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Aliases for PHOX2A Gene

Aliases for PHOX2A Gene

  • Paired Like Homeobox 2a 2 3 5
  • Aristaless Homeobox Protein Homolog 3 4
  • ARIX1 Homeodomain Protein 3 4
  • Paired-Like Homeobox 2A 3 4
  • PMX2A 3 4
  • ARIX 3 4
  • Aristaless (Drosophila) Homeobox, Aristaless Homeobox (Drosophila), Fibrosis Of Extraocular Muscles, Congenital, 2, Autosomal Recessive 2
  • Paired-Like (Aristaless) Homeobox 2a 2
  • Paired Mesoderm Homeobox Protein 2A 3
  • Aristaless Homeobox Homolog 3
  • Arix Homeodomain Protein 3
  • CFEOM2 3
  • NCAM2 3
  • FEOM2 3

External Ids for PHOX2A Gene

Previous HGNC Symbols for PHOX2A Gene

  • ARIX
  • FEOM2

Previous GeneCards Identifiers for PHOX2A Gene

  • GC11M073490
  • GC11M072172
  • GC11M071676
  • GC11M071627
  • GC11M071950
  • GC11M068243

Summaries for PHOX2A Gene

Entrez Gene Summary for PHOX2A Gene

  • The protein encoded by this gene contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system. It regulates the expression of tyrosine hydroxylase and dopamine beta-hydroxylase, two catecholaminergic biosynthetic enzymes essential for the differentiation and maintenance of the noradrenergic neurotransmitter phenotype. The encoded protein has also been shown to regulate transcription of the alpha3 nicotinic acetylcholine receptor gene. Mutations in this gene have been associated with autosomal recessive congenital fibrosis of the extraocular muscles. [provided by RefSeq, Jul 2008]

GeneCards Summary for PHOX2A Gene

PHOX2A (Paired Like Homeobox 2a) is a Protein Coding gene. Diseases associated with PHOX2A include Fibrosis Of Extraocular Muscles, Congenital, 2 and Tukel Syndrome. Among its related pathways are Sudden Infant Death Syndrome (SIDS) Susceptibility Pathways. GO annotations related to this gene include transcription factor activity, sequence-specific DNA binding and RNA polymerase II regulatory region sequence-specific DNA binding. An important paralog of this gene is PHOX2B.

UniProtKB/Swiss-Prot for PHOX2A Gene

  • May be involved in regulating the specificity of expression of the catecholamine biosynthetic genes. Acts as a transcription activator/factor. Could maintain the noradrenergic phenotype.

Gene Wiki entry for PHOX2A Gene

Additional gene information for PHOX2A Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for PHOX2A Gene

Genomics for PHOX2A Gene

Regulatory Elements for PHOX2A Gene

Enhancers for PHOX2A Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH11H072143 1.3 Ensembl ENCODE dbSUPER 10.4 +101.0 100956 2 RB1 BATF RAD21 RFX5 SCRT2 ZNF143 FOS ATF7 RUNX3 CREM FOLR3 NUMA1 LOC100128494 IL18BP ZNF705E ANAPC15 LAMTOR1 LRTOMT PHOX2A RNF121
GH11H071991 1.4 FANTOM5 Ensembl ENCODE 9.6 +254.0 253989 1 PKNOX1 TBL1XR1 BACH1 BMI1 BATF YY1 EED ATF7 ETV6 RUNX3 FOLR3 LRTOMT NUMA1 RNF121 LOC100133315 PHOX2A OR7E128P IL18BP PIR62264
GH11H072037 1.3 ENCODE dbSUPER 9.9 +204.8 204815 6 HDGF PKNOX1 FOXA2 ATF1 MLX ARID4B SIN3A FEZF1 YY1 ZNF121 LRTOMT NUMA1 FAM86C1 LOC100128494 LAMTOR1 ANAPC15 FOLR3 IL18BP RNF121 PHOX2A
GH11H072413 1.2 Ensembl ENCODE 10.3 -168.7 -168695 1 HDGF PKNOX1 ATF1 FOXA2 ARID4B DMAP1 ZNF2 ZNF143 ATF7 RUNX3 LOC100128494 ZNF705E NUMA1 PHOX2A ENSG00000256403 CLPB
GH11H071962 1.3 Ensembl ENCODE dbSUPER 9.2 +282.7 282721 1 BMI1 BATF ATF7 RUNX3 CREM IKZF2 CEBPB JUNB ZNF217 SP1 RNF121 LOC100128494 NUMA1 LOC100133315 ZNF705E LRTOMT ANAPC15 LAMTOR1 PHOX2A FAM86C1
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around PHOX2A on UCSC Golden Path with GeneCards custom track

