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STRs in panel
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Inborn errors of metabolism

Gene: HYKK

Red List (low evidence)

HYKK (hydroxylysine kinase)
EnsemblGeneIds (GRCh38): ENSG00000188266
EnsemblGeneIds (GRCh37): ENSG00000188266
OMIM: 614681, Gene2Phenotype
HYKK is in 2 panels

1 review

Rebecca Foulger (Genomics England curator)

Red List (low evidence)

No phenotype associated with this gene
Created: 23 Feb 2017, 5:14 p.m.

Mode of inheritance
Unknown

Details

Mode of Inheritance
Unknown
Sources
  • London North GLH
  • NHS GMS
Phenotypes
  • Hydroxylysinuria (Disorders of histidine, tryptophan or lysine metabolism)
OMIM
614681
Clinvar variants
Variants in HYKK
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 HYKK. Source London North GLH was added to HYKK.

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: HYKK was added gene: HYKK was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: HYKK was set to Unknown Publications for gene: HYKK were set to 27604308 Phenotypes for gene: HYKK were set to Hydroxylysinuria (Disorders of histidine, tryptophan or lysine metabolism)