Homo sapiens basic helix-loop-helix family member a9 (BHLHA9), RefSeqG - Nucleotide

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SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably. [Orphanet J Rare Dis. 2022]
SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.
Bukowska-Olech E, Sowińska-Seidler A, Wierzba J, Jamsheer A. Orphanet J Rare Dis. 2022 Aug 26; 17(1):325. Epub 2022 Aug 26.
Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly. [Congenit Anom (Kyoto). 2021]
Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly.
Sedighzadeh SS, Sedaghat A, Zamani M, Seifi T, Shariati G, Zeighami J, Mazaheri N, Galehdari H. Congenit Anom (Kyoto). 2021 Nov; 61(6):220-225. Epub 2021 Aug 8.
A reference map of the human binary protein interactome. [Nature. 2020]
A reference map of the human binary protein interactome.
Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, et al. Nature. 2020 Apr; 580(7803):402-408. Epub 2020 Apr 8.

Protein
Protein sequence from Nucleotide coding region
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Mus musculus
Mus musculus

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Genome Links for Protein (Select 569006475) (1)
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Nucleotide