SEMA4A

semaphorin 4A
OMIM: 607292, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Amber SEMA4A in Mendeliome


Version 1.3795

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Cone-rod dystrophy 10, 610283
  • Retinitis pigmentosa 35, 610282

Amber SEMA4A in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 0.225

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Royal Melbourne Hospital
    Phenotypes
    • Cone-rod dystrophy 10, 610283
    • Retinitis pigmentosa 35, 610282

    Green SEMA4A in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.111

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Cone-rod dystrophy 10, 610283 (3)

    Amber SEMA4A in Cone-rod Dystrophy


    Level 2: Ophthalmological disorders
    Version 0.58

    Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Royal Melbourne Hospital
    Phenotypes
    • Cone-rod dystrophy 10, 610283

    Red SEMA4A in Prepair 1000+


    Level 2: Screening
    Version 2.15

    3 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Mackenzie's Mission
    Phenotypes
    • Cone-rod dystrophy 10, 610283
    • Retinitis pigmentosa 35, 610282

    Red SEMA4A in Colorectal Cancer and Polyposis


    Level 2: Cancer Predisposition
    Version 1.4

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • ClinGen
    Phenotypes
    • Lynch syndrome, MONDO:0005835
    Tags
    • disputed