Genomic Location for PHOX2A Gene

Chromosome:
11
Start:
72,239,077 bp from pter
End:
72,245,664 bp from pter
Size:
6,588 bases
Orientation:
Minus strand

Genomic View for PHOX2A Gene

Genes around PHOX2A on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
PHOX2A Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for PHOX2A Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for PHOX2A Gene

Proteins for PHOX2A Gene

  • Protein details for PHOX2A Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    O14813-PHX2A_HUMAN
    Recommended name:
    Paired mesoderm homeobox protein 2A
    Protein Accession:
    O14813
    Secondary Accessions:
    • A8K3N0
    • Q8IVZ2

    Protein attributes for PHOX2A Gene

    Size:
    284 amino acids
    Molecular mass:
    29653 Da
    Quaternary structure:
    No Data Available

neXtProt entry for PHOX2A Gene

Post-translational modifications for PHOX2A Gene

  • Modification sites at PhosphoSitePlus
  • Modification sites at neXtProt

Other Protein References for PHOX2A Gene

ENSEMBL proteins:
REFSEQ proteins:

Antibody Products

  • Abcam antibodies for PHOX2A

No data available for DME Specific Peptides for PHOX2A Gene

Domains & Families for PHOX2A Gene

Gene Families for PHOX2A Gene

HGNC:
Human Protein Atlas (HPA):
  • Disease related genes
  • Predicted intracellular proteins
  • Transcription factors

Suggested Antigen Peptide Sequences for PHOX2A Gene

GenScript: Design optimal peptide antigens:

Graphical View of Domain Structure for InterPro Entry

O14813

UniProtKB/Swiss-Prot:

PHX2A_HUMAN :
  • Belongs to the paired homeobox family.
Family:
  • Belongs to the paired homeobox family.
genes like me logo Genes that share domains with PHOX2A: view

Function for PHOX2A Gene

Molecular function for PHOX2A Gene

UniProtKB/Swiss-Prot Function:
May be involved in regulating the specificity of expression of the catecholamine biosynthetic genes. Acts as a transcription activator/factor. Could maintain the noradrenergic phenotype.

Gene Ontology (GO) - Molecular Function for PHOX2A Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000977 RNA polymerase II regulatory region sequence-specific DNA binding IDA 16280598
GO:0003677 DNA binding IEA --
GO:0003700 transcription factor activity, sequence-specific DNA binding NAS 8661014
GO:0043565 sequence-specific DNA binding IEA --
genes like me logo Genes that share ontologies with PHOX2A: view
genes like me logo Genes that share phenotypes with PHOX2A: view

Human Phenotype Ontology for PHOX2A Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for PHOX2A Gene

MGI Knock Outs for PHOX2A:

Animal Model Products

CRISPR Products

Targeted motifs for PHOX2A Gene
HOMER Transcription Factor Regulatory Elements motif PHOX2A
  • Consensus sequence: YTAATYNRATTA Submotif: canonical Cell Type: Neuron GEO ID: GSE31456

Inhibitory RNA Products

Clone Products

  • Applied Biological Materials Clones for PHOX2A
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

No data available for Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog and Transcription Factor Targets for PHOX2A Gene

Localization for PHOX2A Gene

Subcellular locations from UniProtKB/Swiss-Prot for PHOX2A Gene

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for PHOX2A gene
Compartment Confidence
nucleus 5
cytoskeleton 1

Subcellular locations from the

Human Protein Atlas (HPA)
  • Nuclear membrane (2)
  • Nucleus (2)
  • Vesicles (2)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for PHOX2A Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000790 nuclear chromatin IDA 16280598
GO:0005634 nucleus IEA --
genes like me logo Genes that share ontologies with PHOX2A: view

Pathways & Interactions for PHOX2A Gene

genes like me logo Genes that share pathways with PHOX2A: view

Pathways by source for PHOX2A Gene

SIGNOR curated interactions for PHOX2A Gene

Is inactivated by:

