Genes in panel
STRs in panel
Prev Next

Skeletal dysplasia

Gene: WISP3

Green List (high evidence)

WISP3 (WNT1 inducible signaling pathway protein 3)
EnsemblGeneIds (GRCh38): ENSG00000112761
EnsemblGeneIds (GRCh37): ENSG00000112761
OMIM: 603400, Gene2Phenotype
WISP3 is in 5 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Comment when marking as ready: HGNC approved name CCN6
Created: 3 May 2020, 3:45 a.m. | Last Modified: 3 May 2020, 3:45 a.m.
Panel Version: 0.19

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Arthropathy, progressive pseudorheumatoid, of childhood 208230
  • Spondyloepiphyseal dysplasia tarda with progressive arthropathy 208230
Tags
new gene name
OMIM
603400
Clinvar variants
Variants in WISP3
Penetrance
None
Panels with this gene

History Filter Activity

3 May 2020, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: wisp3 has been classified as Green List (High Evidence).

3 May 2020, Gel status: 3

Added Tag

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Tag new gene name tag was added to gene: WISP3.

17 Dec 2019, Gel status: 3

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: WISP3 was added gene: WISP3 was added to Skeletal dysplasia. Sources: NHS GMS,Expert Review Green Mode of inheritance for gene: WISP3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: WISP3 were set to Arthropathy, progressive pseudorheumatoid, of childhood 208230; Spondyloepiphyseal dysplasia tarda with progressive arthropathy 208230