Growth failure in early childhood
Gene: CREBBPEnsemblGeneIds (GRCh38): ENSG00000005339
EnsemblGeneIds (GRCh37): ENSG00000005339
OMIM: 600140, Gene2Phenotype
CREBBP is in 18 panels
1 review
Rebecca Foulger (Genomics England curator)
Following discussion with members of the Endocrine Specialist Group at the Webex call on 23.05.19, it was agreed that this gene was outside the scope of this clinical indication. Therefore demoted gene from Green to Red.Created: 30 May 2019, 9:49 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Red
- Phenotypes
-
- Rubenstein Taybi
- OMIM
- 600140
- Clinvar variants
- Variants in CREBBP
- Penetrance
- None
- Panels with this gene
-
- Ectodermal dysplasia
- Early onset or syndromic epilepsy
- Sarcoma cancer susceptibility
- Skeletal dysplasia
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Structural eye disease
- Monogenic short stature
- Familial Hirschsprung Disease
- Severe microcephaly
- Familial rhabdomyosarcoma
- Sarcoma susceptibility
- Osteogenesis imperfecta
- Intellectual disability
- IUGR and IGF abnormalities
- DDG2P
- Glaucoma (developmental)
- Fetal anomalies
- Radial dysplasia
History Filter Activity
Added New Source, Status Update
Rebecca Foulger (Genomics England curator)Source Expert Review Red was added to CREBBP. Rating Changed from Green List (high evidence) to Red List (low evidence)
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: CREBBP was added gene: CREBBP was added to Growth failure in early childhood. Sources: Expert Review Green Mode of inheritance for gene: CREBBP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: CREBBP were set to Rubenstein Taybi