Gene Ontology (GO) - Biological Process for PHOX2A Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0003357 noradrenergic neuron differentiation NAS 16280598
GO:0006351 transcription, DNA-templated IEA --
GO:0006355 regulation of transcription, DNA-templated IEA --
GO:0021523 somatic motor neuron differentiation IEA --
GO:0021623 oculomotor nerve formation IEA --
genes like me logo Genes that share ontologies with PHOX2A: view

Drugs & Compounds for PHOX2A Gene

(3) Drugs for PHOX2A Gene - From: Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
genes like me logo Genes that share compounds with PHOX2A: view

Transcripts for PHOX2A Gene

mRNA/cDNA for PHOX2A Gene

Unigene Clusters for PHOX2A Gene

Paired-like homeobox 2a:
Representative Sequences:

CRISPR Products

Inhibitory RNA Products

Clone Products

  • Applied Biological Materials Clones for PHOX2A
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

Alternative Splicing Database (ASD) splice patterns (SP) for PHOX2A Gene

No ASD Table

Relevant External Links for PHOX2A Gene

GeneLoc Exon Structure for
PHOX2A
ECgene alternative splicing isoforms for
PHOX2A

Expression for PHOX2A Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for PHOX2A Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for PHOX2A Gene

This gene is overexpressed in Adrenal Gland (x15.2), Colon - Sigmoid (x9.1), Esophagus - Muscularis (x5.7), and Esophagus - Gastroesophageal Junction (x5.1).

Protein differential expression in normal tissues from HIPED for PHOX2A Gene

This gene is overexpressed in Monocytes (54.6) and Adipocyte (14.4).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, and MOPED for PHOX2A Gene



Protein tissue co-expression partners for PHOX2A Gene

NURSA nuclear receptor signaling pathways regulating expression of PHOX2A Gene:

PHOX2A

SOURCE GeneReport for Unigene cluster for PHOX2A Gene:

Hs.731115

Evidence on tissue expression from TISSUES for PHOX2A Gene

  • Nervous system(4.5)

Phenotype-based relationships between genes and organs from Gene ORGANizer for PHOX2A Gene

Germ Layers:
  • ectoderm
  • mesoderm
Systems:
  • digestive
  • integumentary
  • nervous
  • skeletal muscle
  • skeleton
Organs:
Head and neck:
  • brain
  • cranial nerve
  • eye
  • eyelid
  • face
  • forehead
  • head
  • lip
  • skull
Thorax:
  • chest wall
  • rib
  • rib cage
  • sternum
Pelvis:
  • pelvis
  • rectum
Limb:
  • digit
  • finger
  • foot
  • hand
  • lower limb
  • toe
  • upper limb
General:
  • hair
  • peripheral nervous system
  • skin
  • spinal column
  • vertebrae
genes like me logo Genes that share expression patterns with PHOX2A: view

Primer Products

No data available for mRNA Expression by UniProt/SwissProt for PHOX2A Gene

Orthologs for PHOX2A Gene

This gene was present in the common ancestor of animals.

Orthologs for PHOX2A Gene

Organism Taxonomy Gene Similarity Type Details
dog
(Canis familiaris)
Mammalia PHOX2A 33 34
  • 93.08 (n)
chimpanzee
(Pan troglodytes)
Mammalia PHOX2A 34
  • 93 (a)
OneToOne
cow
(Bos Taurus)
Mammalia PHOX2A 33 34
  • 92.96 (n)
mouse
(Mus musculus)
Mammalia Phox2a 33 16 34
  • 91.19 (n)
rat
(Rattus norvegicus)
Mammalia Phox2a 33
  • 90.48 (n)
oppossum
(Monodelphis domestica)
Mammalia PHOX2A 34
  • 75 (a)
OneToOne
lizard
(Anolis carolinensis)
Reptilia -- 34
  • 35 (a)
ManyToMany
tropical clawed frog
(Silurana tropicalis)
Amphibia phox2a 33
  • 67.64 (n)
zebrafish
(Danio rerio)
Actinopterygii phox2a 33 34
  • 70.16 (n)
fruit fly
(Drosophila melanogaster)
Insecta PHDP 34
  • 34 (a)
OneToMany
worm
(Caenorhabditis elegans)
Secernentea ceh-17 34
  • 34 (a)
OneToMany
Species where no ortholog for PHOX2A was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • chicken (Gallus gallus)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • platypus (Ornithorhynchus anatinus)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for PHOX2A Gene

