Homo sapiens (human): 10367
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Entry
10367 CDS
T01001
Symbol
MICU1, CALC, CBARA1, EFHA3, MPXPS, ara_CALC
Name
(RefSeq) mitochondrial calcium uptake 1
KO
K22827
calcium uptake protein 1, mitochondrial
Organism
hsa
Homo sapiens (human)
Disease
H02447
Myopathy with extrapyramidal signs
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
10367 (MICU1)
09183 Protein families: signaling and cellular processes
04990 Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
10367 (MICU1)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Inner mambrane
Mitochondrial calcium uniporter complex
10367 (MICU1)
Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
EF-hand domain-containing proteins
Calcium binding proteins
10367 (MICU1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EF-hand_1
EF-hand_6
EF-hand_5
EF-hand_7
EF-hand_8
EF-hand_4
Dockerin_1
DUF6559
Motif
Other DBs
NCBI-GeneID:
10367
NCBI-ProteinID:
NP_001182447
OMIM:
605084
HGNC:
1530
Ensembl:
ENSG00000107745
UniProt:
Q9BPX6
Structure
PDB
LinkDB
All DBs
Position
10:complement(72367340..72626079)
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AA seq
476 aa
AA seq
DB search
MFRLNSLSALAELAVGSRWYHGGSQPIQIRRRLMMVAFLGASAVTASTGLLWKRAHAESP
PCVDNLKSDIGDKGKNKDEGDVCNHEKKTADLAPHPEEKKKKRSGFRDRKVMEYENRIRA
YSTPDKIFRYFATLKVISEPGEAEVFMTPEDFVRSITPNEKQPEHLGLDQYIIKRFDGKK
ISQEREKFADEGSIFYTLGECGLISFSDYIFLTTVLSTPQRNFEIAFKMFDLNGDGEVDM
EEFEQVQSIIRSQTSMGMRHRDRPTTGNTLKSGLCSALTTYFFGADLKGKLTIKNFLEFQ
RKLQHDVLKLEFERHDPVDGRITERQFGGMLLAYSGVQSKKLTAMQRQLKKHFKEGKGLT
FQEVENFFTFLKNINDVDTALSFYHMAGASLDKVTMQQVARTVAKVELSDHVCDVVFALF
DCDGNGELSNKEFVSIMKQRLMRGLEKPKDMGFTRLMQAMWKCAQETAWDFALPKQ
NT seq
1431 nt
NT seq
+upstream
nt +downstream
nt
atgtttcgtctgaactcactttctgctttggcagaactggctgtgggttctcgatggtac
catggaggatcacagcccatccagatccggcgaagactaatgatggtggctttcctggga
gcatctgcagtaactgcaagtactggtcttttgtggaagagggcccatgcagaatctcca
ccatgtgtagacaacctaaaaagtgacatcggtgataaagggaagaataaagatgaaggg
gatgtttgtaaccatgagaaaaagactgcagatcttgcccctcacccagaagagaaaaag
aagaaacgttctggattcagagacagaaaagtgatggaatatgagaataggattcgagcc
tactccacgccagacaaaatcttccgatattttgccaccttgaaagtcatcagtgagcct
ggtgaagcagaagtgtttatgacaccagaagattttgtgcgatccataacacccaatgaa
aaacaaccagaacacttgggtctggatcaatatataataaaacgctttgatggaaagaaa
atttcccaggaacgagaaaaatttgctgatgaaggcagtatattttacacccttggagaa
tgtgggctcatatccttttcagactacattttcctcacaactgttctttccactcctcag
agaaattttgaaattgccttcaagatgtttgatttgaatggagatggagaagtagatatg
gaagaatttgaacaggttcagagcatcattcgctcccaaaccagtatgggtatgcgccac
agagatcgtccaactactggcaacaccctcaagtctggcttgtgttcagccctcacaacc
tacttttttggagctgatctgaagggaaagctgacaatcaaaaacttcctcgaatttcag
cgtaaactgcagcatgatgttctgaagcttgagtttgaacgccatgaccctgtggatggg
agaattactgagaggcagtttggtggcatgctacttgcctacagtggggtgcagtccaag
aagctgaccgccatgcagaggcagctcaagaagcacttcaaagaaggaaagggtctgaca
tttcaggaggtggagaacttctttactttcctaaagaacattaatgatgtggacactgca
ttgagtttttaccatatggctggagcatctcttgataaagtgaccatgcagcaggtggcc
aggacagtggctaaagtggagctctcagaccacgtgtgtgatgtggtgtttgcactcttt
gactgtgatggcaatggcgaactgagcaataaggaatttgtttccatcatgaagcaacgg
ctgatgagaggcctggaaaagcccaaagacatgggtttcactcgcctcatgcaggccatg
tggaaatgtgcacaggaaactgcctgggacttcgctttacccaaacagtaa
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