Homo sapiens (human): 517
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Entry
517 CDS
T01001
Symbol
ATP5MC2, ATP5A, ATP5G2
Name
(RefSeq) ATP synthase membrane subunit c locus 2
KO
K02128
F-type H+-transporting ATPase subunit c
Organism
hsa
Homo sapiens (human)
Pathway
hsa00190
Oxidative phosphorylation
hsa01100
Metabolic pathways
hsa04714
Thermogenesis
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05208
Chemical carcinogenesis - reactive oxygen species
hsa05415
Diabetic cardiomyopathy
Module
hsa_M00158
F-type ATPase, eukaryotes
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
517 (ATP5MC2)
09150 Organismal Systems
09159 Environmental adaptation
04714 Thermogenesis
517 (ATP5MC2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
517 (ATP5MC2)
09164 Neurodegenerative disease
05010 Alzheimer disease
517 (ATP5MC2)
05012 Parkinson disease
517 (ATP5MC2)
05014 Amyotrophic lateral sclerosis
517 (ATP5MC2)
05016 Huntington disease
517 (ATP5MC2)
05020 Prion disease
517 (ATP5MC2)
05022 Pathways of neurodegeneration - multiple diseases
517 (ATP5MC2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
517 (ATP5MC2)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ATP-synt_C
Motif
Other DBs
NCBI-GeneID:
517
NCBI-ProteinID:
NP_001317198
OMIM:
603193
HGNC:
842
Ensembl:
ENSG00000135390
UniProt:
Q06055
LinkDB
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Position
12:complement(53665170..53681423)
Genome browser
AA seq
141 aa
AA seq
DB search
MFACSKFVSTPSLVKSTSQLLSRPLSAVVLKRPEILTDESLSSLAVSCPLTSLVSSRSFQ
TSAISRDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYAILGF
ALSEAMGLFCLMVAFLILFAM
NT seq
426 nt
NT seq
+upstream
nt +downstream
nt
atgttcgcctgctccaagtttgtctccactccctccttggtcaagagcacctcacagctg
ctgagccgtccgctatctgcagtggtgctgaaacgaccggagatactgacagatgagagc
ctcagcagcttggcagtctcatgtccccttacctcacttgtctctagccgcagcttccaa
accagcgccatttcaagggacatcgacacagcagccaagttcattggagctggggctgcc
acagttggggtggctggttctggggctgggattggaactgtgtttgggagcctcatcatt
ggttatgccaggaacccttctctgaagcaacagctcttctcctacgccattctgggcttt
gccctctcggaggccatggggctcttttgtctgatggtagcctttctcatcctctttgcc
atgtga
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