Choose one of the five choices you want to search:

Gene, Transcriptome, Protein, Pathway or Disease. 

Gene basic information

LiverAtlas Gene ID

HuLG000361

Entrez Gene ID

513

Official Gene Symbol

ATP5D

Gene name

ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit

Gene Type

protein-coding

Chromosome

19

Genomics Location

19p13.3

Protein products

ATP synthase subunit delta, mitochondrial

Related liver disease name

Hepatocellular carcinoma

Database cross reference

HGNC:837
MIM:603150
Ensembl:ENSG00000099624
HPRD:04397
RefSeq Genomic nucleotide accession:AC_000062
RefSeq Genomic nucleotide gi:89161197

Liver relevance

HCC significant genes

Yes/No

Yes

Evidence

EHCO

Quality score

 

Ontology annotation

GO ID

GO annotation

GO:0000275

mitochondrial proton-transporting ATP synthase complex, catalytic core F(1)

GO:0005215

transporter activity

GO:0005524

ATP binding

GO:0005739

mitochondrion

GO:0005743

mitochondrial inner membrane

GO:0005753

mitochondrial proton-transporting ATP synthase complex

GO:0005759

mitochondrial matrix

GO:0006119

oxidative phosphorylation

GO:0006172

ADP biosynthetic process

GO:0006200

ATP catabolic process

GO:0006754

ATP biosynthetic process

GO:0006811

ion transport

GO:0015992

proton transport

GO:0016020

membrane

GO:0016887

ATPase activity

GO:0022857

transmembrane transporter activity

GO:0022904

respiratory electron transport chain

GO:0032403

protein complex binding

GO:0042776

mitochondrial ATP synthesis coupled proton transport

GO:0043531

ADP binding

GO:0046688

response to copper ion

GO:0046933

hydrogen ion transporting ATP synthase activity, rotational mechanism

GO:0046961

proton-transporting ATPase activity, rotational mechanism