Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7869
Gene name Gene Name - the full gene name approved by the HGNC.
Semaphorin 3B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SEMA3B
Synonyms (NCBI Gene) Gene synonyms aliases
LUCA-1, SEMA5, SEMAA, SemA, semaV
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p21.31
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the class-3 semaphorin/collapsin family, whose members function in growth cone guidance during neuronal development. This family member inhibits axonal extension and has been shown to act as a tumor suppressor b
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016807 hsa-miR-335-5p Microarray 18185580
MIRT1334623 hsa-miR-1178 CLIP-seq
MIRT1334624 hsa-miR-150 CLIP-seq
MIRT1334625 hsa-miR-1915 CLIP-seq
MIRT1334626 hsa-miR-3120-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001755 Process Neural crest cell migration IBA
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IEA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005783 Component Endoplasmic reticulum TAS 8633026
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601281 10724 ENSG00000012171
Protein
UniProt ID Q13214
Protein name Semaphorin-3B (Sema A(V)) (Semaphorin-V) (Sema V)
Protein function Inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01403 Sema 57 495 Sema domain Family
PF00047 ig 577 657 Immunoglobulin domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed abundantly but differentially in a variety of neural and nonneural tissues.
Sequence
Sequence length 749
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Axon guidance  
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Insomnia Insomnia N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Rheumatoid Inhibit 38283352
Breast Neoplasms Inhibit 18922901, 36123344
Breast Neoplasms Associate 32867770, 35990656
Calcinosis Cutis Stimulate 18458115
Carcinogenesis Associate 31217417
Carcinoma Hepatocellular Associate 20532728
Carcinoma Non Small Cell Lung Associate 20521346
Carcinoma Ovarian Epithelial Associate 39519394
Endometrial Neoplasms Inhibit 21933904
Endometrial Neoplasms Associate 31217417