Gene Gene information from NCBI Gene database.
Entrez ID 6586
Gene name Slit guidance ligand 3
Gene symbol SLIT3
Synonyms (NCBI Gene)
MEGF5SLIL2SLIT1Slit-3slit2
Chromosome 5
Chromosome location 5q34-q35.1
Summary The protein encoded by this gene is secreted, likely interacting with roundabout homolog receptors to effect cell migration. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
miRNA miRNA information provided by mirtarbase database.
19
miRTarBase ID miRNA Experiments Reference
MIRT053057 hsa-miR-218-2-3p ImmunohistochemistryLuciferase reporter assayqRT-PCRWestern blot 23720784
MIRT2109754 hsa-miR-362-5p CLIP-seq
MIRT2109755 hsa-miR-500b CLIP-seq
MIRT2109756 hsa-miR-501-5p CLIP-seq
MIRT2333092 hsa-miR-3667-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
42
GO ID Ontology Definition Evidence Reference
GO:0003180 Process Aortic valve morphogenesis IEA
GO:0003180 Process Aortic valve morphogenesis ISS
GO:0003181 Process Atrioventricular valve morphogenesis IEA
GO:0003181 Process Atrioventricular valve morphogenesis ISS
GO:0005509 Function Calcium ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603745 11087 ENSG00000184347
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75094
Protein name Slit homolog 3 protein (Slit-3) (Multiple epidermal growth factor-like domains protein 5) (Multiple EGF-like domains protein 5)
Protein function May act as molecular guidance cue in cellular migration, and function may be mediated by interaction with roundabout homolog receptors.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01462 LRRNT 33 60 Leucine rich repeat N-terminal domain Family
PF13855 LRR_8 61 121 Leucine rich repeat Repeat
PF13855 LRR_8 109 169 Leucine rich repeat Repeat
PF13855 LRR_8 157 217 Leucine rich repeat Repeat
PF01463 LRRCT 239 264 Leucine rich repeat C-terminal domain Family
PF01462 LRRNT 279 306 Leucine rich repeat N-terminal domain Family
PF13855 LRR_8 307 367 Leucine rich repeat Repeat
PF13855 LRR_8 331 391 Leucine rich repeat Repeat
PF01463 LRRCT 461 486 Leucine rich repeat C-terminal domain Family
PF13855 LRR_8 532 593 Leucine rich repeat Repeat
PF13855 LRR_8 581 641 Leucine rich repeat Repeat
PF13855 LRR_8 605 665 Leucine rich repeat Repeat
PF01463 LRRCT 687 712 Leucine rich repeat C-terminal domain Family
PF01462 LRRNT 724 751 Leucine rich repeat N-terminal domain Family
PF13855 LRR_8 752 811 Leucine rich repeat Repeat
PF13855 LRR_8 799 859 Leucine rich repeat Repeat
PF01463 LRRCT 881 906 Leucine rich repeat C-terminal domain Family
PF12661 hEGF 925 944 Human growth factor-like EGF Domain
PF00008 EGF 959 992 EGF-like domain Domain
PF00008 EGF 1000 1030 EGF-like domain Domain
PF00008 EGF 1038 1070 EGF-like domain Domain
PF00008 EGF 1078 1108 EGF-like domain Domain
PF00008 EGF 1123 1153 EGF-like domain Domain
PF02210 Laminin_G_2 1186 1314 Laminin G domain Domain
PF00008 EGF 1371 1401 EGF-like domain Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in thyroid. {ECO:0000269|PubMed:9813312}.
