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B9D1

Official Full Name
B9 domain containing 1
Organism
Homo sapiens
GeneID
27077
Background
This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]
Synonyms
B9; MKS9; EPPB9; MKSR1; JBTS27; MKSR-1;

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