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FBXO7

FBXO7

Protein-coding gene in the species Homo sapiens

only protein 7 is a protein that in humans is encoded by the FBXO7 gene. Mutations in FBXO7 have been associated with Parkinson's disease. This gene encodes

FBXO7

List of human protein-coding genes 3

Q9UKT5 5522 FBXO5 HGNC:13584; Q9UKT4 5523 FBXO6 HGNC:13585; Q9NRD1 5524 FBXO7 HGNC:13586; Q9Y3I1 5525 FBXO8 HGNC:13587; Q9NRD0 5526 FBXO9 HGNC:13588;

List of human protein-coding genes 3

List_of_human_protein-coding_genes_3

PINK1

Protein-coding gene in the species Homo sapiens

Chu CT, Chen BB, Mallampalli RK (4 June 2020). "Chemical inhibition of FBXO7 reduces inflammation and confers neuroprotection by stabilizing the mitochondrial

PINK1

S-phase kinase-associated protein 1

Protein-coding gene in the species Homo sapiens

to interact with: BTRC, CACYBP, CDCA3, CDK9, CUL1, FBXL3, FBXO4, FBXO5, FBXO7, FBXW2, FBXW7, and SKP2. GRCh38: Ensembl release 89: ENSG00000113558 – Ensembl

S-phase kinase-associated protein 1

S-phase_kinase-associated_protein_1

Causes of Parkinson's disease

Factors causing Parkinson's disease

PINK1 (PARK6), PARK7 (DJ-1), ATP13A2 (PARK9), PLA2G6 (PARK14, IPLA2), FBXO7 (PARK15, FBX7), DNAJC6 (PARK19, DJC6), SYNJ1 (PARK20), and VPS13C (PARK23)

Causes of Parkinson's disease

Causes_of_Parkinson's_disease

List of OMIM disorder codes

disease 13; 610297; HTRA2 Parkinson disease 15, autosomal recessive; 260300; FBXO7 Parkinson disease 4; 605543; SNCA Parkinson disease 6, early onset; 605909;

List of OMIM disorder codes

List_of_OMIM_disorder_codes