HLCS

On this page, you will find information about a genetic change that was identified in a UDN participant. We are trying to find others with the same or similar condition.

Sharing information on this website is not a requirement of UDN participation. Only descriptions about participants who give explicit consent will appear here.

A heterozygous change in the HLCS gene was identified in a UDN participant with decline in language and memory (cognitive regression), sudden muscle jerks (myoclonus), and increased muscle tone in lower limbs (limb hypertonia)

Date of Report

Mar 20, 2023

Full Name

holocarboxylase synthetase

Location

Chromosome 21 (21q22.13)

Function

The HLCS gene links biotin to propionyl-CoA carboxylase, pyruvate carboxylase, alpha-methylcrotonyl-CoA carboxylase and acetyl-CoA carboxylase (Suzuki et al., 1994).

Database Links

GeneCards: HLCS

MedlinePlus Genetics: HLCS

NCBI Gene: 3141

OMIM: 609018

UniProtKB/Swiss-Prot: P50747

Clinical Significance

A heterozygous change in this gene was identified in a UDN participant. Research is underway to see if this change is causing symptoms in this participant.

Gene HLCS

Inheritance Pattern Autosomal recessive

Position (hg19) chr21:g.38139542G>A

Transcript NM_000411.8

DNA Change c.1496C>T

Protein Change p.Ala499Val

Contact Us

Interested in learning more about this gene or sharing what you know? Contact us!