about
P688
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesiaA Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE.PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery.PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum.
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Proline-rich transmembrane protein 2
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
Proline-rich transmembrane protein 2
@en
type
label
Proline-rich transmembrane protein 2
@en
altLabel
DSPB3
@en
Prrt2
@en
dispanin subfamily B member 3
@en
proline-rich transmembrane protein 2
@en
prefLabel
Proline-rich transmembrane protein 2
@en
P637
P680
P681
P682
P705
P352
P31
P352
P637
NP_001096033
XP_017167769
XP_030098823
XP_030098824
P681
P682
P702
P703
P705
ENSMUSP00000124520
ENSMUSP00000143833
ENSMUSP00000144042
ENSMUSP00000144451