1. Gene
  2. SLIT1 - slit guidance ligand 1 Gene

SLIT1 - slit guidance ligand 1 Gene

Homo sapiens

Also known as MEGF4; SLIL1; SLIT3; SLIT-1

Gene ID: 6585 | Gene type: protein coding

About SLIT1

Cytogenetic location: 10q24.1 Genomic coordinates (GRCh38): 10:96,998,038-97,185,959 (from NCBI)

This gene has 7 transcripts (splice variants), 255 orthologues and 25 paralogues. Biased expression in brain (RPKM 15.8) and thyroid (RPKM 1.3).

Summary

Enables Roundabout binding activity. Involved in axon extension involved in axon guidance; motor neuron axon guidance; and negative chemotaxis. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

SLIT1 Products(1)

mRNA Protein Name
NM_003061.3 NP_003052.2 slit homolog 1 protein precursor
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables Roundabout binding IPI
IPI: Inferred from physical interaction
15207848 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
21653829 GOA
Biological Process GO Annotation Evidence Reference Source
involved in axon extension involved in axon guidance IDA
IDA: Inferred from direct assay
16840550 GOA
involved in axon guidance IDA
IDA: Inferred from direct assay
11748139 GOA
NOT involved in chemorepulsion involved in embryonic olfactory bulb interneuron precursor migration IDA
IDA: Inferred from direct assay
11748139 GOA
involved in motor neuron axon guidance IMP
IMP: Inferred from mutant phenotype
16162649 GOA
involved in negative chemotaxis IDA
IDA: Inferred from direct assay
11748139 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLIT1 Protein Structure

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (33 - 60)

LRR_8

LRR_8: Leucine rich repeat (62 - 121)

LRR_8

LRR_8: Leucine rich repeat (159 - 217)

LRRCT

LRRCT: Leucine rich repeat C-terminal domain (239 - 264)

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (282 - 308)

LRR_8

LRR_8: Leucine rich repeat (334 - 393)

LRRCT

LRRCT: Leucine rich repeat C-terminal domain (464 - 488)

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (513 - 539)

LRR_4

LRR_4: Leucine Rich repeats (2 copies) (544 - 581)

LRR_8

LRR_8: Leucine rich repeat (590 - 649)

LRRCT

LRRCT: Leucine rich repeat C-terminal domain (695 - 720)

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (733 - 760)

LRR_8

LRR_8: Leucine rich repeat (786 - 844)

LRRCT

LRRCT: Leucine rich repeat C-terminal domain (891 - 915)

EGF

EGF: EGF-like domain (929 - 959)

EGF

EGF: EGF-like domain (1047 - 1079)

EGF

EGF: EGF-like domain (1087 - 1116)

Laminin_G_2

Laminin_G_2: Laminin G domain (1195 - 1322)

hEGF

hEGF: Human growth factor-like EGF (1400 - 1412)

hEGF

hEGF: Human growth factor-like EGF (1442 - 1453)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1534 a.a.
Protein Preferred Names Protein Names

slit homolog 1 protein

multiple EGF-like domains protein 4

SLIT1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SLIT1 O75093 KRTAP10-8 Homo sapiens P60410 32296183
Intra
SLIT1 O75093 KRTAP10-8 Homo sapiens P60410 32296183
Intra
SLIT1 O75093 KRTAP10-8 Homo sapiens P60410 32296183
Intra
SLIT1 O75093 ADAMTSL4 Homo sapiens Q6UY14-3 32296183
Intra
SLIT1 O75093 ADAMTSL4 Homo sapiens Q6UY14-3 32296183
Intra
SLIT1 O75093 ADAMTSL4 Homo sapiens Q6UY14-3 32296183
Intra
SLIT1 O75093 KRTAP13-3 Homo sapiens Q3SY46 32296183
Intra
SLIT1 O75093 KRTAP13-3 Homo sapiens Q3SY46 32296183
Intra
SLIT1 O75093 KRTAP13-3 Homo sapiens Q3SY46 32296183
Intra
SLIT1 O75093 KRTAP13-2 Homo sapiens Q52LG2 32296183
Intra
SLIT1 O75093 KRTAP13-2 Homo sapiens Q52LG2 32296183
Intra
SLIT1 O75093 KRTAP13-2 Homo sapiens Q52LG2 32296183
Intra
SLIT1 O75093 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
SLIT1 O75093 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
SLIT1 O75093 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
SLIT1 O75093 CHRDL2 Homo sapiens Q6WN34-2 32296183
Intra
SLIT1 O75093 CHRDL2 Homo sapiens Q6WN34-2 32296183
Intra
SLIT1 O75093 CHRDL2 Homo sapiens Q6WN34-2 32296183
Intra
SLIT1 O75093 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
SLIT1 O75093 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
SLIT1 O75093 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
SLIT1 O75093 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
SLIT1 O75093 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
SLIT1 O75093 ZNF620 Homo sapiens Q6ZNG0 32296183
Intra
SLIT1 O75093 ZNF620 Homo sapiens Q6ZNG0 32296183
Intra
SLIT1 O75093 ZNF620 Homo sapiens Q6ZNG0 32296183
Intra
SLIT1 O75093 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
SLIT1 O75093 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
SLIT1 O75093 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
SLIT1 O75093 HOXA1 Homo sapiens P49639 32296183
Intra
SLIT1 O75093 HOXA1 Homo sapiens P49639 32296183
Intra
SLIT1 O75093 HOXA1 Homo sapiens P49639 32296183
Intra
SLIT1 O75093 HOXA1 Homo sapiens P49639 21653829
Intra
SLIT1 O75093 FHL5 Homo sapiens Q5TD97 32296183
Intra
SLIT1 O75093 FHL5 Homo sapiens Q5TD97 32296183
Intra
SLIT1 O75093 FHL5 Homo sapiens Q5TD97 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hepatic Adenomas, Familial

Hepatic Adenoma, Somatic

Familial Hepatic Adenoma

Familial Liver Cell Adenomas

Liver Cell Adenomas, Familial

Hepatic Adenomas Familial

HEPAF

Ha

Hepatocellular Adenomas

Hepatocellular Adenoma

Diaphragm Disease

Abnormality Of The Diaphragm

Disease Of Diaphragm

Diaphragmatic Disorder

Disorder Of Diaphragm

Diaphragmatic Hernia, Congenital

Congenital Diaphragmatic Hernia

Diaphragmatic Hernia

Cdh

Congenital Diaphragmatic Defect

Hernia, Diaphragmatic

Dih

Hernia, Congenital Diaphragmatic

Hcd

Diaphragmatic Defect, Congenital

Diaphragm, Unilateral Agenesis Of

Hemidiaphragm, Agenesis Of

Diaphragmatic Hernia 1

Agenesis Of Hemidiaphragm

Unilateral Agenesis Of Diaphragm

Hernia Diaphragmatic

Hernia Diaphragmatic Congenital

Hernia, Diaphragmatic, Type 1

Hiatus Hernia

Oesophageal Hiatus Hernia

Paraoesophageal Hernia

Sliding Hiatus Hernia

Congenital Diaphragm Hernia

Congenital Diaphragm Defect With Hernia

Gross Congenital Diaphragm Defect

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus SLIT1 VGNC VGNC:55971
Felis catus SLIT1 VGNC VGNC:107071
Rattus norvegicus SLIT1 RGD RGD:69307
Macaca mulatta SLIT1 VGNC VGNC:77643
Canis familiaris SLIT1 VGNC VGNC:53014
Mus musculus SLIT1 MGD MGI:1315203