Health / Medical Topics |
PRKAR1A/RARA Fusion Gene
A fusion gene that results from a cryptic rearrangement of chromosome 17 which fuses the first 100 nucleotides of exon 3 of the PRKAR1A gene to exon 3 of the RARA gene. This rearrangement is associated with acute promyelocytic leukemia. (NCI Thesaurus)
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Human PRKAR1A wild-type allele is located within 17q23-q24 and is approximately 21 kb in length. This allele, which encodes cAMP-dependent protein kinase…
This gene plays a role in the regulation of protein kinase A.
Human PRKACG wild-type allele is located within 9q13 and is approximately 2 kb in length. This allele, which encodes cAMP-dependent protein kinase,…
This gene is involved in brain memory function, spermatogenesis and male gonad development.
Human PRKACB wild-type allele is located in the vicinity of 1p36.1 and is approximately 160 kb in length. This allele, which encodes…
This gene plays a role in the regulation of diverse cell processes including cell growth, proliferation, differentiation and motility.