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PLCB1

PLCB1

Protein-coding gene in the species Homo sapiens

5-bisphosphate phospholipase beta-1 is an enzyme that in humans is encoded by the PLCB1 gene. The protein encoded by this gene catalyzes the formation of inositol

PLCB1

Phospholipase C

Class of enzymes

differential splicing such that a mammal may have up to 30 PLC enzymes. beta: PLCB1, PLCB2, PLCB3, PLCB4 gamma: PLCG1, PLCG2 delta: PLCD1, PLCD3, PLCD4 epsilon:

Phospholipase C

Phospholipase_C

Ohtahara syndrome

Medical condition

CDKL5, SLC25A22, STXBP1, SPTAN1, KCNQ2, ARHGEF9, PCDH19, PNKP, SCN2A, PLCB1, SCN8A, ST3GAL3, TBC1D24, BRAT1 and likely others. Less often, the root

Ohtahara syndrome

Ohtahara_syndrome

Malignant migrating partial seizures in infancy

Medical condition

of the KCNT1 gene has shown to be associated. Another gene implicated is PLCB1. MMPSI is diagnosed based on signs, symptoms, and electroencephalogram (EEG)

Malignant migrating partial seizures in infancy

Malignant_migrating_partial_seizures_in_infancy

TRPM7

Protein-coding gene in the species Homo sapiens

intracellular ATP and by the kinase mutants. TRPM7 has been shown to interact with PLCB1 and PLCB2. Patients with pathogenic variants in the TRPM7 gene suffer from

TRPM7

Phosphoinositide phospholipase C

Protein family

localization sequences. PLC-η has been implicated in neuronal functioning. PLCB1; PLCB2; PLCB3; PLCB4; PLCD1; PLCD3; PLCD4; PLCE1; PLCG1; PLCG2; PLCH1; PLCH2;

Phosphoinositide phospholipase C

Phosphoinositide_phospholipase_C

List of human protein-coding genes 6

Q6P1J6 12277 PLBD1 HGNC:26215; Q6P4A8 12278 PLBD2 HGNC:27283; Q8NHP8 12279 PLCB1 HGNC:15917; Q9NQ66 12280 PLCB2 HGNC:9055; Q00722 12281 PLCB3 HGNC:9056;

List of human protein-coding genes 6

List_of_human_protein-coding_genes_6

C2 domain

Protein domain

PIK3C2A; PIK3C2B; PIK3C2G; PLA2G4A; PLA2G4B; PLA2G4D; PLA2G4E; PLA2G4F; PLCB1; PLCB2; PLCB3; PLCB4; PLCD1; PLCD3; PLCD4; PLCE1; PLCG1; PLCG2; PLCH1; PLCH2;

C2 domain