Gene Gene information from NCBI Gene database.
Entrez ID 6585
Gene name Slit guidance ligand 1
Gene symbol SLIT1
Synonyms (NCBI Gene)
MEGF4SLIL1SLIT-1SLIT3
Chromosome 10
Chromosome location 10q24.1
miRNA miRNA information provided by mirtarbase database.
160
miRTarBase ID miRNA Experiments Reference
MIRT039395 hsa-miR-421 CLASH 23622248
MIRT653389 hsa-miR-4713-5p HITS-CLIP 23824327
MIRT636220 hsa-miR-1238-3p HITS-CLIP 23824327
MIRT653388 hsa-miR-629-3p HITS-CLIP 23824327
MIRT639917 hsa-miR-141-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
38
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding IEA
GO:0005509 Function Calcium ion binding NAS 9813312
GO:0005515 Function Protein binding IPI 21653829, 32296183
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603742 11085 ENSG00000187122
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75093
Protein name Slit homolog 1 protein (Slit-1) (Multiple epidermal growth factor-like domains protein 4) (Multiple EGF-like domains protein 4)
Protein function Thought to act as molecular guidance cue in cellular migration, and function appears to be mediated by interaction with roundabout homolog receptors. During neural development involved in axonal navigation at the ventral midline of the neural tu
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 281 308 Leucine rich repeat N-terminal domain Family
PF13855 LRR_8 309 369 Leucine rich repeat Repeat
PF13855 LRR_8 357 412 Leucine rich repeat Repeat
PF13855 LRR_8 381 441 Leucine rich repeat Repeat
PF01463 LRRCT 463 488 Leucine rich repeat C-terminal domain Family
PF13855 LRR_8 589 649 Leucine rich repeat Repeat
PF13855 LRR_8 613 673 Leucine rich repeat Repeat
PF01463 LRRCT 695 720 Leucine rich repeat C-terminal domain Family
PF01462 LRRNT 733 760 Leucine rich repeat N-terminal domain Family
PF13855 LRR_8 761 820 Leucine rich repeat Repeat
PF13855 LRR_8 808 868 Leucine rich repeat Repeat
PF01463 LRRCT 890 915 Leucine rich repeat C-terminal domain Family
PF00008 EGF 929 960 EGF-like domain Domain
PF00008 EGF 968 1001 EGF-like domain Domain
PF00008 EGF 1009 1039 EGF-like domain Domain
PF00008 EGF 1047 1079 EGF-like domain Domain
PF00008 EGF 1087 1117 EGF-like domain Domain
PF12661 hEGF 1136 1157 Human growth factor-like EGF Domain
PF02210 Laminin_G_2 1194 1322 Laminin G domain Domain
PF12661 hEGF 1347 1368 Human growth factor-like EGF Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in adult forebrain. Expressed in fetal brain, lung and kidney. {ECO:0000269|PubMed:9813312}.
Sequence
MALTPGWGSSAGPVRPELWLLLWAAAWRLGASACPALCTCTGTTVDCHGTGLQAIPKNIP
RNTERLELNGNNITRIHKNDFAGLKQLRVLQLMENQIGAVERGAFDDMKELERLRLNRNQ
L
HMLPELLFQNNQALSRLDLSENAIQAIPRKAFRGATDLKNLQLDKNQISCIEEGAFRAL
RGLEVLTLNNNNITTIPVSSFNHMPKLRTFRLHSNHL
FCDCHLAWLSQWLRQRPTIGLFT
QCSGPASLRGLNVAEVQKSEFSCS
GQGEAGRVPTCTLSSGSCPAMCTCSNGIVDCRGKGL
TAIPANLP
ETMTEIRLELNGIKSIPPGAFSPYRKLRRIDLSNNQIAEIAPDAFQGLRSLN
SLVLYGNKI
TDLPRGVFGGLYTLQLLLLNANKINCIRPDAFQDLQNLSLLSLYDNKIQSL
AKGTFTSLRAIQTLHLAQNPF
ICDCNLKWLADFLRTNPIETSGARCASPRRLANKRIGQI
KSKKFRCS
AKEQYFIPGTEDYQLNSECNSDVVCPHKCRCEANVVECSSLKLTKIPERIPQ
STAELRLNNNEISILEATGMFKKLTHLKKINLSNNKVSEIEDGAFEGAASVSELHLTANQ
LESIRSGMFRGL
DGLRTLMLRNNRISCIHNDSFTGLRNVRLLSLYDNQITTVSPGAFDTL
QSLSTLNLLANPF
NCNCQLAWLGGWLRKRKIVTGNPRCQNPDFLRQIPLQDVAFPDFRCE
EGQEEGGCLPRPQCPQECACLDTVVRCSNKHLRALPKGIPKNVTELYLDGNQFTLVPGQL
STFKYLQLVDLSNNKISSLSNSSFTNM
SQLTTLILSYNALQCIPPLAFQGLRSLRLLSLH
GNDISTLQEGIFADVTSLSHLAIGANPL
YCDCHLRWLSSWVKTGYKEPGIARCAGPQDME
GKLLLTTPAKKFECQ
GPPTLAVQAKCDLCLSSPCQNQGTCHNDPLEVYRCACPSGYKGRD
CEVSLDSCSSGPCENGGTCHAQEGEDAPFTCSCPTGFEGPTCGVNTDDCVDHACANGGVC
VDGVGNYTCQCPLQYEGKA
CEQLVDLCSPDLNPCQHEAQCVGTPDGPRCECMPGYAGDNC
SENQDDCRDHRCQNGAQCMDEVNSYSCLCAEGYSGQLCEIPPHLPAPKSPCEGTECQNGA
NCVDQGNRPVCQCLPGF
GGPECEKLLSVNFVDRDTYLQFTDLQNWPRANITLQVSTAEDN
GILLYNGDNDHIAVELYQGHVRVSYDPGSYPSSAIYSAETINDGQFHTVELVAFDQMVNL
SIDGGSPMTMDNFGKHYTLNSEAPLYVGGMPVDVNSAAFRLWQILNGTGFHGCIRNLYIN
NE
LQDFTKTQMKPGVVPGCEPCRKLYCLHGICQPNATPGPMCHCEAGWVGLHCDQPADGP
CHGHKCVHGQCVPLDALSYSCQCQDGYSGALCNQAGALAEPCRGLQCLHGHCQASGTKGA
HCVCDPGFSGELCEQESECRGDPVRDFHQVQRGYAICQTTRPLSWVECRGSCPGQGCCQG
LRLKRRKFTFECSDGTSFAEEVEKPTKCGCALCA
Sequence length 1534
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.
1
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Monomelic amyotrophy Likely pathogenic rs2493101808 RCV003224774
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 19114000
Coronary Artery Disease Associate 35793981
Developmental Disabilities Associate 32973238
Glioma Associate 35996510
Leukemia Myeloid Acute Associate 30820596
Neoplasms Associate 15534609
Parkinson Disease Associate 26961748
Pituitary Neoplasms Associate 33168897