea M, Dabbagh O, AlQudairy H, AlHargan A, Alotaibi W, Sami R, AlOtaibi R, Ali MM, AlHindi H, Colak D, et al. Genes (Basel). 2021 Nov 10; 12(11). Epub 2021 Nov 10.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the MEGF10 gene.
RefSeq protein product
See the reference protein sequence for multiple epidermal growth factor-like domains protein 10 isoform X2 (XP_011541996.1).

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
Functional Class
Functional class of the sequence domain architecture
Gene
Link to related Genes
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed
SNP
Related SNPs

Ensembl [Ensembl]
Ensembl
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone

PREDICTED: Homo sapiens multiple EGF like domains 10 (MEGF10), transcript varian...
PREDICTED: Homo sapiens multiple EGF like domains 10 (MEGF10), transcript variant X2, mRNA
gi|767936684|ref|XM_011543694.1|

Nucleotide
H2AC17[gene] (19)
ClinVar
interleukin-18-binding protein precursor [Mus musculus]
interleukin-18-binding protein precursor [Mus musculus]
gi|6754314|ref|NP_034661.1|

Protein

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide