Pan paniscus (bonobo): 100990265
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Entry
100990265 CDS
T02283
Symbol
MCU
Name
(RefSeq) calcium uniporter protein, mitochondrial isoform X1
KO
K20858
calcium uniporter protein, mitochondrial
Organism
pps
Pan paniscus (bonobo)
Pathway
pps04020
Calcium signaling pathway
pps04218
Cellular senescence
pps04621
NOD-like receptor signaling pathway
pps05010
Alzheimer disease
pps05012
Parkinson disease
pps05014
Amyotrophic lateral sclerosis
pps05017
Spinocerebellar ataxia
pps05020
Prion disease
pps05022
Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:
pps00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
100990265 (MCU)
09140 Cellular Processes
09143 Cell growth and death
04218 Cellular senescence
100990265 (MCU)
09150 Organismal Systems
09151 Immune system
04621 NOD-like receptor signaling pathway
100990265 (MCU)
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
100990265 (MCU)
05012 Parkinson disease
100990265 (MCU)
05014 Amyotrophic lateral sclerosis
100990265 (MCU)
05017 Spinocerebellar ataxia
100990265 (MCU)
05020 Prion disease
100990265 (MCU)
05022 Pathways of neurodegeneration - multiple diseases
100990265 (MCU)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
pps03029
]
100990265 (MCU)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
pps02000
]
100990265 (MCU)
Mitochondrial biogenesis [BR:
pps03029
]
Mitochondrial protein import machinery
Inner mambrane
Mitochondrial calcium uniporter complex
100990265 (MCU)
Transporters [BR:
pps02000
]
Other transporters
Pores ion channels [TC:
1
]
100990265 (MCU)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MCU
Spectrin_Anc-1
SPX
Motif
Other DBs
NCBI-GeneID:
100990265
NCBI-ProteinID:
XP_003816026
Ensembl:
ENSPPAG00000036235
LinkDB
All DBs
Position
8:84870738..85063141
Genome browser
AA seq
346 aa
AA seq
DB search
MAAAAGRSLLLLLSSRGGGGGGALTAGCFPGLGVSRHRQQQHHRTVHQRIASWQNLGAVY
CSTVVPSDDVTVVYQNGLPVISVRLPSRRERCQFTLKPISDSVGVFLRQLQEEDRGIDRV
AIYSPDGVRVAASTGIDLLLLDDFKLVINDLTYHVRPPKRDLLSHENAATLNDVKTLVQQ
LYTTLCIEQHQLNKERELIERLEDLKEQLAPLEKVRIEISRKAEKRTTLVLWGGLAYMAT
QFGILARLTWWEYSWDIMEPVTYFITYGSAMAMYAYFVMTRQEYVYPEARDRQYLLFFHK
GAKKSRFDLEKYNQLKDAIAQAEMDLKRLRDPLQVHLPLRQIGEKD
NT seq
1041 nt
NT seq
+upstream
nt +downstream
nt
atggcggccgccgcaggtagatcgctcctgctgctcctctcctctcggggcggcggcggt
ggcggggcgctgactgccggctgcttccctgggctgggcgtcagccgccaccggcagcag
cagcaccaccggacggtacaccagaggatcgcttcctggcagaatttgggagctgtttat
tgcagtactgttgtgccctctgatgatgttacagtggtttatcaaaatgggttacctgtg
atatctgtgaggctaccatcccggcgtgaacgctgtcagttcacactcaagcctatctct
gactctgttggtgtatttttacgacaactgcaagaagaggatcggggaattgacagagtt
gctatctattcaccagatggtgttcgcgttgctgcttcaacaggaatagacctcctcctc
cttgatgactttaagctggtcattaatgacttaacatatcacgtacgaccaccaaaaaga
gacctcttaagtcatgaaaatgcagcaacgctgaatgatgtaaagacattggtccagcaa
ctatacaccacactgtgcattgagcagcaccagttaaacaaggaaagggagcttattgaa
agactagaggatctcaaagagcagctggctcccctggaaaaggtacgaattgagattagc
agaaaagctgagaagaggaccactttggtgctatggggtggccttgcctacatggccaca
cagtttggcattttggcccggcttacctggtgggaatattcctgggacatcatggagcca
gtaacatacttcatcacttatggaagtgccatggcaatgtatgcatattttgtaatgaca
cgccaggaatatgtttatccagaagccagagacagacaatacttactatttttccataaa
ggagccaaaaagtcacgttttgacctagagaaatacaatcaactcaaggatgcaattgct
caggcagaaatggaccttaagagactgagagacccattacaagtacatctgcctctccga
caaattggtgaaaaagattga
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