about
P688
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humansArx is required for normal enteroendocrine cell development in mice and humansHigh-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathiesThe simultaneous loss of Arx and Pax4 genes promotes a somatostatin-producing cell fate specification at the expense of the alpha- and beta-cell lineages in the mouse endocrine pancreasA regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARXArx homeobox gene is essential for development of mouse olfactory systemInactivation of Arx, the murine ortholog of the X-linked lissencephaly with ambiguous genitalia gene, leads to severe disorganization of the ventral telencephalon with impaired neuronal migration and differentiation
P921
Q28207647-D62BFCFB-A2A7-4168-993B-12B19F074B49Q28506459-07E7968A-D11E-40A7-ADDC-CFC9D35E0BF7Q28506691-EE04A004-62FF-4208-93F7-2154DDF985C5Q28507673-3D00CC99-8970-4875-AB40-BE7E77A397AFQ28508740-70AB92BA-3407-43DB-896D-59C8C9991313Q28589047-42E1F13B-57CA-4AC6-BAF2-26F4E98E90F7Q28591633-7C8D1B2F-5DC0-4C41-B42D-E69F738FAB7C
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Aristaless related homeobox
@nl
protèin
@ace
protéine
@fr
بروتين في فأر المنازل
@ar
name
Aristaless related homeobox
@en
type
label
Aristaless related homeobox
@en
altLabel
Aristaless-related homeobox
@en
Arx
@en
homeobox protein ARX
@en
prefLabel
Aristaless related homeobox
@en
P527
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NP_001292869
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ENSMUSP00000049039
ENSMUSP00000109580