ATP5ME

ATP synthase membrane subunit e, the group of Mitochondrial complex V: ATP synthase subunits

Basic information

Region (hg38): 4:672436-674330

Previous symbols: [ "ATP5I" ]

Links

ENSG00000169020 ∙ NCBI:521 ∙ OMIM:601519 ∙ HGNC:846 ∙ Uniprot:P56385 ∙ AlphaFold ∙ GenCC ∙ jax ∙ Sfari ∙ GnomAD ∙ Pubmed ∙ ClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the ATP5ME gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ATP5ME gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type	Pathogenic	Likely pathogenic	VUS	Likely benign	Benign	Sum
synonymous						0
missense			9			9
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	9	0	0

Variants in ATP5ME

This is a list of pathogenic ClinVar variants found in the ATP5ME region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position	Type	Phenotype	Significance	ClinVar
4-672506-T-A		not specified	Uncertain significance (Jul 12, 2023)
4-672512-G-T		not specified	Uncertain significance (Jan 27, 2025)
4-672517-C-T		not specified	Uncertain significance (Aug 14, 2023)
4-673332-A-G		not specified	Uncertain significance (Oct 28, 2024)
4-673345-T-G		not specified	Uncertain significance (Mar 23, 2022)
4-673370-C-G		not specified	Uncertain significance (Dec 21, 2023)
4-673384-C-T		not specified	Uncertain significance (Dec 18, 2023)
4-673390-G-A		not specified	Uncertain significance (Feb 25, 2025)
4-673918-G-A		not specified	Uncertain significance (Jan 16, 2024)
4-673942-G-A		not specified	Uncertain significance (Feb 19, 2025)
4-674222-G-C		not specified	Uncertain significance (Nov 14, 2024)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
ATP5ME	protein_coding	protein_coding	ENST00000304312	4	1903

pLI Probability LOF Intolerant	pRec Probability LOF Recessive	Individuals with no LOFs	Individuals with Homozygous LOFs	Individuals with Heterozygous LOFs	Defined	p
0.0858	0.773	125669	0	4	125673	0.0000159

	Z-Score	Observed	Expected	Observed/Expected	Mutation Rate	Total Possible in Transcript
Missense	-0.585	51	40.5	1.26	0.00000208	431
Missense in Polyphen		16	11.355	1.409		142
Synonymous	-1.41	22	15.1	1.46	6.59e-7	136
Loss of Function	1.09	2	4.49	0.445	1.90e-7	53

LoF frequencies by population

Ethnicity	Sum of pLOFs	p
African & African-American	0.0000289	0.0000289
Ashkenazi Jewish	0.00	0.00
East Asian	0.00	0.00
Finnish	0.00	0.00
European (Non-Finnish)	0.0000264	0.0000264
Middle Eastern	0.00	0.00
South Asian	0.00	0.00
Other	0.00	0.00

dbNSFP

Source: dbNSFP

• Function: FUNCTION: Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Part of the complex F(0) domain. Minor subunit located with subunit a in the membrane.
• Pathway: Thermogenesis - Homo sapiens (human);Doxorubicin Pathway (Cardiomyocyte Cell), Pharmacodynamics;Oxidative phosphorylation - Homo sapiens (human);Electron Transport Chain;Oxidative phosphorylation;adenosine ribonucleotides <i>de novo</i> biosynthesis;Formation of ATP by chemiosmotic coupling;The citric acid (TCA) cycle and respiratory electron transport;Purine metabolism;Metabolism;superpathway of purine nucleotide salvage;Cristae formation;Mitochondrial biogenesis;Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.;purine nucleotides <i>de novo</i> biosynthesis;Organelle biogenesis and maintenance (Consensus)

Intolerance Scores

• rvis_EVS: 0.19
• rvis_percentile_EVS: 66.57

Haploinsufficiency Scores

• pHI: 0.681
• hipred: Y
• hipred_score: 0.518
• ghis: 0.459

Essentials

• essential_gene_gene_trap: N

Mouse Genome Informatics

• Gene name: Atp5k

Gene ontology

• Biological process: ATP biosynthetic process;cristae formation;mitochondrial ATP synthesis coupled proton transport
• Cellular component: mitochondrial proton-transporting ATP synthase complex, coupling factor F(o);mitochondrion;mitochondrial inner membrane;mitochondrial proton-transporting ATP synthase complex
• Molecular function: proton transmembrane transporter activity;ATPase activity;transmembrane transporter activity