ENSEMBL:
Gene Tree for PHOX2A (if available)
TreeFam:
Gene Tree for PHOX2A (if available)

Paralogs for PHOX2A Gene

Paralogs for PHOX2A Gene

(6) SIMAP similar genes for PHOX2A Gene using alignment to 3 proteins:

genes like me logo Genes that share paralogs with PHOX2A: view

Variants for PHOX2A Gene

Sequence variations from dbSNP and Humsavar for PHOX2A Gene

SNP ID Clin Chr 11 pos Sequence Context AA Info Type
rs104894269 Pathogenic, Fibrosis of extraocular muscles, congenital, 2 (CFEOM2) [MIM:602078] 72,243,790(-) CTCGG(C/T)AGGTG reference, missense
rs886038557 Likely benign 72,243,769(-) CGGCC(A/C)AACCC intron-variant
rs140850664 Benign 72,244,023(+) GGGGG(C/T)GGGGG utr-variant-5-prime
rs182932220 Benign 72,243,849(+) GAGCC(A/G)AGCGC reference, synonymous-codon
rs1000006533 -- 72,245,809(+) GAGTG(A/C)GCCTC upstream-variant-2KB

Structural Variations from Database of Genomic Variants (DGV) for PHOX2A Gene

Variant ID Type Subtype PubMed ID
esv26290 CNV loss 19812545
nsv1069605 CNV deletion 25765185
nsv555405 CNV loss 21841781
nsv951038 CNV deletion 24416366

Variation tolerance for PHOX2A Gene

Gene Damage Index Score: 2.47; 43.31% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for PHOX2A Gene

Human Gene Mutation Database (HGMD)
PHOX2A
SNPedia medical, phenotypic, and genealogical associations of SNPs for
PHOX2A

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for PHOX2A Gene

Disorders for PHOX2A Gene

MalaCards: The human disease database

(17) MalaCards diseases for PHOX2A Gene - From: HGMD, OMIM, ClinVar, GeneTests, Orphanet, Swiss-Prot, DISEASES, Novoseek, and GeneCards

Disorder Aliases PubMed IDs
fibrosis of extraocular muscles, congenital, 2
  • congenital fibrosis of the extraocular muscles 2
tukel syndrome
  • congenital fibrosis of the extraocular muscles
phox2a-related congenital fibrosis of the extraocular muscles
brown syndrome
  • brown tendon sheath syndrome
hypotropia
- elite association - COSMIC cancer census association via MalaCards

UniProtKB/Swiss-Prot

PHX2A_HUMAN
  • Fibrosis of extraocular muscles, congenital, 2 (CFEOM2) [MIM:602078]: A congenital ocular motility disorder marked by restrictive ophthalmoplegia affecting extraocular muscles innervated by the oculomotor and/or trochlear nerves. It is clinically characterized by anchoring of the eyes in downward gaze, ptosis, and backward tilt of the head. Congenital fibrosis of extraocular muscles type 2 may result from the defective development of the oculomotor (nIII), trochlear (nIV) and abducens (nVI) cranial nerve nuclei. {ECO:0000269 PubMed:11600883}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Relevant External Links for PHOX2A

Genetic Association Database (GAD)
PHOX2A
Human Genome Epidemiology (HuGE) Navigator
PHOX2A
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
PHOX2A
genes like me logo Genes that share disorders with PHOX2A: view

No data available for Genatlas for PHOX2A Gene

Publications for PHOX2A Gene

  1. Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. (PMID: 15240857) Weese-Mayer DE … Marazita ML (Pediatric research 2004) 3 22 45 60
  2. A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2). (PMID: 14597037) Yazdani A … Traboulsi EI (American journal of ophthalmology 2003) 3 22 45 60
  3. Molecular analysis of congenital central hypoventilation syndrome. (PMID: 14566559) Sasaki A … Hayasaka K (Human genetics 2003) 3 4 22 60
  4. Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2. (PMID: 11600883) Nakano M … Engle EC (Nature genetics 2001) 2 3 4 60
  5. Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13. (PMID: 8661014) Johnson KR … Lewis EJ (Genomics 1996) 2 3 4 60

Products for PHOX2A Gene

Sources for PHOX2A Gene

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