KEGG   Homo sapiens (human): 205327
Entry
205327            CDS       T01001                                 
Symbol
C2orf69, COXPD53
Name
(RefSeq) chromosome 2 open reading frame 69
Organism
hsa  Homo sapiens (human)
Disease
H00891  Combined oxidative phosphorylation deficiency
SSDB
Motif
Pfam: C2orf69
Other DBs
NCBI-GeneID: 205327
NCBI-ProteinID: NP_710156
OMIM: 619219
HGNC: 26799
Ensembl: ENSG00000178074
UniProt: Q8N8R5
Position
2:199911293..199928273
AA seq 385 aa
MWGFRLLRSPPLLLLLPQLGIGNASSCSQARTMNPGGSGGARCSLSAEVRRRQCLQLSTV
PGADPQRSNELLLLAAAGEGLERQDLPGDPAKEEPQPPPQHHVLYFPGDVQNYHEIMTRH
PENYQWENWSLENVATILAHRFPNSYIWVIKCSRMHLHKFSCYDNFVKSNMFGAPEHNTD
FGAFKHLYMLLVNAFNLSQNSLSKKSLNVWNKDSIASNCRSSPSHTTNGCQGEKVRTCEK
SDESAMSFYPPSLNDASFTLIGFSKGCVVLNQLLFELKEAKKDKNIDAFIKSIRTMYWLD
GGHSGGSNTWVTYPEVLKEFAQTGIIVHTHVTPYQVRDPMRSWIGKEHKKFVQILGDLGM
QVTSQIHFTKEAPSIENHFRVHEVF
NT seq 1158 nt   +upstreamnt  +downstreamnt
atgtgggggttcaggctcctgcggtcgccgccgttgctgctcctgctgccgcagctcgga
atcggaaacgcctcgtcctgctctcaggccagaaccatgaacccgggcggcagcggcggc
gcgcgatgctccctctcggccgaggtgcgccgccgtcagtgcctgcagctttccaccgtg
cctggagccgatccgcagcgcagcaacgaattgctcctgttggcggcggccggggaggga
ctggagcggcaggacctccccggggacccagcgaaggaggagccgcagccgccgccccag
catcacgtcctctatttccctggggatgtgcagaattaccatgaaattatgactcgtcat
cctgagaattatcaatgggaaaactggagtctagaaaatgttgctaccattttagcccac
cggttccccaatagttatatttgggtgataaaatgttcccgaatgcatttgcacaaattc
agctgctatgacaattttgtgaaaagtaacatgtttggtgccccagaacacaatactgac
tttggagcttttaagcacctttatatgttattagttaatgcttttaatttaagtcagaat
agtttatcaaagaaaagtttgaatgtttggaataaggactccatagcatctaactgtaga
tccagtccttctcatactacgaatggttgccagggagaaaaagtgaggacctgtgaaaaa
tctgatgagtctgccatgagtttttatccaccatcactaaatgacgcatcttttactttg
attggattcagtaaaggttgtgttgttttgaatcagttgctttttgaattgaaagaagcc
aagaaagacaagaacatagatgcttttatcaaaagcataagaacaatgtattggctggat
ggtggtcattctggaggaagcaatacttgggttacttatccagaagtcttgaaagaattt
gcacaaacaggaattatcgttcacactcatgtaacaccttaccaagtacgtgatccaatg
agatcttggattggaaaggagcacaagaaatttgttcagatacttggggatcttggtatg
caggtgactagccaaattcattttacaaaggaagctccttccatagagaatcacttcagg
gttcatgaagtattttga

  All links  
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (12)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (9)   
   RefSeq(nuc) (1)   
   GenBank (4)   
   EMBL (4)   
Protein domain (1)   
   Pfam (1)   
All databases (29)   

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