Capra hircus (goat): 102184878
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Entry
102184878 CDS
T02910
Symbol
MCU
Name
(RefSeq) calcium uniporter protein, mitochondrial
KO
K20858
calcium uniporter protein, mitochondrial
Organism
chx
Capra hircus (goat)
Pathway
chx04020
Calcium signaling pathway
chx04218
Cellular senescence
chx04621
NOD-like receptor signaling pathway
chx05010
Alzheimer disease
chx05012
Parkinson disease
chx05014
Amyotrophic lateral sclerosis
chx05017
Spinocerebellar ataxia
chx05020
Prion disease
chx05022
Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:
chx00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
102184878 (MCU)
09140 Cellular Processes
09143 Cell growth and death
04218 Cellular senescence
102184878 (MCU)
09150 Organismal Systems
09151 Immune system
04621 NOD-like receptor signaling pathway
102184878 (MCU)
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
102184878 (MCU)
05012 Parkinson disease
102184878 (MCU)
05014 Amyotrophic lateral sclerosis
102184878 (MCU)
05017 Spinocerebellar ataxia
102184878 (MCU)
05020 Prion disease
102184878 (MCU)
05022 Pathways of neurodegeneration - multiple diseases
102184878 (MCU)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
chx03029
]
102184878 (MCU)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
chx02000
]
102184878 (MCU)
Mitochondrial biogenesis [BR:
chx03029
]
Mitochondrial protein import machinery
Inner mambrane
Mitochondrial calcium uniporter complex
102184878 (MCU)
Transporters [BR:
chx02000
]
Other transporters
Pores ion channels [TC:
1
]
102184878 (MCU)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MCU
Spectrin_Anc-1
SPX
Motif
Other DBs
NCBI-GeneID:
102184878
NCBI-ProteinID:
XP_017897974
UniProt:
A0A452F8G5
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Position
28:complement(16711089..16899705)
Genome browser
AA seq
351 aa
AA seq
DB search
MAAAAGRSLLLLLSSRGGGGGGAGGCGALTAGCFPALGVSRHRQQQHHRTVHQRLSSWPN
LGVVYCSTVVPSDDVTVVYQNGLPVISVRLPSRRERCQFTLKPISDSVGVFLRQLQEEDR
GIDRVAIYSPDGVRVAASTGIDLLLLDDFKLVINDLTYHVRPPKRDLLSHENAATLNDVK
TLVQQLYTTLCIEQHQLNKERELIERLEDLKEQLAPLEKVRIEISRKAEKRTTLVLWGGL
AYMATQFGILARLTWWEYSWDIMEPVTYFITYGSAMAMYAYFVMTRQEYVYPEARDRQYL
LFFHKGAKKSRFDLEKYNELKDAIAQAEMDLKRLRDPLQVHLPLRQIGEKD
NT seq
1056 nt
NT seq
+upstream
nt +downstream
nt
atggcggccgccgcaggtagatcgctcctgctgctcctctcctcccggggcggcggcggc
gggggcgccggcggctgcggagcgctgactgcgggctgcttccccgctctgggcgtcagc
cgccaccggcagcagcagcaccaccggacggtacaccagaggctctcttcttggcctaat
ttgggagttgtttattgcagtactgttgtgccctctgatgatgtgacagtggtgtatcag
aatgggttgcctgtgatatctgtgaggctaccatcccggcgtgaacgctgtcagttcaca
ctcaaacccatctcagactctgttggtgtgtttttacgacaactacaagaagaggatcgg
ggaattgacagagttgcaatctattcaccagatggcgttcgagttgctgcctcaacagga
atagacctcctcctccttgacgactttaagctggtcattaatgacttaacgtatcatgta
cgaccaccaaagagagacctcttaagccatgaaaatgcagcaacactgaatgatgtaaag
acactggtccagcagctctacacaaccctgtgcatcgagcagcaccagctaaacaaggag
agggagctcattgaaagattagaagatctcaaagaacagctggcgcccctggaaaaggta
cgaattgaaatcagcagaaaagctgagaagaggaccactttggtgctatggggtggactt
gcgtacatggccacacagtttggcattttggcccggctcacctggtgggaatattcttgg
gacatcatggagccagtcacctacttcatcacttacggaagcgccatggcgatgtacgca
tattttgtaatgacacgccaggaatatgtttatccagaagccagagacagacaatactta
ttattcttccataaaggagccaaaaagtcacgttttgacctagagaaatacaatgaactc
aaggatgcaattgctcaggcagaaatggaccttaagagactgagagacccattacaagta
catctgcccctccgacaaattggtgaaaaagattga
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