about
sameAs
P688
Identification of a dominant negative homeodomain mutation in Rieger syndromeDominant negative dimerization of a mutant homeodomain protein in Axenfeld-Rieger syndromePituitary dwarfism in the R271W Pit-1 gene mutationStructure and regulation of the human growth hormone-releasing hormone receptor geneThe molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activitiesCharacterization of the gene encoding human pituitary-specific transcription factor, Pit-1Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD
P921
Q24291120-E193AA36-258F-4B4D-9ECA-CB6D4CB47026Q24296487-82C74080-B510-4838-8E8D-8C62E9CB64CBQ24311746-23D0CCC0-775C-49A5-8DA4-FBE362BECD8FQ24313531-32B8F78D-2757-4ACC-A12E-4FFB8F4B5814Q24318726-F0F7AA8F-219A-472B-8DDD-7341F7DB1704Q28116081-37783A90-95A8-4065-9F46-7EEBD5CE4541Q28118827-28B00D2E-28A5-438F-8559-1290501720CB
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in POU class 1 homeobox 1
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
POU class 1 homeobox 1
@en
POU class 1 homeobox 1
@nl
type
label
POU class 1 homeobox 1
@en
POU class 1 homeobox 1
@nl
altLabel
GHF-1
@en
POU domain, class 1, transcription factor 1
@en
POU1F1
@en
growth hormone factor 1
@en
pituitary transcript factor 1
@en
pituitary-specific positive transcription factor 1
@en
prefLabel
POU class 1 homeobox 1
@en
POU class 1 homeobox 1
@nl
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NP_001116229
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D12.776.260.655.750
D12.776.930.710.750
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ENSP00000263781
ENSP00000342931
ENSP00000452610
ENSP00000454072