KEGG   ORTHOLOGY: K02271Help
Entry
K02271                      KO                                     

Name
COX7B
Definition
cytochrome c oxidase subunit 7b
Pathway
ko00190  Oxidative phosphorylation
ko01100  Metabolic pathways
ko04260  Cardiac muscle contraction
ko04714  Thermogenesis
ko04932  Non-alcoholic fatty liver disease (NAFLD)
ko05010  Alzheimer's disease
ko05012  Parkinson's disease
ko05016  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
  Environmental adaptation
   04714 Thermogenesis
    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
TC: 3.D.4.11
Genes
HSA: 1349(COX7B) 170712(COX7B2)
PTR: 100615314(COX7B2) 465727(COX7B)
PPS: 100982199 100986707
GGO: 101133386 101147253 109024487
PON: 100172849(COX7B) 100451432
NLE: 100591930 100602515
MCC: 100428437(COX7B2) 706099(COX7B)
MCF: 102123270(COX7B2) 102124180
CSAB: 103232235(COX7B) 103246147(COX7B2)
RRO: 104669550 104671254 104680071
CJC: 100390732 100414729(COX7B2)
MMU: 66142(Cox7b) 78174(Cox7b2)
RNO: 100361960(Cox7b2) 303393(Cox7b)
CFA: 100684983 100687434(COX7B2)
BTA: 100300550(COX7B) 767916(COX7B2)
ECB: 100629332(COX7B2) 100630758
MDO: 100012618
OAA: 100073487
GGA: 771947(COX7B)
MGP: 723981
CJO: 107312769
APLA: 101800937
ACYG: 106038569
TGU: 100219756(COX7B)
GFR: 102043872
FAB: 101811767
PHI: 102105750
PMAJ: 107203841
CCW: 104691619
FPG: 101916936
FCH: 102056249
CLV: 102086620
EGZ: 104135698
AAM: 106489312
ASN: 102380429
AMJ: 102572384(COX7B)
PSS: 102452704
CMY: 102946319
CPIC: 101945370
PBI: 103063809
GJA: 107123231
XLA: 108700072 447278(cox7b.L)
XTR: 779702(cox7b)
NPR: 108803510
DRE: 563476(cox7b)
IPU: 108279231(COX7B)
AMEX: 103037916
TRU: 101066275
LCO: 104918951
NCC: 104965587
MZE: 101478334
OLA: 101167565
XMA: 102237993
PRET: 103460001
NFU: 107386688
CSEM: 103394928
LCF: 108893360
HCQ: 109515543
BPEC: 110156470
SASA: 106568019(COX7B) 106603475(CX7B2)
SFM: 108920031
LCM: 102346907
CMK: 103178978
 » 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
Reference
PMID:8382530
  Authors
Sadlock JE, Lightowlers RN, Capaldi RA, Schon EA
  Title
Isolation of a cDNA specifying subunit VIIb of human cytochrome c oxidase.
  Journal
Biochim Biophys Acta 1172:223-5 (1993)
DOI:10.1016/0167-4781(93)90301-S
  Sequence
[hsa:1349]

DBGET integrated database retrieval system