KEGG   ORTHOLOGY: K02271Help
Entry
K02271                      KO                                     

Name
COX7B
Definition
cytochrome c oxidase subunit 7b
Pathway
Oxidative phosphorylation
Cardiac muscle contraction
Non-alcoholic fatty liver disease (NAFLD)
Alzheimer's disease
Parkinson's disease
Huntington's disease
Module
M00154  
Cytochrome c oxidase
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: 
CJC: 
100390732 100414729(COX7B2)
SBQ: 
101048999 101052499
MMU: 
66142(Cox7b) 78174(Cox7b2)
RNO: 
100361960(Cox7b2) 303393(Cox7b)
CGE: 
100764866 100772782
NGI: 
103737829 103737882
HGL: 
101715696 101719726 101722775 106010133
CCAN: 
109680062 109686755
OCU: 
100339628 100342996 100353320 100357660
TUP: 
102475894 102498058
CFA: 
100684983 100687434(COX7B2)
AML: 
100466075 100475526
UMR: 
103672701 103675819
FCA: 
101085531 101098629
PTG: 
102951800 102970291
AJU: 
106986098 106986669
BTA: 
100300550(COX7B) 767916(COX7B2)
BOM: 
102265796 102277731
BIU: 
109560438 109561950
PHD: 
102316805 102331814 102332988 102339388 102340979
CHX: 
102184512 102186286
OAS: 
101116886 101121518
SSC: 
100516480 100517408
CFR: 
102506447 102509421
BACU: 
103011737 103017687 103019246
LVE: 
103071977 103079623 103082153
ECB: 
100629332 100630758
MYB: 
102248066 102249757 102256817 102257114
MYD: 
102769655 102770550
HAI: 
109385653 109395055
RSS: 
109437254 109452238
PALE: 
102883692 102883704 102888814
LAV: 
100658215 100666763
MDO: 
100012618
SHR: 
100932664
OAA: 
100073487
GGA: 
771947(COX7B)
MGP: 
723981
CJO: 
107312769
APLA: 
101800937
ACYG: 
106038569
TGU: 
100219756(COX7B)
GFR: 
102043872
FAB: 
101811767
PHI: 
102105750
CCW: 
104691619
FPG: 
101916936
FCH: 
102056249
CLV: 
102086620
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)
SRX: 
107713147 107726769
SANH: 
107675192 107697350
SGH: 
107582003 107598778
IPU: 
108279231(COX7B)
TRU: 
101066275
TNG: 
GSTEN00014630G001
LCO: 
104918951
NCC: 
104965587
MZE: 
101478334
OLA: 
101167565
XMA: 
102237993
CSEM: 
103394928
LCF: 
108893360
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
  Sequence
[hsa:1349]
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