ATPAF2

GENE INFORMATION

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Gene name

ATPAF2 (HGNC Symbol)

Synonyms

ATP12, Atp12p, LP3663, MGC29736

Description

ATP synthase mitochondrial F1 complex assembly factor 2 (HGNC Symbol)

Entrez gene summary

This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]

Chromosome

17

Cytoband

p11.2

Chromosome location (bp)

17977409 - 18039209

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000171953 (version 78.38)

Entrez gene

91647

UniProt

Q8N5M1 (UniProt - Evidence at protein level)

neXtProt

NX_Q8N5M1

Antibodypedia

ATPAF2 antibodies
 

PROTEIN VIEW

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ATPAF2-001
 
ATPAF2-013
 
ATPAF2-014
 
ATPAF2-015
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ATPAF2-001 ENSP00000417190
ENST00000474627
Q8N5M1
Show all »
Show » Show » 289 32.8 No 0
ATPAF2-013 ENSP00000463861
ENST00000585101
J3KTB2
Show all »
Show » 107 11.6 No 0
ATPAF2-014 ENSP00000466008
ENST00000581698
Show » 59 6.1 No 0
ATPAF2-015 ENSP00000397198
ENST00000444058
C9J2Q2
Show all »
Show » Show » 205 23.2 No 0