MT-RNR2

GPTKB entity

Statements (34)
Predicate Object
gptkbp:instanceOf gptkb:gene
gptkbp:alsoKnownAs HUMANIN
MTRNR2
Mitochondrially encoded 16S rRNA
gptkbp:associatedWith gptkb:Leigh_syndrome
gptkb:MELAS_syndrome
mitochondrial disorders
gptkbp:discoveredIn 1981
gptkbp:encodes gptkb:16S_ribosomal_RNA
Humanin peptide
gptkbp:Entrez_Gene_ID 4549
ENSG00000210082
gptkbp:function involved in mitochondrial protein synthesis
component of mitochondrial ribosome
gptkbp:hasTranscript NR_003613.3
gptkbp:HGNC_ID 7453
https://www.w3.org/2000/01/rdf-schema#label MT-RNR2
gptkbp:Humanin_peptide implicated in Alzheimer's disease
neuroprotective properties
gptkbp:isTranscribedFrom gptkb:16S_rRNA
gptkbp:length 1559 nucleotides
gptkbp:locatedIn gptkb:mitochondrial_DNA
gptkbp:locatedOnChromosome gptkb:mitochondrial_chromosome
gptkbp:OMIM 516000
gptkbp:organism gptkb:Homo_sapiens
gptkbp:produces Humanin peptide
gptkbp:RefSeq gptkb:NC_012920.1
gptkbp:relatedTo aging
neuroprotection
apoptosis inhibition
gptkbp:strand heavy strand
gptkbp:UniProtID P0DP25
gptkbp:bfsParent gptkb:NC_012920
gptkbp:bfsLayer 8