Homo sapiens ATP binding cassette subfamily A member 4 (ABCA4), transc - 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.

Understanding and Rescuing the Splicing Defect Caused by the Frequent ABCA4 Variant c.4253+43G>A Underlying Stargardt Disease. [Nucleic Acid Ther. 2024]
Understanding and Rescuing the Splicing Defect Caused by the Frequent ABCA4 Variant c.4253+43G>A Underlying Stargardt Disease.
Suárez-Herrera N, Garanto A, Collin RWJ. Nucleic Acid Ther. 2024 Apr; 34(2):73-82. Epub 2024 Mar 12.
Protein modeling and in silico analysis to assess pathogenicity of ABCA4 variants in patients with inherited retinal disease. [Mol Vis. 2023]
Protein modeling and in silico analysis to assess pathogenicity of ABCA4 variants in patients with inherited retinal disease.
Cevik S, Wangtiraumnuay N, Van Schelvergem K, Tsukikawa M, Capasso J, Biswas SB, Bodt B, Levin AV, Biswas-Fiss E. Mol Vis. 2023; 29:217-233. Epub 2023 Oct 25.
Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population. [Int J Mol Sci. 2023]
Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population.
Kadyshev VV, Alekseeva EA, Strelnikov VV, Stepanova AA, Polyakov AV, Marakhonov AV, Kutsev SI, Zinchenko RA. Int J Mol Sci. 2023 Nov 12; 24(22). Epub 2023 Nov 12.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the ABCA4 gene (NM_001425324.1).
RefSeq protein product
See the reference protein sequence for retinal-specific phospholipid-transporting ATPase ABCA4 isoform 1 (NP_000341.2).

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
CCDS
Link to Consensus CDS
Components (Core)
Links to Core components
Full text in PMC
Free full text articles in PMC
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
Probe
Related Probe entry
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

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 ATP binding cassette subfamily A member 4 (ABCA4), transcript varia...
Homo sapiens ATP binding cassette subfamily A member 4 (ABCA4), transcript variant 1, mRNA
gi|1519245111|ref|NM_000350.3|

Nucleotide
Staphida everetti voucher LSUMNS B-88279 NADH dehydrogenase subunit 2 (ND2) gene...
Staphida everetti voucher LSUMNS B-88279 NADH dehydrogenase subunit 2 (ND2) gene, partial cds; mitochondrial
gi|1398321533|gb|MG546510.1|

Nucleotide
Staphida everetti voucher LSUMNS B-88237 NADH dehydrogenase subunit 2 (ND2) gene...
Staphida everetti voucher LSUMNS B-88237 NADH dehydrogenase subunit 2 (ND2) gene, partial cds; mitochondrial
gi|1398321531|gb|MG546509.1|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide