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Inborn errors of metabolism

Gene: CLPS

Red List (low evidence)

CLPS (colipase)
EnsemblGeneIds (GRCh38): ENSG00000137392
EnsemblGeneIds (GRCh37): ENSG00000137392
OMIM: 120105, Gene2Phenotype
CLPS is in 2 panels

1 review

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

Not associated with phenotype in OMIM or G2P. No variants reported.
Created: 23 Feb 2017, 5:12 p.m.

Mode of inheritance
Unknown

Phenotypes
Pancreatic colipase deficiency (Other disorders of lipid and lipoprotein metabolism)

Publications

Details

Mode of Inheritance
Unknown
Sources
  • London North GLH
  • NHS GMS
Phenotypes
  • Pancreatic colipase deficiency (Other disorders of lipid and lipoprotein metabolism)
OMIM
120105
Clinvar variants
Variants in CLPS
Penetrance
None
Publications
Panels with this gene

History Filter Activity

13 Feb 2019, Gel status: 1

Added New Source, Added New Source

Ivone Leong (Genomics England Curator)

Source NHS GMS was added to CLPS. Source London North GLH was added to CLPS.

8 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Sarah Leigh: Associated with phenotype in O

16 Dec 2018, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: CLPS was added gene: CLPS was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: CLPS was set to Unknown Publications for gene: CLPS were set to 27604308 Phenotypes for gene: CLPS were set to Pancreatic colipase deficiency (Other disorders of lipid and lipoprotein metabolism)