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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 nameGene Name - the full gene name approved by the HGNC.
Selenoprotein H
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
SELENOH
SynonymsGene synonyms aliases
C11orf31, C17orf10, SELH
ChromosomeChromosome number
11
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q12.1
SummarySummary 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
miRNAmiRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22681889
GO:0005794 Component Golgi apparatus IBA 21873635
Other IDsOther 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
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
Associated diseases
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 28991256, 31268507, 25056061, 30285260, 26198764

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