Warning: The NCBI web site requires JavaScript to function. more...

Result Filters

PREDICTED: Mirounga leonina progestin and adipoQ receptor family member 7 (PAQR7), transcript variant X1, mRNA

NCBI Reference Sequence: XM_035019435.1

GenBank Graphics

Feature

Display: FASTA GenBank Help

Details

Supplemental Content

Change region shown

Customize view

Analyze this sequence

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.

Articles about the PAQR7 gene

TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations. [Bioinformatics. 2019]
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations.
Tang H, Finn RD, Thomas PD. Bioinformatics. 2019 Feb 1; 35(3):518-520.

Reference sequence information

RefSeq protein product
See the reference protein sequence for membrane progestin receptor alpha (XP_034875326.1).

More about the gene PAQR7

PAQR7 gene
Also Known As: GH733_015679

Related information

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.
Gene
Link to related Genes
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

Recent activity

Clear Turn Off Turn On

Coronavirus Disease 2019 (COVID-19) Emergency Use Authorizations (EUAs)
Coronavirus Disease 2019 (COVID-19) Emergency Use Authorizations (EUAs)
Testing Two Patient Surveys for Diagnosing Rare Genetic Conditions
Testing Two Patient Surveys for Diagnosing Rare Genetic Conditions

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...