CG5902 - uncharacterized protein
Is expressed in organism. Human ortholog(s) of this gene implicated in midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis. Orthologous to human AMMECR1 (AMMECR nuclear protein 1) and AMMECR1L (AMMECR1 like). [provided by Alliance of Genome Resources, Dec 2024]
NCBI Orthologs
How was this calculated?genes for:
Protein alignment
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Species | Gene | Architecture | aa |
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