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Gene : DMAC2L Homo sapiens

Name  ? distal membrane arm assembly complex 2 like Cytological Location  14q21.3
Brief Description  distal membrane arm assembly complex 2 like
Description  This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. This gene encodes the subunit s, also known as factor B, of the proton channel. This subunit is necessary for the energy transduction activity of the ATP synthase complexes. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000170866,
  • HSU79253,
  • HSU79253,
  • ATPW,
  • uc001wxw.3,
  • ATPW,
  • U79253,
  • ATP synthase, H+ transporting, mitochondrial Fo complex subunit s (factor B),
  • ATP5S,
  • ATP5S,
  • FB,
  • ATP synthase, H+ transporting, mitochondrial Fo complex, subunit s (factor B),
  • HGNC:18799,
  • NM_015684,
  • DMAC2L,
  • ATP synthase, H+ transporting, mitochondrial F0 complex, subunit s (factor B)
  • identifiers:
  • 27109,
  • ENSG00000125375,
  • DMAC2L

Genome feature

Region: gene ? Length: 16437  
Location: 14:50311521-50327957 Cyto location: 14q21.3

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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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3756 SN Ps

5 Cross References

15 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results