Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10509
Gene name Gene Name - the full gene name approved by the HGNC.
Semaphorin 4B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SEMA4B
Synonyms (NCBI Gene) Gene synonyms aliases
SEMAC, SemC
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q26.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017490 hsa-miR-335-5p Microarray 18185580
MIRT051498 hsa-let-7e-5p CLASH 23622248
MIRT073414 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT073407 hsa-miR-20a-5p HITS-CLIP 22473208
MIRT073414 hsa-miR-106b-5p HITS-CLIP 22473208
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 33845483, 34232536, 36217030
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0007399 Process Nervous system development IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617029 10730 ENSG00000185033
Protein
UniProt ID Q9NPR2
Protein name Semaphorin-4B (Semaphorin-C)
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 72 505 Sema domain Family
PF01437 PSI 525 579 Plexin repeat Family
Sequence
MLRTAMGLRSWLAAPWGALPPRPPLLLLLLLLLLLQPPPPTWALSPRISLPLGSEERPFL
RFEAEHISNYTALLLSRDGRTLYVGAREALFALSSNLSFLPGGEYQELLWGADAEKKQQC
SFKGKDPQRDCQNYIKILLPLSGSHLFTCGTAAFSPMCTYINMENFTLARDEKGNVLLED
GKGRCPFDPNFKSTALVVDGELYTGTVSSFQGNDPAISRSQSLRPTKTESSLNWLQDPAF
VASAYIPESLGSLQGDDDKIYFFFSETGQEFEFFENTIVSRIARICKGDEGGERVLQQRW
TSFLKAQLLCSRPDDGFPFNVLQDVFTLSPSPQDWRDTLFYGVFTSQWHRGTTEGSAVCV
FTMKDVQRVFSGLYKEVNRETQQWYTVTHPVPTPRPGACITNSARERKINSSLQLPDRVL
NFLKDHFLMDGQVRSRMLLLQPQARYQRVAVHRVPGLHHTYDVLFLGTGDGRLHKAVSVG
PRVHIIEELQIFSSGQPVQNLLLDT
HRGLLYAASHSGVVQVPMANCSLYRSCGDCLLARD
PYCAWSGSSCKHVSLYQPQLATRPWIQDIEGASAKDLCS
ASSVVSPSFVPTGEKPCEQVQ
FQPNTVNTLACPLLSNLATRLWLRNGAPVNASASCHVLPTGDLLLVGTQQLGEFQCWSLE
EGFQQLVASYCPEVVEDGVADQTDEGGSVPVIISTSRVSAPAGGKASWGADRSYWKEFLV
MCTLFVLAVLLPVLFLLYRHRNSMKVFLKQGECASVHPKTCPVVLPPETRPLNGLGPPST
PLDHRGYQSLSDSPPGSRVFTESEKRPLSIQDSFVEVSPVCPRPRVRLGSEIRDSVV
Sequence length 837
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
Acne acne vulgaris N/A N/A GWAS
Frontal Fibrosing Alopecia Frontal fibrosing alopecia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Inhibit 36115854
Carcinoma Non Small Cell Lung Associate 24474252, 25095981
Carcinoma Renal Cell Associate 29968393
Cholangiocarcinoma Associate 36817485
Colorectal Neoplasms Associate 29197895
Crohn Disease Associate 36817485
Hypoxia Inhibit 24474252
Inflammation Associate 37173738
Lung Neoplasms Associate 24474252
Lymphatic Metastasis Inhibit 36115854