Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6585
Gene name Gene Name - the full gene name approved by the HGNC.
Slit guidance ligand 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLIT1
Synonyms (NCBI Gene) Gene synonyms aliases
MEGF4, SLIL1, SLIT-1, SLIT3
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q24.1
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding NAS 9813312
GO:0005515 Function Protein binding IPI 32296183
GO:0005615 Component Extracellular space IBA 21873635
GO:0005615 Component Extracellular space NAS 9813312
GO:0007097 Process Nuclear migration IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603742 11085 ENSG00000187122
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Bipolar Disorder Bipolar Disorder GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Ulcerative colitis Ulcerative colitis GWAS
Glioblastoma Glioblastoma CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 GWAS, CBGDA
Associations from Text Mining
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