about
P527
P688
FAM20A mutations can cause enamel-renal syndrome (ERS).Novel FAM20A mutations in hypoplastic amelogenesis imperfectaAutosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A geneWhole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndromeNephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsSecreted kinase phosphorylates extracellular proteins that regulate biomineralizationA secretory kinase complex regulates extracellular protein phosphorylation
P921
Q21144895-A9874D6F-DD4F-4BB9-B641-2703AD70BFA9Q24293129-D239E4B1-5F97-4CB8-A97A-D8D207B921FEQ24293486-A965CCC6-4D9F-4B7F-8E5A-417888526420Q24301630-B4BB8289-DE69-4DD8-ABFA-0281385DDB47Q24319733-05C9804B-87A8-4FB9-A75F-F38A123B4E13Q24321933-884C397C-035E-4B1D-B1F2-47BE8694A923Q24323147-24A47356-3EB1-4FCC-AABE-D62B8810049E
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in FAM20A, golgi associated secretory pathway pseudokinase
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
FAM20A golgi associated secretory pathway pseudokinase
@en
FAM20A golgi associated secretory pathway pseudokinase
@nl
type
label
FAM20A golgi associated secretory pathway pseudokinase
@en
FAM20A golgi associated secretory pathway pseudokinase
@nl
altLabel
FAM20A
@en
family with sequence similarity 20, member A
@en
protein FAM20A
@en
pseudokinase FAM20A
@en
prefLabel
FAM20A golgi associated secretory pathway pseudokinase
@en
FAM20A golgi associated secretory pathway pseudokinase
@nl
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NP_001230675
XP_006722022
XP_011523220
XP_016880270
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P682
P702
P703
P705
ENSP00000464910
ENSP00000467884
ENSP00000468308
ENSP00000481085