Danio rerio eukaryotic translation initiation factor 2, subunit 3 gamm - 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.

Broadening the phenotypic spectrum and physiological insights related to EIF2S3 variants. [Hum Mutat. 2021]
Broadening the phenotypic spectrum and physiological insights related to EIF2S3 variants.
Moortgat S, Manfroid I, Pendeville H, Freeman S, Bourdouxhe J, Benoit V, Merhi A, Philippe C, Faivre L, Maystadt I. Hum Mutat. 2021 Jul; 42(7):827-834. Epub 2021 May 19.
Deconvoluting Wavelengths Leading to Fluorescent Light Induced Inflammation and Cellular Stress in Zebrafish (Danio rerio). [Sci Rep. 2020]
Deconvoluting Wavelengths Leading to Fluorescent Light Induced Inflammation and Cellular Stress in Zebrafish (Danio rerio).
Boswell M, Boswell W, Lu Y, Savage M, Walter RB. Sci Rep. 2020 Feb 24; 10(1):3321. Epub 2020 Feb 24.
Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy. [Am J Med Genet A. 2016]
Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy.
Moortgat S, Désir J, Benoit V, Boulanger S, Pendeville H, Nassogne MC, Lederer D, Maystadt I. Am J Med Genet A. 2016 Nov; 170(11):2927-2933. Epub 2016 Jun 22.

RefSeq protein product
See the reference protein sequence for eukaryotic translation initiation factor 2 subunit 3 (NP_997876.2).

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
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
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

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
UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser

Danio rerio eukaryotic translation initiation factor 2, subunit 3 gamma (eif2s3)...
Danio rerio eukaryotic translation initiation factor 2, subunit 3 gamma (eif2s3), mRNA
gi|803378350|ref|NM_212711.3|

Nucleotide
AAI72737 (1)
Identical Protein Groups
Homo sapiens MAGE family member A11 (MAGEA11), RefSeqGene on chromosome X
Homo sapiens MAGE family member A11 (MAGEA11), RefSeqGene on chromosome X
gi|2301856101|ref|NG_012803.2|

Nucleotide
Inadequate Device Operator Training
Inadequate Device Operator Training

MedGen

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide