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PHOX2A

PHOX2A

Protein-coding gene in humans

mesoderm homeobox protein 2A is a protein that in humans is encoded by the PHOX2A gene. The protein encoded by this gene contains a paired-like homeodomain

PHOX2A

Spinothalamic tract

Sensory pathway from the skin to the thalamus

Iain C.; Denk, Franziska; Todd, Andrew J. (2024). "Deep sequencing of Phox2a nuclei reveals five classes of anterolateral system neurons". Proceedings

Spinothalamic tract

Spinothalamic_tract

Phox

Topics referred to by the same term

refer to: Phox (band) PhoX, a proof assistant based on high order logic PHOX2A, a protein PHOX2B, a protein Phosphinooxazolines, a class of chiral ligands

Phox

List of human transcription factors

specific TF according to literature or domain structure – No motif [695] PHOX2A ENSG00000165462 Homeodomain Known motif – High-throughput in vitro [696]

List of human transcription factors

List_of_human_transcription_factors

Congenital fibrosis of the extraocular muscles

Medical condition

mutations in the KIF21A gene, while CFEOM2 is caused by mutations in the PHOX2A gene. CFEOM3 is caused by mutations in the TUBB3 gene. CFEOM was first named

Congenital fibrosis of the extraocular muscles

Congenital_fibrosis_of_the_extraocular_muscles

PHOX2B

Protein-coding gene in the species Homo sapiens

significant research into Phox2B and CCHS with Keep Me Breathing presenting, too. PHOX2A GRCh38: Ensembl release 89: ENSG00000109132 – Ensembl, May 2017 GRCm38:

PHOX2B

Homeobox

DNA pattern affecting anatomy development

NOBOX; OTP; OTX1, OTX2, CRX; PAX2, PAX3, PAX4, PAX5, PAX6, PAX7, PAX8; PHOX2A, PHOX2B; PITX1, PITX2, PITX3; PROP1; PRRX1, PRRX2; RAX, RAX2; RHOXF1, RHOXF2/2B;

Homeobox

PRDM12

Protein-coding gene in the species Homo sapiens

(2023-12-15). "Prdm12 represses the expression of the visceral neuron determinants Phox2a/b in developing somatosensory ganglia". iScience. 26 (12) 108364. doi:10

PRDM12

List of OMIM disorder codes

135700; KIF21A Fibrosis of extraocular muscles, congenital, 2; 602078; PHOX2A Fibrosis of extraocular muscles, congenital, 3A; 600638; TUBB3 Fibrosis

List of OMIM disorder codes

List_of_OMIM_disorder_codes

HAND2

Protein-coding gene in the species Homo sapiens

pathologies. HAND2 has been shown to interact with GATA4, NKX2.5, PPP2R5D, PHOX2A., TWIST1, and TWIST2. Hand2 interactions with TWIST1 and TWIST2 genes are

HAND2

List of human protein-coding genes 6

12092 PHOSPHO1 HGNC:16815; Q8TCT1 12093 PHOSPHO2 HGNC:28316; Q8TCD6 12094 PHOX2A HGNC:691; O14813 12095 PHOX2B HGNC:9143; Q99453 12096 PHPT1 HGNC:30033;

List of human protein-coding genes 6

List_of_human_protein-coding_genes_6

Soulless

Topics referred to by the same term

dictionary. Soulless may refer to: Soulless (gene), a historic name for PHOX2A, a human transcription factor Soulless (film), a 2012 film Soulless (album)

Soulless