KEGG   ORTHOLOGY: K02271Help
Entry
K02271                      KO                                     

Name
COX7B
Definition
cytochrome c oxidase subunit 7b
Pathway
Oxidative phosphorylation
Metabolic pathways
Cardiac muscle contraction
Non-alcoholic fatty liver disease (NAFLD)
Alzheimer's disease
Parkinson's disease
Huntington's disease
Module
M00154  
Cytochrome c oxidase
Disease
H01904  
Microphthalmia with linear skin defects (MLS) syndrome
Brite
KEGG Orthology (KO) [BR:ko00001]
 Metabolism
  Energy metabolism
   00190 Oxidative phosphorylation
    K02271  COX7B; cytochrome c oxidase subunit 7b
 Organismal Systems
  Circulatory system
   04260 Cardiac muscle contraction
    K02271  COX7B; cytochrome c oxidase subunit 7b
 Human Diseases
  Neurodegenerative diseases
   05010 Alzheimer's disease
    K02271  COX7B; cytochrome c oxidase subunit 7b
   05012 Parkinson's disease
    K02271  COX7B; cytochrome c oxidase subunit 7b
   05016 Huntington's disease
    K02271  COX7B; cytochrome c oxidase subunit 7b
  Endocrine and metabolic diseases
   04932 Non-alcoholic fatty liver disease (NAFLD)
    K02271  COX7B; cytochrome c oxidase subunit 7b
KEGG modules [BR:ko00002]
 Structural complex
  Energy metabolism
   ATP synthesis
    M00154  Cytochrome c oxidase
     K02271  COX7B; cytochrome c oxidase subunit 7b
BRITE hierarchy
Other DBs
GO: 
Genes
HSA: 
1349(COX7B) 170712(COX7B2)
PTR: 
100615314(COX7B2) 465727(COX7B)
PPS: 
GGO: 
PON: 
NLE: 
MCC: 
100428437(COX7B2) 706099(COX7B)
MCF: 
CSAB: 
103232235(COX7B) 103246147(COX7B2)
RRO: 
RBB: 
CJC: 
SBQ: 
MMU: 
66142(Cox7b) 78174(Cox7b2)
RNO: 
100361960(Cox7b2) 303393(Cox7b)
CGE: 
NGI: 
HGL: 
CCAN: 
OCU: 
TUP: 
CFA: 
AML: 
UMR: 
ORO: 
FCA: 
PTG: 
AJU: 
BTA: 
100300550(COX7B) 767916(COX7B2)
BOM: 
BIU: 
PHD: 
CHX: 
OAS: 
SSC: 
CFR: 
CDK: 
BACU: 
LVE: 
ECB: 
EPZ: 
EAI: 
MYB: 
MYD: 
HAI: 
RSS: 
PALE: 
LAV: 
TMU: 
MDO: 
SHR: 
OAA: 
GGA: 
771947(COX7B)
MGP: 
CJO: 
APLA: 
ACYG: 
TGU: 
100219756(COX7B)
GFR: 
FAB: 
PHI: 
PMAJ: 
CCW: 
FPG: 
FCH: 
CLV: 
EGZ: 
AAM: 
ASN: 
AMJ: 
102572384(COX7B)
PSS: 
CMY: 
CPIC: 
PBI: 
GJA: 
XLA: 
108700072 447278(cox7b.L)
XTR: 
779702(cox7b)
NPR: 
DRE: 
563476(cox7b)
SRX: 
SANH: 
SGH: 
CCAR: 
IPU: 
108279231(COX7B)
AMEX: 
TRU: 
TNG: 
LCO: 
NCC: 
MZE: 
OLA: 
XMA: 
PRET: 
NFU: 
CSEM: 
LCF: 
HCQ: 
BPEC: 
SASA: 
106568019(COX7B) 106603475(CX7B2)
SFM: 
LCM: 
CMK: 
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Indrieri A, van Rahden VA, Tiranti V, Morleo M, Iaconis D, Tammaro R, D'Amato I, Conte I, Maystadt I, Demuth S, Zvulunov A, Kutsche K, Zeviani M, Franco B
  Title
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease.
  Journal
Am J Hum Genet 91:942-9 (2012)
DOI:10.1016/j.ajhg.2012.09.016
  Sequence
[hsa:1349]

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