transcription factor HIVEP2 isoform X1 [Homo sapiens]

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.
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.

Nuclear factor kappa B activation appears weaker in schizophrenia patients with high brain cytokines than in non-schizophrenic controls with high brain cytokines. [J Neuroinflammation. 2020]
Nuclear factor kappa B activation appears weaker in schizophrenia patients with high brain cytokines than in non-schizophrenic controls with high brain cytokines.
Murphy CE, Lawther AJ, Webster MJ, Asai M, Kondo Y, Matsumoto M, Walker AK, Weickert CS. J Neuroinflammation. 2020 Jul 17; 17(1):215. Epub 2020 Jul 17.
Expanding the phenotype of intellectual disability caused by HIVEP2 variants. [Am J Med Genet A. 2019]
Expanding the phenotype of intellectual disability caused by HIVEP2 variants.
Goldsmith H, Wells A, Sá MJN, Williams M, Heussler H, Buckman M, Pfundt R, de Vries BBA, Goel H. Am J Med Genet A. 2019 Sep; 179(9):1872-1877. Epub 2019 Jun 17.
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features. [Neurogenetics. 2016]
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features.
Steinfeld H, Cho MT, Retterer K, Person R, Schaefer GB, Danylchuk N, Malik S, Wechsler SB, Wheeler PG, van Gassen KL, et al. Neurogenetics. 2016 Jul; 17(3):159-64. Epub 2016 Mar 22.

RefSeq genomic sequence
See the genomic reference sequence for the HIVEP2 gene (NG_047004.1).
RefSeq mRNA
See reference mRNA sequence for the HIVEP2 gene (XM_024446417.2).

BioProject
Proteins related to BioProjects
Nucleotide
Nucleotide sequence from coding region
Taxonomy
Taxonomy sequences associated with protein record
CDD Search Results
Display conserved domains within a protein
Conserved Domains (Concise)
Link to a concise list of conserved domains in a protein
Conserved Domains (Full)
Link to conserved domains within a protein
Domain Relatives
Display proteins with similar conserved domain architecture
Encoding mRNA
Link from protein to encoding mRNA
Gene
Link to related Genes
Genome
Genome record encoding protein sequence
Protein (UniProtKB)
Protein gi (refseq) to protein gi (UniProtKB)
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

transcription factor HIVEP2 isoform X1 [Homo sapiens]
transcription factor HIVEP2 isoform X1 [Homo sapiens]
gi|1370507987|ref|XP_024302185.1|

Protein
Homo sapiens
Homo sapiens
aTEA 40 uM 12 hour treatment for MDA-MB-435 cells

BioProject

Your browsing activity is empty.

Activity recording is turned off.

Protein