Recombinant fragment corresponding to Human FOXN4 aa 282-379.Sequence: MHKWKRKDLAAIHRSMANPEELDKLISDRPESCRRPGKPGEPEAPVLTHA TTVAVAHGCLAVSQLPPQPLMTLSLQSVPLHHQVQPQAHLAPDSPAPA Database link: Q96NZ1
FOXN4 (forkhead box N4) is a protein-coding gene. Diseases associated with FOXN4 include hallervorden-spatz syndrome, and retinitis. GO annotations related to this gene include double-stranded DNA binding and sequence-specific DNA binding. An important paralog of this gene is FOXN3.
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