SEMA5B
Summary: This gene encodes a member of the semaphorin protein family which regulates axon growth during development of the nervous system. The encoded protein has a characteristic Sema domain near the N-terminus, through which semaphorins bind to plexin, and five thrombospondin type 1 repeats in the C-terminal region of the protein. The protein product may be cleaved and exist as a secreted molecule (PMID: 19463192). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012].
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Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
---|---|---|---|---|---|
Namesemaphorin 5B OMIM IDMIM:609298 Ensembl IDEnsembl:ENSG00000082684 HGNC IDHGNC:HGNC:10737 PHARMGKB IDPA35659 Map Location3q21.1 |
GO terms in SEMA5B
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Term Type | Evidence Type | GO Term ID | GO Des. |
---|---|---|---|
MF | IBA | GO:0030215 | semaphorin receptor binding |
MF | IBA | GO:0045499 | chemorepellent activity |
BP | IBA | GO:0001755 | neural crest cell migration |
BP | IBA | GO:0030335 | positive regulation of cell migration |
BP | IEA | GO:0048675 | axon extension |
BP | IBA | GO:0048843 | negative regulation of axon extension involved in axon guidance |
Gene expression in normal tissue: SEMA5B
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in SEMA5B
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Database | Pathway ID | Pathway Des. |
---|---|---|
reactome | R-HSA-1643685 | Disease |
reactome | R-HSA-3781865 | Diseases of glycosylation |
reactome | R-HSA-3906995 | Diseases associated with O-glycosylation of proteins |
reactome | R-HSA-392499 | Metabolism of proteins |
reactome | R-HSA-5083635 | Defective B3GALTL causes Peters-plus syndrome (PpS) |
reactome | R-HSA-5173105 | O-linked glycosylation |
Gene-Drug: Aster Plot
Gene in drug-gene network: Network Plot

Gene-drug targets distribution
Gene Structure: PDB
Models in SEMA5B
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Model | Level | Reference ID | Tissue | Cancer | Drug | Clinical Response | Source | |
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No matching records found |