Neogale vison (American mink): 122900781
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Entry
122900781 CDS
T08764
Symbol
MCU
Name
(RefSeq) calcium uniporter protein, mitochondrial
KO
K20858
calcium uniporter protein, mitochondrial
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04020
Calcium signaling pathway
nvs04218
Cellular senescence
nvs04621
NOD-like receptor signaling pathway
nvs05010
Alzheimer disease
nvs05012
Parkinson disease
nvs05014
Amyotrophic lateral sclerosis
nvs05017
Spinocerebellar ataxia
nvs05020
Prion disease
nvs05022
Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
122900781 (MCU)
09140 Cellular Processes
09143 Cell growth and death
04218 Cellular senescence
122900781 (MCU)
09150 Organismal Systems
09151 Immune system
04621 NOD-like receptor signaling pathway
122900781 (MCU)
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
122900781 (MCU)
05012 Parkinson disease
122900781 (MCU)
05014 Amyotrophic lateral sclerosis
122900781 (MCU)
05017 Spinocerebellar ataxia
122900781 (MCU)
05020 Prion disease
122900781 (MCU)
05022 Pathways of neurodegeneration - multiple diseases
122900781 (MCU)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
nvs03029
]
122900781 (MCU)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
nvs02000
]
122900781 (MCU)
Mitochondrial biogenesis [BR:
nvs03029
]
Mitochondrial protein import machinery
Inner mambrane
Mitochondrial calcium uniporter complex
122900781 (MCU)
Transporters [BR:
nvs02000
]
Other transporters
Pores ion channels [TC:
1
]
122900781 (MCU)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MCU
Spectrin_Anc-1
SPX
Motif
Other DBs
NCBI-GeneID:
122900781
NCBI-ProteinID:
XP_044095686
UniProt:
A0A8C7AWY9
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All DBs
Position
2:186556260..186761327
Genome browser
AA seq
350 aa
AA seq
DB search
MAAAAGRSLLLLLSSRGGGGGAGGCGALTAGCFPGLGVSRHRQQQHHRTVHQRLSSWQNL
GAVYCSTVVPSDDVTVVYQNGLPVISVRLPSRRERCQFTLKPISDSVGVFLRQLQEEDRG
IDRVAIYSPDGVRVAASTGIDLLLLDDFKLVINDLTYHVRPPKRDLLSHENAATLNDVKT
LVQQLYTTLCIEQHQLNKERELIERLEDLKEQLAPLEKVRIEISRKAEKRTTLVLWGGLA
YMATQFGILARLTWWEYSWDIMEPVTYFITYGSAMAMYAYFVMTRQEYVYPEARDRQYLL
FFHKGAKKSRFDLEKYNQLKDAIAQAEMDLKRLRDPLQVHLPLRQIGEKD
NT seq
1053 nt
NT seq
+upstream
nt +downstream
nt
atggcggccgccgcaggtagatcgctcctgctgctcctctcctcccggggcggcggcggg
ggcgccggcggctgcggagcgctgactgccggctgcttccccgggctgggcgtcagccgc
caccggcagcagcagcaccaccggacggtgcaccagaggctctcctcttggcagaatttg
ggagctgtttattgcagtactgttgtgccctctgatgatgtgacagtggtgtatcaaaat
gggttacctgtgatatctgtgaggctaccatcccgacgtgaacgctgccagttcacactc
aaacctatctcagactccgttggtgtgtttttacgacaactgcaagaagaggatcgggga
attgacagagttgcaatctattcaccagatggcgttcgagttgctgcctcaacagggata
gacctcctactccttgatgactttaagctggtcattaatgacttaacatatcatgtacga
ccaccaaagagagacctcttaagccacgaaaatgcagcaacactgaatgatgtaaagaca
ctcgtccagcagctgtacaccacgctgtgcatcgagcagcaccagttaaacaaggaaagg
gagcttattgaaagattagaggatctcaaagagcagctggctcccctggaaaaggtacga
attgagattagcagaaaagctgagaagaggaccactttggtgctatggggtggacttgcc
tacatggccacacagtttggcattttggcccggcttacctggtgggaatattcctgggac
atcatggagccagtcacctactttatcacttacggaagtgccatggcaatgtatgcatat
tttgtaatgacacgccaggaatatgtttatccagaagccagagacagacaatacttatta
tttttccataaaggagccaaaaagtcacgttttgacctagagaaatataatcaactcaag
gatgcaattgctcaggcagaaatggaccttaagagactgagagacccattacaagtacat
ctgccccttcgacaaattggtgaaaaagattga
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