SEMA4A

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Semaphorin-4A is a protein that in humans is encoded by the SEMA4A gene.[5][6]

AliasesSEMA4A, CORD10, RP35, SEMAB, SEMB, semaphorin 4A
End156,177,752 bp[1]
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SEMA4A
Identifiers
AliasesSEMA4A, CORD10, RP35, SEMAB, SEMB, semaphorin 4A
External IDsOMIM: 607292; MGI: 107560; HomoloGene: 8425; GeneCards: SEMA4A; OMA:SEMA4A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001163489
NM_001163490
NM_001163491
NM_013658

RefSeq (protein)

NP_001156961
NP_001156962
NP_001156963
NP_038686

Location (UCSC)Chr 1: 156.15 – 156.18 MbChr 3: 88.34 – 88.37 Mb
PubMed search[3][4]
Wikidata
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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][6]

Clinical significance

A germline variant in SEMA4A (V78M) has been demonstrated to confer risk for colorectal cancer type X.[7]

Recently it has been identified as a novel therapeutic target in Multiple myeloma.[8]

References

Further reading

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