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Gene : HYLS1 Homo sapiens

Name  ? HYLS1 centriolar and ciliogenesis associated Cytological Location  11q24.2
Brief Description  HYLS1 centriolar and ciliogenesis associated
Description  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]
  • synonyms:
  • OTTHUMG00000165858,
  • HGNC:26558,
  • AK057477,
  • HLS,
  • uc009zbv.4,
  • hydrolethalus syndrome 1,
  • FLJ32915,
  • HYLS1,
  • NM_145014
  • identifiers:
  • 219844,
  • ENSG00000198331,
  • HYLS1

Genome feature

Region: gene ? Length: 17033  
Location: 11:125883614-125900646 Cyto location: 11q24.2


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

914 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results