Oryctolagus cuniculus (rabbit): 100341372
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Entry
100341372 CDS
T03373
Name
(RefSeq) calcium uniporter protein, mitochondrial isoform X1
KO
K20858
calcium uniporter protein, mitochondrial
Organism
ocu
Oryctolagus cuniculus (rabbit)
Pathway
ocu04020
Calcium signaling pathway
ocu04218
Cellular senescence
ocu04621
NOD-like receptor signaling pathway
ocu05010
Alzheimer disease
ocu05012
Parkinson disease
ocu05014
Amyotrophic lateral sclerosis
ocu05017
Spinocerebellar ataxia
ocu05020
Prion disease
ocu05022
Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:
ocu00001
]
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
100341372
05012 Parkinson disease
100341372
05014 Amyotrophic lateral sclerosis
100341372
05017 Spinocerebellar ataxia
100341372
05020 Prion disease
100341372
05022 Pathways of neurodegeneration - multiple diseases
100341372
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
ocu03029
]
100341372
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
ocu02000
]
100341372
Mitochondrial biogenesis [BR:
ocu03029
]
Mitochondrial protein import machinery
Inner mambrane
Mitochondrial calcium uniporter complex
100341372
Transporters [BR:
ocu02000
]
Other transporters
Pores ion channels [TC:
1
]
100341372
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MCU
Spectrin_Anc-1
SPX
Motif
Other DBs
NCBI-GeneID:
100341372
NCBI-ProteinID:
XP_002718476
Ensembl:
ENSOCUG00000014855
UniProt:
G1T890
LinkDB
All DBs
Position
18:complement(11496041..11707546)
Genome browser
AA seq
350 aa
AA seq
DB search
MAAAAGRSLLLLLSSRGGGGGAGGCGALTAGCFPGLSVSRHRQQQHHRTVHQRLSSWQNL
GAMYCSTVVPSDDVTVVYQNGLPVISVRLPSRRERCQFTLKPISDSVGVFLRQLQEEDRG
IDRVAIYSPDGVRVAASTGIDLLLLDDFKLVINDFTYLVRPPKRDLLSHENAATLNDVKT
LVQQLYTTLCIEQHQLNKERELIERLEALKEQLAPLEKVRIEISRKAEKRTTLVLWGGLA
YMATQFGILARLTWWEYSWDIMEPVTYFITYGSAMAMYAYFVMTRQEYVYPEARDRQYLL
FFHKGAKKSRFDLEKYNQLKDAIAQAEMDLKRLRDPLQVHLPLRQIGEKD
NT seq
1053 nt
NT seq
+upstream
nt +downstream
nt
atggcggccgccgcaggtagatcgctcctgctgctgctctcctcccggggcggcggcggg
ggcgccggcggctgcggggcgctgactgccggctgcttccccgggctgagcgtcagccgc
caccggcagcagcagcaccaccggacggtgcaccagaggctgtcttcctggcagaatttg
ggagccatgtattgcagtactgttgtgccctctgatgatgtgacagtggtttatcagaat
ggactacctgtgatatctgtgaggctaccgtcccggcgtgagcgctgccagttcacactc
aaacctatctccgactccgttggtgtctttttacgacaactgcaagaagaggatcgggga
attgacagagtggcaatctattcaccagatggtgtgagagtcgctgcctccacaggaata
gacctcctcctcctcgatgacttcaagctggtcatcaatgacttcacgtatctcgtgcgg
ccaccaaagagagacctcttaagccacgaaaatgcagccacgctgaatgacgtgaagaca
ctggtccagcagctctacaccacgctgtgcattgagcagcaccagctgaacaaggagagg
gagctcattgaaaggctagaggcgctcaaagagcaactggctcccctggaaaaggtacga
attgagattagcagaaaagctgagaagaggaccactttggtgctatggggtggccttgcc
tacatggccacacagtttggcattttggcccggcttacctggtgggaatattcctgggac
atcatggagccagtcacctacttcattacttacggaagcgccatggcaatgtatgcatat
tttgtaatgacacgccaggagtatgtttacccagaagccagagacagacaatacttacta
tttttccataaaggagccaaaaagtcacgttttgacctagagaaatacaaccaactcaag
gatgcaattgctcaggcagaaatggaccttaaacgactgagagacccattgcaagtacat
ctgccccttcgacagattggtgaaaaagattga
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