Homo sapiens Gene: HYLS1
Summary
InnateDB Gene IDBG-75678.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HYLS1
Gene Name hydrolethalus syndrome 1
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000198331
Encoded Proteins
hydrolethalus syndrome 1
hydrolethalus syndrome 1
hydrolethalus syndrome 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:125883614-125900648
Strand Forward strand
Band q24.2
Transcripts
ENST00000356438 ENSP00000348815
ENST00000425380 ENSP00000414884
ENST00000526028 ENSP00000436833
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005886 plasma membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q96M11
TrEMBL A0A024R3K0
UniProt Splice Variant
Entrez Gene 219844
UniGene Hs.98133
RefSeq NM_145014 NM_001134793 XM_005271430 XM_006718777 XM_006718778
HUGO HGNC:26558
OMIM 610693
CCDS CCDS8467
HPRD 08148
IMGT
EMBL AK057477 AK127394 AP000842 BC015047 CH471065
GenPept AAH15047 BAB71503 BAG54500 EAW67665 EAW67666
RNA Seq Atlas 219844