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C5orf42 chromosome 5 open reading frame 42

Also known as: Hug; OFD6; JBTS17

Summary

The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]

Genomic context

Location:
5p13.2
Sequence:
Chromosome: 5; NC_000005.10 (37063928..37249428, complement)
Total number of exons:
60

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