MEGF8, multiple EGF like domains 8

MEGF8, multiple EGF like domains 8

• The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]

• Gene Synonyms (C19orf49, CRPT2, EGFL4, SBP1, multiple epidermal growth factor-like domains protein 8, EGF-like domain-containing protein 4, EGF-like-domain, multiple 4, HBV pre-S2-binding protein 1, HBV pre-s2 binding protein 1, epidermal growth factor-like protein 4, hepatitis B virus pre-S2-binding protein 1,)
• NCBI Gene ID: 1954
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q7Z7M0
• 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.

multiple EGF like domains 8 interacts with:

• ataxin 7
  F-box protein 6
  growth factor independent 1B transcriptional repressor
  mahogunin ring finger 1
  nuclear RNA export factor 1
  pregnancy specific beta-1-glycoprotein 1
  pregnancy specific beta-1-glycoprotein 3
  pregnancy specific beta-1-glycoprotein 8
  protein tyrosine phosphatase receptor type K
  ring finger protein 157
  tafazzin
  vir like m6A methyltransferase associated

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.