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MAA microphthalmia or anophthalmia and associated anomalies [Homo sapiens (human)]

Gene Symbol MAA
Entrez Gene ID 4080
Full Name microphthalmia or anophthalmia and associated anomalies
Synonyms LZMS, MCOPS1
General protein information
Gene Type unknown
Organism Homo sapiens (human)


Summary lac of sum
Disorder MIM:


Disorder Html: Microphthalmia, syndromic 1 (2)

The following MAA gene sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the MAA gene which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.

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