P688
MRI analysis of an inherited speech and language disorder: structural brain abnormalitiesStructure of the forkhead domain of FOXP2 bound to DNAA functional genetic link between distinct developmental language disordersInvestigating protein-protein interactions in live cells using bioluminescence resonance energy transfer[The FoxP2 gene makes humans speak and birds twitter].
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in FOXP2
@nl
protèin
@ace
protéine humaine
@fr
بروتين في الإنسان العاقل
@ar
name
FOXP2
@ca
FOXP2
@cy
FOXP2
@en-ca
FOXP2
@en-gb
FOXP2
@et
FOXP2
@eu
FOXP2
@fa
FOXP2
@fi
FOXP2
@ja
FOXP2
@nl
type
label
FOXP2
@ca
FOXP2
@cy
FOXP2
@en-ca
FOXP2
@en-gb
FOXP2
@et
FOXP2
@eu
FOXP2
@fa
FOXP2
@fi
FOXP2
@ja
FOXP2
@nl
altLabel
CAG repeat protein 44
@en
FOXP2
@en
Forkhead box protein P2
@fr
forkhead box protein P2
@en
forkhead/winged-helix transcription factor
@en
trinucleotide repeat containing 10
@en
trinucleotide repeat-containing gene 10 protein
@en
prefLabel
FOXP2
@ca
FOXP2
@cy
FOXP2
@en-ca
FOXP2
@en-gb
FOXP2
@et
FOXP2
@eu
FOXP2
@fa
FOXP2
@fi
FOXP2
@ja
FOXP2
@nl
P527
P637
P680
P682
P705
P352
P6366
P646
P2888
P31
P352
P6366
P637
NP_001166237
NP_001166238
XP_016868290
P646
P680
P681
P682
P702
P703
P705
ENSP00000265436
ENSP00000353367
ENSP00000367482
ENSP00000375084
ENSP00000377129
ENSP00000377130
ENSP00000377132
ENSP00000377133
ENSP00000377135
ENSP00000385069