KEGG   Neogale vison (American mink): 122891642
Entry
122891642         CDS       T08764                                 
Symbol
ATP5MC2
Name
(RefSeq) ATP synthase F(0) complex subunit C2, mitochondrial
  KO
K02128  F-type H+-transporting ATPase subunit c
Organism
nvs  Neogale vison (American mink)
Pathway
nvs00190  Oxidative phosphorylation
nvs01100  Metabolic pathways
nvs04714  Thermogenesis
nvs05010  Alzheimer disease
nvs05012  Parkinson disease
nvs05014  Amyotrophic lateral sclerosis
nvs05016  Huntington disease
nvs05020  Prion disease
nvs05022  Pathways of neurodegeneration - multiple diseases
nvs05208  Chemical carcinogenesis - reactive oxygen species
nvs05415  Diabetic cardiomyopathy
Module
nvs_M00158  F-type ATPase, eukaryotes
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    122891642 (ATP5MC2)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    122891642 (ATP5MC2)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    122891642 (ATP5MC2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122891642 (ATP5MC2)
   05012 Parkinson disease
    122891642 (ATP5MC2)
   05014 Amyotrophic lateral sclerosis
    122891642 (ATP5MC2)
   05016 Huntington disease
    122891642 (ATP5MC2)
   05020 Prion disease
    122891642 (ATP5MC2)
   05022 Pathways of neurodegeneration - multiple diseases
    122891642 (ATP5MC2)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    122891642 (ATP5MC2)
SSDB
Motif
Pfam: ATP-synt_C
Other DBs
NCBI-GeneID: 122891642
NCBI-ProteinID: XP_044083414
LinkDB
Position
12:100000520..100007855
AA seq 145 aa
MYACAKFVSTPFLVRSTSQLLSRSLSAVVLKPPETLTDEAPYKGLSILAAPRPLTSLIPS
RSFQTSAISRDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYA
ILGFALSEAMGLFCLMVAFLILFAM
NT seq 438 nt   +upstreamnt  +downstreamnt
atgtacgcctgcgcaaagttcgtctccaccccgttcttggtcaggagcacctctcagctg
ttgagcagatcactgtctgcagtggtgctaaaaccacccgagacactgacagatgaggca
ccttataagggcctcagcatcttggcagccccacgtcccctgacctcacttattcctagc
cgaagcttccaaaccagcgccatttcaagggacatcgatacagcagccaagttcattggg
gctggggctgccacggtaggggtggctggctctggggctggaattgggactgtgtttggg
agcctcatcattggttatgccaggaatccctctctgaagcaacagctcttctcctacgcc
attctgggctttgccctctccgaggccatggggctcttttgcctgatggtggcctttctc
atcctcttcgccatgtga

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