Growth failure in early childhood
Gene: SRCAPEnsemblGeneIds (GRCh38): ENSG00000080603
EnsemblGeneIds (GRCh37): ENSG00000080603
OMIM: 611421, Gene2Phenotype
SRCAP is in 7 panels
2 reviews
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 SRCAP should be included on the panel. Therefore kept rating as Green.Created: 30 May 2019, 9:34 a.m.
Ivone Leong (Genomics England Curator)
This gene is part of a consensus list for SRS/SRS-like testing provided by Frederic Brioude. Suggested initial gene rating: Green; Evidence for inclusion: none given; Evidence for exclusion: none given; Technical notes (e.g. non-coding/CNV mutations requiring coverage?): none given; Phenotypes: Floating HarborCreated: 14 May 2019, 1:25 p.m.
Phenotypes
Floating Harbor
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert list
- Expert Review Green
- Phenotypes
-
- Floating-Harbor syndrome, OMIM:136140
- OMIM
- 611421
- Clinvar variants
- Variants in SRCAP
- Penetrance
- None
- Panels with this gene
History Filter Activity
Set Phenotypes
Arina Puzriakova (Genomics England Curator)Phenotypes for gene: SRCAP were changed from Floating Harbor; Floating-Harbor syndrome, 136140 to Floating-Harbor syndrome, OMIM:136140
Added New Source, Set Phenotypes
Ivone Leong (Genomics England Curator)Source Expert list was added to SRCAP. Added phenotypes Floating Harbor for gene: SRCAP
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: SRCAP was added gene: SRCAP was added to Growth failure in early childhood. Sources: Expert Review Green Mode of inheritance for gene: SRCAP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SRCAP were set to Floating-Harbor syndrome, 136140