Homo sapiens (human): 205327
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Entry
205327 CDS
T01001
Symbol
C2orf69, COXPD53
Name
(RefSeq) mitochondrial protein C2orf69 precursor
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)
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SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
C2orf69
Motif
Other DBs
NCBI-GeneID:
205327
NCBI-ProteinID:
NP_710156
OMIM:
619219
HGNC:
26799
Ensembl:
ENSP00000312770.5
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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