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PAX2

PAX2
Protein PAX2 PDB 1k78.png
Identifiers
Aliases PAX2, PAPRS, FSGS7, paired box 2
External IDs MGI: 97486 HomoloGene: 2968 GeneCards: PAX2
Gene location (Human)
Chromosome 10 (human)
Chr. Chromosome 10 (human)
Chromosome 10 (human)
Genomic location for PAX2
Genomic location for PAX2
Band 10q24.31 Start 100,735,603 bp
End 100,829,941 bp
RNA expression pattern
PBB GE PAX2 206229 x at fs.png

PBB GE PAX2 206228 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_011037

RefSeq (protein)

NP_035167

Location (UCSC) Chr 10: 100.74 – 100.83 Mb Chr 10: 44.76 – 44.84 Mb
PubMed search

NM_003989

NM_011037

NP_003981

NP_035167

Paired box gene 2, also known as PAX2 is a protein which in humans is encoded by the PAX2 gene.

The Pax Genes, or Paired-Box Containing Genes, play important roles in the development and proliferation of multiple cell lines, development of organs, and development and organization of the central nervous system. The transcription factor gene Pax2 is important in the regionalized embryological development of the central nervous system. In mammals, the brain is developed in three regions: the forebrain, midbrain, and the hindbrain. Concentration gradients of fibroblast growth factor 8 (FGF8) and Wingless-Type MMTV Integration Site Family, Member 1 (Wnt1) control expression of Pax2 during development of the Mesencephalon, or midbrain. Similar patterning during embryological development can be observed in “basal chordates or ascidians,” in which organization of the central nervous system in ascidian larvae are also controlled by fibroblast growth factor genes. The Pax2 gene encodes for the transcription factor which appears to be essential in the organization of the midbrain and hindbrain regions, and at the earliest can be detected on either side of the sulcus limitans, which separates motor and sensory nerve nuclei.


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