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  2. Congenital diaphragmatic hernia
  3. SLIT3
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Congenital diaphragmatic hernia

Gene: SLIT3

Amber List (moderate evidence)
SLIT3 (slit guidance ligand 3)
EnsemblGeneIds (GRCh38): ENSG00000184347
EnsemblGeneIds (GRCh37): ENSG00000184347
OMIM: 603745, Gene2Phenotype
SLIT3 is in 3 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

I don't know

Two affected individuals, single family, supportive mouse model.
Sources: Literature
Created: 21 Jun 2021, 7:53 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Congenital diaphragmatic hernia

Publications

Created: 21 Jun 2021, 7:53 a.m.

Panel version: 0.80

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Congenital diaphragmatic hernia
OMIM
603745
Clinvar variants
Variants in SLIT3
Penetrance
None
Publications
Panels with this gene

History Filter Activity

21 Jun 2021, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: slit3 has been classified as Amber List (Moderate Evidence).

21 Jun 2021, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: slit3 has been classified as Amber List (Moderate Evidence).

21 Jun 2021, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: SLIT3 was added gene: SLIT3 was added to Congenital diaphragmatic hernia. Sources: Literature Mode of inheritance for gene: SLIT3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SLIT3 were set to 33933663 Phenotypes for gene: SLIT3 were set to Congenital diaphragmatic hernia Review for gene: SLIT3 was set to AMBER