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- Q14916248 subject Q8375682.
- Q14916248 abstract "PAX3 is a gene that belongs to the paired box (PAX) family of transcription factors. This gene was formerly known as splotch. PAX3 has been identified with ear, eye and facial development. Mutations in it can cause Waardenburg syndrome types 1 and 3. It is expressed in early embryonic phases in dermatomyotome of paraxial mesoderm which it helps to demarcate. In that way PAX3 contributes to early striated muscle development since all myoblasts are derived from dermatomyotome of paraxial mesoderm. Alternative splicing results in transcripts encoding isoforms with different C-termini.".
- Q14916248 entrezgene "5077".
- Q14916248 wikiPageExternalLink NBK1531.
- Q14916248 wikiPageWikiLink Q1108970.
- Q14916248 wikiPageWikiLink Q1129238.
- Q14916248 wikiPageWikiLink Q1151801.
- Q14916248 wikiPageWikiLink Q17928793.
- Q14916248 wikiPageWikiLink Q18029032.
- Q14916248 wikiPageWikiLink Q18029035.
- Q14916248 wikiPageWikiLink Q18031655.
- Q14916248 wikiPageWikiLink Q18252931.
- Q14916248 wikiPageWikiLink Q1898141.
- Q14916248 wikiPageWikiLink Q310425.
- Q14916248 wikiPageWikiLink Q3331437.
- Q14916248 wikiPageWikiLink Q3816207.
- Q14916248 wikiPageWikiLink Q407384.
- Q14916248 wikiPageWikiLink Q428914.
- Q14916248 wikiPageWikiLink Q8375682.
- Q14916248 wikiPageWikiLink Q896177.
- Q14916248 wikiPageWikiLink Q903869.
- Q14916248 type Biomolecule.
- Q14916248 type Protein.
- Q14916248 type Thing.
- Q14916248 type Q206229.
- Q14916248 type Q8054.
- Q14916248 comment "PAX3 is a gene that belongs to the paired box (PAX) family of transcription factors. This gene was formerly known as splotch. PAX3 has been identified with ear, eye and facial development. Mutations in it can cause Waardenburg syndrome types 1 and 3. It is expressed in early embryonic phases in dermatomyotome of paraxial mesoderm which it helps to demarcate.".
- Q14916248 label "PAX3".