Homo sapiens (human): 205327
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Entry
205327 CDS
T01001
Symbol
C2orf69, COXPD53
Name
(RefSeq) chromosome 2 open reading frame 69
KO
K28271
mitochondrial protein C2orf69
Organism
hsa
Homo sapiens (human)
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
205327 (C2orf69)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Regulator of mitochondrial biogenesis
Other regulator of mitochondrial biogenesis
205327 (C2orf69)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
C2orf69
Motif
Other DBs
NCBI-GeneID:
205327
NCBI-ProteinID:
NP_710156
OMIM:
619219
HGNC:
26799
Ensembl:
ENSG00000178074
UniProt:
Q8N8R5
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All DBs
Position
2:199911293..199928273
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AA seq
385 aa
AA seq
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MWGFRLLRSPPLLLLLPQLGIGNASSCSQARTMNPGGSGGARCSLSAEVRRRQCLQLSTV
PGADPQRSNELLLLAAAGEGLERQDLPGDPAKEEPQPPPQHHVLYFPGDVQNYHEIMTRH
PENYQWENWSLENVATILAHRFPNSYIWVIKCSRMHLHKFSCYDNFVKSNMFGAPEHNTD
FGAFKHLYMLLVNAFNLSQNSLSKKSLNVWNKDSIASNCRSSPSHTTNGCQGEKVRTCEK
SDESAMSFYPPSLNDASFTLIGFSKGCVVLNQLLFELKEAKKDKNIDAFIKSIRTMYWLD
GGHSGGSNTWVTYPEVLKEFAQTGIIVHTHVTPYQVRDPMRSWIGKEHKKFVQILGDLGM
QVTSQIHFTKEAPSIENHFRVHEVF
NT seq
1158 nt
NT seq
+upstream
nt +downstream
nt
atgtgggggttcaggctcctgcggtcgccgccgttgctgctcctgctgccgcagctcgga
atcggaaacgcctcgtcctgctctcaggccagaaccatgaacccgggcggcagcggcggc
gcgcgatgctccctctcggccgaggtgcgccgccgtcagtgcctgcagctttccaccgtg
cctggagccgatccgcagcgcagcaacgaattgctcctgttggcggcggccggggaggga
ctggagcggcaggacctccccggggacccagcgaaggaggagccgcagccgccgccccag
catcacgtcctctatttccctggggatgtgcagaattaccatgaaattatgactcgtcat
cctgagaattatcaatgggaaaactggagtctagaaaatgttgctaccattttagcccac
cggttccccaatagttatatttgggtgataaaatgttcccgaatgcatttgcacaaattc
agctgctatgacaattttgtgaaaagtaacatgtttggtgccccagaacacaatactgac
tttggagcttttaagcacctttatatgttattagttaatgcttttaatttaagtcagaat
agtttatcaaagaaaagtttgaatgtttggaataaggactccatagcatctaactgtaga
tccagtccttctcatactacgaatggttgccagggagaaaaagtgaggacctgtgaaaaa
tctgatgagtctgccatgagtttttatccaccatcactaaatgacgcatcttttactttg
attggattcagtaaaggttgtgttgttttgaatcagttgctttttgaattgaaagaagcc
aagaaagacaagaacatagatgcttttatcaaaagcataagaacaatgtattggctggat
ggtggtcattctggaggaagcaatacttgggttacttatccagaagtcttgaaagaattt
gcacaaacaggaattatcgttcacactcatgtaacaccttaccaagtacgtgatccaatg
agatcttggattggaaaggagcacaagaaatttgttcagatacttggggatcttggtatg
caggtgactagccaaattcattttacaaaggaagctccttccatagagaatcacttcagg
gttcatgaagtattttga
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