KEGG   Homo sapiens (human): 1349Help
Entry
1349              CDS       T01001                                 

Gene name
COX7B, APLCC
Definition
cytochrome c oxidase subunit VIIb (EC:1.9.3.1)
Orthology
K02271  
cytochrome c oxidase subunit 7b
Organism
hsa  Homo sapiens (human)
Pathway
Oxidative phosphorylation
Metabolic pathways
Cardiac muscle contraction
Non-alcoholic fatty liver disease (NAFLD)
Alzheimer's disease
Parkinson's disease
Huntington's disease
Module
Cytochrome c oxidase
Brite
KEGG Orthology (KO) [BR:hsa00001]
 Metabolism
  Energy metabolism
   00190 Oxidative phosphorylation
    1349 (COX7B)
 Organismal Systems
  Circulatory system
   04260 Cardiac muscle contraction
    1349 (COX7B)
 Human Diseases
  Neurodegenerative diseases
   05010 Alzheimer's disease
    1349 (COX7B)
   05012 Parkinson's disease
    1349 (COX7B)
   05016 Huntington's disease
    1349 (COX7B)
  Endocrine and metabolic diseases
   04932 Non-alcoholic fatty liver disease (NAFLD)
    1349 (COX7B)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: 
Motif
Other DBs
NCBI-GI: 
NCBI-GeneID: 
OMIM: 
HGNC: 
HPRD: 
UniProt: 
Position
Xq21.1
AA seq 80 aa AA seqDB search
MFPLVKSALNRLQVRSIQQTMARQSHQKRTPDFHDKYGNAVLASGATFCIVTWTYVATQV
GIEWNLSPVGRVTPKEWRNQ
NT seq 243 nt NT seq  +upstreamnt  +downstreamnt
atgtttcccttggtcaaaagcgcactaaatcgtctccaagttcgaagcattcagcaaaca
atggcaaggcagagccaccagaaacgtacacctgattttcatgacaaatacggtaatgct
gtattagctagtggagccactttctgtattgttacatggacatatgtagcaacacaagtc
ggaatagaatggaacctgtcccctgttggcagagttaccccaaaggaatggaggaatcag
taa

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