APOO (apolipoprotein O)

2014-08-01  

Identity

HGNC
LOCATION
Xp22.11
LOCUSID
ALIAS
FAM121B,MIC26,MICOS26,Mic23,My025
FUSION GENES

Other Information

Locus ID:

NCBI: 79135
MIM: 300753
HGNC: 28727
Ensembl: ENSG00000184831

Variants:

dbSNP: 79135
ClinVar: 79135
TCGA: ENSG00000184831
COSMIC: APOO

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000184831ENST00000379226Q9BUR5
ENSG00000184831ENST00000439528H7C1U8
ENSG00000184831ENST00000490078G3V1B6
ENSG00000184831ENST00000633372A0A0J9YXS4
ENSG00000184831ENST00000633432A0A0J9YXT7
ENSG00000184831ENST00000634086A0A0J9YWW6

Expression (GTEx)

0
5
10
15
20
25
30
35

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
376491612023A X-linked nonsense APOO/MIC26 variant causes a lethal mitochondrial disease with progeria-like phenotypes.0
376491612023A X-linked nonsense APOO/MIC26 variant causes a lethal mitochondrial disease with progeria-like phenotypes.0
355885782022Role of apolipoprotein O in autophagy via the p38 mitogen-activated protein kinase signaling pathway in myocardial infarction.1
355885782022Role of apolipoprotein O in autophagy via the p38 mitogen-activated protein kinase signaling pathway in myocardial infarction.1
324398082021Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features.19
324398082021Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features.19
327882262020MIC26 and MIC27 cooperate to regulate cardiolipin levels and the landscape of OXPHOS complexes.19
327882262020MIC26 and MIC27 cooperate to regulate cardiolipin levels and the landscape of OXPHOS complexes.19
300922692018Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases.29
300922692018Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases.29
257649792015The non-glycosylated isoform of MIC26 is a constituent of the mammalian MICOS complex and promotes formation of crista junctions.32
257649792015The non-glycosylated isoform of MIC26 is a constituent of the mammalian MICOS complex and promotes formation of crista junctions.32
247431512014Apolipoprotein O is mitochondrial and promotes lipotoxicity in heart.26
247431512014Apolipoprotein O is mitochondrial and promotes lipotoxicity in heart.26
243417432013Microarray analysis provides new insights into the function of apolipoprotein O in HepG2 cell line.6

Citation

Dessen P

APOO (apolipoprotein O)

Atlas Genet Cytogenet Oncol Haematol. 2014-08-01

Online version: http://atlasgeneticsoncology.org/gene/54131