HYLS1
Sign in to saveAlso known as HLS, HYLS1, centriolar and ciliogenesis associated, HYLS1 centriolar and ciliogenesis associated
Hydrolethalus syndrome protein 1 is a protein that in humans is encoded by the HYLS1 gene.
Gene data
HYLS1- Name
- HYLS1 centriolar and ciliogenesis associated
- Type
- protein-coding
- Aliases
- HLS
This gene encodes a protein localized to the cytoplasm. Mutations in this gene are associated with hydrolethalus syndrome. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2008].
via MyGene.info
Gene · Ensembl
HYLS1 centriolar and ciliogenesis associated
- Symbol
- HYLS1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 11:125,883,614-125,900,846
- Strand
- Forward (+)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 9 more facts
- HomoloGene ID
- 82283
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/219844
- genomic end
- 125900646
- genomic start
- 125753509
- chromosome
- human chromosome 11
- cytogenetic location
- 11q24.2
- expressed in
- ganglionic eminence
- genetic association
- hydrolethalus syndrome
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Function
- Clinical significance
- References
- Further reading
Hydrolethalus syndrome protein 1 is a protein that in humans is encoded by the HYLS1 gene.
== Function ==
Excerpted from Wikipedia’s “HYLS1” article, available under the CC BY-SA 4.0 licence.