Homo sapiens deafness, autosomal recessive 31, mRNA (cDNA clone MGC:16 - Nucleotide

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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.

Homo sapiens deafness, autosomal recessive 31, mRNA (cDNA clone MGC:168027 IMAGE...
Homo sapiens deafness, autosomal recessive 31, mRNA (cDNA clone MGC:168027 IMAGE:9020404), complete cds
gi|223462729|gb|BC136416.1|

Nucleotide
major facilitator superfamily domain-containing protein 8 isoform X2 [Homo sapie...
major facilitator superfamily domain-containing protein 8 isoform X2 [Homo sapiens]
gi|2217349967|ref|XP_047305948.1|

Protein

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Nucleotide