KEGG   Homo sapiens (human): 9997
Entry
9997              CDS       T01001                                 
Symbol
SCO2, CEMCOX1, ECGF1, Gliostatin, MC4DN2, MYP6, PD-ECGF, SCO1L, TP, TYMP, TdRPase
Name
(RefSeq) protein SCO2 homolog, mitochondrial precursor
  KO
K23755  protein SCO2
Organism
hsa  Homo sapiens (human)
Pathway
hsa05230  Central carbon metabolism in cancer
Disease
H01200  Fatal infantile cardioencephalomyopathy
H01368  Cytochrome c oxidase (COX) deficiency
H02041  Myopia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09161 Cancer: overview
   05230 Central carbon metabolism in cancer
    9997 (SCO2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    9997 (SCO2)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial quality control factors
  Mitochondrial respiratory chain complex assembly factors
   Complex-IV assembly factors
    9997 (SCO2)
SSDB
Motif
Pfam: SCO1-SenC AhpC-TSA Thioredoxin_8
Other DBs
NCBI-GeneID: 9997
NCBI-ProteinID: NP_001162580
OMIM: 604272
HGNC: 10604
UniProt: O43819
Structure
Position
22:complement(50523568..50526442)
AA seq 266 aa
MLLLTRSPTAWHRLSQLKPRVLPGTLGGQALHLRSWLLSRQGPAETGGQGQPQGPGLRTR
LLITGLFGAGLGGAWLALRAEKERLQQQKRTEALRQAAVGQGDFHLLDHRGRARCKADFR
GQWVLMYFGFTHCPDICPDELEKLVQVVRQLEAEPGLPPVQPVFITVDPERDDVEAMARY
VQDFHPRLLGLTGSTKQVAQASHSYRVYYNAGPKDEDQDYIVDHSIAIYLLNPDGLFTDY
YGRSRSAEQISDSVRRHMAAFRSVLS
NT seq 801 nt   +upstreamnt  +downstreamnt
atgctgctgctgactcggagccccacagcttggcacaggctctctcagctcaagcctcgg
gtcctccctgggaccctgggaggccaggccctgcatctgaggtcctggcttttgtcaagg
cagggccctgcagagacaggtgggcagggccagccccagggccctgggcttcgaacccgg
ctgctgatcacaggcctgttcggggctggactcggtggggcctggctggccctgagggct
gagaaggagaggctgcagcagcaaaagcgaacagaagccctgcgccaggcagctgtgggc
cagggcgacttccacctgctggatcacagaggccgggctcgctgcaaggctgacttccgg
ggccagtgggtgctgatgtactttggcttcactcactgccctgacatctgcccagacgag
ctggagaagctggtgcaggtggtgcggcagctggaagcagagcctggtttgcctccagtg
cagcctgtcttcatcactgtggaccccgagcgggacgacgttgaagccatggcccgctac
gtccaggacttccacccaagactgttgggtctgaccggctccaccaaacaggttgcccag
gctagtcacagttaccgcgtgtactacaatgcaggccccaaggatgaggaccaggactac
atcgtggaccactccattgccatctacctgctcaaccctgacggcctcttcacggattac
tacggccggagcagatcggctgagcagatctcagacagtgtgcggcggcacatggcggct
ttccgcagtgtcctgtcttga

  All links  
Disease (4)   
   OMIM (4)   
Gene (13)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   RIKEN BRC-DNA (7)   
   OC (1)   
Protein sequence (6)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (20)   
   RefSeq(nuc) (4)   
   GenBank (8)   
   EMBL (8)   
3D Structure (1)   
   PDB (1)   
Protein domain (3)   
   Pfam (3)   
All databases (47)   

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