Homo sapiens whirlin (WHRN), transcript variant 2, mRNA

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Novel pathogenic WHRN variant causing hearing loss in a moroccan family. [Mol Biol Rep. 2023]
Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
AitRaise I, Amalou G, Redouane S, Charoute H, Snoussi K, Abdelghaffar H, Bonnet C, Petit C, Barakat A. Mol Biol Rep. 2023 Dec; 50(12):10663-10669. Epub 2023 Nov 4.
Identification of motif-based interactions between SARS-CoV-2 protein domains and human peptide ligands pinpoint antiviral targets. [Nat Commun. 2023]
Identification of motif-based interactions between SARS-CoV-2 protein domains and human peptide ligands pinpoint antiviral targets.
Mihalič F, Benz C, Kassa E, Lindqvist R, Simonetti L, Inturi R, Aronsson H, Andersson E, Chi CN, Davey NE, et al. Nat Commun. 2023 Sep 13; 14(1):5636. Epub 2023 Sep 13.
Phase separation-mediated condensation of Whirlin-Myo15-Eps8 stereocilia tip complex. [Cell Rep. 2021]
Phase separation-mediated condensation of Whirlin-Myo15-Eps8 stereocilia tip complex.
Lin L, Shi Y, Wang M, Wang C, Lu Q, Zhu J, Zhang R. Cell Rep. 2021 Feb 23; 34(8):108770.

RefSeq alternative splicing
See 38 reference mRNA sequence splice variants for the WHRN gene.
RefSeq protein product
See the reference protein sequence for whirlin isoform 2 (NP_001077354.2).

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
Gene
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OMIM
OMIM records associated with Nucleotide sequence
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
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UCSC Genome Browser [UCSC Genome Browser]
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