Gene Gene information from NCBI Gene database.
Entrez ID 6405
Gene name Semaphorin 3F
Gene symbol SEMA3F
Synonyms (NCBI Gene)
SEMA-IVSEMA4SEMAK
Chromosome 3
Chromosome location 3p21.31
Summary This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin loop and a C-terminal basic do
miRNA miRNA information provided by mirtarbase database.
188
miRTarBase ID miRNA Experiments Reference
MIRT519572 hsa-miR-5011-5p HITS-CLIP 23313552
MIRT697191 hsa-miR-3145-3p HITS-CLIP 23313552
MIRT519571 hsa-miR-190a-3p HITS-CLIP 23313552
MIRT519569 hsa-miR-6083 HITS-CLIP 23313552
MIRT519570 hsa-miR-1277-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
44
GO ID Ontology Definition Evidence Reference
GO:0001755 Process Neural crest cell migration IBA
GO:0005102 Function Signaling receptor binding IEA
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space TAS 8786119
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601124 10728 ENSG00000001617
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q13275
Protein name Semaphorin-3F (Sema III/F) (Semaphorin IV) (Sema IV)
Protein function May play a role in cell motility and cell adhesion.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01403 Sema 59 527 Sema domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed abundantly but differentially in a variety of neural and nonneural tissues. There is high expression in mammary gland, kidney, fetal brain, and lung and lower expression in heart and liver.
Sequence
MLVAGLLLWASLLTGAWPSFPTQDHLPATPRVRLSFKELKATGTAHFFNFLLNTTDYRIL
LKDEDHDRMYVGSKDYVLSLDLHDINREPLIIHWAASPQRIEECVLSGKDVNGECGNFVR
LIQPWNRTHLYVCGTGAYNPMCTYVNRGRRAQATPWTQTQAVRGRGSRATDGALRPMPTA
PRQDYIFYLEPERLESGKGKCPYDPKLDTASALINEELYAGVYIDFMGTDAAIFRTLGKQ
TAMRTDQYNSRWLNDPSFIHAELIPDSAERNDDKLYFFFRERSAEAPQSPAVYARIGRIC
LNDDGGHCCLVNKWSTFLKARLVCSVPGEDGIETHFDELQDVFVQQTQDVRNPVIYAVFT
SSGSVFRGSAVCVYSMADIRMVFNGPFAHKEGPNYQWMPFSGKMPYPRPGTCPGGTFTPS
MKSTKDYPDEVINFMRSHPLMYQAVYPLQRRPLVVRTGAPYRLTTIAVDQVDAADGRYEV
LFLGTDRGTVQKVIVLPKDDQELEELMLEEVEVFKDPAPVKTMTISS
KRQQLYVASAVGV
THLSLHRCQAYGAACADCCLARDPYCAWDGQACSRYTASSKRRSRRQDVRHGNPIRQCRG
FNSNANKNAVESVQYGVAGSAAFLECQPRSPQATVKWLFQRDPGDRRREIRAEDRFLRTE
QGLLLRALQLSDRGLYSCTATENNFKHVVTRVQLHVLGRDAVHAALFPPLSMSAPPPPGA
GPPTPPYQELAQLLAQPEVGLIHQYCQGYWRHVPPSPREAPGAPRSPEPQDQKKPRNRRH
HPPDT
Sequence length 785
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Axon guidance  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
118
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely benign rs374308618 RCV005933241
Cervical cancer Likely benign rs374355347 RCV005933435
Familial cancer of breast Likely benign rs200014361 RCV005933498
Hearing impairment Uncertain significance rs1399111219 RCV001375120
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 39232098
Breast Neoplasms Associate 26784191
Calcinosis Cutis Inhibit 20388805
Carcinogenesis Associate 26722466, 30696738, 32297576, 39232098
Carcinoma Adenoid Cystic Associate 28961428
Colorectal Neoplasms Associate 25193853, 33109776
Colorectal Neoplasms Inhibit 26722466
Disease Inhibit 31215376
Endometrial Neoplasms Inhibit 21933904
Endometrial Neoplasms Associate 31215376, 32297576