about
P688
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeSporadic and familial blepharophimosis -ptosis-epicanthus inversus syndrome: FOXL2 mutation screen and MRI study of the superior levator eyelid muscleFOXL2 mutation screening in a large panel of POF patients and XX malesSumoylation of forkhead L2 by Ubc9 is required for its activity as a transcriptional repressor of the Steroidogenic Acute Regulatory geneTranscriptional factor FOXL2 interacts with DP103 and induces apoptosisEvolution and expression of FOXL2FOXL2 activates P450 aromatase gene transcription: towards a better characterization of the early steps of mammalian ovarian development
P921
Q24290819-E5328269-44CF-4961-8D64-9DA4AA7390CCQ24297553-927B4178-72CC-42C6-8372-51730A246F82Q24303685-F87658EE-0EE6-4A14-A7B7-54CD1C49E202Q24315137-3E91D518-EFA9-4ED6-9EAF-2205D42501D2Q24321909-0C164364-73A9-4FFE-ADE1-271A5BF6B401Q24324373-D2D3E825-B334-4AD5-94F1-6E00363A699BQ24337775-01DF4DA5-8840-4769-9E94-1585CF70C2B9
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Forkhead box L2
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Forkhead box L2
@en
Forkhead box L2
@nl
type
label
Forkhead box L2
@en
Forkhead box L2
@nl
altLabel
FOXL2
@en
P-Frk
@en
Pituitary forkhead factor
@en
forkhead box protein L2
@en
forkhead transcription factor FOXL2
@en
prefLabel
Forkhead box L2
@en
Forkhead box L2
@nl
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ENSP00000497217