Variant ID | 29779 |
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Entrez Gene ID | 6586 |
Gene | SLIT3 (GeneCards) |
Location | hg19 5:168678421-168678421
hg38 5:169251417-169251417 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
Method | NextSeq500 |
Mutation(HGVS format) | NC_000005.9:g.168678421 G>A (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 1.2896 |
CADD Raw score (version 1.3) | 0.488623 (Deleterious) |
FATHMM raw prediction score | 0.95414 (Tolerated) |
Deleterious probability by DeFine | 0.8715 (Deleterious) |
Entrez Gene ID | 6586 (NCBI Gene) |
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Official Gene Symbol | SLIT3 (GeneCards) |
Number of variants in SLIT3 in this database | 11 (view all the variants) |
Full name | slit guidance ligand 3 |
Band | 5q34-q35.1 |
Other IDs | Vega: OTTHUMG00000130409 OMIM: 603745 HGNC: HGNC:11087 Ensembl: ENSG00000184347 |
Other names | MEGF5, SLIL2, SLIT1, slit2, Slit-3 |
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] |
Individual ID | 28867142.36 (view all the variants in this individual) |
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Pubmed ID | 28867142 |
Whose mosaic mutation | Male Patient |
Origin of mosaic mutation in patients | de novo |
Phenotype | 3 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
OMIM ID | 209850 |
Pubmed ID | 28867142 |
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Title | Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder |
Journal | American Journal of Human Genetics |
Publication date | 2017.08 |
Disease | Autism Spectrum Disorders |
Incidence | 0.01 |
Number of cases | cases of unknown sex: 247; |