Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
401
Gene name Gene Name - the full gene name approved by the HGNC.
Paired like homeobox 2A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PHOX2A
Synonyms (NCBI Gene) Gene synonyms aliases
ARIX, CFEOM2, FEOM2, NCAM2, PMX2A
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.4
Summary Summary of gene provided in NCBI Entrez 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 tyr
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs104894269 G>A Pathogenic Missense variant, coding sequence variant
rs1178102382 C>G,T Pathogenic Splice acceptor variant
rs1590729541 C>T Pathogenic Splice donor variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023218 hsa-miR-122-5p Microarray 19296470
MIRT025054 hsa-miR-181a-5p Microarray 17612493
MIRT530891 hsa-miR-3936 PAR-CLIP 22012620
MIRT530890 hsa-miR-6782-5p PAR-CLIP 22012620
MIRT530889 hsa-miR-3158-5p PAR-CLIP 22012620
Transcription factors
Transcription factor Regulation Reference
HAND2 Activation 16280598
PHOX2B Unknown 15888479
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IDA 16280598
GO:0000785 Component Chromatin ISA
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IBA
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IDA 16280598
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602753 691 ENSG00000165462
Protein
UniProt ID O14813
Protein name Paired mesoderm homeobox protein 2A (ARIX1 homeodomain protein) (Aristaless homeobox protein homolog) (Paired-like homeobox 2A)
Protein 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.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00046 Homeodomain 91 147 Homeodomain Domain
Sequence
MDYSYLNSYDSCVAAMEASAYGDFGACSQPGGFQYSPLRPAFPAAGPPCPALGSSNCALG
ALRDHQPAPYSAVPYKFFPEPSGLHEKRKQRRIRTTFTSAQLKELERVFAETHYPDIYTR
EELALKIDLTEARVQVWFQNRRAKFRK
QERAASAKGAAGAAGAKKGEARCSSEDDDSKES
TCSPTPDSTASLPPPPAPGLASPRLSPSPLPVALGSGPGPGPGPQPLKGALWAGVAGGGG
GGPGAGAAELLKAWQPAESGPGPFSGVLSSFHRKPGPALKTNLF
Sequence length 284
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Fibrosis Of Extraocular Muscles fibrosis of extraocular muscles, congenital, 2 rs1590729541, rs1178102382 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
congenital fibrosis of the extraocular muscles Associate 15747768, 31541710
Fibrosis Of Extraocular Muscles Congenital 2 Associate 24940936
fourth cranial nerve palsy familial congenital Associate 14736788, 16049556, 18323871
Muscle Neoplasms Associate 14736788
Muscular Atrophy Associate 16049556
Neuroblastoma Associate 20957039, 26902400
Precancerous Conditions Associate 28767682
Retinal Diseases Associate 24940936
Strabismus Associate 24940936
Trochlear Nerve Diseases Associate 14736788