Sequence
MAPGWAGVGAAVRARLALALALASVLSGPPAVACPTKCTCSAASVDCHGLGLRAVPRGIP
RNAERLDLDRNNITRITKMDFAGLKNLRVLHLEDNQVSVIERGAFQDLKQLERLRLNKNK
L
QVLPELLFQSTPKLTRLDLSENQIQGIPRKAFRGITDVKNLQLDNNHISCIEDGAFRAL
RDLEILTLNNNNISRILVTSFNHMPKIRTLRLHSNHL
YCDCHLAWLSDWLRQRRTVGQFT
LCMAPVHLRGFNVADVQKKEYVCP
APHSEPPSCNANSISCPSPCTCSNNIVDCRGKGLME
IPANLP
EGIVEIRLEQNSIKAIPAGAFTQYKKLKRIDISKNQISDIAPDAFQGLKSLTSL
VLYGNKI
TEIVKGLFDGLVSLQLLLLNANKI
NCLRVNTFQDLQNLNLLSLYDNKLQTISK
GLFAPLQSIQTLHLAQNPFVCDCHLKWLADYLQDNPIETSGARCSSPRRLANKRISQIKS
KKFRCS
GSEDYRSRFSSECFMDLVCPEKCRCEGTIVDCSNQKLVRIPSHLPEYVTDLRLN
DNEVSVLEATGIFKKLPNLRKINLSNNKIKEVREGAFDGA
ASVQELMLTGNQLETVHGRV
FRGLSGLKTLMLRSNLIGCVSNDTFAGLSSVRLLSLYDNRITTITPGAFTTLVSLSTINL
LSNPF
NCNCHLAWLGKWLRKRRIVSGNPRCQKPFFLKEIPIQDVAIQDFTCDGNEESSCQ
LSPRCPEQCTCMETVVRCSNKGLRALPRGMPKDVTELYLEGNHLTAVPRELSALRHLTLI
DLSNNSISMLTNYTFSNM
SHLSTLILSYNRLRCIPVHAFNGLRSLRVLTLHGNDISSVPE
GSFNDLTSLSHLALGTNPL
HCDCSLRWLSEWVKAGYKEPGIARCSSPEPMADRLLLTTPT
HRFQCK
GPVDINIVAKCNACLSSPCKNNGTCTQDPVELYRCACPYSYKGKDCTVPINTCI
QNPCQHGGTCHLSDSHKDGFSCSCPLGFEGQR
CEINPDDCEDNDCENNATCVDGINNYVC
ICPPNYTGEL
CDEVIDHCVPELNLCQHEAKCIPLDKGFSCECVPGYSGKLCETDNDDCVA
HKCRHGAQCVDTINGYTCTCPQGFSGPF
CEHPPPMVLLQTSPCDQYECQNGAQCIVVQQE
PTCRCPPGFAGPR
CEKLITVNFVGKDSYVELASAKVRPQANISLQVATDKDNGILLYKGD
NDPLALELYQGHVRLVYDSLSSPPTTVYSVETVNDGQFHSVELVTLNQTLNLVVDKGTPK
SLGKLQKQPAVGINSPLYLGGIPTSTGLSALRQGTDRPLGGFHGCIHEVRINNE
LQDFKA
LPPQSLGVSPGCKSCTVCKHGLCRSVEKDSVVCECRPGWTGPLCDQEARDPCLGHRCHHG
KCVATGTSYMCKCAEGYGGDL
CDNKNDSANACSAFKCHHGQCHISDQGEPYCLCQPGFSG
EHCQQENPCLGQVVREVIRRQKGYASCATASKVPIMECRGGCGPQCCQPTRSKRRKYVFQ
CTDGSSFVEEVERHLECGCLACS
Sequence length 1523
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Axon guidance   Signaling by ROBO receptors
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
20
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Familial congenital diaphragmatic hernia Likely pathogenic rs926590189 RCV001281695
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ATOPIC ECZEMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION CTD, Disgenet, GWAS catalog
CTD, Disgenet, GWAS catalog
CTD, Disgenet, GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR II DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Adenocarcinoma of lung (disorder) Lung adenocarcinoma BEFREE 26045181
★☆☆☆☆
Found in Text Mining only
Adenoma of large intestine Colorectal adenoma BEFREE 24516561
★☆☆☆☆
Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 20298552 Associate
★☆☆☆☆
Found in Text Mining only
Atrial Fibrillation Atrial Fibrillation CTD_human_DG 29892015, 30061737
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Atrial Fibrillation Atrial Fibrillation GWASCAT_DG 30061737
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Bicuspid Aortic Valve Disease Bicuspid aortic valve Pubtator 36071494 Associate
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Bipolar disorder Pubtator 27112568 Associate
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Bipolar Disorder Bipolar Disorder GWASCAT_DG 28115744
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Breast Carcinoma Breast Carcinoma BEFREE 15534609
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 15534609, 36361532, 37178414 Associate
★☆☆☆☆
Found in Text Mining only