Homo sapiens inverted formin 2 (INF2), transcript variant 1, mRNA

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.
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.

INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death. [Cell Mol Life Sci. 2024]
INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death.
Labat-de-Hoz L, Fernández-Martín L, Correas I, Alonso MA. Cell Mol Life Sci. 2024 Jun 25; 81(1):279. Epub 2024 Jun 25.
Functional genetic variants of the disulfidptosis-related INF2 gene predict survival of hepatitis B virus-related hepatocellular carcinoma. [Carcinogenesis. 2024]
Functional genetic variants of the disulfidptosis-related INF2 gene predict survival of hepatitis B virus-related hepatocellular carcinoma.
Wei J, Wen Q, Zhan S, Cao J, Jiang Y, Lian J, Mai Y, Qiu M, Liu Y, Chen P, et al. Carcinogenesis. 2024 Apr 12; 45(4):199-209.
Phosphorylation of INF2 by AMPK promotes mitochondrial fission and oncogenic function in endometrial cancer. [Cell Death Dis. 2024]
Phosphorylation of INF2 by AMPK promotes mitochondrial fission and oncogenic function in endometrial cancer.
Ding Y, Lv Z, Cao W, Shi W, He Q, Gao K. Cell Death Dis. 2024 Jan 17; 15(1):65. Epub 2024 Jan 17.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the INF2 gene.
RefSeq protein product
See the reference protein sequence for inverted formin-2 isoform 1 (NP_071934.3).

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
Functional Class
Functional class of the sequence domain architecture
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

Ensembl [Ensembl]
Ensembl
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 fms related receptor tyrosine kinase 3 (FLT3), RefSeqGene (LRG_457)...
Homo sapiens fms related receptor tyrosine kinase 3 (FLT3), RefSeqGene (LRG_457) on chromosome 13
gi|160358346|ref|NG_007066.1||gnl|L G_457

Nucleotide
Protein Links for Nucleotide (Select 1919262136) (92)
Protein
PREDICTED: Homo sapiens fms related receptor tyrosine kinase 3 (FLT3), transcrip...
PREDICTED: Homo sapiens fms related receptor tyrosine kinase 3 (FLT3), transcript variant X7, mRNA
gi|2462536640|ref|XM_054374316.1|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide