Homo sapiens filamin A interacting protein 1 (FILIP1), transcript vari - Nucleotide

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Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects. [Brain. 2023]
Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects.
Roos A, van der Ven PFM, Alrohaif H, Kölbel H, Heil L, Della Marina A, Weis J, Aßent M, Beck-Wödl S, Barresi R, et al. Brain. 2023 Oct 3; 146(10):4200-4216.
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly. [Hum Genet. 2023]
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly.
Schnabel F, Schuler E, Al-Maawali A, Chaurasia A, Syrbe S, Al-Kindi A, Bhavani GS, Shukla A, Altmüller J, Nürnberg P, et al. Hum Genet. 2023 Apr; 142(4):543-552. Epub 2023 Mar 21.
TRABID targets DDB2 for deubiquitination to promote proliferation of hepatocellular carcinoma cells. [Biochem Biophys Res Commun. 2022]
TRABID targets DDB2 for deubiquitination to promote proliferation of hepatocellular carcinoma cells.
Chen Y, Zhang X. Biochem Biophys Res Commun. 2022 Oct 15; 625:23-30. Epub 2022 Aug 2.

RefSeq protein product
See the reference protein sequence for filamin-A-interacting protein 1 isoform 3 (NP_001287795.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens filamin A interacting protein 1 (FILIP1), transcript variant 4, mRN...
Homo sapiens filamin A interacting protein 1 (FILIP1), transcript variant 4, mRNA
gi|1676440092|ref|NM_001300866.3|

Nucleotide
Structure Links for Protein (Select 255759932) (1)
Structure
BioProjects for Gene (Select 129997587) (4)
BioProject
Taxonomy Links for Protein (Select 1023176007) (1)
Taxonomy
Taxonomy Links for Protein (Select 189008233) (1)
Taxonomy

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Nucleotide