B9D1, B9 domain containing 1

B9D1, B9 domain containing 1

• 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]

• Gene Synonyms (B9, EPPB9, JBTS27, MKS9, MKSR-1, MKSR1, B9 domain-containing protein 1, B9 protein domain 1, MKS1-related protein 1, endothelial precursor protein B9,)
• NCBI Gene ID: 27077
• Species: Homo sapiens (Human)
• UNIPROT ID#>>B4DN64
  UNIPROT ID#>>I3L2R1
  UNIPROT ID#>>A8MYG7
  UNIPROT ID#>>Q9UPM9
  UNIPROT ID#>>A8MTX4
  UNIPROT ID#>>A0A0B4J223
  UNIPROT ID#>>B4DEW0
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

B9 domain containing 1 interacts with:

• B9 domain containing 2
  coenzyme Q6, monooxygenase
  coiled-coil and C2 domain containing 2A
  inversin
  MKS transition zone complex subunit 1
  phosducin like 3
  transmembrane protein 17
  transmembrane protein 231

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.