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SEMA4A

Semaphorin-4A is a protein that in humans is encoded by the SEMA4A gene.[1][2]

Function

Function

SEMA4A is a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in guidance of axonal migration during neuronal development and in immune responses.[supplied by OMIM][2]

Clinical significance

Clinical significance

A germline variant in SEMA4A (V78M) has been demonstrated to confer risk for colorectal cancer type X.[3]

References

References

  1. Püschel AW, Adams RH, Betz H (Jun 1995). “Murine semaphorin D/collapsin is a member of a diverse gene family and creates domains inhibitory for axonal extension”. Neuron. 14 (5): 941–8. doi:10.1016/0896-6273(95)90332-1. PMID 7748561.
  2. 2.0 2.1 “Entrez Gene: SEMA4A sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A”.
  3. Schulz E, Klampfl P, Holzapfel S, Janecke AR, Ulz P, Renner W, Kashofer K, Nojima S, Leitner A, Zebisch A, Wölfler A, Hofer S, Gerger A, Lax S, Beham-Schmid C, Steinke V, Heitzer E, Geigl JB, Windpassinger C, Hoefler G, Speicher MR, Richard Boland C, Kumanogoh A, Sill H (Oct 2014). “Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X.” Nature Communications. 5: 5191. doi:10.1038/ncomms6191. PMC 4214414. PMID 25307848.
Further reading

Further reading


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