XB-FEAT-953026: Difference between revisions
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=Summary for human DYNC2I2 from NCBI= | =Summary for human DYNC2I2 from NCBI= | ||
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Defects in this gene are a cause of short-rib thoracic dysplasia 11 with or without polydactyly. [provided by RefSeq, Mar 2014] | |||
Latest revision as of 12:41, 10 June 2020
dync2i2
This is the community wiki page for the gene dync2i2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
2020/06/04 Human symbol has changed for genepage ID: 953026 From wdr34 to dync2i2
Human name has changed for for genepage ID 943583 From WD repeat domain 34 to dynein 2 intermediate chain 2
Summary for human DYNC2I2 from NCBI
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Defects in this gene are a cause of short-rib thoracic dysplasia 11 with or without polydactyly. [provided by RefSeq, Mar 2014]