SELENOH (selenoprotein H)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
280636
Gene name Gene Name - the full gene name approved by the HGNC.
Selenoprotein H
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SELENOH
Synonyms (NCBI Gene) Gene synonyms aliases
C11orf31, C17orf10, SELH
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q12.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a nucleolar protein, which belongs to the SelWTH family. It functions as an oxidoreductase, and has been shown to protect neurons against UVB-induced damage by inhibiting apoptotic cell death pathways, promote mitochondrial biogenesis an
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(12)
miRTarBase ID miRNA Experiments Reference
MIRT541624 hsa-miR-512-5p PAR-CLIP 21572407
MIRT541623 hsa-miR-510-5p PAR-CLIP 21572407
MIRT541621 hsa-miR-5690 PAR-CLIP 21572407
MIRT541622 hsa-miR-4768-3p PAR-CLIP 21572407
MIRT541620 hsa-miR-4459 PAR-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(2)
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22681889
GO:0005794 Component Golgi apparatus IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
607914 18251 ENSG00000211450
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q8IZQ5
Protein name Selenoprotein H (SelH)
Protein function May be involved in a redox-related process.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10262 Rdx 35 → 119 Rdx family Family
Sequence
Sequence length 122
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (1)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Schizophrenia Schizophrenia N/A N/A GWAS
Show/Hide Text Mining Associations (1)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Drug Hypersensitivity Associate 25336634