about
P688
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephalyIdentification and characterization of multiple novel Rab-myosin Va interactionsLoss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
RAB39B, member RAS oncogene family
@en
RAB39B, member RAS oncogene family
@nl
type
label
RAB39B, member RAS oncogene family
@en
RAB39B, member RAS oncogene family
@nl
altLabel
RAB39B
@en
Waisman syndrome (basal ganglion disorder with mental retardation)
@en
Waisman syndrome
@en
ras-related protein Rab-39B
@en
prefLabel
RAB39B, member RAS oncogene family
@en
RAB39B, member RAS oncogene family
@nl
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ENSP00000358466