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- Table of Contents
Facts about Paired mesoderm homeobox protein 2A.
Could maintain the noradrenergic phenotype. .
Human | |
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Gene Name: | PHOX2A |
Uniprot: | O14813 |
Entrez: | 401 |
Belongs to: |
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paired homeobox family |
aristaless (Drosophila) homeobox, aristaless homeobox (Drosophila), fibrosis ofextraocular muscles, congenital, 2, autosomal recessive; aristaless homeobox homolog; Aristaless homeobox protein homolog; arix homeodomain protein; ARIX1 homeodomain protein; ARIXNCAM2; CFEOM2MGC52227; paired mesoderm homeobox protein 2A; paired-like homeobox 2apaired-like (aristaless) homeobox 2a; PMX2AFEOM2
Mass (kDA):
29.653 kDA
Human | |
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Location: | 11q13.4 |
Sequence: | 11; NC_000011.10 (72239077..72244176, complement) |
Nucleus.
PMID: 8661014 by Johnson K.R., et al. Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13.
PMID: 11600883 by Nakano M., et al. Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.